Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343216-160343421 | Rare:82 | ||||
chr1:160400358-160400608 | Common:1; Rare:62 | ||||
chr1:161021386-161021580 | Common:1; Rare:48 | ||||
chr1:161038894-161039022 | Common:1; Rare:46 | ||||
chr1:161045887-161046042 | Common:1; Rare:40 | ||||
chr1:161089486-161089686 | Rare:54 | ||||
chr1:161118019-161118146 | Rare:64 | ||||
chr1:161132431-161132862 | Common:2; Rare:139 | ||||
chr1:161166268-161166499 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161199053-161199081 | Rare:8 | ||||
chr1:161225768-161226072 | Common:10; Rare:44 | ||||
chr1:161749763-161749829 | Rare:30 | ||||
chr1:163321752-163322023 | Common:1; Rare:73 | ||||
chr1:165768772-165768938 | Common:1; Rare:74 | ||||
chr1:167220678-167220900 | Common:1; Rare:53 |