| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186726655-186726818 | Common:4; Rare:56 | ||||
| chr4:189940579-189941000 | Common:15; Rare:139 | ||||
| chr5:218101-218409 | Common:4; Rare:123; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443095-443275 | Common:9; Rare:81 | ||||
| chr5:612211-612369 | Rare:62 | ||||
| chr5:892535-893005 | Common:5; Rare:150 | ||||
| chr5:1799785-1799988 | Common:7; Rare:96 | ||||
| chr5:1801286-1801455 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422311-5422693 | Common:3; Rare:128 | ||||
| chr5:6632982-6633591 | Common:8; Rare:178; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868991-7869227 | Common:2; Rare:124; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:9546073-9546366 | Common:7; Rare:69 | ||||
| chr5:10249874-10250436 | Common:19; Rare:263; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353564-10353925 | Common:4; Rare:139 | ||||
| chr5:10761074-10761199 | Rare:48 |