Variant report

Variant rs4721631
Chromosome Location chr7:17601239-17601240
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17596600-17601400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr7:17597600-17604200 Weak transcription NHLF lung
3 chr7:17598800-17601600 Enhancers NHEK skin
4 chr7:17598800-17602200 Enhancers HMEC breast
5 chr7:17599000-17601400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:17599000-17604200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:17599000-17617800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr7:17599200-17604200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr7:17599400-17604200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr7:17599400-17604400 Weak transcription Hela-S3 cervix
11 chr7:17600200-17603800 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr7:17600200-17603800 Weak transcription Muscle Satellite Cultured Cells --
13 chr7:17601000-17616800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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