| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154858471-154858747 | Common:1; Rare:92 | ||||
| chr5:157266050-157266155 | Rare:33 | ||||
| chr5:157383146-157383186 | Rare:7 | ||||
| chr5:157383189-157383285 | Rare:23 | ||||
| chr5:157460085-157460243 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:157575680-157575936 | Common:4; Rare:69 | ||||
| chr5:157731646-157731833 | Common:2; Rare:75 | ||||
| chr5:159099778-159099843 | Common:3; Rare:6 | ||||
| chr5:159100073-159100649 | Common:4; Rare:170 | ||||
| chr5:159263197-159263330 | Common:1; Rare:44 | ||||
| chr5:160419049-160419171 | Common:2; Rare:38 | ||||
| chr5:163460033-163460158 | Common:2; Rare:53 | ||||
| chr5:169583627-169583801 | Common:6; Rare:50 | ||||
| chr5:170389264-170389507 | Common:5; Rare:47 | ||||
| chr5:170389620-170389708 | Common:1; Rare:18 |