Variant report

Variant rs11771896
Chromosome Location chr7:41017777-41017778
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:40986200-41020600 Weak transcription Aorta Aorta
2 chr7:41011800-41042000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:41012200-41020200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr7:41016400-41018600 Enhancers Hela-S3 cervix
5 chr7:41017200-41018000 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr7:41017400-41018600 Enhancers Cortex derived primary cultured neurospheres brain
7 chr7:41017400-41018600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:41017400-41019200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr7:41017400-41024400 Weak transcription Pancreatic Islets Pancreatic Islet

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