Variant report

Variant rs6079592
Chromosome Location chr20:14861031-14861032
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14858400-14861400 Enhancers HMEC breast
2 chr20:14858600-14861200 Enhancers NHEK skin
3 chr20:14858600-14861600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr20:14859400-14861200 Enhancers Hela-S3 cervix
5 chr20:14859400-14861800 Enhancers HepG2 liver
6 chr20:14859400-14862600 Enhancers Duodenum Mucosa Duodenum
7 chr20:14860000-14861400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr20:14860200-14862400 Enhancers Fetal Intestine Large intestine
9 chr20:14860200-14865600 Weak transcription Stomach Mucosa stomach
10 chr20:14860600-14861200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr20:14860600-14861200 Enhancers Placenta Amnion Placenta Amnion
12 chr20:14860600-14861600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr20:14860600-14863800 Weak transcription Pancreatic Islets Pancreatic Islet
14 chr20:14860800-14861200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr20:14860800-14861600 Weak transcription Fetal Intestine Small intestine
16 chr20:14860800-14864000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr20:14861000-14861200 Enhancers Brain Hippocampus Middle brain
18 chr20:14861000-14862400 ZNF genes & repeats A549 lung
19 chr20:14861000-14866200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
20 chr20:14861000-14866200 Weak transcription HUVEC blood vessel

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