| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38506012-38506029 | Rare:9 | ||||
| chr22:38506089-38506235 | Rare:45 | ||||
| chr22:38570171-38570483 | Common:5; Rare:57 | ||||
| chr22:38656382-38656716 | Common:1; Rare:79 | ||||
| chr22:38681809-38681991 | Common:1; Rare:76 | ||||
| chr22:38739723-38740157 | Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:38794080-38794315 | Common:1; Rare:61 | ||||
| chr22:38872180-38872447 | Rare:71 | ||||
| chr22:39319594-39319918 | Common:4; Rare:120 | ||||
| chr22:39349668-39350010 | Common:2; Rare:90 | ||||
| chr22:39521030-39521197 | Common:3; Rare:59 | ||||
| chr22:40044151-40044341 | Common:2; Rare:41 | ||||
| chr22:40346441-40346686 | Common:1; Rare:106; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:40636659-40637033 | Common:2; Rare:102 | ||||
| chr22:40856434-40857159 | Common:2; Rare:295; Clinvar:3 |