Variant report

Variant rs6987448
Chromosome Location chr8:49323385-49323386
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49319800-49332400 Weak transcription Fetal Kidney kidney
2 chr8:49321000-49323400 Enhancers HMEC breast
3 chr8:49321800-49323400 Enhancers HSMMtube muscle
4 chr8:49322000-49323600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr8:49322400-49323400 Enhancers Muscle Satellite Cultured Cells --
6 chr8:49322400-49323600 Enhancers HUVEC blood vessel
7 chr8:49322600-49323400 Enhancers HSMM muscle
8 chr8:49322600-49323600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr8:49322600-49323600 Enhancers Osteobl bone
10 chr8:49322800-49329800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr8:49323000-49325000 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr8:49323000-49325800 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr8:49323200-49325200 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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