| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46296711-46296918 | Common:2; Rare:75 | ||||
| chr22:46335632-46335804 | Common:5; Rare:78; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762506-46762693 | Common:3; Rare:68 | ||||
| chr22:50185690-50185942 | Common:4; Rare:106 | ||||
| chr22:50244516-50244659 | Common:1; Rare:46 | ||||
| chr22:50244954-50245070 | Common:2; Rare:45 | ||||
| chr22:50525543-50525674 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50532140-50532263 | Rare:31 | ||||
| chr22:50562886-50563065 | Common:3; Rare:48 | ||||
| chr22:50582786-50583142 | Common:7; Rare:118; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628079-50628280 | Common:9; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783574-50783853 | Common:2; Rare:94 | ||||
| chr3:196692-196914 | Common:1; Rare:68 | ||||
| chr3:196982-197332 | Common:3; Rare:127 | ||||
| chr3:3126806-3126990 | Common:4; Rare:79; Clinvar (benign):2 |