Variant report

Variant rs10765652
Chromosome Location chr11:93833056-93833057
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:93802400-93833400 Weak transcription HMEC breast
2 chr11:93816800-93833400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr11:93819600-93833400 Weak transcription NHEK skin
4 chr11:93820400-93833200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:93827000-93833400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:93832400-93833800 ZNF genes & repeats Fetal Intestine Small intestine
7 chr11:93832600-93833200 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
8 chr11:93832600-93833800 ZNF genes & repeats H1 Cell Line embryonic stem cell
9 chr11:93833000-93833800 ZNF genes & repeats Fetal Intestine Large intestine

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