Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:227947516-227947814 | Common:2; Rare:74 | ||||
chr1:227947823-227948151 | Common:3; Rare:99 | ||||
chr1:228081972-228082173 | Rare:41 | ||||
chr1:228082426-228082982 | Common:6; Rare:184 | ||||
chr1:228082989-228083163 | Rare:62 | ||||
chr1:228087944-228088154 | Common:2; Rare:42 | ||||
chr1:228102404-228102795 | Common:1; Rare:145 | ||||
chr1:228102848-228103517 | Common:3; Rare:237 | ||||
chr1:228109171-228109637 | Rare:127 | ||||
chr1:228139771-228140451 | Common:4; Rare:194 | ||||
chr1:228140460-228140686 | Common:1; Rare:49 | ||||
chr1:228141250-228141410 | Rare:33 | ||||
chr1:228141577-228141727 | Rare:49 | ||||
chr1:228165406-228166356 | Common:2; Rare:349; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
chr1:228213120-228213242 | Rare:29 |