| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:44676945-44677206 | Common:6; Rare:92 | ||||
| chr22:45163599-45164028 | Common:9; Rare:286 | ||||
| chr22:45240820-45241100 | Common:2; Rare:55 | ||||
| chr22:45284802-45284954 | Common:4; Rare:71 | ||||
| chr22:45309529-45310139 | Common:2; Rare:374 | ||||
| chr22:45502503-45502970 | Common:4; Rare:252 | ||||
| chr22:45671648-45671990 | Common:6; Rare:207 | ||||
| chr22:46150279-46150632 | Common:2; Rare:201 | ||||
| chr22:46250226-46250464 | Common:6; Rare:141 | ||||
| chr22:46267808-46268062 | Common:2; Rare:155 | ||||
| chr22:46296489-46297010 | Common:8; Rare:271 | ||||
| chr22:46335558-46335961 | Common:17; Rare:329; Clinvar:22; Clinvar (benign):21; Clinvar (pathogenic):4 | ||||
| chr22:46336057-46336463 | Common:8; Rare:203 | ||||
| chr22:46377535-46377950 | Common:13; Rare:168 | ||||
| chr22:46577056-46577267 | Common:1; Rare:68 |