The 2.0 version of rSNPBase

Variant report

Variant rs6715637
Chromosome Location chr2:21112318-21112319
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:21111800-21112800 Enhancers Esophagus oesophagus
2 chr2:21112000-21113400 Enhancers NHEK skin
3 chr2:21112000-21114800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:21112200-21112400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
5 chr2:21112200-21113000 Enhancers Fetal Thymus thymus
6 chr2:21112200-21113200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:21112200-21113200 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr2:21112200-21113200 Enhancers HMEC breast
9 chr2:21112200-21113400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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Last update: Aug 31, 2015