| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:20786638-20786853 | Rare:84 | ||||
| chr1:20787250-20787490 | Rare:112 | ||||
| chr1:21345447-21345648 | Common:3; Rare:73 | ||||
| chr1:21782959-21783301 | Common:2; Rare:124 | ||||
| chr1:23194802-23194984 | Common:1; Rare:41 | ||||
| chr1:23344214-23344576 | Common:2; Rare:124 | ||||
| chr1:23368213-23368498 | Common:1; Rare:85 | ||||
| chr1:23558948-23559331 | Common:5; Rare:177 | ||||
| chr1:23559335-23559670 | Common:2; Rare:146 | ||||
| chr1:23559842-23560138 | Common:1; Rare:91 | ||||
| chr1:23778281-23778525 | Common:9; Rare:121 | ||||
| chr1:23800723-23800929 | Common:1; Rare:69 | ||||
| chr1:23825407-23825574 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:23959628-23959901 | Common:2; Rare:76 | ||||
| chr1:23980189-23980691 | Common:1; Rare:118 |