| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1201437-1201823 | Common:3; Rare:157; Clinvar (benign):1 | ||||
| chr5:1799786-1800001 | Common:7; Rare:102 | ||||
| chr5:1801286-1801460 | Common:4; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378498-6378686 | Rare:75 | ||||
| chr5:6633012-6633419 | Common:8; Rare:132; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr5:9546072-9546361 | Common:7; Rare:68 | ||||
| chr5:10249865-10250170 | Common:16; Rare:145 | ||||
| chr5:10307636-10307812 | Rare:40 | ||||
| chr5:10307820-10308044 | Common:1; Rare:38 | ||||
| chr5:10353597-10353925 | Common:3; Rare:117 | ||||
| chr5:10761040-10761461 | Common:14; Rare:146 | ||||
| chr5:14581643-14581858 | Rare:93 | ||||
| chr5:14664551-14664927 | Common:5; Rare:154 | ||||
| chr5:16465469-16465944 | Common:1; Rare:141 |