Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20333265-20333471 | Common:1; Rare:40 | ||||
chr14:20343219-20343652 | Common:12; Rare:244 | ||||
chr14:20413418-20413531 | Common:3; Rare:32 | ||||
chr14:20455042-20455287 | Common:2; Rare:73 | ||||
chr14:20684438-20684629 | Common:2; Rare:31; Clinvar (benign):2 | ||||
chr14:20989739-20990062 | Common:5; Rare:82 | ||||
chr14:20999161-20999243 | Rare:18 | ||||
chr14:21024965-21025191 | Rare:84 | ||||
chr14:21025697-21025814 | Common:1; Rare:24 | ||||
chr14:21383884-21384252 | Common:8; Rare:117 | ||||
chr14:21384365-21384448 | Rare:34 | ||||
chr14:21437221-21437396 | Common:3; Rare:75 | ||||
chr14:21456042-21456470 | Common:4; Rare:108 | ||||
chr14:21476580-21476775 | Rare:88 | ||||
chr14:21476868-21477278 | Common:2; Rare:134 |