| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58451485-58451629 | Common:1; Rare:52 | ||||
| chr19:58499212-58499560 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:58519761-58520031 | Rare:71 | ||||
| chr19:58554195-58554437 | Rare:69 | ||||
| chr19:58554951-58555262 | Common:2; Rare:109 | ||||
| chr19:58573264-58573582 | Common:1; Rare:80 | ||||
| chr19:58573585-58573645 | Common:1; Rare:14 | ||||
| chr2:264558-264975 | Common:4; Rare:153 | ||||
| chr2:676981-677292 | Common:2; Rare:117 | ||||
| chr2:677294-677466 | Common:1; Rare:73 | ||||
| chr2:3377791-3377953 | Rare:43 | ||||
| chr2:3379625-3379768 | Common:2; Rare:58 | ||||
| chr2:3519492-3519674 | Common:3; Rare:51 | ||||
| chr2:3558269-3558571 | Common:6; Rare:110 | ||||
| chr2:3575080-3575358 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):5 |