Variant report

Variant rs72674255
Chromosome Location chr14:38066052-38066053
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:38064400-38066400 Bivalent/Poised TSS Colonic Mucosa Colon
2 chr14:38064800-38066200 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
3 chr14:38064800-38066800 Bivalent Enhancer Primary T helper 17 cells PMA-I stimulated --
4 chr14:38065000-38066800 Bivalent/Poised TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr14:38065000-38069600 Bivalent/Poised TSS Primary T cells from cord blood blood
6 chr14:38065200-38066800 Bivalent/Poised TSS Fetal Stomach stomach
7 chr14:38065600-38066600 Flanking Active TSS A549 lung
8 chr14:38065600-38067000 Weak transcription Lung lung
9 chr14:38065600-38067000 Weak transcription Pancreas Pancrea
10 chr14:38065800-38066400 Bivalent/Poised TSS Fetal Intestine Small intestine
11 chr14:38065800-38066600 Enhancers Primary T killer memory cells from peripheral blood blood
12 chr14:38065800-38066600 Flanking Active TSS HepG2 liver
13 chr14:38065800-38066800 Bivalent Enhancer Rectal Mucosa Donor 31 rectum
14 chr14:38065800-38067000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr14:38065800-38067000 Weak transcription Esophagus oesophagus
16 chr14:38065800-38067200 Weak transcription Gastric stomach
17 chr14:38065800-38067600 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
18 chr14:38065800-38068800 Bivalent Enhancer HMEC breast
19 chr14:38066000-38066200 Active TSS Rectal Mucosa Donor 29 rectum
20 chr14:38066000-38066600 Flanking Bivalent TSS/Enh Fetal Intestine Large intestine
21 chr14:38066000-38068600 Enhancers Liver Liver

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