Variant report

Variant rs10810523
Chromosome Location chr9:16034642-16034643
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16023600-16040600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr9:16026200-16039200 Weak transcription Adipose Nuclei Adipose
3 chr9:16026400-16039200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:16030800-16050000 Weak transcription Aorta Aorta
5 chr9:16031600-16035600 Enhancers Fetal Muscle Leg muscle
6 chr9:16032200-16035000 Weak transcription Dnd41 blood
7 chr9:16032200-16039200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr9:16032800-16037400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:16033000-16035200 Weak transcription HMEC breast
10 chr9:16033200-16039200 Weak transcription Stomach Smooth Muscle stomach
11 chr9:16033400-16039200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr9:16033400-16039200 Weak transcription Osteobl bone
13 chr9:16033800-16034800 Enhancers Placenta Placenta
14 chr9:16034000-16043600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
15 chr9:16034400-16034800 Enhancers Fetal Kidney kidney

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