| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11934586-11934754 | Common:2; Rare:60; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:12618202-12618449 | Rare:56 | ||||
| chr1:16352407-16352608 | Common:3; Rare:108 | ||||
| chr1:16613486-16613773 | Common:4; Rare:1 | ||||
| chr1:19210254-19210417 | Rare:63 | ||||
| chr1:19251505-19251838 | Common:6; Rare:109 | ||||
| chr1:19485437-19485765 | Common:1; Rare:123 | ||||
| chr1:19596730-19597068 | Common:3; Rare:121 | ||||
| chr1:21345474-21345655 | Common:1; Rare:70 | ||||
| chr1:23559484-23559648 | Common:1; Rare:66 | ||||
| chr1:23959641-23959868 | Common:2; Rare:63 | ||||
| chr1:25232448-25232657 | Rare:83 | ||||
| chr1:25338244-25338447 | Common:1; Rare:72 | ||||
| chr1:25819833-25820013 | Common:4; Rare:57 | ||||
| chr1:26432091-26432406 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 |