| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45671711-45672134 | Common:3; Rare:157 | ||||
| chr22:45672675-45672683 | Rare:1 | ||||
| chr22:46053777-46053869 | Rare:35 | ||||
| chr22:46054116-46054487 | Common:6; Rare:117 | ||||
| chr22:46151032-46151197 | Rare:30 | ||||
| chr22:46250090-46250574 | Common:6; Rare:136 | ||||
| chr22:46267738-46268090 | Common:2; Rare:102 | ||||
| chr22:46288315-46288570 | Rare:79 | ||||
| chr22:46296359-46296988 | Common:4; Rare:170 | ||||
| chr22:46297203-46297243 | Rare:7 | ||||
| chr22:46335520-46335951 | Common:9; Rare:181; Clinvar:13; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr22:46336535-46336569 | Common:1; Rare:4 | ||||
| chr22:46576763-46577142 | Common:6; Rare:122 | ||||
| chr22:46737407-46737682 | Common:2; Rare:63 | ||||
| chr22:46738194-46738494 | Common:8; Rare:82 |