Variant report

Variant rs11823900
Chromosome Location chr11:15887004-15887005
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:15883400-15887800 Weak transcription Right Atrium heart
2 chr11:15884600-15887600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr11:15885000-15887800 Enhancers Hela-S3 cervix
4 chr11:15885600-15887400 Enhancers Placenta Placenta
5 chr11:15885600-15888000 Enhancers Esophagus oesophagus
6 chr11:15886000-15888000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:15886000-15888400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr11:15886400-15887400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:15886400-15887400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr11:15886600-15887200 Weak transcription H9 Cell Line embryonic stem cell
11 chr11:15886600-15887600 Weak transcription Fetal Intestine Small intestine
12 chr11:15886600-15888000 Enhancers HMEC breast
13 chr11:15886800-15887400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
14 chr11:15886800-15892600 Weak transcription iPS-20b Cell Line embryonic stem cell
15 chr11:15887000-15887200 Enhancers NHEK skin

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