Variant report

Variant rs56786415
Chromosome Location chr2:187170978-187170979
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187168000-187172400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:187168000-187173000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:187168400-187172400 Weak transcription NHEK skin
4 chr2:187169000-187171200 Weak transcription Fetal Intestine Large intestine
5 chr2:187169600-187172400 Weak transcription HepG2 liver
6 chr2:187170400-187171200 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr2:187170600-187173800 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr2:187170800-187171000 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr2:187170800-187173600 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr2:187170800-187174000 Enhancers HUES48 Cell Line embryonic stem cell

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