| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3022918-3023262 | Common:1; Rare:96 | ||||
| chr16:3027314-3027694 | Common:1; Rare:144; Clinvar (pathogenic):1 | ||||
| chr16:3052154-3052359 | Common:2; Rare:46 | ||||
| chr16:3053942-3054004 | Rare:11 | ||||
| chr16:3057496-3057724 | Rare:79 | ||||
| chr16:3078289-3078428 | Common:1; Rare:27 | ||||
| chr16:3463580-3463692 | Rare:17 | ||||
| chr16:3622067-3622212 | Rare:34 | ||||
| chr16:3831716-3832006 | Common:2; Rare:75 | ||||
| chr16:3849565-3849602 | Rare:7 | ||||
| chr16:3849611-3849742 | Rare:30 | ||||
| chr16:3992239-3992562 | Common:6; Rare:87 | ||||
| chr16:4243203-4243395 | Rare:35 | ||||
| chr16:4383534-4383829 | Common:5; Rare:58 | ||||
| chr16:4612131-4612381 | Common:1; Rare:69 |