| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:18387316-18387534 | Common:3; Rare:67 | ||||
| chr6:24495067-24495246 | Common:1; Rare:66; Clinvar:10; Clinvar (benign):4 | ||||
| chr6:24666744-24666983 | Common:2; Rare:119 | ||||
| chr6:24666990-24667200 | Common:2; Rare:70 | ||||
| chr6:24719929-24720348 | Common:6; Rare:155 | ||||
| chr6:24774853-24775017 | Common:2; Rare:52 | ||||
| chr6:24911028-24911243 | Rare:33 | ||||
| chr6:24935892-24935986 | Rare:24 | ||||
| chr6:25278781-25279115 | Common:6; Rare:76 | ||||
| chr6:25962411-25962696 | Rare:36 | ||||
| chr6:26021408-26021653 | Common:2; Rare:65 | ||||
| chr6:26033554-26033792 | Common:6; Rare:94 | ||||
| chr6:26043701-26043960 | Common:3; Rare:94 | ||||
| chr6:26045170-26045412 | Common:1; Rare:81 | ||||
| chr6:26056329-26056546 | Common:3; Rare:149 |