| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186191494-186191818 | Common:5; Rare:108; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:189940631-189941004 | Common:14; Rare:137 | ||||
| chr5:218104-218369 | Common:4; Rare:110; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443095-443272 | Common:9; Rare:79 | ||||
| chr5:612172-612357 | Rare:74 | ||||
| chr5:693289-693510 | Common:4; Rare:63 | ||||
| chr5:892535-892949 | Common:5; Rare:126 | ||||
| chr5:1799785-1799988 | Common:7; Rare:96 | ||||
| chr5:1801295-1801447 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422311-5422660 | Common:3; Rare:114 | ||||
| chr5:6378498-6378699 | Rare:81 | ||||
| chr5:6449067-6449146 | Rare:13 | ||||
| chr5:6632994-6633384 | Common:8; Rare:126; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:7851070-7851173 | Common:1; Rare:16 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 |