Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:1048865-1049092 | Common:2; Rare:118 | ||||
chr10:1049334-1049490 | Common:5; Rare:72 | ||||
chr10:1056702-1056866 | Common:3; Rare:61 | ||||
chr10:6202769-6202936 | Common:4; Rare:43 | ||||
chr10:7787934-7788263 | Common:1; Rare:136 | ||||
chr10:8053442-8053664 | Rare:60 | ||||
chr10:11164830-11165148 | Common:1; Rare:68 | ||||
chr10:11165351-11165507 | Rare:48 | ||||
chr10:12129458-12129726 | Rare:109 | ||||
chr10:12195825-12195969 | Rare:34 | ||||
chr10:13099943-13100205 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):4 | ||||
chr10:13300037-13300171 | Rare:50; Clinvar:1 | ||||
chr10:14008133-14008320 | Rare:50 | ||||
chr10:14008406-14008477 | Rare:15 | ||||
chr10:14008484-14008626 | Common:1; Rare:33 |