| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39519832-39520653 | Common:4; Rare:297 | ||||
| chr22:39521023-39521159 | Common:3; Rare:53 | ||||
| chr22:39532100-39532420 | Common:3; Rare:86 | ||||
| chr22:39532652-39533143 | Common:3; Rare:173 | ||||
| chr22:39900957-39901215 | Common:1; Rare:43 | ||||
| chr22:40044046-40044472 | Common:2; Rare:101 | ||||
| chr22:40044484-40044865 | Common:2; Rare:93 | ||||
| chr22:40045263-40045564 | Common:3; Rare:75 | ||||
| chr22:40177792-40178039 | Rare:63 | ||||
| chr22:40178237-40178584 | Rare:67 | ||||
| chr22:40345917-40346044 | Rare:30 | ||||
| chr22:40346257-40346611 | Common:1; Rare:142; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:40346704-40346859 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr22:40346874-40346983 | Common:1; Rare:23 | ||||
| chr22:40370529-40370765 | Rare:83 |