| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46053749-46053901 | Rare:57 | ||||
| chr22:46250261-46250425 | Common:3; Rare:54 | ||||
| chr22:46267836-46268048 | Common:1; Rare:68 | ||||
| chr22:46296672-46296924 | Common:2; Rare:90 | ||||
| chr22:46335621-46335770 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762455-46762676 | Common:3; Rare:83 | ||||
| chr22:50185703-50185966 | Common:4; Rare:108 | ||||
| chr22:50244960-50245114 | Common:2; Rare:62 | ||||
| chr22:50582784-50583136 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50783592-50783859 | Common:2; Rare:87 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr3:4303270-4303407 | Common:1; Rare:57 | ||||
| chr3:4467213-4467282 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493177-4493348 | Rare:60 | ||||
| chr3:5187327-5187614 | Common:4; Rare:118 |