| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45992049-45992182 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
| chr21:45992187-45992397 | Common:1; Rare:72; Clinvar:9; Clinvar (benign):3 | ||||
| chr21:46129738-46129960 | Common:3; Rare:85 | ||||
| chr22:22298066-22298210 | Common:2; Rare:54 | ||||
| chr22:25447997-25448161 | Common:4; Rare:61 | ||||
| chr22:26673003-26673104 | Common:1; Rare:32 | ||||
| chr22:28799407-28799533 | Rare:25 | ||||
| chr22:30196849-30197077 | Common:2; Rare:27 | ||||
| chr22:30205541-30205767 | Common:1; Rare:44 | ||||
| chr22:30246106-30246190 | Common:1; Rare:14 | ||||
| chr22:30249183-30249378 | Rare:51 | ||||
| chr22:30253299-30253537 | Common:1; Rare:52 | ||||
| chr22:30420556-30420772 | Common:2; Rare:34 | ||||
| chr22:30969036-30969278 | Common:2; Rare:69 | ||||
| chr22:36288832-36289297 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):8 |