| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42649310-42649482 | Common:1; Rare:67 | ||||
| chr22:43089406-43089507 | Common:1; Rare:22 | ||||
| chr22:43892032-43892325 | Common:1; Rare:50 | ||||
| chr22:43955326-43955556 | Common:3; Rare:70 | ||||
| chr22:45163758-45164003 | Common:2; Rare:95 | ||||
| chr22:46296663-46296924 | Common:2; Rare:94 | ||||
| chr22:46335621-46335816 | Common:5; Rare:91; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762467-46762669 | Common:3; Rare:75 | ||||
| chr22:50525536-50525710 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783606-50783859 | Common:2; Rare:75 | ||||
| chr3:3126784-3126985 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr3:9363020-9363105 | Rare:31 | ||||
| chr3:9397430-9397673 | Rare:82 | ||||
| chr3:9792379-9792570 | Rare:54 | ||||
| chr3:10026340-10026489 | Rare:39 |