| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19986269-19986669 | Common:8; Rare:201 | ||||
| chr22:19987060-19987630 | Common:7; Rare:399 | ||||
| chr22:20016407-20017104 | Common:45; Rare:1247 | ||||
| chr22:20020806-20021231 | Common:11; Rare:702 | ||||
| chr22:20021246-20021418 | Common:2; Rare:27 | ||||
| chr22:20021430-20021850 | Common:2; Rare:138 | ||||
| chr22:20052530-20053010 | Common:1; Rare:118; Clinvar (pathogenic):1 | ||||
| chr22:20079503-20080335 | Common:10; Rare:913 | ||||
| chr22:20080407-20080556 | Common:1; Rare:40 | ||||
| chr22:20080465-20080607 | Common:2; Rare:46 | ||||
| chr22:20080977-20081265 | Common:3; Rare:117 | ||||
| chr22:20111996-20113738 | Common:30; Rare:1175 | ||||
| chr22:20114938-20115370 | Common:1; Rare:184 | ||||
| chr22:20115383-20116385 | Common:8; Rare:684 | ||||
| chr22:20116545-20116945 | Common:6; Rare:171 |