Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:98933518-98933799 | Rare:60 | ||||
chr5:100900663-100900851 | Rare:34 | ||||
chr5:108727788-108727907 | Common:1; Rare:19 | ||||
chr5:108727913-108727935 | Rare:7 | ||||
chr5:112162128-112162225 | Rare:15 | ||||
chr5:127229233-127229355 | Common:1; Rare:24 | ||||
chr5:128083062-128083196 | Common:8; Rare:40 | ||||
chr5:131379719-131379937 | Rare:40 | ||||
chr5:131747383-131747528 | Rare:14 | ||||
chr5:132426703-132426840 | Rare:21 | ||||
chr5:137752741-137752804 | Rare:7 | ||||
chr5:137752996-137753217 | Common:1; Rare:77 | ||||
chr5:139325516-139325793 | Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
chr5:139368692-139368740 | Rare:12 | ||||
chr5:139392973-139393152 | Rare:61 |