| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:154612469-154612869 | Common:1; Rare:112; Clinvar:4 | ||||
| chr4:155953480-155954190 | Common:12; Rare:267 | ||||
| chr4:158201309-158201976 | Common:8; Rare:165 | ||||
| chr4:158209980-158210840 | Common:19; Rare:545 | ||||
| chr4:158671032-158671616 | Common:8; Rare:120 | ||||
| chr4:158671700-158672470 | Common:31; Rare:952; Clinvar:15; Clinvar (benign):9 | ||||
| chr4:158672514-158673138 | Common:12; Rare:191 | ||||
| chr4:158722581-158723527 | Common:13; Rare:972 | ||||
| chr4:158723513-158724189 | Common:3; Rare:155 | ||||
| chr4:158768726-158769126 | Common:6; Rare:492 | ||||
| chr4:158769240-158769724 | Common:6; Rare:172 | ||||
| chr4:158805573-158805973 | Common:3; Rare:111 | ||||
| chr4:159103470-159105272 | Common:49; Rare:1176 | ||||
| chr4:163165950-163166647 | Common:15; Rare:737 | ||||
| chr4:163166750-163167240 | Common:16; Rare:443 |