Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:50115932-50116111 | Common:3; Rare:39 | ||||
chr20:50510076-50510415 | Common:3; Rare:129 | ||||
chr20:50731711-50731770 | Rare:17 | ||||
chr20:50958467-50958874 | Common:1; Rare:156; Clinvar:2; Clinvar (benign):4 | ||||
chr20:53593769-53593894 | Common:1; Rare:44 | ||||
chr20:56392174-56392687 | Common:6; Rare:134 | ||||
chr20:57710515-57710653 | Rare:33 | ||||
chr20:57711391-57711498 | Rare:22 | ||||
chr20:58515337-58515500 | Common:3; Rare:29 | ||||
chr20:58651107-58651305 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr20:59042711-59043058 | Common:1; Rare:127 | ||||
chr20:59940266-59940481 | Rare:87 | ||||
chr20:62143299-62143739 | Common:5; Rare:185 | ||||
chr20:62182959-62183050 | Rare:21 | ||||
chr20:62238241-62238583 | Common:1; Rare:94 |