Human hg19 chr3:178984659-178984878 UCSC Genome Browser v478

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UCSC Genome Browser on Human (GRCh37/hg19)
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chr3:178,984,659-178,984,878 220 bp.

Custom Tracks

100_hg19_chr19_nmt=3

10_hg19_chr17_nmt=4

118_hg19_chr22_nmt=4

11_hg19_chr10_nmt=3

128_hg19_chr14_nmt=11

12_hg19_chr3_nmt=22

13_hg19_chr3_nmt=23

148_hg19_chr2_nmt=3

14_hg19_chr2_nmt=6

15_hg19_chr19_nmt=3

167_hg19_chr14_nmt=11

16_hg19_chr5_nmt=21

17_hg19_chr3_nmt=26

18_hg19_chr17_nmt=21

19_hg19_chr10_nmt=9

1_hg19_chr15_nmt=4

20_hg19_chr1_nmt=4

21_hg19_chr20_nmt=3

22_hg19_chr19_nmt=32

23_hg19_chr14_nmt=3

24_hg19_chr9_nmt=4

25_hg19_chr5_nmt=29

26_hg19_chr17_nmt=14

27_hg19_chr2_nmt=3

28_hg19_chr12_nmt=7

29_hg19_chrX_nmt=23

2_hg19_chr8_nmt=3

30_hg19_chr11_nmt=4

31_hg19_chr22_nmt=20

32_hg19_chr8_nmt=3

33_hg19_chr6_nmt=8

34_hg19_chr17_nmt=3

35_hg19_chrY_nmt=8

36_hg19_chr17_nmt=5

37_hg19_chr1_nmt=21

38_hg19_chr17_nmt=8

39_hg19_chr1_nmt=3

3_hg19_chr14_nmt=9

40_hg19_chr22_nmt=12

41_hg19_chr1_nmt=3

42_hg19_chr2_nmt=3

43_hg19_chr17_nmt=5

44_hg19_chr12_nmt=6

45_hg19_chr3_nmt=10

46_hg19_chrX_nmt=20

47_hg19_chr14_nmt=17

48_hg19_chr2_nmt=3

49_hg19_chr3_nmt=12

4_hg19_chr3_nmt=3

50_hg19_chr2_nmt=4

5_hg19_chr16_nmt=4

69_hg19_chr1_nmt=29

6_hg19_chr11_nmt=4

7_hg19_chr11_nmt=8

8_hg19_chr2_nmt=5

94_hg19_chr12_nmt=28

9_hg19_chr20_nmt=6

ALL_mutations_hg19

Mapping and Sequencing

p14 Fix Patches

p14 Alt Haplotypes

Chromosome Band

ENCODE Pilot
[No data-chr3]

Exome Probesets

Fosmid End Pairs

GRC Map Contigs

liftOver & ReMap

Problematic Regions

Genes and Gene Predictions

updated GENCODE V47lift37

updated NCBI RefSeq

updated GENCODE Versions

IKMC Genes Mapped

LRG Transcripts

MGC/ORFeome Genes

Pfam in UCSC Gene

Prediction Archive

Retroposed Genes

UCSC Alt Events

Phenotypes, Variants, and Literature

ClinVar Variants

Constraint scores

Deleteriousness Predictions

Development Delay

Dosage Sensitivity

Gene Interactions

Haploinsufficiency

new MITOMAP
[No data-chr3]

Polygenic Risk Scores

new Splicing Impact

UniProt Variants

updated Variants in Papers

Variation

Array Probesets

dbVar Common Struct Var

Genome In a Bottle

Genome Variants

HGDP Allele Freq

Platinum Genomes

mRNA and EST

H-Inv

Human RNA Editing

SIB Alt-Splicing

Expression

CSHL Small RNA-seq

EPDnew Promoters

GTEx Transcript

GWIPS-viz Riboseq

Regulation

ENCODE Regulation

ENC DNase/FAIRE

ENC RNA Binding

Genome Segments

GTEx Combined eQTL

GTEx Tissue eQTL

JASPAR Transcription Factors

Stanf Nucleosome

SUNY SwitchGear

TS miRNA Targets

UCSF Brain Methyl

UMMS Brain Hist

VISTA Enhancers

Comparative Genomics

Cons Indels MmCf

Primate Chain/Net

Placental Chain/Net

Vertebrate Chain/Net

CHM13 alignments

Neandertal Assembly and Analysis

Cand. Gene Flow
[No data-chr3]

H-C Coding Diffs

Neandertal Methyl

Neandertal Mito
[No data-chr3]

Sel Swp Scan (S)

Denisova Assembly and Analysis

Denisova Methyl

Denisova Variants

Mod Hum Variants

Repeats

Interrupted Rpts