| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177516881-177517084 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177600021-177600188 | Common:4; Rare:56; Clinvar (benign):4 | ||||
| chr5:178153821-178154110 | Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr5:178204337-178204534 | Common:3; Rare:69 | ||||
| chr5:179559559-179559794 | Common:1; Rare:68 | ||||
| chr5:179623613-179623980 | Common:4; Rare:133 | ||||
| chr5:179698580-179699099 | Common:4; Rare:184 | ||||
| chr5:179806318-179806448 | Rare:41 | ||||
| chr5:179806890-179807070 | Common:3; Rare:64 | ||||
| chr5:179820803-179820922 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179858797-179859031 | Rare:123 | ||||
| chr5:179907828-179908045 | Common:3; Rare:106 | ||||
| chr5:180071698-180071862 | Common:1; Rare:73 | ||||
| chr5:180810115-180810236 | Common:1; Rare:31 | ||||
| chr5:180861146-180861430 | Common:2; Rare:113 |