| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48780240-48780572 | Common:2; Rare:99 | ||||
| chr4:48830821-48831249 | Common:1; Rare:133 | ||||
| chr4:48831653-48831702 | Rare:11 | ||||
| chr4:51842791-51843225 | Common:1; Rare:130 | ||||
| chr4:52038248-52038346 | Rare:37; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52659194-52659402 | Common:1; Rare:72 | ||||
| chr4:53365997-53366204 | Rare:48 | ||||
| chr4:53377434-53377718 | Common:3; Rare:86 | ||||
| chr4:54064481-54064798 | Common:4; Rare:102 | ||||
| chr4:55346175-55346347 | Common:3; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395845-55395957 | Common:1; Rare:30; Clinvar:2 | ||||
| chr4:55546801-55546982 | Common:2; Rare:63 | ||||
| chr4:55948736-55948952 | Common:1; Rare:42 | ||||
| chr4:56387414-56387545 | Rare:44 | ||||
| chr4:56435458-56435974 | Common:6; Rare:170 |