Variant report

Variant rs185249826
Chromosome Location chr7:110175030-110175031
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:110172600-110175400 Flanking Active TSS Dnd41 blood
2 chr7:110173600-110175200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:110173800-110175200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr7:110174000-110175200 Enhancers HepG2 liver
5 chr7:110174000-110175400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr7:110174000-110176000 Enhancers Fetal Heart heart
7 chr7:110174200-110175200 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr7:110174400-110175200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr7:110174400-110175200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr7:110174400-110175400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr7:110174600-110175400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr7:110174600-110176000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr7:110174800-110175200 Flanking Active TSS A549 lung
14 chr7:110174800-110176200 Enhancers HMEC breast
15 chr7:110174800-110176200 Enhancers NHEK skin

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