| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:188109484-188109646 | Common:3; Rare:33 | ||||
| chr4:189940588-189941000 | Common:15; Rare:137 | ||||
| chr5:218104-218385 | Common:4; Rare:120; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443059-443272 | Common:10; Rare:93 | ||||
| chr5:612170-612369 | Rare:79 | ||||
| chr5:891228-891612 | Common:2; Rare:118 | ||||
| chr5:892512-893013 | Common:5; Rare:161 | ||||
| chr5:1799771-1799988 | Common:8; Rare:102 | ||||
| chr5:1801286-1801549 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:2752177-2752258 | Rare:23 | ||||
| chr5:5422269-5422693 | Common:3; Rare:141 | ||||
| chr5:6378467-6378706 | Rare:98 | ||||
| chr5:6632872-6633405 | Common:11; Rare:174; Clinvar:10; Clinvar (benign):7 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:10249834-10250445 | Common:19; Rare:291; Clinvar:5; Clinvar (benign):2 |