Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113490699-113491029 | Common:1; Rare:121 | ||||
chr13:114281529-114281650 | Common:1; Rare:66 | ||||
chr13:114281828-114282061 | Common:6; Rare:110 | ||||
chr14:20343190-20343644 | Common:12; Rare:267 | ||||
chr14:20455042-20455316 | Common:2; Rare:79 | ||||
chr14:20684418-20684639 | Common:2; Rare:38; Clinvar (benign):2 | ||||
chr14:20802779-20802970 | Common:1; Rare:26 | ||||
chr14:21025016-21025352 | Rare:103 | ||||
chr14:21025687-21025803 | Rare:22 | ||||
chr14:21456042-21456247 | Common:4; Rare:58 | ||||
chr14:21476619-21476660 | Rare:19 | ||||
chr14:21476868-21477271 | Common:2; Rare:131 | ||||
chr14:21511289-21511513 | Rare:57 | ||||
chr14:22589161-22589494 | Common:4; Rare:104 | ||||
chr14:22766541-22766719 | Common:1; Rare:94 |