Variant report
Variant | rs58555528 |
---|---|
Chromosome Location | chr1:63226707-63226708 |
allele | C/T |
Outlinks | Ensembl   UCSC |
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 |