| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748728-124749017 | Common:3; Rare:65 | ||||
| chr5:126423185-126423497 | Rare:64 | ||||
| chr5:126594998-126595382 | Common:5; Rare:158; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):5 | ||||
| chr5:126776760-126777214 | Common:4; Rare:159; Clinvar:6; Clinvar (benign):7 | ||||
| chr5:127030515-127030775 | Common:2; Rare:63 | ||||
| chr5:127290650-127290856 | Rare:44 | ||||
| chr5:127517884-127517992 | Common:1; Rare:25 | ||||
| chr5:128082970-128083451 | Common:8; Rare:154 | ||||
| chr5:128083542-128083822 | Common:2; Rare:126 | ||||
| chr5:128538202-128538427 | Common:5; Rare:73 | ||||
| chr5:129459482-129460476 | Common:7; Rare:229 | ||||
| chr5:131165063-131165382 | Common:3; Rare:117; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:131170679-131171021 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr5:131635173-131635446 | Common:1; Rare:103 | ||||
| chr5:131796936-131797263 | Rare:96 |