| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:160119394-160119584 | Rare:45 | ||||
| chr5:160419022-160419171 | Common:2; Rare:49 | ||||
| chr5:163460021-163460299 | Common:2; Rare:91 | ||||
| chr5:163505444-163505705 | Common:1; Rare:91 | ||||
| chr5:168579267-168579493 | Common:1; Rare:56 | ||||
| chr5:170389254-170389506 | Common:5; Rare:47 | ||||
| chr5:170389656-170389731 | Common:1; Rare:17 | ||||
| chr5:171387512-171388006 | Rare:234; Clinvar:1 | ||||
| chr5:172006492-172006950 | Common:2; Rare:125 | ||||
| chr5:172454349-172454655 | Common:10; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172641069-172641320 | Common:3; Rare:67 | ||||
| chr5:172770584-172770931 | Common:3; Rare:93 | ||||
| chr5:172771000-172771014 | Rare:2 | ||||
| chr5:172771089-172771438 | Common:4; Rare:147 | ||||
| chr5:172834163-172834430 | Common:1; Rare:65 |