Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236281927-236282258 | Common:6; Rare:98 | ||||
chr1:236604486-236604624 | Common:4; Rare:41 | ||||
chr1:236795067-236795422 | Common:6; Rare:145; Clinvar:3 | ||||
chr1:239386434-239386603 | Common:1; Rare:26 | ||||
chr1:241848123-241848204 | Rare:16 | ||||
chr1:243255040-243255433 | Common:1; Rare:96 | ||||
chr1:243255752-243256140 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244050936-244051398 | Rare:70 | ||||
chr1:244451879-244452078 | Rare:68 | ||||
chr1:244835128-244835333 | Rare:83 | ||||
chr1:244835583-244835736 | Common:1; Rare:67; Clinvar (benign):4 | ||||
chr1:244863001-244863268 | Common:4; Rare:113 | ||||
chr1:244864393-244864728 | Common:1; Rare:138 | ||||
chr1:244970251-244970413 | Common:3; Rare:76 | ||||
chr1:246566209-246566515 | Common:1; Rare:102 |