| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:150149551-150149873 | Common:2; Rare:98 | ||||
| chr1:150149985-150150141 | Common:1; Rare:37 | ||||
| chr1:150150646-150150830 | Common:4; Rare:49 | ||||
| chr1:150159537-150159829 | Common:1; Rare:77 | ||||
| chr1:150234492-150235175 | Common:2; Rare:125 | ||||
| chr1:150236015-150236397 | Common:1; Rare:95 | ||||
| chr1:150236543-150236646 | Common:1; Rare:17 | ||||
| chr1:150268210-150268356 | Common:1; Rare:23 | ||||
| chr1:150268362-150268460 | Rare:19 | ||||
| chr1:150268739-150269218 | Common:2; Rare:125 | ||||
| chr1:150272599-150272682 | Common:1; Rare:17 | ||||
| chr1:150293687-150293982 | Common:2; Rare:90 | ||||
| chr1:150321341-150321673 | Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:150363874-150364346 | Common:6; Rare:146 | ||||
| chr1:150364552-150365109 | Common:2; Rare:148 |