| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43015044-43015395 | Common:2; Rare:139 | ||||
| chr22:43089317-43089507 | Common:3; Rare:64 | ||||
| chr22:43143361-43143439 | Common:2; Rare:24 | ||||
| chr22:43812214-43812441 | Common:3; Rare:76 | ||||
| chr22:43955326-43955566 | Common:3; Rare:75 | ||||
| chr22:44024130-44024414 | Common:2; Rare:88 | ||||
| chr22:44181163-44181434 | Common:5; Rare:66 | ||||
| chr22:44498054-44498479 | Common:3; Rare:152 | ||||
| chr22:44668480-44668785 | Common:5; Rare:118 | ||||
| chr22:45163674-45164199 | Common:7; Rare:199 | ||||
| chr22:46053742-46053909 | Rare:62 | ||||
| chr22:46250226-46250408 | Common:2; Rare:50 | ||||
| chr22:46267832-46268037 | Common:1; Rare:62 | ||||
| chr22:46296711-46296918 | Common:2; Rare:75 | ||||
| chr22:46335621-46335770 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 |