| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6632966-6633460 | Common:8; Rare:158; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868995-7869204 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr5:9546069-9546313 | Common:6; Rare:55 | ||||
| chr5:10249879-10250169 | Common:16; Rare:140 | ||||
| chr5:10250173-10250371 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353850-10353920 | Common:1; Rare:27 | ||||
| chr5:10354027-10354344 | Rare:114 | ||||
| chr5:16465790-16465871 | Rare:11 | ||||
| chr5:31532049-31532367 | Common:3; Rare:94 | ||||
| chr5:32174244-32174402 | Common:1; Rare:60 | ||||
| chr5:32711181-32711536 | Common:1; Rare:65 | ||||
| chr5:33440624-33441095 | Common:7; Rare:129 | ||||
| chr5:34656117-34656459 | Common:3; Rare:93 | ||||
| chr5:34915201-34915371 | Rare:49 | ||||
| chr5:34915493-34915768 | Common:1; Rare:74 |