| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29995610-29995707 | Rare:44 | ||||
| chr16:29996070-29996296 | Common:2; Rare:80 | ||||
| chr16:30064343-30064493 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr16:30069659-30069976 | Common:1; Rare:111; Clinvar:3; Clinvar (benign):6 | ||||
| chr16:30075889-30076059 | Common:1; Rare:57 | ||||
| chr16:30355203-30355450 | Common:2; Rare:85 | ||||
| chr16:30407470-30407645 | Rare:59 | ||||
| chr16:30445872-30446050 | Common:1; Rare:41 | ||||
| chr16:30534822-30535084 | Common:2; Rare:82 | ||||
| chr16:30571588-30571884 | Rare:82 | ||||
| chr16:30698069-30698240 | Rare:95 | ||||
| chr16:30698455-30698723 | Common:1; Rare:98 | ||||
| chr16:30699058-30699386 | Rare:78; Clinvar (benign):1 | ||||
| chr16:30748093-30748441 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762080-30762348 | Common:3; Rare:90 |