Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160128832-160129042 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:173864904-173865052 | Common:2; Rare:46 | ||||
chr1:184504066-184504280 | Rare:38 | ||||
chr1:184664132-184664195 | Rare:16 | ||||
chr1:185316103-185316366 | Common:1; Rare:62 | ||||
chr1:197201257-197201529 | Common:1; Rare:93 | ||||
chr1:204288317-204288597 | Common:2; Rare:54 | ||||
chr1:204451055-204451099 | Rare:5 | ||||
chr1:207064629-207065017 | Common:1; Rare:94 | ||||
chr1:207822669-207823045 | Common:1; Rare:74 | ||||
chr1:207823977-207824239 | Common:3; Rare:36 | ||||
chr1:211382746-211382858 | Common:1; Rare:48 | ||||
chr1:218345307-218345339 | Rare:5 | ||||
chr1:220253455-220253558 | Common:1; Rare:27 | ||||
chr1:220880011-220880085 | Rare:23 |