| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156860670-156860907 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr1:157045231-157045294 | Common:1; Rare:15 | ||||
| chr1:157045513-157045993 | Rare:150 | ||||
| chr1:157138283-157138769 | Common:6; Rare:152 | ||||
| chr1:157138833-157139134 | Common:1; Rare:83 | ||||
| chr1:157993035-157993722 | Common:5; Rare:148 | ||||
| chr1:158999722-159000037 | Common:2; Rare:65 | ||||
| chr1:159009458-159009493 | Rare:8 | ||||
| chr1:159009762-159009932 | Rare:42 | ||||
| chr1:159009936-159010145 | Common:1; Rare:38 | ||||
| chr1:159010180-159010258 | Rare:15 | ||||
| chr1:159780729-159781186 | Common:5; Rare:132 | ||||
| chr1:159854681-159854892 | Rare:70 | ||||
| chr1:159854907-159855048 | Common:1; Rare:43 | ||||
| chr1:159923720-159923919 | Common:1; Rare:34 |