| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45691599-45691708 | Common:1; Rare:20 | ||||
| chr19:45691800-45692118 | Rare:113 | ||||
| chr19:45692200-45692776 | Common:4; Rare:143 | ||||
| chr19:45692842-45693089 | Common:1; Rare:46 | ||||
| chr19:45730788-45731137 | Common:1; Rare:75 | ||||
| chr19:45768199-45768309 | Rare:40; Clinvar (benign):2 | ||||
| chr19:45768413-45768501 | Rare:33; Clinvar:1 | ||||
| chr19:45768702-45769097 | Common:3; Rare:135; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:45769179-45769689 | Common:2; Rare:206 | ||||
| chr19:45770546-45771020 | Common:4; Rare:205; Clinvar:2 | ||||
| chr19:45779552-45779776 | Common:2; Rare:67 | ||||
| chr19:45792328-45792382 | Rare:11 | ||||
| chr19:45792694-45793102 | Common:2; Rare:117 | ||||
| chr19:45862607-45862768 | Common:1; Rare:45 | ||||
| chr19:45863025-45863428 | Common:5; Rare:125 |