Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117367323-117367490 | Common:4; Rare:58 | ||||
chr1:117605771-117606079 | Rare:95 | ||||
chr1:117929546-117929800 | Common:2; Rare:75 | ||||
chr1:119140640-119140748 | Rare:30 | ||||
chr1:121184907-121185088 | Rare:62 | ||||
chr1:145823869-145824088 | Rare:80 | ||||
chr1:145824091-145824331 | Rare:69 | ||||
chr1:145858996-145859172 | Rare:51 | ||||
chr1:145918680-145919042 | Common:2; Rare:82 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145957961-145958295 | Rare:78 | ||||
chr1:145964573-145964767 | Rare:46 | ||||
chr1:145994927-145995478 | Rare:230 | ||||
chr1:145995998-145996883 | Common:2; Rare:341 | ||||
chr1:147172420-147172779 | Common:1; Rare:92 |