| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:59624041-59624228 | Common:1; Rare:35 | ||||
| chr5:59649596-59649886 | Common:1; Rare:42 | ||||
| chr5:59684113-59684278 | Common:1; Rare:25 | ||||
| chr5:59790575-59791259 | Rare:173 | ||||
| chr5:59793125-59793310 | Rare:32 | ||||
| chr5:59798890-59799290 | Common:3; Rare:119 | ||||
| chr5:61304608-61305140 | Common:2; Rare:191 | ||||
| chr5:65925558-65925844 | Rare:114 | ||||
| chr5:66882610-66882960 | Common:2; Rare:82 | ||||
| chr5:68319698-68319955 | Common:2; Rare:42 | ||||
| chr5:68434198-68434566 | Common:8; Rare:96 | ||||
| chr5:72956673-72956774 | Rare:16 | ||||
| chr5:77180147-77180406 | Common:1; Rare:59 | ||||
| chr5:77180860-77181340 | Common:8; Rare:183 | ||||
| chr5:78984540-78985090 | Common:15; Rare:250; Clinvar:11; Clinvar (benign):1; Clinvar (pathogenic):6 |