Variant report

Variant rs7018958
Chromosome Location chr9:86021211-86021212
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:86013400-86041000 Weak transcription Aorta Aorta
2 chr9:86016600-86023600 Weak transcription HepG2 liver
3 chr9:86017400-86034400 Weak transcription Psoas Muscle Psoas
4 chr9:86018800-86021600 Enhancers Fetal Brain Male brain
5 chr9:86019000-86022600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr9:86019400-86037600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:86020000-86021400 Enhancers Fetal Muscle Leg muscle
8 chr9:86020400-86021800 Weak transcription Left Ventricle heart
9 chr9:86020600-86021400 Enhancers Pancreas Pancrea
10 chr9:86020600-86021600 Enhancers Fetal Brain Female brain
11 chr9:86020600-86021800 Enhancers Monocytes-CD14+_RO01746 blood
12 chr9:86020800-86022800 Enhancers Primary monocytes fromperipheralblood blood
13 chr9:86020800-86024200 Enhancers Primary neutrophils fromperipheralblood blood
14 chr9:86021000-86021600 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr9:86021000-86022000 Enhancers Right Atrium heart
16 chr9:86021200-86021800 Enhancers Skeletal Muscle Male skeletal muscle
17 chr9:86021200-86041600 Weak transcription Right Ventricle heart

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