| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12867567-12867798 | Common:1; Rare:87 | ||||
| chr19:12885102-12885466 | Rare:104; Clinvar (pathogenic):2 | ||||
| chr19:12885595-12885708 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:13012887-13013109 | Common:5; Rare:47 | ||||
| chr19:13095592-13095727 | Rare:38 | ||||
| chr19:13099541-13099730 | Rare:55 | ||||
| chr19:13104474-13104798 | Common:1; Rare:80 | ||||
| chr19:13105261-13105401 | Rare:67 | ||||
| chr19:13151237-13151405 | Rare:30 | ||||
| chr19:13152532-13153294 | Common:2; Rare:206 | ||||
| chr19:13153372-13153728 | Common:1; Rare:177 | ||||
| chr19:13154419-13154583 | Common:1; Rare:48 | ||||
| chr19:13154964-13155371 | Common:3; Rare:113 | ||||
| chr19:13155502-13155840 | Common:1; Rare:70 | ||||
| chr19:13155971-13156390 | Common:3; Rare:100 |