Variant report

Variant rs8025686
Chromosome Location chr15:56291175-56291176
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:56286600-56292000 Weak transcription Esophagus oesophagus
2 chr15:56287000-56291600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr15:56287000-56291800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr15:56287400-56291600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr15:56287600-56291800 Weak transcription Placenta Amnion Placenta Amnion
6 chr15:56288000-56291600 Weak transcription A549 lung
7 chr15:56288400-56291800 Enhancers Hela-S3 cervix
8 chr15:56288800-56292800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr15:56289000-56295000 Enhancers HMEC breast
10 chr15:56289200-56295000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr15:56289400-56291800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr15:56289400-56291800 Enhancers NHEK skin
13 chr15:56290200-56292000 Enhancers Fetal Intestine Large intestine
14 chr15:56290400-56295000 Enhancers Placenta Placenta
15 chr15:56290600-56291200 Enhancers Breast Myoepithelial Primary Cells Breast

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