| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42614826-42615247 | Common:3; Rare:182 | ||||
| chr22:42649297-42649482 | Common:1; Rare:69 | ||||
| chr22:42720795-42720975 | Common:1; Rare:60 | ||||
| chr22:42857169-42857430 | Common:3; Rare:108 | ||||
| chr22:42959818-42959979 | Common:1; Rare:30 | ||||
| chr22:43015044-43015384 | Common:2; Rare:132 | ||||
| chr22:43089325-43089480 | Common:3; Rare:53 | ||||
| chr22:43812228-43812441 | Common:3; Rare:71 | ||||
| chr22:43955326-43955567 | Common:3; Rare:75 | ||||
| chr22:44024130-44024431 | Common:2; Rare:92 | ||||
| chr22:44312811-44313032 | Common:1; Rare:45 | ||||
| chr22:44668441-44668782 | Common:5; Rare:131 | ||||
| chr22:45163674-45164125 | Common:7; Rare:171 | ||||
| chr22:45502764-45503061 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr22:45671795-45672055 | Common:3; Rare:94 |