| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186723754-186723903 | Common:4; Rare:61 | ||||
| chr4:189940579-189941000 | Common:15; Rare:139 | ||||
| chr5:218104-218361 | Common:4; Rare:103; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443103-443272 | Common:9; Rare:74 | ||||
| chr5:892726-892872 | Common:3; Rare:51 | ||||
| chr5:1799795-1799971 | Common:4; Rare:87 | ||||
| chr5:1801300-1801484 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422342-5422705 | Common:2; Rare:119 | ||||
| chr5:7869000-7869206 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr5:9546073-9546361 | Common:7; Rare:68 | ||||
| chr5:10249874-10250170 | Common:16; Rare:141 | ||||
| chr5:10353573-10353917 | Common:3; Rare:132 | ||||
| chr5:14581643-14581863 | Rare:96 | ||||
| chr5:14664582-14664674 | Common:1; Rare:38 | ||||
| chr5:16465715-16465871 | Rare:25 |