| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50197727-50197940 | Common:1; Rare:74 | ||||
| chr22:50198204-50198421 | Common:1; Rare:93 | ||||
| chr22:50306313-50306451 | Common:1; Rare:27 | ||||
| chr22:50308632-50308853 | Common:3; Rare:46 | ||||
| chr22:50314494-50314640 | Common:1; Rare:67 | ||||
| chr22:50539649-50539939 | Common:3; Rare:47 | ||||
| chr22:50541220-50541397 | Common:5; Rare:27 | ||||
| chr22:50627347-50627561 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr22:50698486-50698717 | Common:1; Rare:51; Clinvar:1 | ||||
| chr22:50722557-50722691 | Common:2; Rare:43 | ||||
| chr22:50724187-50724237 | Rare:4 | ||||
| chr22:50728865-50728948 | Rare:10 | ||||
| chr3:3133206-3133497 | Common:6; Rare:70 | ||||
| chr3:3135054-3135107 | Rare:15 | ||||
| chr3:3152582-3152658 | Common:1; Rare:23 |