| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:633506-633745 | Common:8; Rare:111 | ||||
| chr19:663133-663427 | Common:2; Rare:113 | ||||
| chr19:680478-680756 | Common:2; Rare:95 | ||||
| chr19:893159-893484 | Common:3; Rare:138 | ||||
| chr19:913155-913289 | Rare:43 | ||||
| chr19:984260-984348 | Rare:31 | ||||
| chr19:1067091-1067182 | Common:1; Rare:28 | ||||
| chr19:1103787-1104115 | Common:4; Rare:139 | ||||
| chr19:1105183-1105404 | Common:1; Rare:92 | ||||
| chr19:1105406-1105738 | Common:3; Rare:160; Clinvar (pathogenic):1 | ||||
| chr19:1132102-1132452 | Common:2; Rare:136 | ||||
| chr19:1169196-1169306 | Common:1; Rare:27 | ||||
| chr19:1248451-1248583 | Common:1; Rare:44 | ||||
| chr19:1260928-1261169 | Common:3; Rare:81 | ||||
| chr19:1269068-1269410 | Common:2; Rare:133 |