| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31489744-31490122 | Common:1; Rare:150 | ||||
| chr22:31496399-31496602 | Common:2; Rare:57 | ||||
| chr22:31662213-31662337 | Common:1; Rare:49 | ||||
| chr22:31750066-31750208 | Common:3; Rare:50 | ||||
| chr22:31753839-31753996 | Rare:53 | ||||
| chr22:31944328-31944817 | Common:5; Rare:181 | ||||
| chr22:31945343-31945387 | Rare:15 | ||||
| chr22:32474639-32474731 | Common:2; Rare:26 | ||||
| chr22:33058343-33058519 | Common:3; Rare:42 | ||||
| chr22:35399905-35400197 | Rare:102 | ||||
| chr22:36387981-36388341 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr22:36481604-36481729 | Common:2; Rare:32 | ||||
| chr22:36482082-36482236 | Common:1; Rare:40 | ||||
| chr22:36507031-36507173 | Common:3; Rare:48 | ||||
| chr22:36529090-36529483 | Common:5; Rare:117 |