Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:52972652-52972841 | Common:2; Rare:45 | ||||
chr20:53593804-53593909 | Common:1; Rare:41 | ||||
chr20:54208057-54208121 | Rare:16 | ||||
chr20:56392187-56392385 | Rare:48 | ||||
chr20:56468394-56468734 | Rare:112 | ||||
chr20:58651080-58651313 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr20:58651591-58652034 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):4 | ||||
chr20:58888778-58889121 | Common:1; Rare:103 | ||||
chr20:58892344-58892659 | Common:2; Rare:86 | ||||
chr20:58910068-58910374 | Rare:82 | ||||
chr20:58981098-58981354 | Common:2; Rare:114 | ||||
chr20:59032219-59032568 | Common:3; Rare:148; Clinvar:1; Clinvar (benign):5 | ||||
chr20:59042746-59043041 | Common:1; Rare:109 | ||||
chr20:59940238-59940594 | Common:1; Rare:123 | ||||
chr20:59940774-59940933 | Common:1; Rare:42 |