| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:165631116-165631293 | Common:4; Rare:56 | ||||
| chr1:165698406-165698757 | Common:5; Rare:135 | ||||
| chr1:165768681-165769049 | Common:2; Rare:135; Clinvar:1 | ||||
| chr1:165827716-165827829 | Common:1; Rare:32 | ||||
| chr1:166839322-166839547 | Rare:64 | ||||
| chr1:167220779-167220923 | Rare:35 | ||||
| chr1:167630113-167630375 | Common:4; Rare:49 | ||||
| chr1:167935931-167936266 | Common:1; Rare:98 | ||||
| chr1:167936548-167936994 | Common:1; Rare:160 | ||||
| chr1:168178748-168179176 | Common:4; Rare:131 | ||||
| chr1:168225714-168226062 | Common:4; Rare:111 | ||||
| chr1:168728873-168728973 | Common:1; Rare:33 | ||||
| chr1:169367750-169368254 | Common:3; Rare:103 | ||||
| chr1:169485626-169486197 | Common:4; Rare:170; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:169794683-169794736 | Rare:13 |