| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45671797-45672066 | Common:3; Rare:98 | ||||
| chr22:46053778-46053909 | Rare:45 | ||||
| chr22:46150289-46150629 | Common:1; Rare:113 | ||||
| chr22:46250240-46250404 | Common:2; Rare:47 | ||||
| chr22:46267870-46268042 | Common:1; Rare:56 | ||||
| chr22:46296589-46296930 | Common:2; Rare:106 | ||||
| chr22:46335601-46335825 | Common:5; Rare:105; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46738026-46738271 | Common:5; Rare:61 | ||||
| chr22:46762455-46762747 | Common:3; Rare:109 | ||||
| chr22:49918361-49918822 | Common:5; Rare:165; Clinvar (benign):1 | ||||
| chr22:50185725-50185953 | Common:4; Rare:95 | ||||
| chr22:50190422-50190621 | Common:3; Rare:62 | ||||
| chr22:50244516-50244662 | Common:1; Rare:48 | ||||
| chr22:50244954-50245070 | Common:2; Rare:45 | ||||
| chr22:50257157-50257482 | Common:2; Rare:92 |