| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:206664897-206665148 | Not yet | Common:4; Rare:38 | 176 | ||
| chr1:223027793-223027919 | Not yet | Common:3; Rare:36 | 106 | ||
| chr1:223992564-223992775 | Not yet | Common:3; Rare:78 | 140 | ||
| chr1:226965219-226965734 | Not yet | Common:2; Rare:168; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | 195 | ||
| chr1:226984594-226984941 | Not yet | Common:2; Rare:122; Clinvar (pathogenic):5 | 175 | ||
| chr1:228369152-228369469 | Not yet | Common:1; Rare:63 | 170 | ||
| chr1:228370222-228370455 | Not yet | Common:1; Rare:54 | 138 | ||
| chr1:229431719-229432432 | Not yet | Common:6; Rare:168; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):7 | 214 | ||
| chr1:231421026-231421249 | Not yet | Rare:59; Clinvar:1; Clinvar (benign):1 | 150 | ||
| chr1:231813946-231814199 | Not yet | Common:1; Rare:50 | 167 | ||
| chr1:231822833-231822985 | Not yet | Common:2; Rare:27 | 131 | ||
| chr1:236998050-236998133 | Not yet | Rare:22 | 59 | ||
| chr1:236998173-236998208 | Not yet | Rare:7 | 54 | ||
| chr10:20890640-20890722 | Not yet | Common:2; Rare:7 | 71 | ||
| chr10:24118390-24118537 | Not yet | Rare:36 | 129 |