| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:84569957-84570275 | Common:4; Rare:81 | ||||
| chr15:84631314-84631508 | Common:3; Rare:62 | ||||
| chr15:90085280-90085474 | Common:4; Rare:47; Clinvar:2; Clinvar (benign):3 | ||||
| chr15:90184027-90184254 | Common:2; Rare:55 | ||||
| chr15:92882387-92882738 | Common:3; Rare:109 | ||||
| chr15:97965666-97965946 | Common:3; Rare:82 | ||||
| chr15:97968990-97969221 | Common:3; Rare:55 | ||||
| chr15:97970343-97970639 | Common:3; Rare:66 | ||||
| chr15:99105703-99106009 | Common:8; Rare:132 | ||||
| chr15:99106542-99106732 | Common:1; Rare:41 | ||||
| chr15:99109079-99109217 | Common:4; Rare:31 | ||||
| chr15:99126430-99126792 | Common:2; Rare:88 | ||||
| chr15:100887470-100887656 | Rare:49; Clinvar (pathogenic):2 | ||||
| chr16:1155021-1155224 | Common:1; Rare:91 | ||||
| chr16:1172161-1172319 | Common:3; Rare:51 |