| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856919-40857154 | Common:1; Rare:94; Clinvar:3 | ||||
| chr22:41468812-41469140 | Rare:74 | ||||
| chr22:41560903-41561072 | Common:2; Rare:43 | ||||
| chr22:41621000-41621368 | Common:7; Rare:136 | ||||
| chr22:41800506-41800626 | Rare:38 | ||||
| chr22:41947093-41947225 | Rare:50 | ||||
| chr22:42090740-42091049 | Common:1; Rare:103; Clinvar (pathogenic):1 | ||||
| chr22:42614856-42615244 | Common:3; Rare:159 | ||||
| chr22:42649333-42649482 | Common:1; Rare:58 | ||||
| chr22:45163777-45164003 | Common:2; Rare:82 | ||||
| chr22:46053794-46053901 | Rare:38 | ||||
| chr22:46054122-46054445 | Common:6; Rare:102 | ||||
| chr22:46267870-46268027 | Common:1; Rare:47 | ||||
| chr22:46296744-46296922 | Rare:59 | ||||
| chr22:46335621-46335797 | Common:5; Rare:80; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 |