| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69189509-69189615 | Common:1; Rare:35 | ||||
| chr5:69217622-69217835 | Common:4; Rare:68 | ||||
| chr5:69332739-69332855 | Rare:32 | ||||
| chr5:69369464-69369852 | Common:1; Rare:161 | ||||
| chr5:69560083-69560257 | Common:2; Rare:46 | ||||
| chr5:71587188-71587396 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:72816524-72816678 | Common:3; Rare:48 | ||||
| chr5:73498305-73498508 | Common:3; Rare:67 | ||||
| chr5:73565623-73565836 | Common:5; Rare:98 | ||||
| chr5:74767030-74767351 | Common:3; Rare:99 | ||||
| chr5:75336919-75337277 | Common:3; Rare:123 | ||||
| chr5:75511614-75511913 | Common:1; Rare:111 | ||||
| chr5:75717345-75717666 | Common:5; Rare:83 | ||||
| chr5:76875181-76875225 | Rare:14 | ||||
| chr5:77030284-77030421 | Rare:44 |