Variant report

Variant rs73307694
Chromosome Location chr7:17604118-17604119
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17597600-17604200 Weak transcription NHLF lung
2 chr7:17599000-17604200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr7:17599000-17617800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr7:17599200-17604200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr7:17599400-17604200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr7:17599400-17604400 Weak transcription Hela-S3 cervix
7 chr7:17601000-17616800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr7:17602200-17604200 Weak transcription HMEC breast
9 chr7:17602400-17604200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr7:17603800-17604800 Enhancers Primary monocytes fromperipheralblood blood
11 chr7:17603800-17605000 Enhancers Primary hematopoietic stem cells blood
12 chr7:17603800-17605000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr7:17603800-17605000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr7:17603800-17605200 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr7:17603800-17605200 Enhancers Muscle Satellite Cultured Cells --

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