| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69166865-69167458 | Common:4; Rare:181 | ||||
| chr5:69189446-69189652 | Common:1; Rare:66 | ||||
| chr5:69217667-69217860 | Common:2; Rare:74 | ||||
| chr5:69234769-69234949 | Common:1; Rare:52 | ||||
| chr5:69332727-69332839 | Rare:28 | ||||
| chr5:69369212-69369344 | Common:4; Rare:40 | ||||
| chr5:69369423-69369893 | Common:1; Rare:194 | ||||
| chr5:69369999-69370075 | Rare:15 | ||||
| chr5:69492690-69492808 | Rare:35 | ||||
| chr5:69560088-69560286 | Common:2; Rare:49 | ||||
| chr5:71455573-71455745 | Rare:54 | ||||
| chr5:71455894-71455969 | Rare:32 | ||||
| chr5:71587119-71587420 | Common:2; Rare:105; Clinvar (benign):2 | ||||
| chr5:72106973-72107514 | Common:3; Rare:186 | ||||
| chr5:72816500-72816799 | Common:4; Rare:112 |