| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698165-30698240 | Rare:54 | ||||
| chr16:30698283-30698598 | Common:1; Rare:120 | ||||
| chr16:30748134-30748457 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762060-30762355 | Common:3; Rare:97 | ||||
| chr16:30893966-30894275 | Common:5; Rare:81 | ||||
| chr16:30923242-30923588 | Common:1; Rare:86 | ||||
| chr16:31033432-31033583 | Common:1; Rare:60 | ||||
| chr16:31074187-31074450 | Common:1; Rare:73 | ||||
| chr16:31179820-31180152 | Common:1; Rare:121 | ||||
| chr16:31442757-31443059 | Common:1; Rare:49 | ||||
| chr16:31459319-31459510 | Common:1; Rare:81 | ||||
| chr16:31472109-31472186 | Rare:21 | ||||
| chr16:31508365-31508484 | Common:2; Rare:49 | ||||
| chr16:46689131-46689297 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973626-46973775 | Rare:71 |