Variant report

Variant rs10260765
Chromosome Location chr7:110173993-110173994
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:110170600-110174000 Weak transcription HepG2 liver
2 chr7:110171800-110174000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr7:110172600-110174000 Enhancers HMEC breast
4 chr7:110172600-110175400 Flanking Active TSS Dnd41 blood
5 chr7:110173400-110174000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:110173600-110174000 Enhancers NHEK skin
7 chr7:110173600-110175200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:110173800-110174200 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr7:110173800-110175200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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