| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8681912-8682579 | Common:13; Rare:202 | ||||
| chr16:8851584-8852025 | Common:11; Rare:272 | ||||
| chr16:8991920-8992320 | Common:2; Rare:90 | ||||
| chr16:9003420-9003690 | Common:6; Rare:101 | ||||
| chr16:9027110-9027450 | Common:6; Rare:120 | ||||
| chr16:9047720-9048180 | Common:16; Rare:198 | ||||
| chr16:9092981-9093945 | Common:9; Rare:454 | ||||
| chr16:9275929-9276107 | Rare:34 | ||||
| chr16:10461514-10462201 | Common:1; Rare:136 | ||||
| chr16:10468682-10469116 | Common:9; Rare:228 | ||||
| chr16:10537742-10538280 | Common:10; Rare:259; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:10575850-10576873 | Common:12; Rare:239 | ||||
| chr16:10577080-10577540 | Common:4; Rare:120 | ||||
| chr16:10578420-10578720 | Common:4; Rare:64 | ||||
| chr16:10578660-10579112 | Common:12; Rare:222 |