Variant report

Variant rs73218129
Chromosome Location chr2:20567189-20567190
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20551600-20568800 Weak transcription Psoas Muscle Psoas
2 chr2:20556800-20569200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr2:20564400-20567200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:20564400-20567200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:20564400-20567200 Enhancers HMEC breast
6 chr2:20564800-20567200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:20564800-20567200 Enhancers NHEK skin
8 chr2:20565000-20567200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr2:20565000-20570200 Enhancers Placenta Placenta
10 chr2:20565200-20578400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr2:20565800-20569400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr2:20565800-20570000 Weak transcription NHLF lung
13 chr2:20565800-20575200 Weak transcription NH-A brain
14 chr2:20566000-20567200 ZNF genes & repeats GM12878-XiMat blood
15 chr2:20566400-20567200 Enhancers Esophagus oesophagus
16 chr2:20566600-20567200 Enhancers Placenta Amnion Placenta Amnion
17 chr2:20566600-20567600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
18 chr2:20567000-20571200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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