| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:95072590-95072735 | Rare:40 | ||||
| chr1:95072864-95073042 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr1:95233935-95234363 | Common:6; Rare:133 | ||||
| chr1:95234398-95234516 | Common:2; Rare:29 | ||||
| chr1:96721445-96721477 | Rare:10 | ||||
| chr1:96721524-96721885 | Common:3; Rare:160 | ||||
| chr1:96722000-96722099 | Rare:26 | ||||
| chr1:97920354-97920590 | Common:1; Rare:44 | ||||
| chr1:97920876-97921189 | Common:2; Rare:120; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr1:97921295-97921515 | Common:2; Rare:46 | ||||
| chr1:98661545-98661732 | Common:2; Rare:64 | ||||
| chr1:99766496-99766739 | Common:1; Rare:44 | ||||
| chr1:99849806-99850153 | Common:2; Rare:109 | ||||
| chr1:99850172-99850306 | Rare:22; Clinvar:1 | ||||
| chr1:99850317-99850442 | Rare:39; Clinvar:2; Clinvar (benign):2 |