Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25338168-25338500 | Common:2; Rare:112 | ||||
chr1:25819889-25820034 | Common:3; Rare:45 | ||||
chr1:26110921-26111233 | Common:2; Rare:96 | ||||
chr1:26111676-26111869 | Common:1; Rare:69 | ||||
chr1:26279928-26280203 | Rare:147 | ||||
chr1:26317798-26318063 | Common:3; Rare:47 | ||||
chr1:26432098-26432433 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472127-26472627 | Common:5; Rare:168 | ||||
chr1:26473020-26473258 | Common:1; Rare:125 | ||||
chr1:26542879-26543140 | Common:2; Rare:62 | ||||
chr1:26545712-26545899 | Common:1; Rare:39 | ||||
chr1:26695608-26695712 | Rare:35 | ||||
chr1:26787877-26788207 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26889808-26889917 | Rare:40 | ||||
chr1:26900060-26900224 | Rare:63 |