| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69369463-69369877 | Common:1; Rare:172 | ||||
| chr5:69492444-69492643 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr5:69492679-69492815 | Rare:43 | ||||
| chr5:69560044-69560280 | Common:2; Rare:60 | ||||
| chr5:71455514-71455852 | Rare:99 | ||||
| chr5:71455858-71456322 | Common:2; Rare:146; Clinvar (benign):1 | ||||
| chr5:71587188-71587446 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:72107184-72107519 | Common:2; Rare:137 | ||||
| chr5:72179380-72179706 | Common:1; Rare:70 | ||||
| chr5:72816496-72816733 | Common:4; Rare:92 | ||||
| chr5:72955862-72956105 | Common:1; Rare:108 | ||||
| chr5:73498315-73498652 | Common:3; Rare:103 | ||||
| chr5:73498780-73498790 | Rare:2 | ||||
| chr5:73565374-73565436 | Rare:12 | ||||
| chr5:73565597-73565817 | Common:5; Rare:94 |