| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24427476-24427627 | Common:1; Rare:35 | ||||
| chr22:24427835-24428299 | Common:1; Rare:110 | ||||
| chr22:24555066-24555514 | Common:4; Rare:167 | ||||
| chr22:24555593-24556048 | Rare:146 | ||||
| chr22:24593108-24593308 | Common:1; Rare:51 | ||||
| chr22:24593355-24593535 | Common:2; Rare:26 | ||||
| chr22:24603078-24603253 | Common:4; Rare:31 | ||||
| chr22:24607451-24607731 | Common:2; Rare:68 | ||||
| chr22:24607841-24607933 | Common:1; Rare:16 | ||||
| chr22:25405328-25405542 | Common:6; Rare:106 | ||||
| chr22:25564480-25565120 | Common:2; Rare:211 | ||||
| chr22:25565368-25565544 | Common:1; Rare:47 | ||||
| chr22:26428820-26429310 | Common:4; Rare:159 | ||||
| chr22:26479937-26480030 | Rare:17 | ||||
| chr22:26483495-26483954 | Common:9; Rare:151; Clinvar:7; Clinvar (benign):2 |