| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50628026-50628366 | Common:26; Rare:344; Clinvar:9; Clinvar (benign):3 | ||||
| chr22:50674811-50674978 | Rare:90 | ||||
| chr22:50675030-50675530 | Common:4; Rare:227; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:50783596-50783821 | Common:4; Rare:148 | ||||
| chr3:3126685-3127101 | Common:18; Rare:413; Clinvar (benign):12 | ||||
| chr3:3127285-3127491 | Common:1; Rare:50 | ||||
| chr3:4303253-4303701 | Common:7; Rare:363 | ||||
| chr3:4466580-4466960 | Common:2; Rare:214 | ||||
| chr3:4467006-4467385 | Common:4; Rare:335; Clinvar:14; Clinvar (benign):4 | ||||
| chr3:4493061-4493540 | Common:4; Rare:341; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:4711437-4711901 | Common:11; Rare:236; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:4978535-4978926 | Common:9; Rare:248 | ||||
| chr3:4979061-4979693 | Common:7; Rare:330 | ||||
| chr3:4980257-4980674 | Common:6; Rare:214 | ||||
| chr3:5187261-5187761 | Common:20; Rare:530 |