| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131165087-131165383 | Common:5; Rare:196; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:131170670-131171016 | Common:2; Rare:148; Clinvar (benign):4 | ||||
| chr5:131263866-131264176 | Common:2; Rare:204 | ||||
| chr5:131635037-131635449 | Common:2; Rare:265 | ||||
| chr5:131796908-131797301 | Rare:205 | ||||
| chr5:132227714-132227921 | Common:4; Rare:91 | ||||
| chr5:132293910-132294530 | Common:4; Rare:250 | ||||
| chr5:132369525-132369970 | Common:17; Rare:249; Clinvar:9; Clinvar (benign):11 | ||||
| chr5:132370100-132370350 | Common:4; Rare:181; Clinvar:19; Clinvar (benign):6; Clinvar (pathogenic):13 | ||||
| chr5:132410727-132410931 | Rare:70 | ||||
| chr5:132490769-132491016 | Rare:63 | ||||
| chr5:132556770-132557080 | Common:2; Rare:199; Clinvar:2 | ||||
| chr5:132557125-132557650 | Common:3; Rare:293; Clinvar:26; Clinvar (benign):16; Clinvar (pathogenic):6 | ||||
| chr5:132737485-132737740 | Rare:135 | ||||
| chr5:132777197-132777448 | Common:1; Rare:115 |