| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10353597-10353901 | Common:3; Rare:111 | ||||
| chr5:16465661-16465887 | Rare:50 | ||||
| chr5:16616977-16617262 | Common:2; Rare:77; Clinvar (benign):5 | ||||
| chr5:31532037-31532381 | Common:3; Rare:98 | ||||
| chr5:32173810-32174120 | Rare:95 | ||||
| chr5:32174229-32174416 | Common:1; Rare:71 | ||||
| chr5:32711203-32711321 | Rare:18 | ||||
| chr5:32712224-32712318 | Rare:23 | ||||
| chr5:33440606-33441125 | Common:7; Rare:144 | ||||
| chr5:33891937-33892303 | Rare:87 | ||||
| chr5:34008027-34008251 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656061-34656497 | Common:4; Rare:119 | ||||
| chr5:34839278-34839357 | Common:2; Rare:25 | ||||
| chr5:34915215-34915321 | Rare:30 | ||||
| chr5:34915462-34915766 | Common:1; Rare:85 |