| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:168225685-168226117 | Common:10; Rare:278 | ||||
| chr1:169105460-169105961 | Common:6; Rare:150 | ||||
| chr1:169106103-169106480 | Common:11; Rare:363 | ||||
| chr1:169367711-169368341 | Common:11; Rare:333 | ||||
| chr1:169485705-169486487 | Common:7; Rare:501; Clinvar:17; Clinvar (benign):12 | ||||
| chr1:169711476-169712175 | Common:1; Rare:224 | ||||
| chr1:169794520-169795318 | Common:14; Rare:369 | ||||
| chr1:169893540-169893797 | Common:12; Rare:227 | ||||
| chr1:169893820-169894029 | Common:2; Rare:64 | ||||
| chr1:169894128-169894430 | Common:8; Rare:199 | ||||
| chr1:170074450-170074782 | Common:5; Rare:152 | ||||
| chr1:170531466-170531867 | Common:8; Rare:112 | ||||
| chr1:170531991-170532470 | Common:11; Rare:407; Clinvar:5 | ||||
| chr1:170532490-170533020 | Common:2; Rare:123 | ||||
| chr1:171257110-171257530 | Common:2; Rare:77 |