Variant report
| Variant | rs61765580 |
|---|---|
| Chromosome Location | chr1:57669162-57669163 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:57647000-57670600 | Weak transcription | Fetal Intestine Small | intestine |
| 2 | chr1:57657400-57670200 | Weak transcription | Fetal Intestine Large | intestine |
| 3 | chr1:57663600-57669800 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
| 4 | chr1:57664600-57678400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 5 | chr1:57665200-57670400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 6 | chr1:57665400-57669200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 7 | chr1:57665600-57671600 | Weak transcription | Fetal Heart | heart |
| 8 | chr1:57667800-57670800 | Weak transcription | Fetal Brain Female | brain |
| 9 | chr1:57668400-57669200 | Bivalent Enhancer | HUES48 Cell Line | embryonic stem cell |
| 10 | chr1:57668600-57671600 | Weak transcription | Fetal Brain Male | brain |
| 11 | chr1:57668800-57669400 | Bivalent Enhancer | H1 Cell Line | embryonic stem cell |
| 12 | chr1:57669000-57669200 | Flanking Bivalent TSS/Enh | iPS DF 19.11 Cell Line | embryonic stem cell |
| 13 | chr1:57669000-57669400 | Bivalent Enhancer | ES-UCSF4 Cell Line | embryonic stem cell |
