Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999679-175000152 | Common:3; Rare:151 | ||||
chr1:176207226-176207344 | Common:1; Rare:61 | ||||
chr1:178093610-178093789 | Common:1; Rare:45 | ||||
chr1:178341318-178341461 | Rare:27 | ||||
chr1:178725131-178725347 | Common:10; Rare:78 | ||||
chr1:178871037-178871192 | Rare:29 | ||||
chr1:179293672-179293876 | Common:3; Rare:66 | ||||
chr1:179365669-179365988 | Common:6; Rare:78 | ||||
chr1:179575917-179576139 | Common:2; Rare:46 | ||||
chr1:179882158-179882324 | Common:1; Rare:32 | ||||
chr1:179882493-179882898 | Rare:205; Clinvar:9; Clinvar (benign):2 | ||||
chr1:180502348-180502668 | Common:1; Rare:112 | ||||
chr1:181088494-181088700 | Rare:67 | ||||
chr1:182839164-182839391 | Common:1; Rare:99 | ||||
chr1:183472258-183472515 | Common:2; Rare:92 |