| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303664-177303830 | Common:4; Rare:75 | ||||
| chr5:180810108-180810294 | Common:5; Rare:56 | ||||
| chr6:1624682-1624952 | Common:3; Rare:52 | ||||
| chr6:2245567-2245817 | Rare:85 | ||||
| chr6:4021174-4021418 | Rare:105 | ||||
| chr6:5003642-5003825 | Common:5; Rare:53 | ||||
| chr6:5260681-5261061 | Common:6; Rare:135; Clinvar (benign):4 | ||||
| chr6:5261250-5261618 | Common:10; Rare:105 | ||||
| chr6:7541424-7541713 | Rare:87; Clinvar (benign):1 | ||||
| chr6:7910780-7910906 | Rare:43 | ||||
| chr6:8435412-8435648 | Common:3; Rare:83 | ||||
| chr6:13615165-13615530 | Common:3; Rare:147 | ||||
| chr6:16761424-16761758 | Common:2; Rare:103 | ||||
| chr6:24666862-24667292 | Common:3; Rare:167 | ||||
| chr6:25279239-25279494 | Common:2; Rare:97 |