| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499216-58499526 | Common:2; Rare:93; Clinvar:3 | ||||
| chr2:264558-264976 | Common:4; Rare:154 | ||||
| chr2:677362-677557 | Common:1; Rare:82 | ||||
| chr2:3377799-3377953 | Rare:39 | ||||
| chr2:3379640-3379780 | Common:2; Rare:60 | ||||
| chr2:3519495-3519636 | Common:2; Rare:43 | ||||
| chr2:3558251-3558481 | Common:5; Rare:101 | ||||
| chr2:3575114-3575358 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423393-9423697 | Rare:95 | ||||
| chr2:9474500-9474605 | Common:6; Rare:55 | ||||
| chr2:9555599-9555966 | Common:2; Rare:122 | ||||
| chr2:9843250-9843539 | Common:6; Rare:86 | ||||
| chr2:16665798-16665989 | Common:4; Rare:39 | ||||
| chr2:17540470-17540798 | Common:2; Rare:70 | ||||
| chr2:17753721-17754159 | Common:3; Rare:141; Clinvar (benign):1 |