| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186723759-186723950 | Common:5; Rare:78 | ||||
| chr4:189940593-189941012 | Common:16; Rare:145 | ||||
| chr5:218094-218409 | Common:4; Rare:126; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443069-443280 | Common:10; Rare:97 | ||||
| chr5:461823-461911 | Rare:18 | ||||
| chr5:465201-465425 | Common:1; Rare:74 | ||||
| chr5:612222-612351 | Rare:51 | ||||
| chr5:693289-693540 | Common:6; Rare:75 | ||||
| chr5:892541-892923 | Common:5; Rare:118 | ||||
| chr5:1799791-1799986 | Common:4; Rare:91 | ||||
| chr5:1801300-1801549 | Common:4; Rare:129; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:2751818-2752139 | Common:1; Rare:101 | ||||
| chr5:6632994-6633684 | Common:9; Rare:214; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:6633739-6633862 | Rare:51 | ||||
| chr5:7868995-7869209 | Common:2; Rare:110; Clinvar (benign):1 |