| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2269499-2269697 | Common:3; Rare:87 | ||||
| chr19:2270010-2270303 | Common:5; Rare:89 | ||||
| chr19:2325166-2325276 | Common:1; Rare:18 | ||||
| chr19:2328388-2328731 | Common:2; Rare:151 | ||||
| chr19:2427518-2427804 | Common:4; Rare:112 | ||||
| chr19:2841152-2841557 | Common:2; Rare:127 | ||||
| chr19:2944910-2945220 | Common:6; Rare:104 | ||||
| chr19:3136035-3136387 | Common:6; Rare:85 | ||||
| chr19:3136546-3136603 | Rare:20 | ||||
| chr19:3178682-3178865 | Rare:70 | ||||
| chr19:3366475-3366606 | Common:3; Rare:25 | ||||
| chr19:3478424-3478679 | Common:2; Rare:64 | ||||
| chr19:3479048-3479445 | Common:2; Rare:66 | ||||
| chr19:3572623-3572988 | Common:2; Rare:101 | ||||
| chr19:3981947-3982424 | Common:2; Rare:180; Clinvar:1; Clinvar (benign):5 |