| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52751330-52751870 | Common:8; Rare:269 | ||||
| chr4:52862102-52862363 | Common:26; Rare:288 | ||||
| chr4:53365935-53366340 | Common:3; Rare:198 | ||||
| chr4:53377431-53377839 | Common:7; Rare:214 | ||||
| chr4:53378010-53378420 | Common:12; Rare:187 | ||||
| chr4:53591417-53591735 | Common:8; Rare:161 | ||||
| chr4:54064484-54064807 | Common:5; Rare:175 | ||||
| chr4:54657956-54659070 | Common:15; Rare:346; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:55346145-55346441 | Common:8; Rare:255; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr4:55346450-55346860 | Common:4; Rare:210; Clinvar:1 | ||||
| chr4:55395513-55395694 | Common:1; Rare:79 | ||||
| chr4:55395713-55396209 | Common:12; Rare:329; Clinvar:6; Clinvar (benign):2 | ||||
| chr4:55398049-55398963 | Common:17; Rare:221 | ||||
| chr4:55545610-55546163 | Common:4; Rare:189 | ||||
| chr4:55546316-55546549 | Common:2; Rare:74 |