Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207822670-207822882 | Common:1; Rare:42 | ||||
chr1:210233732-210234125 | Common:8; Rare:112 | ||||
chr1:212638503-212638785 | Common:2; Rare:31 | ||||
chr1:223766287-223766414 | Common:2; Rare:38 | ||||
chr1:223992554-223992905 | Common:5; Rare:116 | ||||
chr1:225842164-225842407 | Rare:70 | ||||
chr1:225844633-225844755 | Rare:37 | ||||
chr1:225850066-225850341 | Common:3; Rare:72 | ||||
chr1:225856696-225856942 | Common:6; Rare:79 | ||||
chr1:234531202-234531364 | Common:1; Rare:25 | ||||
chr1:244451039-244451248 | Common:2; Rare:52 | ||||
chr1:244863744-244863839 | Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
chr1:244970941-244971245 | Rare:87 | ||||
chr10:3129568-3129914 | Common:2; Rare:135 | ||||
chr10:3783015-3783325 | Common:1; Rare:50 |