Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161132221-161132742 | Common:1; Rare:141 | ||||
chr1:161132746-161132897 | Common:1; Rare:42 | ||||
chr1:161132900-161133148 | Common:1; Rare:46 | ||||
chr1:161153749-161154175 | Common:1; Rare:134; Clinvar (pathogenic):1 | ||||
chr1:161154373-161154428 | Rare:8 | ||||
chr1:161154447-161154501 | Rare:10 | ||||
chr1:161159340-161159586 | Common:2; Rare:77 | ||||
chr1:161159751-161159798 | Rare:10 | ||||
chr1:161159827-161159877 | Rare:9 | ||||
chr1:161165889-161166140 | Common:1; Rare:61 | ||||
chr1:161166164-161166614 | Common:4; Rare:110; Clinvar:5; Clinvar (benign):2 | ||||
chr1:161167085-161167127 | Rare:11 | ||||
chr1:161177228-161177315 | Rare:25 | ||||
chr1:161177368-161177635 | Common:1; Rare:81 | ||||
chr1:161177760-161177905 | Rare:19 |