Variant report

Variant rs7586583
Chromosome Location chr2:31217341-31217342
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31156000-31221400 Weak transcription Pancreas Pancrea
2 chr2:31203600-31221400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:31203600-31227200 Weak transcription HMEC breast
4 chr2:31207800-31218400 Weak transcription Esophagus oesophagus
5 chr2:31211200-31233800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr2:31211400-31221600 Weak transcription NHEK skin
7 chr2:31211600-31221600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:31213800-31217400 Weak transcription Fetal Lung lung
9 chr2:31213800-31217600 Weak transcription Primary neutrophils fromperipheralblood blood
10 chr2:31216000-31221000 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr2:31216600-31217800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr2:31217200-31217600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland

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