Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:176207510-176207710 | Common:2; Rare:86 | ||||
chr1:178093621-178093815 | Common:3; Rare:64 | ||||
chr1:178094387-178094561 | Rare:75 | ||||
chr1:178341305-178341598 | Common:1; Rare:60 | ||||
chr1:178869184-178869359 | Common:1; Rare:28 | ||||
chr1:178870970-178871134 | Rare:29 | ||||
chr1:178871148-178871334 | Rare:40 | ||||
chr1:179081956-179082078 | Common:1; Rare:37 | ||||
chr1:179143052-179143221 | Rare:34 | ||||
chr1:179293614-179293907 | Common:3; Rare:96 | ||||
chr1:179365662-179365975 | Common:7; Rare:79 | ||||
chr1:179591575-179591852 | Common:1; Rare:68 | ||||
chr1:179877756-179877887 | Rare:30 | ||||
chr1:179882199-179882445 | Rare:49 | ||||
chr1:179882478-179882957 | Common:1; Rare:237; Clinvar:10; Clinvar (benign):4 |