Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20787244-20787403 | Rare:83 | ||||
chr1:21290203-21290389 | Rare:38 | ||||
chr1:21345476-21345655 | Common:1; Rare:70 | ||||
chr1:21783086-21783272 | Common:2; Rare:66 | ||||
chr1:23368225-23368466 | Rare:72 | ||||
chr1:23559478-23559648 | Common:1; Rare:69 | ||||
chr1:23691738-23691826 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23800730-23800959 | Common:1; Rare:80 | ||||
chr1:23959641-23959894 | Common:2; Rare:70 | ||||
chr1:23980251-23980455 | Rare:67 | ||||
chr1:24642882-24643218 | Rare:99 | ||||
chr1:25232448-25232642 | Rare:79 | ||||
chr1:25247451-25247641 | Common:2; Rare:68 | ||||
chr1:25338188-25338437 | Common:1; Rare:90 | ||||
chr1:25859362-25859552 | Common:3; Rare:78 |