| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:61725000-61725333 | Common:1; Rare:142 | ||||
| chr1:61725346-61725530 | Common:2; Rare:26 | ||||
| chr1:61725570-61725621 | Common:2; Rare:7 | ||||
| chr1:61742347-61742574 | Common:1; Rare:65 | ||||
| chr1:61742729-61742980 | Common:1; Rare:73 | ||||
| chr1:62194724-62194824 | Rare:33 | ||||
| chr1:62435960-62436495 | Common:5; Rare:159 | ||||
| chr1:62436588-62437159 | Common:1; Rare:144 | ||||
| chr1:62688280-62688588 | Common:1; Rare:109 | ||||
| chr1:62783928-62784278 | Rare:103 | ||||
| chr1:63367283-63367811 | Common:3; Rare:141; Clinvar (benign):1 | ||||
| chr1:63367849-63367950 | Common:1; Rare:14 | ||||
| chr1:63523102-63523671 | Common:4; Rare:163 | ||||
| chr1:63593140-63593447 | Rare:101; Clinvar (benign):1 | ||||
| chr1:63593559-63594129 | Common:6; Rare:207; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 |