Variant report

Variant rs7807962
Chromosome Location chr7:17604524-17604525
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17599000-17617800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr7:17601000-17616800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:17603800-17604800 Enhancers Primary monocytes fromperipheralblood blood
4 chr7:17603800-17605000 Enhancers Primary hematopoietic stem cells blood
5 chr7:17603800-17605000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr7:17603800-17605000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr7:17603800-17605200 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr7:17603800-17605200 Enhancers Muscle Satellite Cultured Cells --
9 chr7:17604200-17604800 Enhancers HSMM muscle
10 chr7:17604200-17604800 Enhancers NHLF lung
11 chr7:17604200-17605000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr7:17604200-17605000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr7:17604200-17605000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr7:17604200-17605000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr7:17604400-17604800 Enhancers Hela-S3 cervix
16 chr7:17604400-17605000 Enhancers NH-A brain

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