Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42998639-42998837 | Rare:45 | ||||
chr17:43011974-43012209 | Common:1; Rare:54 | ||||
chr17:43125474-43125590 | Rare:16; Clinvar (benign):1 | ||||
chr17:43170297-43170375 | Rare:16 | ||||
chr17:43171024-43171245 | Rare:68 | ||||
chr17:43778917-43779076 | Rare:34 | ||||
chr17:44070636-44070918 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44078866-44079153 | Common:3; Rare:75 | ||||
chr17:44123577-44123844 | Common:3; Rare:77 | ||||
chr17:44186658-44187002 | Common:1; Rare:127 | ||||
chr17:44219007-44219266 | Common:1; Rare:82 | ||||
chr17:44220830-44221039 | Rare:65 | ||||
chr17:44324774-44325023 | Common:2; Rare:87 | ||||
chr17:44350277-44350454 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
chr17:44503363-44503676 | Rare:131 |