| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499182-58499655 | Common:3; Rare:168; Clinvar:7; Clinvar (benign):2 | ||||
| chr19:58519767-58520061 | Rare:80 | ||||
| chr19:58538324-58538516 | Common:1; Rare:47 | ||||
| chr19:58554921-58555275 | Common:2; Rare:123 | ||||
| chr19:58558956-58559151 | Common:1; Rare:55 | ||||
| chr19:58573368-58573637 | Common:2; Rare:62 | ||||
| chr2:677315-677606 | Common:2; Rare:118 | ||||
| chr2:2331198-2331357 | Rare:32 | ||||
| chr2:3377754-3378009 | Common:1; Rare:72 | ||||
| chr2:3379600-3379780 | Common:2; Rare:73 | ||||
| chr2:3519485-3519674 | Common:3; Rare:56 | ||||
| chr2:3558251-3558735 | Common:6; Rare:170 | ||||
| chr2:3575080-3575447 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3594924-3595040 | Rare:39 | ||||
| chr2:3595095-3595146 | Rare:18 |