| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:90085279-90085463 | Common:4; Rare:46; Clinvar:2; Clinvar (benign):3 | ||||
| chr15:90184027-90184253 | Common:2; Rare:55 | ||||
| chr15:92882372-92882738 | Common:3; Rare:113 | ||||
| chr15:93086326-93086534 | Common:1; Rare:45 | ||||
| chr15:96327012-96327125 | Rare:23 | ||||
| chr15:96327323-96327503 | Common:3; Rare:26 | ||||
| chr15:99097192-99097388 | Common:3; Rare:44 | ||||
| chr15:99126443-99126788 | Common:1; Rare:83 | ||||
| chr15:99138118-99138382 | Common:2; Rare:66 | ||||
| chr15:99806877-99807032 | Common:3; Rare:19 | ||||
| chr16:1172145-1172312 | Common:3; Rare:56 | ||||
| chr16:1200458-1200806 | Common:4; Rare:185; Clinvar:2; Clinvar (benign):10 | ||||
| chr16:1207080-1207427 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:1361745-1362091 | Common:4; Rare:179; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):7 | ||||
| chr16:2123506-2123642 | Rare:48 |