| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:566708-567527 | Common:13; Rare:649 | ||||
| chr16:569249-570140 | Common:18; Rare:741 | ||||
| chr16:578790-579389 | Common:8; Rare:374; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:588801-589789 | Common:14; Rare:1046 | ||||
| chr16:589753-590429 | Common:24; Rare:963 | ||||
| chr16:636128-636599 | Common:28; Rare:629 | ||||
| chr16:636635-637381 | Common:12; Rare:555 | ||||
| chr16:641644-642483 | Common:27; Rare:993 | ||||
| chr16:642580-643040 | Common:2; Rare:143 | ||||
| chr16:660651-661301 | Common:199; Rare:1496 | ||||
| chr16:667780-668236 | Common:4; Rare:511 | ||||
| chr16:675182-675839 | Common:4; Rare:497 | ||||
| chr16:679734-680572 | Common:71; Rare:1156 | ||||
| chr16:680936-682453 | Common:8; Rare:794; Clinvar:2; Clinvar (pathogenic):11 | ||||
| chr16:682420-683116 | Common:5; Rare:431 |