| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28925199-28925369 | Rare:51 | ||||
| chr16:28974712-28974786 | Rare:38 | ||||
| chr16:29807928-29808119 | Rare:118 | ||||
| chr16:29995610-29995707 | Rare:44 | ||||
| chr16:29996075-29996252 | Common:2; Rare:61 | ||||
| chr16:30065578-30065835 | Rare:86 | ||||
| chr16:30075875-30076040 | Rare:55 | ||||
| chr16:30096922-30097118 | Rare:30 | ||||
| chr16:30355210-30355433 | Common:1; Rare:77 | ||||
| chr16:30445866-30445985 | Rare:35 | ||||
| chr16:30762058-30762357 | Common:3; Rare:97 | ||||
| chr16:30923242-30923578 | Common:1; Rare:83 | ||||
| chr16:31074187-31074432 | Common:1; Rare:67 | ||||
| chr16:31508374-31508454 | Rare:32 | ||||
| chr16:46689130-46689304 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 |