Variant report
| Variant | rs17098239 |
|---|---|
| Chromosome Location | chr1:76625917-76625918 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:76619800-76646400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 2 | chr1:76620600-76627800 | Weak transcription | Brain Dorsolateral Prefrontal Cortex | brain |
| 3 | chr1:76620800-76627800 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 4 | chr1:76621000-76626000 | Weak transcription | Fetal Intestine Small | intestine |
| 5 | chr1:76621000-76627000 | Weak transcription | Fetal Muscle Leg | muscle |
| 6 | chr1:76621000-76627600 | Weak transcription | Fetal Lung | lung |
| 7 | chr1:76621000-76630600 | Weak transcription | Psoas Muscle | Psoas |
| 8 | chr1:76621000-76630800 | Weak transcription | Primary B cells from cord blood | blood |
| 9 | chr1:76625200-76626400 | Enhancers | Primary T cells from cord blood | blood |
| 10 | chr1:76625400-76626000 | Weak transcription | Fetal Intestine Large | intestine |
