| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:219928526-219928990 | Common:2; Rare:280 | ||||
| chr1:220046242-220046849 | Common:6; Rare:754 | ||||
| chr1:220089552-220090257 | Common:11; Rare:324 | ||||
| chr1:220090276-220090676 | Common:1; Rare:90 | ||||
| chr1:220093715-220094242 | Common:25; Rare:341; Clinvar (benign):4 | ||||
| chr1:220094250-220094440 | Common:3; Rare:93; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:220094460-220094840 | Common:1; Rare:97; Clinvar (benign):2 | ||||
| chr1:220271786-220272186 | Common:3; Rare:98 | ||||
| chr1:220272307-220272710 | Rare:609; Clinvar:35 | ||||
| chr1:220879120-220879550 | Common:24; Rare:414 | ||||
| chr1:220879609-220879728 | Rare:28 | ||||
| chr1:220879920-220880560 | Common:4; Rare:214 | ||||
| chr1:221712150-221712601 | Common:2; Rare:163 | ||||
| chr1:221736873-221736983 | Common:1; Rare:29 | ||||
| chr1:221741435-221741889 | Common:4; Rare:170 |