| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67561884-67562079 | Rare:67 | ||||
| chr16:67562249-67562644 | Common:1; Rare:121 | ||||
| chr16:67562750-67562886 | Rare:35 | ||||
| chr16:67562930-67563479 | Common:3; Rare:174 | ||||
| chr16:67644770-67645193 | Common:2; Rare:95 | ||||
| chr16:67659774-67659974 | Rare:61; Clinvar (pathogenic):1 | ||||
| chr16:67660147-67660466 | Rare:172; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:67660738-67661084 | Common:2; Rare:120 | ||||
| chr16:67666218-67666356 | Common:1; Rare:56 | ||||
| chr16:67666585-67666826 | Common:1; Rare:46 | ||||
| chr16:67677826-67678092 | Common:1; Rare:41 | ||||
| chr16:67719271-67719573 | Common:1; Rare:81 | ||||
| chr16:67805891-67806045 | Rare:24 | ||||
| chr16:67806437-67806863 | Rare:100 | ||||
| chr16:67806955-67807182 | Rare:71 |