| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104400-49104660 | Rare:162; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr3:49104724-49104949 | Rare:175; Clinvar (benign):6 | ||||
| chr3:49120734-49120997 | Rare:152 | ||||
| chr3:49132320-49132600 | Common:2; Rare:187; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:49166284-49166454 | Common:2; Rare:83 | ||||
| chr3:49339994-49340162 | Common:4; Rare:124 | ||||
| chr3:49340460-49340990 | Common:3; Rare:164 | ||||
| chr3:49357600-49357880 | Common:1; Rare:176 | ||||
| chr3:49358150-49358518 | Common:8; Rare:360 | ||||
| chr3:49411837-49412436 | Common:4; Rare:408 | ||||
| chr3:49429228-49429435 | Rare:100 | ||||
| chr3:49429563-49429963 | Common:3; Rare:139 | ||||
| chr3:49469883-49470399 | Common:4; Rare:276 | ||||
| chr3:49470378-49470778 | Common:1; Rare:128; Clinvar (benign):2 | ||||
| chr3:49510151-49510677 | Common:2; Rare:180; Clinvar:2; Clinvar (benign):7 |