| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185535370-185535632 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:189940605-189941000 | Common:15; Rare:136 | ||||
| chr5:218123-218408 | Common:3; Rare:115; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443095-443280 | Common:9; Rare:85 | ||||
| chr5:612215-612354 | Rare:55 | ||||
| chr5:892607-892923 | Common:5; Rare:103 | ||||
| chr5:1799778-1799993 | Common:8; Rare:101 | ||||
| chr5:1801300-1801455 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422153-5422460 | Common:2; Rare:100 | ||||
| chr5:6378498-6378686 | Rare:75 | ||||
| chr5:6448936-6449146 | Rare:29 | ||||
| chr5:7851032-7851216 | Common:2; Rare:37 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:9546102-9546299 | Common:6; Rare:43 | ||||
| chr5:10249847-10250190 | Common:16; Rare:157 |