| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:86617803-86618175 | Common:2; Rare:133 | ||||
| chr5:87267755-87267968 | Common:4; Rare:80 | ||||
| chr5:87268674-87268955 | Common:1; Rare:127; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:87408148-87408224 | Rare:22 | ||||
| chr5:87412779-87413106 | Common:4; Rare:108 | ||||
| chr5:88250702-88250822 | Rare:23 | ||||
| chr5:88251195-88251488 | Common:1; Rare:48 | ||||
| chr5:88827143-88827315 | Rare:32 | ||||
| chr5:88883087-88883303 | Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:88889302-88889529 | Common:2; Rare:69 | ||||
| chr5:90409302-90409423 | Common:1; Rare:30 | ||||
| chr5:90409657-90410112 | Common:11; Rare:159 | ||||
| chr5:90473850-90473906 | Rare:14 | ||||
| chr5:90473979-90474097 | Common:1; Rare:44 | ||||
| chr5:90474301-90474493 | Rare:77 |