The 2.0 version of rSNPBase

Variant report

Variant rs12076307
Chromosome Location chr1:94214656-94214657
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94199400-94217400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:94208200-94215600 Weak transcription Aorta Aorta
3 chr1:94210800-94215600 Weak transcription Thymus Thymus
4 chr1:94211800-94215600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr1:94212600-94215200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:94212600-94217200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:94213000-94216200 Weak transcription Esophagus oesophagus
8 chr1:94213200-94216800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:94213400-94215600 Weak transcription HMEC breast
10 chr1:94213400-94217800 Enhancers Primary B cells from peripheral blood blood
11 chr1:94213600-94215400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:94213600-94215600 Weak transcription HepG2 liver
13 chr1:94214000-94215800 Weak transcription Lung lung
14 chr1:94214400-94215400 Enhancers Primary B cells from cord blood blood
15 chr1:94214400-94215800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr1:94214400-94218000 Enhancers Fetal Thymus thymus
17 chr1:94214600-94215200 Enhancers GM12878-XiMat blood

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Last update: Aug 31, 2015