Variant report

Variant rs2523642
Chromosome Location chr6:31351181-31351182
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31345000-31361600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:31345600-31353200 Weak transcription Right Atrium heart
3 chr6:31345800-31367400 Weak transcription Gastric stomach
4 chr6:31348000-31354200 Weak transcription Lung lung
5 chr6:31348400-31354000 Weak transcription Adipose Nuclei Adipose
6 chr6:31348800-31364400 Weak transcription Primary T cells from cord blood blood
7 chr6:31350200-31354200 Strong transcription Breast Myoepithelial Primary Cells Breast
8 chr6:31350200-31367400 Weak transcription Aorta Aorta
9 chr6:31350600-31361600 Weak transcription Ovary ovary
10 chr6:31350800-31351400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:31351000-31351200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr6:31351000-31351200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
13 chr6:31351000-31351200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr6:31351000-31366000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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