| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12736840-12737095 | Common:2; Rare:88 | ||||
| chr19:12766381-12766563 | Rare:29 | ||||
| chr19:12775482-12775806 | Common:6; Rare:168 | ||||
| chr19:12777980-12778300 | Common:2; Rare:119 | ||||
| chr19:12778361-12778539 | Common:4; Rare:56 | ||||
| chr19:12791251-12791521 | Rare:101 | ||||
| chr19:12792400-12793000 | Common:2; Rare:178 | ||||
| chr19:12801766-12801994 | Common:2; Rare:153 | ||||
| chr19:12833540-12833950 | Rare:193 | ||||
| chr19:12838200-12838580 | Common:2; Rare:155 | ||||
| chr19:12881380-12881655 | Rare:98 | ||||
| chr19:12890760-12891232 | Common:2; Rare:131; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:12919227-12919462 | Common:2; Rare:234 | ||||
| chr19:12928319-12928845 | Common:1; Rare:261 | ||||
| chr19:12933619-12933851 | Common:2; Rare:131 |