| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147234808-147234970 | Common:2; Rare:37 | ||||
| chr5:147234971-147235137 | Rare:55 | ||||
| chr5:147878587-147878711 | Common:1; Rare:19 | ||||
| chr5:148383704-148384033 | Rare:86 | ||||
| chr5:149063043-149063374 | Rare:68; Clinvar:1 | ||||
| chr5:149271664-149271951 | Common:3; Rare:96 | ||||
| chr5:149345404-149345557 | Common:1; Rare:58 | ||||
| chr5:149550278-149550381 | Rare:18 | ||||
| chr5:149551092-149551321 | Common:2; Rare:56 | ||||
| chr5:149551324-149551656 | Rare:78 | ||||
| chr5:149960575-149960923 | Rare:116; Clinvar:7 | ||||
| chr5:150000404-150000497 | Common:2; Rare:17 | ||||
| chr5:150357450-150357760 | Rare:103; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412623-150413057 | Common:2; Rare:95 | ||||
| chr5:150449662-150449795 | Common:4; Rare:46 |