Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:107672131-107672273 | Rare:42 | ||||
chr5:108728231-108728365 | Rare:50 | ||||
chr5:112161701-112161781 | Rare:22 | ||||
chr5:112162118-112162229 | Rare:19 | ||||
chr5:112162234-112162279 | Rare:12 | ||||
chr5:119300248-119300327 | Rare:21 | ||||
chr5:122801881-122802088 | Common:1; Rare:52 | ||||
chr5:127966557-127966743 | Rare:34 | ||||
chr5:128084458-128084704 | Common:2; Rare:79 | ||||
chr5:131159881-131160088 | Rare:38 | ||||
chr5:131160599-131160713 | Rare:10 | ||||
chr5:131313129-131313250 | Rare:39 | ||||
chr5:131527372-131527629 | Common:1; Rare:50 | ||||
chr5:132587578-132587954 | Common:1; Rare:80; Clinvar:18; Clinvar (benign):6 | ||||
chr5:132609115-132609397 | Common:1; Rare:87; Clinvar:21; Clinvar (benign):10; Clinvar (pathogenic):7 |