| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:169367600-169368265 | Common:17; Rare:560 | ||||
| chr1:169368172-169368323 | Common:2; Rare:57 | ||||
| chr1:169368338-169368738 | Common:4; Rare:93 | ||||
| chr1:169485692-169486280 | Common:6; Rare:680; Clinvar:22; Clinvar (benign):8 | ||||
| chr1:169661714-169662114 | Common:3; Rare:81 | ||||
| chr1:169794258-169794473 | Common:1; Rare:36 | ||||
| chr1:169794470-169795450 | Common:31; Rare:779 | ||||
| chr1:169795713-169796301 | Common:13; Rare:207 | ||||
| chr1:169893200-169894524 | Common:42; Rare:1294 | ||||
| chr1:170074450-170075010 | Common:9; Rare:396 | ||||
| chr1:170531468-170532610 | Common:41; Rare:1237; Clinvar:10 | ||||
| chr1:171313920-171314190 | Common:1; Rare:57 | ||||
| chr1:171484720-171485672 | Common:5; Rare:683 | ||||
| chr1:171485970-171486262 | Common:3; Rare:67 | ||||
| chr1:171541442-171541895 | Rare:181 |