Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113490672-113491148 | Common:5; Rare:182 | ||||
chr13:113584506-113584712 | Rare:58 | ||||
chr13:113863934-113864195 | Common:2; Rare:65 | ||||
chr13:114314389-114314560 | Rare:60 | ||||
chr14:20343548-20343652 | Rare:41 | ||||
chr14:20454789-20455319 | Common:7; Rare:139 | ||||
chr14:20455474-20455691 | Rare:64 | ||||
chr14:20684478-20684608 | Common:1; Rare:19; Clinvar (benign):1 | ||||
chr14:21476619-21476747 | Rare:58 | ||||
chr14:21476878-21477257 | Common:2; Rare:118 | ||||
chr14:22589129-22589428 | Common:4; Rare:96 | ||||
chr14:22766537-22766760 | Common:1; Rare:126 | ||||
chr14:22872592-22872675 | Rare:26 | ||||
chr14:22929345-22929604 | Rare:61 | ||||
chr14:22982482-22982900 | Common:3; Rare:142 |