| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30375817-30376527 | Rare:176 | ||||
| chr16:30534824-30535084 | Common:2; Rare:82 | ||||
| chr16:30698457-30698580 | Rare:54 | ||||
| chr16:30762058-30762343 | Common:3; Rare:93 | ||||
| chr16:30893966-30894275 | Common:5; Rare:81 | ||||
| chr16:30923242-30923556 | Common:1; Rare:81 | ||||
| chr16:31033452-31033608 | Common:1; Rare:58 | ||||
| chr16:31074187-31074432 | Common:1; Rare:67 | ||||
| chr16:31214120-31214172 | Rare:11 | ||||
| chr16:31442755-31443059 | Common:1; Rare:50 | ||||
| chr16:31471907-31472189 | Rare:65 | ||||
| chr16:31508389-31508490 | Common:4; Rare:39 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973626-46973757 | Rare:62 | ||||
| chr16:47461020-47461366 | Common:2; Rare:133; Clinvar (benign):2 |