| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69560139-69560269 | Common:1; Rare:34 | ||||
| chr5:71455590-71455786 | Rare:61 | ||||
| chr5:71455884-71455981 | Rare:41 | ||||
| chr5:71587188-71587506 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:71719085-71719329 | Common:1; Rare:59 | ||||
| chr5:72107176-72107312 | Rare:45 | ||||
| chr5:72308286-72308615 | Common:3; Rare:104 | ||||
| chr5:72816510-72816718 | Common:4; Rare:76 | ||||
| chr5:72848072-72848249 | Common:3; Rare:63 | ||||
| chr5:72955854-72956099 | Common:1; Rare:109 | ||||
| chr5:73498305-73498660 | Common:3; Rare:115 | ||||
| chr5:73565365-73565825 | Common:7; Rare:141 | ||||
| chr5:73625891-73626262 | Common:4; Rare:93 | ||||
| chr5:74640723-74640821 | Rare:26 | ||||
| chr5:74685480-74685537 | Rare:15 |