Variant report

Variant rs16871785
Chromosome Location chr8:105765178-105765179
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:105760000-105766400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr8:105760600-105766600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr8:105764200-105765400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr8:105764400-105765200 Enhancers Muscle Satellite Cultured Cells --
5 chr8:105764400-105765200 Enhancers HMEC breast
6 chr8:105764400-105765400 Enhancers Osteobl bone
7 chr8:105764600-105765200 Enhancers NHDF-Ad bronchial
8 chr8:105764600-105765400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr8:105764600-105765400 Enhancers NH-A brain
10 chr8:105764600-105765600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr8:105764800-105765400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr8:105764800-105765400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr8:105765000-105765200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr8:105765000-105766400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr8:105765000-105766400 Weak transcription NHEK skin

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