| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39946480-39947035 | Common:6; Rare:485 | ||||
| chr22:39947212-39947612 | Common:1; Rare:65 | ||||
| chr22:39965710-39966060 | Common:1; Rare:74 | ||||
| chr22:39994150-39994450 | Common:2; Rare:57 | ||||
| chr22:40043803-40044441 | Common:12; Rare:440 | ||||
| chr22:40044469-40044878 | Common:13; Rare:573 | ||||
| chr22:40044920-40045230 | Common:1; Rare:89 | ||||
| chr22:40045203-40045796 | Common:9; Rare:384 | ||||
| chr22:40177625-40178025 | Rare:377 | ||||
| chr22:40345752-40346203 | Common:4; Rare:175 | ||||
| chr22:40346278-40347000 | Common:8; Rare:800; Clinvar:43; Clinvar (benign):36; Clinvar (pathogenic):5 | ||||
| chr22:40370348-40371440 | Common:3; Rare:534 | ||||
| chr22:40436490-40437041 | Common:3; Rare:244 | ||||
| chr22:40463025-40463425 | Common:3; Rare:99 | ||||
| chr22:40463520-40463920 | Common:1; Rare:78 |