Variant report

Variant rs6943331
Chromosome Location chr7:17665703-17665704
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17662800-17666000 Enhancers Hela-S3 cervix
2 chr7:17663000-17666600 Enhancers NHDF-Ad bronchial
3 chr7:17663200-17665800 Enhancers Osteobl bone
4 chr7:17663200-17666200 Enhancers NHLF lung
5 chr7:17663200-17666400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr7:17663800-17666000 Enhancers HMEC breast
7 chr7:17664600-17665800 Enhancers Fetal Kidney kidney
8 chr7:17664600-17665800 Flanking Active TSS NH-A brain
9 chr7:17664600-17666000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr7:17665000-17665800 Flanking Active TSS Muscle Satellite Cultured Cells --
11 chr7:17665200-17666000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr7:17665200-17666200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:17665400-17665800 Enhancers Primary hematopoietic stem cells blood
14 chr7:17665400-17665800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr7:17665400-17665800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr7:17665400-17666000 Enhancers Primary hematopoietic stem cells short term culture blood
17 chr7:17665600-17665800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr7:17665600-17669000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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