| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30355849-30355956 | Rare:25 | ||||
| chr16:30374669-30374802 | Rare:28 | ||||
| chr16:30445871-30446054 | Common:1; Rare:44 | ||||
| chr16:30534671-30535098 | Common:3; Rare:130 | ||||
| chr16:30585532-30585911 | Common:1; Rare:86 | ||||
| chr16:30610352-30610536 | Rare:45 | ||||
| chr16:30650752-30650903 | Rare:44 | ||||
| chr16:30697933-30698252 | Common:1; Rare:139 | ||||
| chr16:30698455-30698729 | Common:1; Rare:99 | ||||
| chr16:30699003-30699379 | Rare:100; Clinvar (benign):1 | ||||
| chr16:30762080-30762355 | Common:3; Rare:93 | ||||
| chr16:30893941-30894275 | Common:5; Rare:91 | ||||
| chr16:30896437-30896645 | Common:1; Rare:50 | ||||
| chr16:30923251-30923588 | Common:1; Rare:83 | ||||
| chr16:30949034-30949117 | Rare:16 |