| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52553766-52553839 | Rare:12 | ||||
| chr1:52697889-52697975 | Common:3; Rare:18 | ||||
| chr1:52697979-52698209 | Common:1; Rare:53 | ||||
| chr1:52698219-52698531 | Common:3; Rare:106; Clinvar (pathogenic):1 | ||||
| chr1:52726265-52726567 | Common:9; Rare:114 | ||||
| chr1:52726734-52726797 | Rare:10 | ||||
| chr1:52921044-52921235 | Common:2; Rare:41 | ||||
| chr1:52921325-52921893 | Common:2; Rare:172 | ||||
| chr1:52927219-52927365 | Common:3; Rare:52 | ||||
| chr1:52927650-52927917 | Common:4; Rare:51 | ||||
| chr1:53014747-53015060 | Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:53015294-53015343 | Rare:10 | ||||
| chr1:53196654-53196950 | Rare:114; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:53197039-53197088 | Rare:13; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr1:53197131-53197289 | Common:1; Rare:30 |