The 2.0 version of rSNPBase

Variant report

Variant rs6576742
Chromosome Location chr1:85485383-85485384
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85480800-85485400 Weak transcription Fetal Intestine Large intestine
2 chr1:85481800-85487200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:85482600-85487600 Weak transcription HMEC breast
4 chr1:85483600-85494800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:85483800-85488800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:85485000-85485400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:85485000-85486000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr1:85485000-85486000 Strong transcription Breast Myoepithelial Primary Cells Breast
9 chr1:85485000-85486400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr1:85485000-85486400 Strong transcription Fetal Intestine Small intestine
11 chr1:85485200-85486400 Strong transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr1:85485200-85486400 Enhancers NHDF-Ad bronchial

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Last update: Aug 31, 2015