Variant report

Variant rs71484150
Chromosome Location chr11:119727707-119727708
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:119722200-119729600 Weak transcription H9 Cell Line embryonic stem cell
2 chr11:119724800-119727800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr11:119724800-119729600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr11:119725600-119727800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr11:119725600-119728800 Weak transcription Esophagus oesophagus
6 chr11:119725800-119727800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:119725800-119728200 Weak transcription Brain Hippocampus Middle brain
8 chr11:119725800-119728600 Weak transcription Fetal Intestine Large intestine
9 chr11:119725800-119728800 Weak transcription Fetal Intestine Small intestine
10 chr11:119725800-119733200 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr11:119726000-119729600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr11:119726400-119747000 Weak transcription Right Atrium heart
13 chr11:119727400-119727800 Weak transcription Right Ventricle heart
14 chr11:119727600-119727800 Enhancers Left Ventricle heart

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