| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30558268-30558646 | Common:4; Rare:96 | ||||
| chr16:30585561-30585949 | Common:1; Rare:83 | ||||
| chr16:30610352-30610544 | Rare:48 | ||||
| chr16:30698008-30698235 | Common:1; Rare:108 | ||||
| chr16:30698467-30698580 | Rare:51 | ||||
| chr16:30748134-30748441 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761454-30761600 | Rare:60 | ||||
| chr16:30762058-30762329 | Common:3; Rare:93 | ||||
| chr16:30787146-30787272 | Rare:17 | ||||
| chr16:30893942-30894268 | Common:5; Rare:88 | ||||
| chr16:30923236-30923610 | Common:1; Rare:88 | ||||
| chr16:31033456-31033591 | Common:1; Rare:51 | ||||
| chr16:31074184-31074483 | Common:1; Rare:84 | ||||
| chr16:31108285-31108471 | Rare:42 | ||||
| chr16:31179827-31180182 | Common:3; Rare:149; Clinvar:2; Clinvar (benign):2 |