| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37675365-37675680 | Common:3; Rare:92 | ||||
| chr22:37745967-37746285 | Common:4; Rare:111 | ||||
| chr22:37805562-37805829 | Rare:86 | ||||
| chr22:37849293-37849480 | Rare:113 | ||||
| chr22:37953609-37953737 | Rare:53 | ||||
| chr22:38468029-38468258 | Common:1; Rare:69 | ||||
| chr22:38656391-38656725 | Common:1; Rare:75 | ||||
| chr22:38681781-38682268 | Common:3; Rare:177 | ||||
| chr22:38755435-38755622 | Common:1; Rare:42 | ||||
| chr22:39399673-39399831 | Common:3; Rare:71 | ||||
| chr22:40346441-40346556 | Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40819283-40819506 | Common:11; Rare:108 | ||||
| chr22:40856430-40856695 | Rare:125 | ||||
| chr22:40856939-40857159 | Common:1; Rare:93; Clinvar:3 | ||||
| chr22:41091518-41091779 | Common:5; Rare:96 |