The 2.0 version of rSNPBase

Variant report

Variant rs7521107
Chromosome Location chr1:94461318-94461319
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94446200-94463400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:94452400-94463800 Enhancers HMEC breast
3 chr1:94452800-94462400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:94452800-94464000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr1:94457000-94461400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
6 chr1:94458200-94462000 Enhancers NHEK skin
7 chr1:94458600-94461800 Enhancers HSMM muscle
8 chr1:94458800-94477000 Weak transcription Right Atrium heart
9 chr1:94459000-94461800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:94459600-94461400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr1:94459600-94463400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr1:94460000-94461400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:94460400-94462000 Enhancers NH-A brain
14 chr1:94461000-94461600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:94461200-94461400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
16 chr1:94461200-94461600 Flanking Active TSS HSMMtube muscle

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Last update: Aug 31, 2015