| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:206664897-206665148 | Common:4; Rare:38 | ||||
| chr1:223027793-223027919 | Common:3; Rare:36 | ||||
| chr1:223992564-223992775 | Common:3; Rare:78 | ||||
| chr1:226965219-226965734 | Common:2; Rare:168; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:226984594-226984941 | Common:2; Rare:122; Clinvar (pathogenic):5 | ||||
| chr1:228369152-228369469 | Common:1; Rare:63 | ||||
| chr1:228370222-228370455 | Common:1; Rare:54 | ||||
| chr1:229431719-229432432 | Common:6; Rare:168; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):7 | ||||
| chr1:231421026-231421249 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:231813946-231814199 | Common:1; Rare:50 | ||||
| chr1:231822833-231822985 | Common:2; Rare:27 | ||||
| chr1:236998050-236998133 | Rare:22 | ||||
| chr1:236998173-236998208 | Rare:7 | ||||
| chr10:20890640-20890722 | Common:2; Rare:7 | ||||
| chr10:24118390-24118537 | Rare:36 |