Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75784605-75784872 | Common:2; Rare:113 | ||||
chr17:75855323-75855658 | Common:1; Rare:78 | ||||
chr17:75979096-75979283 | Rare:51; Clinvar:4 | ||||
chr17:76103712-76103867 | Common:4; Rare:49 | ||||
chr17:76501385-76501558 | Rare:60; Clinvar (benign):3 | ||||
chr17:76726775-76726858 | Common:4; Rare:45 | ||||
chr17:76737309-76737546 | Common:3; Rare:94 | ||||
chr17:76737914-76738119 | Common:3; Rare:57 | ||||
chr17:78187045-78187364 | Common:3; Rare:100 | ||||
chr17:78782219-78782549 | Common:6; Rare:102 | ||||
chr17:79009761-79009924 | Common:7; Rare:44 | ||||
chr17:80035855-80036030 | Common:1; Rare:61 | ||||
chr17:80220320-80220468 | Common:1; Rare:56; Clinvar:1 | ||||
chr17:81656521-81656680 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
chr17:81666565-81666753 | Common:1; Rare:79 |