Variant report

Variant rs13382254
Chromosome Location chr2:20322712-20322713
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20320400-20326400 Enhancers Placenta Placenta
2 chr2:20322000-20323000 Enhancers Placenta Amnion Placenta Amnion
3 chr2:20322000-20323400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:20322000-20323400 Enhancers Esophagus oesophagus
5 chr2:20322000-20327600 Weak transcription Fetal Intestine Small intestine
6 chr2:20322200-20323000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:20322200-20323200 Enhancers NHEK skin
8 chr2:20322200-20325000 Weak transcription Stomach Mucosa stomach
9 chr2:20322400-20322800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:20322600-20323000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:20322600-20323000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr2:20322600-20323000 Enhancers Pancreas Pancrea
13 chr2:20322600-20324800 Weak transcription Duodenum Mucosa Duodenum
14 chr2:20322600-20327600 Weak transcription Liver Liver

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