| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:160419049-160419279 | Common:4; Rare:86 | ||||
| chr5:160421680-160421956 | Common:1; Rare:80 | ||||
| chr5:160422048-160422379 | Common:1; Rare:89 | ||||
| chr5:163437297-163437647 | Rare:104 | ||||
| chr5:163459784-163460721 | Common:8; Rare:285 | ||||
| chr5:163505440-163505667 | Common:1; Rare:75 | ||||
| chr5:168291529-168291606 | Rare:19 | ||||
| chr5:168486337-168486526 | Common:3; Rare:70; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr5:168579269-168579931 | Common:4; Rare:188 | ||||
| chr5:169583592-169583834 | Common:6; Rare:78 | ||||
| chr5:171387498-171388235 | Common:2; Rare:316; Clinvar:1 | ||||
| chr5:171388323-171388694 | Common:1; Rare:103 | ||||
| chr5:172006498-172006982 | Common:2; Rare:136 | ||||
| chr5:172188190-172188511 | Common:1; Rare:89 | ||||
| chr5:172454318-172454704 | Common:12; Rare:112; Clinvar:1; Clinvar (benign):3 |