| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31107344-31107646 | Common:2; Rare:107 | ||||
| chr22:31290718-31290937 | Rare:92 | ||||
| chr22:31292391-31292467 | Rare:20 | ||||
| chr22:31292469-31292512 | Rare:14 | ||||
| chr22:31399466-31399677 | Rare:64 | ||||
| chr22:31496462-31496556 | Common:1; Rare:23 | ||||
| chr22:31630803-31631038 | Common:5; Rare:57 | ||||
| chr22:31662204-31662337 | Common:1; Rare:53 | ||||
| chr22:31750066-31750328 | Common:3; Rare:73 | ||||
| chr22:31753822-31754026 | Common:1; Rare:74 | ||||
| chr22:32474893-32475019 | Rare:45; Clinvar:1 | ||||
| chr22:32801489-32801714 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:35399918-35400164 | Rare:82 | ||||
| chr22:35648279-35648535 | Common:2; Rare:43 | ||||
| chr22:36319538-36319926 | Common:2; Rare:91; Clinvar (benign):3 |