| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186723769-186723953 | Common:5; Rare:72 | ||||
| chr4:189940543-189940991 | Common:13; Rare:143 | ||||
| chr5:218106-218415 | Common:4; Rare:123; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443102-443278 | Common:9; Rare:79 | ||||
| chr5:892631-892917 | Common:5; Rare:93 | ||||
| chr5:1799791-1799949 | Common:4; Rare:79 | ||||
| chr5:1801295-1801486 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:6378498-6378699 | Rare:81 | ||||
| chr5:6632994-6633313 | Common:6; Rare:100; Clinvar:7; Clinvar (benign):3 | ||||
| chr5:7868995-7869204 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr5:9545964-9546333 | Common:9; Rare:89 | ||||
| chr5:10353577-10353905 | Common:3; Rare:126 | ||||
| chr5:16465469-16465904 | Rare:124 | ||||
| chr5:31532052-31532381 | Common:3; Rare:97 | ||||
| chr5:32174267-32174389 | Common:1; Rare:46 |