Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817198-42817527 | Rare:109 | ||||
chr1:42846387-42846638 | Common:1; Rare:73 | ||||
chr1:42958855-42959042 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43358666-43359000 | Common:7; Rare:102 | ||||
chr1:43367961-43368180 | Rare:56 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43524947-43525142 | Rare:31 | ||||
chr1:43649852-43650211 | Rare:88 | ||||
chr1:43946629-43946983 | Rare:94 | ||||
chr1:43974788-43975042 | Common:3; Rare:68 | ||||
chr1:44631924-44632135 | Common:1; Rare:76 | ||||
chr1:44674381-44674814 | Common:3; Rare:122 | ||||
chr1:44739676-44739864 | Common:1; Rare:66 | ||||
chr1:44775447-44775607 | Rare:60 | ||||
chr1:44775822-44776140 | Common:2; Rare:115 |