Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:1594435-1594649 | Common:3; Rare:86 | ||||
chr5:1633909-1634049 | Common:2; Rare:45 | ||||
chr5:2124906-2125125 | Common:1; Rare:43 | ||||
chr5:8457537-8457765 | Common:2; Rare:86 | ||||
chr5:11236618-11236726 | Rare:25 | ||||
chr5:11346208-11346403 | Rare:38 | ||||
chr5:13931159-13931461 | Common:3; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
chr5:14142843-14142959 | Common:1; Rare:24 | ||||
chr5:14250117-14250321 | Common:1; Rare:46 | ||||
chr5:14264737-14264880 | Common:1; Rare:46 | ||||
chr5:16465100-16465148 | Rare:16 | ||||
chr5:17802301-17802545 | Common:3; Rare:36 | ||||
chr5:17807176-17807206 | Rare:8 | ||||
chr5:17807215-17807362 | Common:1; Rare:26 | ||||
chr5:17990289-17990487 | Common:1; Rare:37 |