| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48430022-48430251 | Common:1; Rare:55 | ||||
| chr3:48440011-48440319 | Common:2; Rare:116 | ||||
| chr3:48504072-48504288 | Common:2; Rare:71 | ||||
| chr3:48635407-48635564 | Rare:52 | ||||
| chr3:48847663-48847965 | Common:1; Rare:82 | ||||
| chr3:48918758-48918912 | Common:2; Rare:91 | ||||
| chr3:48983030-48983233 | Rare:38 | ||||
| chr3:49007213-49007426 | Common:2; Rare:84 | ||||
| chr3:49021503-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49022056-49022211 | Rare:64; Clinvar (pathogenic):1 | ||||
| chr3:49093564-49093643 | Rare:40 | ||||
| chr3:49104615-49104891 | Common:1; Rare:111; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120747-49120991 | Rare:74 | ||||
| chr3:49132790-49133161 | Rare:83; Clinvar:3 | ||||
| chr3:49411839-49412213 | Common:1; Rare:124 |