The 2.0 version of rSNPBase

Variant report

Variant rs187956
Chromosome Location chr1:77508652-77508653
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77497000-77516800 Weak transcription Fetal Stomach stomach
2 chr1:77503800-77512200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr1:77505800-77508800 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr1:77506000-77509800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:77506000-77558600 Weak transcription Stomach Smooth Muscle stomach
6 chr1:77506200-77510200 Weak transcription Rectal Smooth Muscle rectum
7 chr1:77506400-77509800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:77506400-77510000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:77506600-77509800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:77506600-77509800 Weak transcription Aorta Aorta
11 chr1:77506600-77510000 Weak transcription NHEK skin
12 chr1:77506800-77509600 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr1:77506800-77509800 Weak transcription HMEC breast
14 chr1:77508600-77547600 Weak transcription Ovary ovary

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Last update: Aug 31, 2015