| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46267841-46268032 | Common:1; Rare:58 | ||||
| chr22:46296711-46296959 | Common:2; Rare:87 | ||||
| chr22:46335621-46335792 | Common:4; Rare:78; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46762455-46762701 | Common:3; Rare:92 | ||||
| chr22:50244973-50245091 | Common:1; Rare:48 | ||||
| chr22:50525531-50525661 | Common:4; Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50562887-50563038 | Common:3; Rare:44 | ||||
| chr22:50582784-50583146 | Common:7; Rare:123; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50783581-50783859 | Common:2; Rare:93 | ||||
| chr3:3126813-3127017 | Common:4; Rare:94; Clinvar (benign):4 | ||||
| chr3:4303256-4303405 | Common:1; Rare:58 | ||||
| chr3:4493156-4493503 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4814432-4814665 | Common:5; Rare:74; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:4979254-4979530 | Common:2; Rare:59 | ||||
| chr3:5187304-5187663 | Common:5; Rare:139 |