Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:37671614-37671939 | Common:12; Rare:120 | ||||
chr2:38875886-38876036 | Common:1; Rare:51 | ||||
chr2:39437121-39437464 | Common:3; Rare:121 | ||||
chr2:43226597-43226865 | Common:2; Rare:105 | ||||
chr2:46616979-46617215 | Common:6; Rare:85 | ||||
chr2:46915733-46915858 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
chr2:53786992-53787086 | Rare:37 | ||||
chr2:53970983-53971089 | Common:3; Rare:40 | ||||
chr2:54457047-54457276 | Common:1; Rare:93 | ||||
chr2:61017429-61017747 | Common:1; Rare:91; Clinvar:1 | ||||
chr2:61144935-61145116 | Common:2; Rare:53 | ||||
chr2:61177203-61177539 | Common:5; Rare:140 | ||||
chr2:61888382-61888699 | Common:1; Rare:146 | ||||
chr2:63588731-63589010 | Rare:86 | ||||
chr2:63840822-63841025 | Common:1; Rare:56 |