Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201118620-201118792 | Rare:26 | ||||
chr2:201451444-201451820 | Common:2; Rare:96 | ||||
chr2:201642637-201642770 | Rare:68 | ||||
chr2:201780890-201781247 | Common:3; Rare:109; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202238447-202238656 | Rare:74; Clinvar:1 | ||||
chr2:202911624-202911971 | Common:1; Rare:73 | ||||
chr2:202912128-202912293 | Common:2; Rare:56 | ||||
chr2:203014552-203014925 | Common:1; Rare:119 | ||||
chr2:203328091-203328400 | Common:2; Rare:113 | ||||
chr2:206085772-206085965 | Common:1; Rare:55 | ||||
chr2:206159384-206159989 | Common:3; Rare:182 | ||||
chr2:206765276-206765654 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165937-207166088 | Rare:26 | ||||
chr2:207529713-207530100 | Common:3; Rare:116 | ||||
chr2:207625227-207625565 | Common:1; Rare:92 |