Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161020836-161021008 | Rare:51 | ||||
chr1:161038894-161039011 | Rare:43 | ||||
chr1:161040267-161040450 | Rare:38 | ||||
chr1:161045860-161046042 | Common:1; Rare:46 | ||||
chr1:161088927-161089217 | Common:2; Rare:56 | ||||
chr1:161089223-161089750 | Common:1; Rare:141 | ||||
chr1:161117956-161118140 | Rare:89 | ||||
chr1:161132435-161132705 | Common:1; Rare:94 | ||||
chr1:161153736-161154108 | Common:1; Rare:114; Clinvar (pathogenic):1 | ||||
chr1:161159392-161159555 | Common:1; Rare:51 | ||||
chr1:161166263-161166516 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161167527-161167658 | Common:1; Rare:43 | ||||
chr1:161199051-161199320 | Rare:43 | ||||
chr1:161225768-161226072 | Common:10; Rare:44 | ||||
chr1:161314333-161314412 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 |