| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50525840-50526941 | Common:20; Rare:971; Clinvar:22; Clinvar (benign):37; Clinvar (pathogenic):38 | ||||
| chr22:50526904-50527143 | Rare:75 | ||||
| chr22:50562729-50563251 | Common:49; Rare:825 | ||||
| chr22:50582360-50582750 | Common:2; Rare:355; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr22:50582743-50583254 | Common:51; Rare:913; Clinvar:14; Clinvar (benign):17 | ||||
| chr22:50627960-50628500 | Common:51; Rare:660; Clinvar:14; Clinvar (benign):4 | ||||
| chr22:50783537-50783937 | Common:13; Rare:522 | ||||
| chr3:3109710-3110228 | Common:8; Rare:190 | ||||
| chr3:3110220-3110640 | Common:2; Rare:159 | ||||
| chr3:3126665-3127129 | Common:38; Rare:892; Clinvar (benign):24 | ||||
| chr3:3179514-3180051 | Common:13; Rare:486; Clinvar:13 | ||||
| chr3:4303089-4304059 | Common:21; Rare:1035 | ||||
| chr3:4466550-4466970 | Common:1; Rare:157 | ||||
| chr3:4466990-4467150 | Common:1; Rare:94; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:4467080-4467601 | Common:8; Rare:601; Clinvar:14; Clinvar (benign):6 |