| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92898015-92898045 | Common:1; Rare:6 | ||||
| chr15:93862906-93863113 | Common:1; Rare:45 | ||||
| chr15:100940925-100941131 | Common:2; Rare:42 | ||||
| chr15:101201340-101201661 | Common:1; Rare:61 | ||||
| chr16:2515216-2515458 | Rare:72 | ||||
| chr16:2516492-2516852 | Common:2; Rare:90 | ||||
| chr16:3960900-3961130 | Common:4; Rare:47 | ||||
| chr16:4682166-4682355 | Common:2; Rare:68 | ||||
| chr16:4797954-4798122 | Rare:94; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr16:4812227-4812313 | Rare:42 | ||||
| chr16:4852794-4852935 | Common:1; Rare:38 | ||||
| chr16:8632675-8632840 | Common:1; Rare:24 | ||||
| chr16:8839822-8840004 | Common:7; Rare:36 | ||||
| chr16:11841698-11841911 | Common:1; Rare:81 | ||||
| chr16:17343753-17344019 | Common:3; Rare:51 |