| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:8440715-8440844 | Rare:52 | ||||
| chr4:10116687-10117089 | Common:8; Rare:190 | ||||
| chr4:10457337-10457518 | Common:3; Rare:71 | ||||
| chr4:13627706-13627837 | Common:1; Rare:41 | ||||
| chr4:15427908-15428060 | Rare:17 | ||||
| chr4:15655220-15655481 | Common:2; Rare:102 | ||||
| chr4:15681418-15681875 | Common:4; Rare:152 | ||||
| chr4:17614549-17614678 | Common:2; Rare:68 | ||||
| chr4:17810525-17811050 | Common:4; Rare:155 | ||||
| chr4:18020651-18020727 | Rare:14 | ||||
| chr4:18021722-18022003 | Common:2; Rare:94 | ||||
| chr4:23890016-23890278 | Common:1; Rare:40 | ||||
| chr4:25160370-25160728 | Common:3; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234104 | Rare:106 | ||||
| chr4:25914034-25914292 | Common:2; Rare:112 |