| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87872241-87872302 | Common:3; Rare:22 | ||||
| chr16:87872325-87872367 | Rare:10 | ||||
| chr16:87872701-87872751 | Common:2; Rare:12 | ||||
| chr16:87945515-87945656 | Common:2; Rare:46 | ||||
| chr16:87956645-87956741 | Common:1; Rare:26 | ||||
| chr16:87956904-87957076 | Common:1; Rare:45 | ||||
| chr16:88024701-88024794 | Rare:20 | ||||
| chr16:88025105-88025459 | Common:4; Rare:72 | ||||
| chr16:88430281-88430402 | Common:2; Rare:38; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:88430570-88430648 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:88533705-88533798 | Rare:34 | ||||
| chr16:88534044-88534388 | Common:1; Rare:168 | ||||
| chr16:88769707-88769839 | Common:1; Rare:43 | ||||
| chr16:88770684-88770722 | Rare:10 | ||||
| chr16:88770896-88771153 | Common:2; Rare:74 |