| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50526068-50526230 | Common:4; Rare:133; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr22:50526424-50526650 | Common:2; Rare:120; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr22:50532237-50532781 | Common:6; Rare:184 | ||||
| chr22:50562887-50563107 | Common:3; Rare:54 | ||||
| chr22:50582967-50583176 | Common:3; Rare:75 | ||||
| chr22:50600410-50600920 | Common:1; Rare:130 | ||||
| chr22:50601360-50601770 | Common:4; Rare:103 | ||||
| chr22:50628100-50628320 | Common:9; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50673835-50674626 | Common:4; Rare:249 | ||||
| chr22:50674670-50675030 | Common:2; Rare:100 | ||||
| chr22:50783614-50783814 | Common:2; Rare:61 | ||||
| chr3:197797-198562 | Common:8; Rare:383 | ||||
| chr3:1092863-1093051 | Common:1; Rare:58 | ||||
| chr3:2098654-2098876 | Common:4; Rare:88 | ||||
| chr3:2511356-2511782 | Common:11; Rare:225 |