Variant report

Variant rs4908940
Chromosome Location chr3:17797271-17797272
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17791200-17800800 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr3:17795400-17800800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr3:17796800-17798200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr3:17796800-17798200 Enhancers NHEK skin
5 chr3:17796800-17798400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr3:17796800-17798600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr3:17796800-17798600 Enhancers HMEC breast
8 chr3:17797000-17797600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr3:17797000-17798000 Enhancers GM12878-XiMat blood
10 chr3:17797000-17798400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:17797200-17797400 Enhancers Sigmoid Colon Sigmoid Colon
12 chr3:17797200-17797600 Enhancers Primary T cells from cord blood blood
13 chr3:17797200-17797800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
14 chr3:17797200-17797800 Enhancers Primary T regulatory cells fromperipheralblood blood
15 chr3:17797200-17797800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr3:17797200-17798000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
17 chr3:17797200-17798000 Enhancers Dnd41 blood

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