| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1362103-1362318 | Rare:69 | ||||
| chr19:1383255-1383560 | Common:2; Rare:147 | ||||
| chr19:1383794-1383967 | Rare:65; Clinvar (benign):2 | ||||
| chr19:1401497-1401633 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1407144-1407608 | Common:3; Rare:187 | ||||
| chr19:1407639-1407836 | Rare:52 | ||||
| chr19:1407852-1408118 | Common:2; Rare:88 | ||||
| chr19:1415313-1415795 | Common:13; Rare:107 | ||||
| chr19:1438249-1438523 | Common:1; Rare:119 | ||||
| chr19:1479136-1479364 | Common:1; Rare:89 | ||||
| chr19:1479552-1479649 | Rare:23 | ||||
| chr19:1490293-1490511 | Common:3; Rare:77 | ||||
| chr19:1490644-1491225 | Common:8; Rare:189 | ||||
| chr19:1566962-1567339 | Common:1; Rare:111 | ||||
| chr19:1567543-1567865 | Common:2; Rare:85 |