Variant report

Variant rs7039636
Chromosome Location chr9:117905891-117905892
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117890200-117909000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:117900000-117908400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:117904000-117907400 Enhancers Cortex derived primary cultured neurospheres brain
4 chr9:117904200-117907000 Enhancers Brain Hippocampus Middle brain
5 chr9:117904200-117909200 Weak transcription Aorta Aorta
6 chr9:117904400-117906000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr9:117904800-117907600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr9:117904800-117910000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:117904800-117910200 Enhancers NHDF-Ad bronchial
10 chr9:117905000-117906000 Enhancers HSMM muscle
11 chr9:117905000-117907800 Enhancers Dnd41 blood
12 chr9:117905000-117910000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr9:117905000-117910200 Enhancers Osteobl bone
14 chr9:117905400-117907000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr9:117905400-117908000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr9:117905400-117908200 Weak transcription NHLF lung
17 chr9:117905600-117906800 Weak transcription Rectal Smooth Muscle rectum
18 chr9:117905600-117908400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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