Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:30150987-30151049 | Common:1; Rare:13 | ||||
chr2:30151751-30152072 | Rare:68 | ||||
chr2:30152170-30152302 | Rare:26 | ||||
chr2:30158335-30158981 | Common:1; Rare:133 | ||||
chr2:32463029-32463149 | Rare:14 | ||||
chr2:33477686-33477911 | Common:3; Rare:50 | ||||
chr2:33530916-33531056 | Common:1; Rare:23 | ||||
chr2:42102063-42102105 | Rare:9 | ||||
chr2:42170226-42170348 | Rare:28 | ||||
chr2:43896688-43896857 | Rare:39; Clinvar (benign):1 | ||||
chr2:44778834-44778963 | Rare:26 | ||||
chr2:44975785-44975877 | Common:2; Rare:26 | ||||
chr2:46943988-46944139 | Common:1; Rare:35 | ||||
chr2:47818778-47818974 | Common:2; Rare:40 | ||||
chr2:47906500-47906812 | Common:2; Rare:107 |