Variant report

Variant rs1414245
Chromosome Location chr9:21750069-21750070
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21744200-21752200 Enhancers HMEC breast
2 chr9:21746600-21751200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:21747200-21752000 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr9:21747800-21751800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr9:21748400-21754400 Weak transcription Hela-S3 cervix
6 chr9:21748600-21754400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr9:21748800-21754400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr9:21749600-21751400 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr9:21749800-21750400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr9:21749800-21750600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr9:21750000-21750400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
12 chr9:21750000-21750400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr9:21750000-21750400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr9:21750000-21750400 Enhancers Osteobl bone
15 chr9:21750000-21751200 Enhancers NHEK skin

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