| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30355219-30355442 | Common:1; Rare:81 | ||||
| chr16:30374474-30374860 | Common:2; Rare:75 | ||||
| chr16:30375809-30376534 | Rare:179 | ||||
| chr16:30534867-30535089 | Common:3; Rare:75 | ||||
| chr16:30762070-30762325 | Common:3; Rare:88 | ||||
| chr16:30787144-30787426 | Common:1; Rare:55 | ||||
| chr16:30893940-30894252 | Common:5; Rare:84 | ||||
| chr16:31033460-31033576 | Rare:44 | ||||
| chr16:31074187-31074432 | Common:1; Rare:67 | ||||
| chr16:31108373-31108471 | Rare:32 | ||||
| chr16:31213920-31214172 | Common:1; Rare:40 | ||||
| chr16:31442766-31443059 | Common:1; Rare:47 | ||||
| chr16:31471907-31472191 | Rare:66 | ||||
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46689140-46689416 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 |