The 2.0 version of rSNPBase

Variant report

Variant rs7537692
Chromosome Location chr1:85488678-85488679
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85483600-85494800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:85483800-85488800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:85485400-85491400 Strong transcription Fetal Intestine Large intestine
4 chr1:85485400-85513000 Weak transcription Pancreas Pancrea
5 chr1:85485800-85505200 Weak transcription Duodenum Mucosa Duodenum
6 chr1:85486000-85513000 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:85486400-85499200 Weak transcription NHDF-Ad bronchial
8 chr1:85486400-85500400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:85487800-85490800 Strong transcription Fetal Intestine Small intestine
10 chr1:85488000-85493000 Weak transcription HMEC breast
11 chr1:85488400-85488800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
12 chr1:85488400-85489000 Enhancers Primary T cells fromperipheralblood blood
13 chr1:85488400-85489000 Enhancers Primary Natural Killer cells fromperipheralblood blood

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Last update: Aug 31, 2015