| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:90717128-90717365 | Rare:56 | ||||
| chr15:90902591-90902645 | Rare:14 | ||||
| chr15:91022502-91022664 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:101295191-101295373 | Rare:55 | ||||
| chr16:53656-53902 | Common:7; Rare:67 | ||||
| chr16:138598-138809 | Common:10; Rare:64 | ||||
| chr16:234466-234524 | Rare:26 | ||||
| chr16:381827-382175 | Common:8; Rare:121 | ||||
| chr16:401630-401945 | Common:2; Rare:140 | ||||
| chr16:636249-636473 | Common:4; Rare:66 | ||||
| chr16:679765-680162 | Common:8; Rare:106 | ||||
| chr16:680383-680601 | Common:1; Rare:69 | ||||
| chr16:681469-681849 | Common:2; Rare:158; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:684117-684501 | Common:3; Rare:195 | ||||
| chr16:721066-721191 | Common:3; Rare:36 |