| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30591837-30591929 | Common:2; Rare:36 | ||||
| chr22:31081179-31081345 | Common:1; Rare:43 | ||||
| chr22:31107421-31107672 | Common:2; Rare:78 | ||||
| chr22:31292469-31292513 | Rare:14 | ||||
| chr22:31399466-31399669 | Rare:62 | ||||
| chr22:31489775-31489948 | Rare:66 | ||||
| chr22:31496409-31496567 | Common:1; Rare:40 | ||||
| chr22:31662211-31662373 | Common:2; Rare:63 | ||||
| chr22:31753792-31753982 | Rare:65 | ||||
| chr22:32474944-32475337 | Common:2; Rare:137; Clinvar (benign):1 | ||||
| chr22:32801456-32801710 | Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:35257394-35257531 | Common:1; Rare:41 | ||||
| chr22:35299716-35299967 | Common:2; Rare:67 | ||||
| chr22:35300050-35300326 | Common:2; Rare:88 | ||||
| chr22:35399915-35400185 | Rare:94 |