Variant report

Variant rs56688888
Chromosome Location chr7:17665154-17665155
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17662800-17665200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr7:17662800-17666000 Enhancers Hela-S3 cervix
3 chr7:17663000-17666600 Enhancers NHDF-Ad bronchial
4 chr7:17663200-17665200 Enhancers HSMM muscle
5 chr7:17663200-17665600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr7:17663200-17665800 Enhancers Osteobl bone
7 chr7:17663200-17666200 Enhancers NHLF lung
8 chr7:17663200-17666400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr7:17663800-17666000 Enhancers HMEC breast
10 chr7:17664000-17665600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr7:17664200-17665200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr7:17664200-17665200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:17664400-17665600 Enhancers NHEK skin
14 chr7:17664600-17665800 Enhancers Fetal Kidney kidney
15 chr7:17664600-17665800 Flanking Active TSS NH-A brain
16 chr7:17664600-17666000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr7:17665000-17665800 Flanking Active TSS Muscle Satellite Cultured Cells --

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