| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58519761-58520011 | Rare:66 | ||||
| chr19:58549997-58550284 | Common:2; Rare:106 | ||||
| chr19:58554955-58555220 | Common:2; Rare:86 | ||||
| chr19:58558961-58559126 | Common:1; Rare:46 | ||||
| chr19:58573298-58573412 | Rare:27 | ||||
| chr19:58573502-58573587 | Common:1; Rare:20 | ||||
| chr2:677358-677557 | Common:1; Rare:84 | ||||
| chr2:1744389-1744634 | Common:1; Rare:84 | ||||
| chr2:3377811-3378035 | Common:2; Rare:62 | ||||
| chr2:3379611-3379786 | Common:2; Rare:74 | ||||
| chr2:3519477-3519660 | Common:2; Rare:57 | ||||
| chr2:3558230-3558515 | Common:5; Rare:126 | ||||
| chr2:3575129-3575358 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423132-9423316 | Common:1; Rare:41 | ||||
| chr2:9423442-9423683 | Rare:76 |