Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:214280970-214281259 | Common:2; Rare:123 | ||||
chr1:214551222-214551349 | Common:1; Rare:46 | ||||
chr1:214551554-214551939 | Common:2; Rare:123 | ||||
chr1:217631020-217631385 | Common:3; Rare:104 | ||||
chr1:218345764-218346134 | Common:5; Rare:108; Clinvar:10; Clinvar (benign):4 | ||||
chr1:218346838-218346943 | Rare:25; Clinvar:6; Clinvar (pathogenic):1 | ||||
chr1:219173757-219173900 | Common:1; Rare:76 | ||||
chr1:219174770-219174985 | Rare:36 | ||||
chr1:220093889-220094246 | Common:12; Rare:116; Clinvar (benign):2 | ||||
chr1:221742060-221742288 | Rare:60 | ||||
chr1:222589851-222589972 | Common:2; Rare:32 | ||||
chr1:222617791-222618119 | Common:3; Rare:80 | ||||
chr1:222644146-222644392 | Common:1; Rare:74 | ||||
chr1:222712459-222712881 | Common:3; Rare:149 | ||||
chr1:222713243-222713425 | Common:1; Rare:56 |