| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11797136-11797634 | Common:12; Rare:495 | ||||
| chr16:11850224-11851444 | Common:17; Rare:506 | ||||
| chr16:11851427-11851753 | Common:1; Rare:343 | ||||
| chr16:11887008-11887413 | Common:4; Rare:170 | ||||
| chr16:11914436-11915530 | Common:23; Rare:555 | ||||
| chr16:11915664-11916388 | Common:16; Rare:699 | ||||
| chr16:11976476-11977025 | Common:14; Rare:388 | ||||
| chr16:12039156-12039532 | Common:3; Rare:82 | ||||
| chr16:12803495-12803751 | Common:7; Rare:162 | ||||
| chr16:12803777-12804069 | Common:9; Rare:142 | ||||
| chr16:12901284-12901921 | Common:5; Rare:333 | ||||
| chr16:12902066-12902419 | Common:2; Rare:156 | ||||
| chr16:12903073-12903233 | Common:1; Rare:40 | ||||
| chr16:13919825-13920269 | Common:3; Rare:177; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:14070951-14071464 | Common:16; Rare:377 |