Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:56333957-56334161 | Rare:61 | ||||
chr12:56468478-56468648 | Rare:70 | ||||
chr12:56521801-56522051 | Common:3; Rare:59 | ||||
chr12:56688090-56688464 | Common:5; Rare:129 | ||||
chr12:56752315-56752457 | Rare:46 | ||||
chr12:57111196-57111472 | Common:4; Rare:56 | ||||
chr12:57248707-57249119 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
chr12:57430758-57431068 | Common:1; Rare:75 | ||||
chr12:57520444-57520720 | Common:2; Rare:83 | ||||
chr12:57772081-57772215 | Rare:52 | ||||
chr12:57846372-57846479 | Rare:34 | ||||
chr12:58920153-58920340 | Common:2; Rare:57 | ||||
chr12:58920500-58920665 | Common:2; Rare:61 | ||||
chr12:62260059-62260427 | Common:1; Rare:133 | ||||
chr12:64222237-64222366 | Rare:44 |