| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31749993-31750286 | Common:3; Rare:82 | ||||
| chr22:31753760-31754118 | Common:1; Rare:127 | ||||
| chr22:32412136-32412330 | Common:2; Rare:61 | ||||
| chr22:32474702-32474870 | Common:3; Rare:52; Clinvar:5; Clinvar (benign):2 | ||||
| chr22:32474897-32475348 | Common:2; Rare:160; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:32801481-32801708 | Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:32801835-32802122 | Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:35299719-35299979 | Common:2; Rare:70 | ||||
| chr22:35399903-35400195 | Rare:102 | ||||
| chr22:35648279-35648550 | Common:2; Rare:46 | ||||
| chr22:35840357-35840566 | Rare:39 | ||||
| chr22:36239506-36239777 | Common:2; Rare:69 | ||||
| chr22:36387811-36388410 | Common:5; Rare:159; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481562-36481729 | Common:2; Rare:45 | ||||
| chr22:36507031-36507184 | Common:3; Rare:55 |