Variant report

Variant rs11733805
Chromosome Location chr4:110795858-110795859
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:110786200-110796600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr4:110789800-110798400 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr4:110791800-110797200 Weak transcription Primary T cells from cord blood blood
4 chr4:110791800-110799600 Weak transcription Brain Angular Gyrus brain
5 chr4:110793800-110797600 Enhancers Pancreas Pancrea
6 chr4:110794400-110796600 Enhancers K562 blood
7 chr4:110794800-110796600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr4:110794800-110796600 Enhancers NHEK skin
9 chr4:110794800-110796800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:110795000-110796600 Enhancers Esophagus oesophagus
11 chr4:110795000-110796600 Enhancers Skeletal Muscle Female skeletal muscle
12 chr4:110795400-110796600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr4:110795600-110796000 Enhancers Skeletal Muscle Male skeletal muscle
14 chr4:110795600-110796600 Enhancers Placenta Amnion Placenta Amnion

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