Variant report

Variant rs58555528
Chromosome Location chr1:63226707-63226708
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:63219600-63226800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:63222600-63226800 Weak transcription H9 Cell Line embryonic stem cell
3 chr1:63225400-63226800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr1:63225800-63227400 Enhancers Esophagus oesophagus
5 chr1:63225800-63231400 Weak transcription Right Atrium heart
6 chr1:63226200-63226800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:63226400-63228800 Enhancers Placenta Placenta
8 chr1:63226600-63227800 ZNF genes & repeats H1 Cell Line embryonic stem cell
9 chr1:63226600-63227800 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
10 chr1:63226600-63228200 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
11 chr1:63226600-63228600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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