Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178725114-178725371 | Common:10; Rare:89 | ||||
chr1:179229564-179229822 | Common:6; Rare:68 | ||||
chr1:179293639-179293849 | Common:2; Rare:81 | ||||
chr1:179877766-179877919 | Rare:31 | ||||
chr1:179882471-179882870 | Rare:185; Clinvar:8; Clinvar (benign):2 | ||||
chr1:179954650-179954848 | Common:1; Rare:46 | ||||
chr1:180154731-180154976 | Common:3; Rare:101 | ||||
chr1:180502347-180502665 | Common:1; Rare:109 | ||||
chr1:180502816-180502963 | Rare:58 | ||||
chr1:180631966-180632270 | Common:2; Rare:107 | ||||
chr1:181022818-181023192 | Common:25; Rare:178 | ||||
chr1:181482554-181482967 | Common:2; Rare:131 | ||||
chr1:181483479-181483674 | Common:3; Rare:40 | ||||
chr1:181483907-181484131 | Rare:57 | ||||
chr1:182391744-182392053 | Common:4; Rare:108; Clinvar:4; Clinvar (benign):4 |