| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30123118-30123378 | Common:6; Rare:77 | ||||
| chr16:30193650-30193897 | |||||
| chr16:30355218-30355446 | Common:2; Rare:82 | ||||
| chr16:30407513-30407637 | Rare:44 | ||||
| chr16:30445872-30446052 | Common:1; Rare:41 | ||||
| chr16:30534828-30535105 | Common:3; Rare:89 | ||||
| chr16:30571557-30571718 | Rare:48 | ||||
| chr16:30572131-30572241 | Rare:38 | ||||
| chr16:30610339-30610550 | Rare:52 | ||||
| chr16:30698008-30698226 | Common:1; Rare:106 | ||||
| chr16:30698461-30698646 | Common:1; Rare:71 | ||||
| chr16:30698999-30699146 | Rare:54 | ||||
| chr16:30748068-30748462 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761437-30761600 | Rare:66 | ||||
| chr16:30762060-30762357 | Common:3; Rare:97 |