| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104615-49104854 | Common:1; Rare:101; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120747-49121136 | Rare:106; Clinvar:1 | ||||
| chr3:49125294-49125782 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:49129607-49129958 | Rare:98; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:49132790-49133104 | Rare:71; Clinvar:2 | ||||
| chr3:49166274-49166442 | Common:1; Rare:46 | ||||
| chr3:49171480-49171684 | Common:3; Rare:48; Clinvar (pathogenic):1 | ||||
| chr3:49340000-49340232 | Common:2; Rare:87 | ||||
| chr3:49357485-49357798 | Rare:127 | ||||
| chr3:49358016-49358486 | Common:4; Rare:241 | ||||
| chr3:49411820-49412438 | Common:2; Rare:215 | ||||
| chr3:49429250-49429419 | Rare:42 | ||||
| chr3:49469997-49470325 | Common:1; Rare:100 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49688650-49688770 | Common:2; Rare:35 |