Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179881845-179882103 | Common:3; Rare:71 | ||||
chr1:179882206-179882311 | Rare:19 | ||||
chr1:179882488-179882966 | Common:1; Rare:243; Clinvar:11; Clinvar (benign):4 | ||||
chr1:179954708-179954834 | Rare:26 | ||||
chr1:182391291-182391441 | Rare:30 | ||||
chr1:182789641-182789798 | Common:2; Rare:56 | ||||
chr1:182839205-182839367 | Common:1; Rare:66 | ||||
chr1:182839577-182839725 | Common:2; Rare:66 | ||||
chr1:183635643-183636079 | Common:3; Rare:120 | ||||
chr1:184051612-184051739 | Common:3; Rare:44 | ||||
chr1:184386883-184387354 | Common:1; Rare:106 | ||||
chr1:185156923-185157303 | Common:1; Rare:105 | ||||
chr1:186375221-186375471 | Rare:56 | ||||
chr1:186375686-186375926 | Common:1; Rare:65 | ||||
chr1:186680391-186680628 | Common:3; Rare:55 |