| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39638823-39639149 | Common:1; Rare:118 | ||||
| chr4:39697890-39698389 | Common:2; Rare:172 | ||||
| chr4:40056634-40056955 | Common:4; Rare:98 | ||||
| chr4:40515887-40516185 | Common:1; Rare:63 | ||||
| chr4:40629394-40629581 | Common:1; Rare:27 | ||||
| chr4:40629666-40629914 | Common:1; Rare:62 | ||||
| chr4:40630158-40630546 | Common:2; Rare:75 | ||||
| chr4:41256721-41257133 | Common:5; Rare:134; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:41260645-41261019 | Rare:66; Clinvar:1 | ||||
| chr4:41261692-41261731 | Common:1; Rare:7; Clinvar (benign):1 | ||||
| chr4:41261740-41261951 | Rare:81; Clinvar:1 | ||||
| chr4:41359547-41359766 | Rare:33 | ||||
| chr4:41360668-41360930 | Common:1; Rare:75 | ||||
| chr4:41934935-41935230 | Common:3; Rare:80 | ||||
| chr4:41935328-41935416 | Rare:23 |