| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1344883-1345226 | Common:2; Rare:116 | ||||
| chr5:1799747-1799988 | Common:9; Rare:110 | ||||
| chr5:1801287-1801486 | Common:4; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:1882999-1883146 | Common:1; Rare:31 | ||||
| chr5:6378479-6378669 | Rare:81 | ||||
| chr5:6633012-6633429 | Common:8; Rare:134; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:7868977-7869204 | Common:2; Rare:117; Clinvar (benign):1 | ||||
| chr5:9546073-9546380 | Common:7; Rare:71 | ||||
| chr5:9546445-9546530 | Common:2; Rare:17 | ||||
| chr5:10249856-10250388 | Common:19; Rare:253; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353573-10353979 | Common:3; Rare:155 | ||||
| chr5:10761074-10761465 | Common:13; Rare:127 | ||||
| chr5:14664572-14664718 | Common:3; Rare:68 | ||||
| chr5:16465509-16465544 | Rare:11 | ||||
| chr5:16465701-16465949 | Common:1; Rare:58 |