Variant report

Variant rs8056766
Chromosome Location chr16:70664806-70664807
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:70647400-70669200 Weak transcription Right Atrium heart
2 chr16:70659200-70668800 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr16:70661200-70669000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr16:70661800-70665000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr16:70663000-70666400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr16:70663000-70669000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr16:70663400-70668800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr16:70664800-70665200 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
9 chr16:70664800-70665200 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
10 chr16:70664800-70665400 ZNF genes & repeats Fetal Intestine Small intestine

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