| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39521040-39521379 | Common:6; Rare:119 | ||||
| chr22:39946643-39947019 | Common:1; Rare:71 | ||||
| chr22:40044129-40044341 | Common:2; Rare:48 | ||||
| chr22:40044560-40044990 | Common:3; Rare:103 | ||||
| chr22:40177793-40178053 | Rare:69 | ||||
| chr22:40346445-40346655 | Rare:97; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40463401-40463486 | Rare:15 | ||||
| chr22:40636661-40637033 | Common:2; Rare:102 | ||||
| chr22:40819321-40819553 | Common:11; Rare:112 | ||||
| chr22:40856379-40857159 | Common:3; Rare:323; Clinvar:3 | ||||
| chr22:40951015-40951404 | Common:2; Rare:134 | ||||
| chr22:40951611-40951716 | Common:1; Rare:29 | ||||
| chr22:41091406-41091862 | Common:6; Rare:170 | ||||
| chr22:41286160-41286522 | Common:2; Rare:115 | ||||
| chr22:41381897-41382047 | Common:2; Rare:71 |