| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58519600-58519685 | Rare:18 | ||||
| chr19:58519767-58520030 | Rare:70 | ||||
| chr19:58549997-58550284 | Common:2; Rare:106 | ||||
| chr19:58554933-58555344 | Common:2; Rare:138 | ||||
| chr19:58558282-58558675 | Rare:121 | ||||
| chr19:58558889-58559150 | Common:1; Rare:82 | ||||
| chr19:58573305-58573587 | Common:1; Rare:70 | ||||
| chr2:677346-677557 | Common:1; Rare:91 | ||||
| chr2:1373662-1374121 | Common:4; Rare:109 | ||||
| chr2:3377811-3377966 | Rare:41 | ||||
| chr2:3379644-3379791 | Common:2; Rare:62 | ||||
| chr2:3519370-3519628 | Common:2; Rare:81 | ||||
| chr2:3558225-3558565 | Common:6; Rare:135 | ||||
| chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423124-9423587 | Common:1; Rare:121 |