| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49018496-49018630 | Rare:58 | ||||
| chr3:49021490-49021720 | Rare:58; Clinvar:1 | ||||
| chr3:49021993-49022366 | Rare:140; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:49029319-49029564 | Common:2; Rare:168 | ||||
| chr3:49093579-49093766 | Common:1; Rare:60 | ||||
| chr3:49104442-49104910 | Common:1; Rare:187; Clinvar:8; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:49120754-49120997 | Rare:74 | ||||
| chr3:49132836-49133163 | Rare:73; Clinvar:3 | ||||
| chr3:49166284-49166429 | Common:1; Rare:40 | ||||
| chr3:49340009-49340272 | Common:3; Rare:91 | ||||
| chr3:49358037-49358464 | Common:4; Rare:218 | ||||
| chr3:49411839-49412429 | Common:2; Rare:210 | ||||
| chr3:49429260-49429430 | Rare:38 | ||||
| chr3:49469988-49470325 | Common:1; Rare:105 | ||||
| chr3:49673763-49674035 | Common:5; Rare:56 |