Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:32188121-32188424 | Rare:57 | ||||
chr20:32475282-32475602 | Common:1; Rare:76 | ||||
chr20:32855602-32855629 | Common:1; Rare:3 | ||||
chr20:33410281-33410486 | Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr20:33812311-33812446 | Rare:16 | ||||
chr20:34096654-34096949 | Rare:53 | ||||
chr20:34102212-34102242 | Rare:5 | ||||
chr20:34290593-34290941 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
chr20:34489039-34489148 | Common:1; Rare:19 | ||||
chr20:34706757-34706845 | Rare:13 | ||||
chr20:34727690-34727843 | Rare:29 | ||||
chr20:34854842-34855066 | Rare:53 | ||||
chr20:34856571-34856834 | Common:1; Rare:52 | ||||
chr20:34860711-34860793 | Common:1; Rare:11 | ||||
chr20:35003301-35003426 | Common:2; Rare:48 |