| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30445871-30446050 | Common:1; Rare:42 | ||||
| chr16:30526762-30526897 | Common:4; Rare:40 | ||||
| chr16:30527251-30527371 | Rare:35 | ||||
| chr16:30534467-30535105 | Common:4; Rare:213 | ||||
| chr16:30572133-30572388 | Rare:68 | ||||
| chr16:30585487-30585908 | Common:1; Rare:102 | ||||
| chr16:30610339-30610562 | Rare:59 | ||||
| chr16:30658646-30658720 | Rare:23 | ||||
| chr16:30698057-30698252 | Rare:102 | ||||
| chr16:30698441-30698727 | Common:1; Rare:104 | ||||
| chr16:30698999-30699416 | Rare:109; Clinvar (benign):1 | ||||
| chr16:30761442-30761582 | Rare:55 | ||||
| chr16:30762052-30762348 | Common:3; Rare:94 | ||||
| chr16:30787110-30787272 | Rare:26 | ||||
| chr16:30893932-30894275 | Common:5; Rare:93 |