| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40777921-40778319 | Common:1; Rare:109 | ||||
| chr19:40799062-40799266 | Common:5; Rare:73 | ||||
| chr19:41193094-41193267 | Common:1; Rare:54 | ||||
| chr19:41219155-41219411 | Common:1; Rare:69 | ||||
| chr19:41262326-41262615 | Rare:51 | ||||
| chr19:41264320-41264887 | Common:4; Rare:181 | ||||
| chr19:41265198-41265525 | Rare:64 | ||||
| chr19:41310093-41310322 | Rare:94 | ||||
| chr19:41310397-41310507 | Rare:25 | ||||
| chr19:41353499-41354173 | Common:2; Rare:179 | ||||
| chr19:41363791-41364014 | Common:1; Rare:80; Clinvar:1 | ||||
| chr19:41364065-41364164 | Common:1; Rare:28; Clinvar:4 | ||||
| chr19:41375842-41375972 | Rare:17 | ||||
| chr19:41397303-41397851 | Common:12; Rare:174; Clinvar (benign):5 | ||||
| chr19:41439526-41439657 | Rare:39 |