| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147683102-147683395 | Rare:52 | ||||
| chr4:147822207-147822428 | Rare:29 | ||||
| chr4:151100825-151101161 | Rare:71 | ||||
| chr4:153684171-153684299 | Rare:40 | ||||
| chr4:168903619-168903881 | Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:168915639-168915932 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:173509619-173509689 | Common:1; Rare:19 | ||||
| chr4:184537513-184537749 | Common:4; Rare:63 | ||||
| chr5:757047-757179 | Common:2; Rare:22 | ||||
| chr5:784685-784853 | Common:2; Rare:51 | ||||
| chr5:1594456-1594640 | Common:3; Rare:74 | ||||
| chr5:1633922-1634056 | Common:2; Rare:46 | ||||
| chr5:8457582-8457751 | Common:2; Rare:53 | ||||
| chr5:14011736-14011840 | Common:1; Rare:33 | ||||
| chr5:14186247-14186378 | Common:1; Rare:25 |