Variant report

Variant rs7709576
Chromosome Location chr5:150959716-150959717
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:150951200-150960400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:150951600-150960400 Genic enhancers NHEK skin
3 chr5:150956800-150960200 Genic enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr5:150957200-150960400 Genic enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr5:150958000-150960800 Weak transcription Fetal Thymus thymus
6 chr5:150959400-150965600 Weak transcription Pancreas Pancrea
7 chr5:150959600-150960000 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr5:150959600-150960000 Genic enhancers Esophagus oesophagus
9 chr5:150959600-150960800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr5:150959600-150961200 Genic enhancers HMEC breast
11 chr5:150959600-150962000 Enhancers Placenta Placenta
12 chr5:150959600-150967400 Enhancers Breast Myoepithelial Primary Cells Breast

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