| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:159100089-159100705 | Common:4; Rare:178 | ||||
| chr5:159263236-159263330 | Common:1; Rare:30 | ||||
| chr5:160400026-160400210 | Common:3; Rare:54 | ||||
| chr5:163437292-163437647 | Rare:105 | ||||
| chr5:163460026-163460173 | Common:2; Rare:62 | ||||
| chr5:170297716-170297897 | Common:1; Rare:32 | ||||
| chr5:170389264-170389506 | Common:5; Rare:47 | ||||
| chr5:170389600-170389774 | Common:3; Rare:37 | ||||
| chr5:171387501-171388006 | Rare:239; Clinvar:1 | ||||
| chr5:172006559-172006950 | Common:2; Rare:99 | ||||
| chr5:172188211-172188532 | Common:1; Rare:86 | ||||
| chr5:172454362-172454668 | Common:12; Rare:79; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172770350-172770931 | Common:5; Rare:153 | ||||
| chr5:172770969-172771069 | Rare:22 | ||||
| chr5:172771079-172771409 | Common:4; Rare:133 |