Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119686712-119687112 | Common:2; Rare:108 | ||||
chr1:119712568-119712956 | Common:3; Rare:143 | ||||
chr1:119737080-119737370 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:119779940-119780310 | Rare:119 | ||||
chr1:119868301-119868521 | Common:1; Rare:35 | ||||
chr1:119968767-119968895 | Rare:16 | ||||
chr1:120340962-120341067 | Common:1; Rare:36 | ||||
chr1:120415510-120415960 | Common:7; Rare:124 | ||||
chr1:120558519-120558921 | Common:2; Rare:188 | ||||
chr1:120844300-120844542 | Rare:16 | ||||
chr1:120850810-120851367 | Rare:99 | ||||
chr1:121021637-121021887 | Rare:58 | ||||
chr1:121097648-121098122 | Common:9; Rare:423 | ||||
chr1:121586764-121587169 | Common:5; Rare:284 | ||||
chr1:144077110-144077650 | Rare:12 |