Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42682608-42682731 | Common:1; Rare:50 | ||||
chr1:42683269-42683465 | Common:3; Rare:78 | ||||
chr1:42766978-42767309 | Common:4; Rare:113; Clinvar (benign):1 | ||||
chr1:42816961-42817136 | Common:1; Rare:49 | ||||
chr1:42817198-42817260 | Rare:18 | ||||
chr1:42846401-42846649 | Common:1; Rare:69 | ||||
chr1:42958821-42959063 | Common:3; Rare:68; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43358662-43358986 | Common:7; Rare:102 | ||||
chr1:43367923-43368197 | Rare:69 | ||||
chr1:43389757-43389955 | Common:3; Rare:90 | ||||
chr1:43946585-43947022 | Rare:122 | ||||
chr1:44031433-44031668 | Common:2; Rare:48 | ||||
chr1:44631915-44632088 | Common:2; Rare:59 | ||||
chr1:44674411-44674731 | Common:3; Rare:84 | ||||
chr1:44775462-44775607 | Rare:55 |