| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4290110-4290291 | Common:3; Rare:73 | ||||
| chr4:4541957-4542143 | Common:1; Rare:78 | ||||
| chr4:6640549-6640726 | Common:3; Rare:74 | ||||
| chr4:6987026-6987284 | Common:1; Rare:77 | ||||
| chr4:7068017-7068398 | Common:9; Rare:129 | ||||
| chr4:8428422-8428564 | Common:2; Rare:56 | ||||
| chr4:8440717-8440977 | Rare:98 | ||||
| chr4:15655289-15655466 | Common:1; Rare:82 | ||||
| chr4:15681458-15681863 | Common:3; Rare:141 | ||||
| chr4:15702967-15703128 | Common:2; Rare:33 | ||||
| chr4:17614551-17614678 | Common:2; Rare:67 | ||||
| chr4:17810687-17811065 | Common:4; Rare:119 | ||||
| chr4:24584465-24584708 | Common:1; Rare:77 | ||||
| chr4:25160385-25160704 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914308 | Common:2; Rare:110 |