Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38873306-38873554 | Common:3; Rare:85 | ||||
chr1:39026228-39026401 | Common:1; Rare:45 | ||||
chr1:40040444-40040807 | Common:3; Rare:111 | ||||
chr1:40161152-40161402 | Common:1; Rare:66 | ||||
chr1:40257909-40258282 | Common:4; Rare:100; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508661-40508814 | Common:4; Rare:42 | ||||
chr1:40691596-40691864 | Common:1; Rare:118 | ||||
chr1:40979621-40979765 | Common:1; Rare:51 | ||||
chr1:42682158-42682436 | Common:2; Rare:70 | ||||
chr1:42766970-42767337 | Common:6; Rare:128; Clinvar (benign):1 | ||||
chr1:42816938-42817136 | Common:1; Rare:55 | ||||
chr1:42817203-42817686 | Rare:133 | ||||
chr1:42846392-42846636 | Common:1; Rare:68 | ||||
chr1:42958800-42959078 | Common:4; Rare:76; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172071-43172334 | Common:3; Rare:103 |