| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69332739-69332834 | Rare:23 | ||||
| chr5:69369443-69369877 | Common:1; Rare:183 | ||||
| chr5:69369991-69370090 | Rare:20 | ||||
| chr5:69560082-69560257 | Common:2; Rare:47 | ||||
| chr5:71455563-71455697 | Rare:37 | ||||
| chr5:71587188-71587498 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:72107022-72107715 | Common:3; Rare:229 | ||||
| chr5:72179304-72179595 | Rare:67 | ||||
| chr5:72816500-72816793 | Common:4; Rare:111 | ||||
| chr5:72848088-72848180 | Common:3; Rare:40 | ||||
| chr5:72955862-72956096 | Common:1; Rare:102 | ||||
| chr5:73448775-73448889 | Rare:23 | ||||
| chr5:73498305-73498670 | Common:3; Rare:120 | ||||
| chr5:73565405-73565826 | Common:7; Rare:132 | ||||
| chr5:74640660-74640953 | Common:2; Rare:99 |