Variant report

Variant rs10962157
Chromosome Location chr9:15786817-15786818
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15756200-15790800 Weak transcription Primary hematopoietic stem cells blood
2 chr9:15777000-15810600 Weak transcription Pancreas Pancrea
3 chr9:15779000-15791200 Weak transcription Stomach Smooth Muscle stomach
4 chr9:15781200-15790800 Weak transcription Fetal Thymus thymus
5 chr9:15783200-15788600 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr9:15783600-15802000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr9:15784600-15790200 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr9:15785000-15808600 Weak transcription Aorta Aorta
9 chr9:15785600-15788000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr9:15785600-15788000 Weak transcription Duodenum Mucosa Duodenum
11 chr9:15786200-15789200 Weak transcription Psoas Muscle Psoas
12 chr9:15786600-15787000 ZNF genes & repeats Left Ventricle heart
13 chr9:15786600-15787200 Strong transcription Breast Myoepithelial Primary Cells Breast
14 chr9:15786600-15789600 Weak transcription Ovary ovary
15 chr9:15786800-15787000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr9:15786800-15787000 Genic enhancers Esophagus oesophagus
17 chr9:15786800-15787000 ZNF genes & repeats Gastric stomach
18 chr9:15786800-15787200 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --

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