| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007016-49007361 | Common:2; Rare:107 | ||||
| chr3:49018552-49018608 | Rare:21 | ||||
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49022096-49022142 | Rare:18 | ||||
| chr3:49025155-49025440 | Common:1; Rare:60 | ||||
| chr3:49028300-49028392 | Rare:26 | ||||
| chr3:49029378-49029432 | Common:1; Rare:39 | ||||
| chr3:49029433-49029452 | Rare:9 | ||||
| chr3:49104326-49104568 | Rare:80; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:49104616-49104934 | Common:1; Rare:127; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49122283-49122467 | Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:49132979-49133270 | Rare:52; Clinvar:1 | ||||
| chr3:49166284-49166387 | Common:1; Rare:30 | ||||
| chr3:49358096-49358418 | Common:4; Rare:170 | ||||
| chr3:49411878-49412379 | Common:2; Rare:180 |