Variant report

Variant rs17200944
Chromosome Location chr3:17852126-17852127
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17850200-17852400 Enhancers Fetal Heart heart
2 chr3:17850200-17853200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr3:17850400-17852200 Enhancers K562 blood
4 chr3:17850400-17853000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr3:17850400-17853000 Enhancers NH-A brain
6 chr3:17850400-17853200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr3:17850400-17853200 Enhancers NHDF-Ad bronchial
8 chr3:17850400-17853200 Enhancers Osteobl bone
9 chr3:17850400-17853600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr3:17850600-17852200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr3:17850800-17852200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr3:17851000-17853000 Enhancers Muscle Satellite Cultured Cells --
13 chr3:17851400-17852200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr3:17851400-17852600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr3:17851400-17861000 Weak transcription Right Atrium heart
16 chr3:17851800-17853200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr3:17852000-17852400 Enhancers HSMM muscle
18 chr3:17852000-17852600 Enhancers HUVEC blood vessel

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