| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161117956-161118206 | Rare:329 | ||||
| chr1:161118210-161119012 | Common:8; Rare:359 | ||||
| chr1:161131417-161131965 | Common:1; Rare:186 | ||||
| chr1:161132393-161132693 | Common:3; Rare:256 | ||||
| chr1:161132684-161133279 | Common:6; Rare:267 | ||||
| chr1:161153711-161153824 | Rare:25 | ||||
| chr1:161153833-161154110 | Common:1; Rare:88; Clinvar (pathogenic):1 | ||||
| chr1:161154060-161154420 | Common:5; Rare:202; Clinvar (pathogenic):1 | ||||
| chr1:161159340-161159589 | Common:3; Rare:130 | ||||
| chr1:161165849-161166070 | Common:2; Rare:106 | ||||
| chr1:161166219-161166695 | Common:6; Rare:194; Clinvar:8; Clinvar (benign):3 | ||||
| chr1:161201900-161202528 | Common:9; Rare:439; Clinvar:14; Clinvar (benign):26 | ||||
| chr1:161209058-161210223 | Common:4; Rare:470; Clinvar:2; Clinvar (benign):11; Clinvar (pathogenic):6 | ||||
| chr1:161225701-161226076 | Common:20; Rare:103 | ||||
| chr1:161227719-161227869 | Rare:42 |