| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30658547-30659113 | Common:1; Rare:182 | ||||
| chr16:30659291-30659692 | Common:2; Rare:116 | ||||
| chr16:30659791-30659909 | Common:1; Rare:53 | ||||
| chr16:30660091-30660294 | Common:3; Rare:62 | ||||
| chr16:30697984-30698530 | Common:1; Rare:233 | ||||
| chr16:30698545-30698760 | Common:2; Rare:68 | ||||
| chr16:30698947-30699218 | Rare:97; Clinvar (benign):1 | ||||
| chr16:30699249-30699573 | Common:1; Rare:73 | ||||
| chr16:30740424-30740693 | Rare:58 | ||||
| chr16:30740791-30741140 | Common:2; Rare:69 | ||||
| chr16:30748050-30748493 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:30748751-30748833 | Rare:27 | ||||
| chr16:30762023-30762383 | Common:3; Rare:117 | ||||
| chr16:30786717-30786820 | Common:2; Rare:24 | ||||
| chr16:30786945-30787034 | Rare:22 |