| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:984106-984414 | Common:4; Rare:109 | ||||
| chr19:1021027-1021519 | Common:15; Rare:185 | ||||
| chr19:1026258-1026351 | Common:2; Rare:28 | ||||
| chr19:1026372-1026720 | Common:1; Rare:120 | ||||
| chr19:1039846-1040228 | Common:2; Rare:120 | ||||
| chr19:1040540-1040610 | Rare:16 | ||||
| chr19:1040957-1041281 | Common:3; Rare:72 | ||||
| chr19:1066956-1067381 | Common:3; Rare:112 | ||||
| chr19:1077002-1077305 | Rare:68 | ||||
| chr19:1095292-1095635 | Common:8; Rare:147 | ||||
| chr19:1095862-1096105 | Common:3; Rare:44 | ||||
| chr19:1103704-1104162 | Common:9; Rare:181 | ||||
| chr19:1132132-1132462 | Common:2; Rare:132 | ||||
| chr19:1174112-1174454 | Common:2; Rare:144 | ||||
| chr19:1205453-1205893 | Common:3; Rare:143; Clinvar:1; Clinvar (benign):1 |