| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1801286-1801465 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:2752223-2752270 | Rare:12 | ||||
| chr5:5422311-5422705 | Common:3; Rare:134 | ||||
| chr5:6378476-6378699 | Rare:94 | ||||
| chr5:6632996-6633313 | Common:6; Rare:100; Clinvar:7; Clinvar (benign):3 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:9546001-9546361 | Common:9; Rare:91 | ||||
| chr5:10249837-10250445 | Common:19; Rare:287; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353573-10353970 | Common:3; Rare:154 | ||||
| chr5:10441803-10441946 | Rare:42 | ||||
| chr5:10761039-10761496 | Common:14; Rare:156 | ||||
| chr5:14664538-14664919 | Common:5; Rare:160 | ||||
| chr5:16465689-16465913 | Rare:50 | ||||
| chr5:16616976-16617203 | Common:2; Rare:65; Clinvar (benign):5 | ||||
| chr5:16935823-16936498 | Common:4; Rare:200 |