| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43621842-43622142 | Common:2; Rare:105; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690823-43690986 | Common:2; Rare:86; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338086-44338190 | Common:2; Rare:38 | ||||
| chr3:44338421-44338800 | Common:6; Rare:127 | ||||
| chr3:44477596-44477752 | Common:1; Rare:39 | ||||
| chr3:44584710-44584990 | Rare:51 | ||||
| chr3:44624952-44625103 | Common:2; Rare:45 | ||||
| chr3:44712569-44712720 | Common:1; Rare:58 | ||||
| chr3:44729549-44729667 | Common:1; Rare:46 | ||||
| chr3:44761583-44761809 | Common:3; Rare:83 | ||||
| chr3:44861796-44861925 | Common:2; Rare:60 | ||||
| chr3:44976091-44976295 | Common:3; Rare:86 | ||||
| chr3:45689169-45689459 | Common:2; Rare:96 | ||||
| chr3:45995802-45995927 | Common:1; Rare:31; Clinvar:1 | ||||
| chr3:46208302-46208592 | Common:3; Rare:44 |