Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161045887-161046050 | Common:1; Rare:44 | ||||
chr1:161117977-161118141 | Rare:87 | ||||
chr1:161132574-161132862 | Common:2; Rare:84 | ||||
chr1:161199053-161199183 | Rare:23 | ||||
chr1:161225787-161226082 | Common:9; Rare:42 | ||||
chr1:161314265-161314405 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161749756-161749837 | Rare:35 | ||||
chr1:161750231-161750422 | Rare:47 | ||||
chr1:161766136-161766372 | Common:3; Rare:68 | ||||
chr1:162561346-162561740 | Common:4; Rare:149 | ||||
chr1:162790558-162790789 | Common:4; Rare:67 | ||||
chr1:162855768-162855973 | Rare:42 | ||||
chr1:163321732-163322105 | Common:1; Rare:101 | ||||
chr1:165630891-165631277 | Common:6; Rare:99 | ||||
chr1:165768760-165768942 | Common:1; Rare:77 |