Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42798654-42798778 | Rare:40 | ||||
chr17:42833276-42833547 | Rare:88 | ||||
chr17:42964436-42964512 | Rare:36 | ||||
chr17:43125351-43125701 | Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171034-43171267 | Common:1; Rare:74 | ||||
chr17:43778911-43779041 | Rare:28 | ||||
chr17:44070584-44070947 | Common:3; Rare:122; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123599-44123863 | Common:3; Rare:76 | ||||
chr17:44186672-44187002 | Common:1; Rare:117 | ||||
chr17:44187161-44187315 | Common:1; Rare:41 | ||||
chr17:44221273-44221427 | Rare:46 | ||||
chr17:44324771-44324982 | Common:2; Rare:76 | ||||
chr17:44345057-44345321 | Rare:55; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503371-44503714 | Rare:134 | ||||
chr17:44899374-44899736 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 |