Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:50450322-50450466 | Common:1; Rare:65 | ||||
chr7:56051405-56051884 | Common:1; Rare:180; Clinvar:5; Clinvar (benign):1 | ||||
chr7:56106413-56106713 | Common:8; Rare:103 | ||||
chr7:66114794-66114898 | Common:1; Rare:50 | ||||
chr7:66115177-66115354 | Common:1; Rare:41 | ||||
chr7:66681942-66682175 | Common:5; Rare:97 | ||||
chr7:66921154-66921424 | Common:1; Rare:81 | ||||
chr7:66996557-66996865 | Common:2; Rare:68 | ||||
chr7:72828175-72828472 | Rare:76 | ||||
chr7:73308794-73308870 | Rare:31 | ||||
chr7:73578536-73578953 | Common:14; Rare:117 | ||||
chr7:73683399-73683659 | Common:3; Rare:118 | ||||
chr7:74254385-74254497 | Rare:49 | ||||
chr7:75914944-75915164 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr7:76047939-76048197 | Common:2; Rare:90 |