| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940620-189941035 | Common:16; Rare:151 | ||||
| chr5:218123-218409 | Common:3; Rare:115; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443103-443280 | Common:9; Rare:80 | ||||
| chr5:612201-612351 | Rare:59 | ||||
| chr5:892658-892917 | Common:5; Rare:87 | ||||
| chr5:1799791-1799993 | Common:4; Rare:94 | ||||
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378498-6378675 | Rare:69 | ||||
| chr5:7851039-7851173 | Common:2; Rare:24 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:10249866-10250160 | Common:16; Rare:141 | ||||
| chr5:10250230-10250377 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:10353590-10353907 | Common:3; Rare:117 | ||||
| chr5:10441807-10441969 | Common:1; Rare:48 | ||||
| chr5:14183558-14183753 | Common:3; Rare:34 |