| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69332738-69332834 | Rare:23 | ||||
| chr5:69369203-69369294 | Common:4; Rare:29 | ||||
| chr5:69369365-69369934 | Common:2; Rare:224 | ||||
| chr5:69370016-69370197 | Rare:34 | ||||
| chr5:69492707-69492895 | Rare:53 | ||||
| chr5:69560036-69560294 | Common:3; Rare:66 | ||||
| chr5:71455475-71455789 | Rare:90 | ||||
| chr5:71586609-71586822 | Common:1; Rare:43 | ||||
| chr5:71587188-71587435 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:72106973-72107242 | Common:1; Rare:72 | ||||
| chr5:72107265-72107537 | Common:2; Rare:112 | ||||
| chr5:72816468-72816736 | Common:4; Rare:100 | ||||
| chr5:72871329-72871350 | Rare:3 | ||||
| chr5:72955869-72956099 | Common:1; Rare:98 | ||||
| chr5:73120489-73120628 | Common:1; Rare:34 |