| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69332739-69332840 | Rare:25 | ||||
| chr5:69369464-69369906 | Common:1; Rare:177 | ||||
| chr5:69369970-69370052 | Common:1; Rare:20 | ||||
| chr5:69492698-69492815 | Rare:35 | ||||
| chr5:69560076-69560277 | Common:2; Rare:51 | ||||
| chr5:71455514-71455726 | Rare:61 | ||||
| chr5:71587192-71587413 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr5:72107202-72107522 | Common:2; Rare:132 | ||||
| chr5:72816496-72816728 | Common:4; Rare:88 | ||||
| chr5:72955860-72956091 | Common:1; Rare:103 | ||||
| chr5:73498315-73498568 | Common:3; Rare:78 | ||||
| chr5:73565370-73565836 | Common:7; Rare:143 | ||||
| chr5:74640573-74640896 | Common:1; Rare:106 | ||||
| chr5:74767038-74767363 | Common:3; Rare:102 | ||||
| chr5:75236860-75237087 | Common:6; Rare:85 |