| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:54164452-54164667 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:54171452-54171475 | Common:1; Rare:4 | ||||
| chr20:54171509-54171689 | Common:2; Rare:56; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr20:54171867-54171932 | Common:1; Rare:9 | ||||
| chr20:54172451-54172972 | Common:3; Rare:108; Clinvar (pathogenic):2 | ||||
| chr20:54173258-54173442 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:54173446-54174215 | Common:8; Rare:202; Clinvar:9; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr20:56392145-56392704 | Common:6; Rare:152 | ||||
| chr20:56468504-56468763 | Rare:94 | ||||
| chr20:57351189-57351412 | Common:2; Rare:66 | ||||
| chr20:57709878-57710335 | Common:1; Rare:127 | ||||
| chr20:57710514-57710678 | Rare:44 | ||||
| chr20:57711036-57711113 | Common:2; Rare:17 | ||||
| chr20:57711336-57711876 | Common:4; Rare:109 | ||||
| chr20:58309418-58309727 | Common:2; Rare:118 |