| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41219106-41219256 | Rare:26 | ||||
| chr19:41219275-41219403 | Common:1; Rare:43 | ||||
| chr19:41220345-41220693 | Common:1; Rare:96 | ||||
| chr19:41262285-41262617 | Rare:60 | ||||
| chr19:41298342-41298611 | Rare:45 | ||||
| chr19:41309937-41310279 | Rare:115 | ||||
| chr19:41363794-41363992 | Common:1; Rare:70; Clinvar:1 | ||||
| chr19:41397332-41397406 | Common:2; Rare:29 | ||||
| chr19:41397550-41397848 | Common:7; Rare:103; Clinvar (benign):5 | ||||
| chr19:41439886-41439973 | Common:2; Rare:43 | ||||
| chr19:41860023-41860287 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:41860977-41861232 | Rare:81; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41884167-41884452 | Rare:74 | ||||
| chr19:41958706-41958762 | Rare:25 | ||||
| chr19:41959260-41959401 | Common:1; Rare:56 |