| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28800439-28800696 | Common:5; Rare:102 | ||||
| chr22:29267835-29268345 | Common:2; Rare:149 | ||||
| chr22:29766956-29767602 | Common:5; Rare:216 | ||||
| chr22:30356817-30357007 | Common:1; Rare:70 | ||||
| chr22:30606927-30607126 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:30607131-30607247 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:31630781-31631072 | Common:7; Rare:75 | ||||
| chr22:35840358-35840732 | Common:2; Rare:81 | ||||
| chr22:37019439-37019842 | Common:5; Rare:111 | ||||
| chr22:37675399-37675703 | Common:4; Rare:88 | ||||
| chr22:37849301-37849475 | Rare:103 | ||||
| chr22:37953512-37953755 | Common:1; Rare:92 | ||||
| chr22:38656391-38656741 | Common:1; Rare:80 | ||||
| chr22:38681795-38682256 | Common:3; Rare:169 | ||||
| chr22:39502139-39502374 | Rare:64 |