| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30748118-30748447 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762052-30762360 | Common:3; Rare:98 | ||||
| chr16:30893916-30894276 | Common:5; Rare:98 | ||||
| chr16:30896441-30896630 | Common:1; Rare:46 | ||||
| chr16:30923242-30923592 | Common:1; Rare:87 | ||||
| chr16:30949229-30949462 | Common:1; Rare:92 | ||||
| chr16:31033234-31033582 | Common:2; Rare:104 | ||||
| chr16:31073730-31073837 | Rare:31 | ||||
| chr16:31074187-31074457 | Common:1; Rare:75 | ||||
| chr16:31179839-31180147 | Common:1; Rare:112 | ||||
| chr16:31442740-31443059 | Common:1; Rare:54 | ||||
| chr16:31471901-31472189 | Rare:65 | ||||
| chr16:31508351-31508505 | Common:4; Rare:69 | ||||
| chr16:46621337-46621517 | Rare:64 | ||||
| chr16:46689131-46689394 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):1 |