Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42577671-42577858 | Common:1; Rare:92 | ||||
chr17:42798672-42798778 | Rare:33 | ||||
chr17:42833378-42833468 | Rare:39 | ||||
chr17:43125344-43125643 | Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43545621-43545809 | Common:1; Rare:46 | ||||
chr17:44070612-44070942 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186663-44186982 | Common:1; Rare:122 | ||||
chr17:44324777-44324989 | Common:2; Rare:77 | ||||
chr17:44503377-44503630 | Rare:111 | ||||
chr17:44899375-44899729 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060987-45061339 | Common:2; Rare:93 | ||||
chr17:46225353-46225479 | Common:1; Rare:33 | ||||
chr17:46818724-46818924 | Rare:42 | ||||
chr17:46923048-46923187 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47649607-47649941 | Common:1; Rare:129 |