Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42964422-42964512 | Rare:41 | ||||
chr17:42980478-42980538 | Rare:22 | ||||
chr17:42998390-42998522 | Common:4; Rare:44 | ||||
chr17:43125344-43125592 | Rare:49; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171043-43171236 | Rare:56 | ||||
chr17:43398890-43398994 | Rare:27 | ||||
chr17:43778925-43779111 | Common:1; Rare:46 | ||||
chr17:44070612-44070911 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123588-44123824 | Common:3; Rare:70 | ||||
chr17:44186666-44187032 | Common:1; Rare:128 | ||||
chr17:44220845-44221147 | Common:1; Rare:106 | ||||
chr17:44221211-44221398 | Rare:54 | ||||
chr17:44222103-44222351 | Rare:50 | ||||
chr17:44308441-44308619 | Common:1; Rare:54 | ||||
chr17:44324765-44324982 | Common:2; Rare:79 |