Variant report
| Variant | rs72674478 |
|---|---|
| Chromosome Location | chr1:76649065-76649066 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:76636600-76652800 | Weak transcription | Primary B cells from cord blood | blood |
| 2 | chr1:76643800-76651800 | Weak transcription | Fetal Kidney | kidney |
| 3 | chr1:76644400-76651000 | Weak transcription | Fetal Lung | lung |
| 4 | chr1:76644800-76653200 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 5 | chr1:76645400-76652600 | Weak transcription | HUVEC | blood vessel |
| 6 | chr1:76646600-76652600 | Weak transcription | Brain Hippocampus Middle | brain |
| 7 | chr1:76646600-76658000 | Weak transcription | Fetal Stomach | stomach |
| 8 | chr1:76646800-76652800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 9 | chr1:76646800-76653200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 10 | chr1:76647000-76665600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 11 | chr1:76649000-76652600 | Weak transcription | Brain Cingulate Gyrus | brain |
