| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159000180-159000261 | Rare:21 | ||||
| chr6:159726948-159727175 | Rare:89 | ||||
| chr6:159727353-159727616 | Common:5; Rare:116 | ||||
| chr6:159789553-159789975 | Common:4; Rare:143 | ||||
| chr6:166342510-166342659 | Common:3; Rare:59 | ||||
| chr6:169702026-169702317 | Common:5; Rare:126 | ||||
| chr6:169751537-169751644 | Rare:39; Clinvar (benign):1 | ||||
| chr6:170554221-170554393 | Common:1; Rare:56 | ||||
| chr7:1570007-1570110 | Common:1; Rare:30 | ||||
| chr7:2242168-2242256 | Common:2; Rare:54 | ||||
| chr7:4775522-4775652 | Common:4; Rare:54; Clinvar:1 | ||||
| chr7:5513741-5513870 | Common:1; Rare:57 | ||||
| chr7:6009029-6009363 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):15 | ||||
| chr7:6104627-6104981 | Common:5; Rare:129 | ||||
| chr7:6484070-6484391 | Common:2; Rare:132 |