Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42773362-42773484 | Rare:37 | ||||
chr17:42833373-42833501 | Rare:51 | ||||
chr17:42964409-42964520 | Rare:55 | ||||
chr17:42998330-42998548 | Common:4; Rare:66 | ||||
chr17:43125344-43125714 | Rare:87; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170303-43170497 | Common:2; Rare:39 | ||||
chr17:43170982-43171251 | Rare:87 | ||||
chr17:43778878-43779062 | Rare:42 | ||||
chr17:44070612-44070918 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44111228-44111453 | Rare:61 | ||||
chr17:44186666-44187002 | Common:1; Rare:121 | ||||
chr17:44187161-44187274 | Rare:31 | ||||
chr17:44324717-44324987 | Common:4; Rare:96 | ||||
chr17:44350506-44351455 | Common:1; Rare:297; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
chr17:44352050-44352451 | Rare:138; Clinvar:13; Clinvar (benign):5; Clinvar (pathogenic):2 |