| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:32623842-32624026 | Common:2; Rare:30 | ||||
| chr14:34969188-34969228 | Common:1; Rare:4 | ||||
| chr14:49633949-49634050 | Common:1; Rare:47; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:50000041-50000298 | Common:2; Rare:40 | ||||
| chr14:50000882-50001125 | Rare:47 | ||||
| chr14:61570518-61570540 | Rare:4 | ||||
| chr14:73245975-73246113 | Common:2; Rare:61 | ||||
| chr14:73713271-73713590 | Common:2; Rare:90 | ||||
| chr14:74616614-74616738 | Common:1; Rare:22 | ||||
| chr15:23686298-23686511 | Common:1; Rare:62 | ||||
| chr15:34795537-34795562 | Common:1; Rare:2; Clinvar (benign):1 | ||||
| chr15:51094651-51094988 | Common:8; Rare:88 | ||||
| chr15:73927694-73927875 | Common:1; Rare:55 | ||||
| chr15:82750435-82750591 | Common:2; Rare:40 | ||||
| chr15:89801152-89801635 | Rare:148 |