Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147172360-147172765 | Common:1; Rare:111 | ||||
chr1:147270311-147270486 | Common:1; Rare:38 | ||||
chr1:147270878-147270974 | Rare:31; Clinvar:1 | ||||
chr1:147669562-147669613 | Common:1; Rare:12 | ||||
chr1:147669616-147669693 | Common:2; Rare:11 | ||||
chr1:147670218-147670278 | Rare:16 | ||||
chr1:149886659-149886924 | Common:1; Rare:82 | ||||
chr1:149887960-149888215 | Rare:52 | ||||
chr1:149927703-149927829 | Rare:50; Clinvar (benign):3 | ||||
chr1:149936812-149937183 | Common:1; Rare:70 | ||||
chr1:150067114-150067358 | Common:4; Rare:45 | ||||
chr1:150067650-150067888 | Rare:67 | ||||
chr1:150150077-150150286 | Common:2; Rare:64 | ||||
chr1:150151010-150151093 | Rare:31 | ||||
chr1:150235734-150235900 | Common:2; Rare:28 |