Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:130101441-130101663 | Common:1; Rare:38 | ||||
chr8:140664916-140665238 | Common:1; Rare:79 | ||||
chr8:140715015-140715151 | Rare:18 | ||||
chr8:140963716-140964076 | Common:2; Rare:53 | ||||
chr8:141206062-141206137 | Rare:28 | ||||
chr8:143817076-143817372 | Rare:71 | ||||
chr8:143927612-143927995 | Common:4; Rare:164; Clinvar:31; Clinvar (benign):9 | ||||
chr8:143929236-143929426 | Common:1; Rare:86; Clinvar:5; Clinvar (benign):1 | ||||
chr8:143951762-143951951 | Common:1; Rare:49 | ||||
chr8:144105705-144105956 | Common:2; Rare:82; Clinvar (benign):1 | ||||
chr8:144511123-144511302 | Rare:75 | ||||
chr8:144685805-144686037 | Common:3; Rare:55 | ||||
chr8:145002825-145002955 | Common:1; Rare:41 | ||||
chr9:2827446-2827755 | Common:2; Rare:82 | ||||
chr9:3822739-3823013 | Common:1; Rare:59 |