Variant report

Variant rs542638162
Chromosome Location chr20:14859511-14859512
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14857400-14859600 Weak transcription HUES64 Cell Line embryonic stem cell
2 chr20:14857400-14861000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr20:14858000-14859600 Enhancers Cortex derived primary cultured neurospheres brain
4 chr20:14858400-14859600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr20:14858400-14861400 Enhancers HMEC breast
6 chr20:14858600-14859600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr20:14858600-14860000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr20:14858600-14861200 Enhancers NHEK skin
9 chr20:14858600-14861600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr20:14858800-14859600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr20:14858800-14859800 Weak transcription NH-A brain
12 chr20:14859000-14860600 Weak transcription NHDF-Ad bronchial
13 chr20:14859200-14860000 Enhancers Pancreatic Islets Pancreatic Islet
14 chr20:14859400-14859600 Enhancers Fetal Intestine Small intestine
15 chr20:14859400-14860400 Enhancers Liver Liver
16 chr20:14859400-14861000 Flanking Active TSS A549 lung
17 chr20:14859400-14861200 Enhancers Hela-S3 cervix
18 chr20:14859400-14861800 Enhancers HepG2 liver
19 chr20:14859400-14862600 Enhancers Duodenum Mucosa Duodenum

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