| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101948057-101948374 | Common:2; Rare:95 | ||||
| chr15:34794018-34794171 | Common:3; Rare:22 | ||||
| chr15:34794678-34794949 | Rare:68; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:34795432-34795609 | Common:2; Rare:45; Clinvar:4; Clinvar (benign):4 | ||||
| chr15:40511664-40511861 | Common:1; Rare:45 | ||||
| chr15:43879615-43879992 | Common:1; Rare:79 | ||||
| chr15:50686038-50686155 | Common:1; Rare:24 | ||||
| chr15:51094660-51094963 | Common:7; Rare:80 | ||||
| chr15:63049328-63049489 | Rare:35 | ||||
| chr15:73927792-73927860 | Rare:15 | ||||
| chr15:82750496-82750580 | Common:1; Rare:20 | ||||
| chr15:84631314-84631485 | Common:3; Rare:50 | ||||
| chr15:90084830-90085101 | Rare:90; Clinvar:2 | ||||
| chr15:90087111-90087573 | Common:4; Rare:113; Clinvar (benign):4 | ||||
| chr15:90088342-90088748 | Common:1; Rare:130; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 |