| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:214281465-214281684 | Common:2; Rare:89 | ||||
| chr1:214551514-214551878 | Common:2; Rare:126 | ||||
| chr1:214602908-214603304 | Common:3; Rare:109 | ||||
| chr1:214603437-214603529 | Common:1; Rare:15 | ||||
| chr1:215567361-215567494 | Rare:50 | ||||
| chr1:215567498-215567773 | Common:1; Rare:88 | ||||
| chr1:217630972-217631385 | Common:4; Rare:123 | ||||
| chr1:218285031-218285402 | Common:5; Rare:137 | ||||
| chr1:219173740-219173958 | Common:2; Rare:121 | ||||
| chr1:220046384-220046828 | Common:1; Rare:129 | ||||
| chr1:220089741-220090135 | Common:2; Rare:76 | ||||
| chr1:220093884-220094239 | Common:11; Rare:115; Clinvar (benign):1 | ||||
| chr1:220094415-220094591 | Rare:56; Clinvar (benign):3 | ||||
| chr1:220272307-220272705 | Rare:112; Clinvar:5 | ||||
| chr1:220690175-220690403 | Rare:89 |