Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44002819-44003006 | Common:4; Rare:50 | ||||
chr19:44072035-44072187 | Common:1; Rare:36 | ||||
chr19:44113120-44113460 | Common:5; Rare:78 | ||||
chr19:44141500-44141643 | Common:1; Rare:19 | ||||
chr19:44304984-44305141 | Rare:43 | ||||
chr19:44356661-44356809 | Common:1; Rare:25 | ||||
chr19:44643793-44643997 | Rare:53 | ||||
chr19:44954911-44955026 | Common:2; Rare:33 | ||||
chr19:45092853-45093220 | Common:3; Rare:111 | ||||
chr19:45370529-45370722 | Common:1; Rare:59 | ||||
chr19:45406359-45406685 | Common:2; Rare:80 | ||||
chr19:45496996-45497227 | Common:1; Rare:78 | ||||
chr19:45584768-45585077 | Common:4; Rare:116; Clinvar:2; Clinvar (benign):4 | ||||
chr19:45692332-45692706 | Common:1; Rare:85 | ||||
chr19:45768231-45768276 | Rare:20 |