Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42455993-42456590 | Common:1; Rare:182 | ||||
chr1:42658280-42658466 | Common:2; Rare:53 | ||||
chr1:42682136-42682465 | Common:2; Rare:89 | ||||
chr1:42682576-42682766 | Common:1; Rare:73 | ||||
chr1:42683249-42683466 | Common:3; Rare:90 | ||||
chr1:42767010-42767309 | Common:4; Rare:95; Clinvar (benign):1 | ||||
chr1:42817024-42817136 | Common:1; Rare:26 | ||||
chr1:42817225-42817461 | Rare:90 | ||||
chr1:42846392-42846666 | Common:1; Rare:79 | ||||
chr1:42958785-42959100 | Common:4; Rare:83; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172221-43172341 | Common:1; Rare:61 | ||||
chr1:43358655-43359006 | Common:7; Rare:113 | ||||
chr1:43367961-43368216 | Rare:68 | ||||
chr1:43389757-43389964 | Common:4; Rare:92 | ||||
chr1:43707363-43707547 | Common:2; Rare:49 |