| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499212-58499535 | Common:2; Rare:99; Clinvar:3 | ||||
| chr19:58519761-58520022 | Rare:68 | ||||
| chr19:58554939-58555262 | Common:2; Rare:114 | ||||
| chr2:677358-677564 | Common:1; Rare:87 | ||||
| chr2:1744255-1744638 | Common:2; Rare:125 | ||||
| chr2:3377811-3378119 | Common:2; Rare:95 | ||||
| chr2:3379611-3379795 | Common:2; Rare:74 | ||||
| chr2:3519477-3519586 | Common:2; Rare:45 | ||||
| chr2:3558252-3558658 | Common:6; Rare:150 | ||||
| chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423143-9423302 | Common:1; Rare:33 | ||||
| chr2:9423398-9423719 | Rare:101 | ||||
| chr2:9555621-9555992 | Common:2; Rare:122 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:9843250-9843544 | Common:6; Rare:88 |