| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31489768-31490180 | Common:3; Rare:167 | ||||
| chr22:31496387-31496591 | Common:2; Rare:59 | ||||
| chr22:31630822-31631038 | Common:5; Rare:54 | ||||
| chr22:31750021-31750157 | Common:2; Rare:46 | ||||
| chr22:31750162-31750330 | Common:1; Rare:39 | ||||
| chr22:31753802-31754107 | Common:1; Rare:108 | ||||
| chr22:31944328-31944817 | Common:5; Rare:181 | ||||
| chr22:32412119-32412315 | Common:2; Rare:64 | ||||
| chr22:32474938-32475379 | Common:3; Rare:161; Clinvar (benign):1 | ||||
| chr22:35257383-35257513 | Common:1; Rare:33 | ||||
| chr22:35380796-35381103 | Common:11; Rare:115 | ||||
| chr22:35399915-35400206 | Rare:99 | ||||
| chr22:36387931-36388330 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481333-36481668 | Common:4; Rare:96 | ||||
| chr22:36507031-36507168 | Common:3; Rare:47 |