| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31346572-31346754 | Common:5; Rare:29 | ||||
| chr22:31399389-31399660 | Common:1; Rare:78 | ||||
| chr22:31489929-31490164 | Common:3; Rare:97 | ||||
| chr22:31496399-31496571 | Common:1; Rare:44 | ||||
| chr22:31630829-31631019 | Common:4; Rare:50 | ||||
| chr22:31662204-31662377 | Common:2; Rare:67 | ||||
| chr22:31753809-31754107 | Common:1; Rare:105 | ||||
| chr22:32412161-32412311 | Common:2; Rare:47 | ||||
| chr22:32474647-32475091 | Common:4; Rare:145; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:32801489-32801710 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:35257387-35257541 | Common:1; Rare:47 | ||||
| chr22:35399905-35400197 | Rare:102 | ||||
| chr22:36387935-36388314 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481567-36481734 | Common:2; Rare:46 | ||||
| chr22:36482021-36482236 | Common:1; Rare:53 |