| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1801309-1801455 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378487-6378686 | Rare:85 | ||||
| chr5:7869000-7869194 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:9545988-9546299 | Common:8; Rare:76 | ||||
| chr5:10249875-10250190 | Common:16; Rare:144 | ||||
| chr5:10250213-10250333 | Common:3; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:10353597-10353892 | Common:3; Rare:106 | ||||
| chr5:16465538-16465871 | Rare:89 | ||||
| chr5:31532052-31532332 | Common:3; Rare:76 | ||||
| chr5:32174277-32174395 | Common:1; Rare:43 | ||||
| chr5:33440606-33441058 | Common:6; Rare:117 | ||||
| chr5:34915493-34915733 | Common:1; Rare:54 | ||||
| chr5:36151875-36152180 | Rare:95 | ||||
| chr5:36876640-36876915 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877069-36877144 | Rare:29; Clinvar:1 |