Variant report

Variant rs7865094
Chromosome Location chr9:110530761-110530762
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110518200-110544600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr9:110523200-110535200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:110529000-110531000 Enhancers Adipose Nuclei Adipose
4 chr9:110530400-110530800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
5 chr9:110530400-110530800 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr9:110530400-110530800 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr9:110530400-110530800 Enhancers Placenta Placenta
8 chr9:110530400-110531000 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr9:110530400-110531000 Enhancers ES-WA7 Cell Line embryonic stem cell
10 chr9:110530400-110531000 Enhancers Lung lung
11 chr9:110530400-110531000 Enhancers HUVEC blood vessel
12 chr9:110530600-110530800 Weak transcription Left Ventricle heart
13 chr9:110530600-110531000 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr9:110530600-110531000 Enhancers Fetal Muscle Leg muscle
15 chr9:110530600-110531200 Enhancers H1 Cell Line embryonic stem cell

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