| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:44181619-44181903 | Common:4; Rare:74 | ||||
| chr22:44668458-44668782 | Common:5; Rare:121 | ||||
| chr22:44764973-44765242 | Common:1; Rare:56 | ||||
| chr22:45163669-45164236 | Common:7; Rare:216 | ||||
| chr22:45309716-45309983 | Common:1; Rare:103 | ||||
| chr22:45413574-45413722 | Rare:58 | ||||
| chr22:45672014-45672076 | Rare:30 | ||||
| chr22:46053736-46053901 | Rare:64 | ||||
| chr22:46054215-46054432 | Common:5; Rare:69 | ||||
| chr22:46250245-46250445 | Common:3; Rare:67 | ||||
| chr22:46267870-46268037 | Common:1; Rare:52 | ||||
| chr22:46296738-46296921 | Common:1; Rare:63 | ||||
| chr22:46335601-46335813 | Common:5; Rare:101; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762496-46762712 | Common:3; Rare:82 | ||||
| chr22:49918367-49918684 | Common:2; Rare:114; Clinvar (benign):1 |