| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:170389368-170389464 | Common:2; Rare:14 | ||||
| chr5:171387556-171388006 | Rare:217; Clinvar:1 | ||||
| chr5:172006509-172006950 | Common:2; Rare:117 | ||||
| chr5:172188180-172188504 | Common:1; Rare:90 | ||||
| chr5:172454362-172454655 | Common:10; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172770584-172770931 | Common:3; Rare:93 | ||||
| chr5:172770967-172771014 | Rare:16 | ||||
| chr5:172771018-172771069 | Rare:6 | ||||
| chr5:172771072-172771486 | Common:5; Rare:158 | ||||
| chr5:172834162-172834430 | Common:1; Rare:65 | ||||
| chr5:172958773-172958913 | Common:1; Rare:42 | ||||
| chr5:172959362-172959493 | Common:2; Rare:46 | ||||
| chr5:172983716-172983961 | Common:1; Rare:88 | ||||
| chr5:173056137-173056437 | Common:1; Rare:81 | ||||
| chr5:173057111-173057410 | Common:1; Rare:79 |