Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:65081234-65081393 | Common:2; Rare:52 | ||||
chr7:65750284-65750483 | Common:3; Rare:40 | ||||
chr7:65750916-65751144 | Common:4; Rare:98 | ||||
chr7:65770719-65770916 | Common:6; Rare:62 | ||||
chr7:66493507-66493751 | Common:4; Rare:101 | ||||
chr7:66592308-66592411 | Common:2; Rare:38 | ||||
chr7:66654275-66654573 | Common:2; Rare:95 | ||||
chr7:66844821-66845050 | Rare:95 | ||||
chr7:67302409-67302696 | Common:5; Rare:94 | ||||
chr7:73005886-73006154 | Rare:22 | ||||
chr7:74040191-74040261 | Rare:10 | ||||
chr7:74059744-74059939 | Rare:55; Clinvar (benign):1 | ||||
chr7:74062290-74062521 | Rare:44 | ||||
chr7:74890532-74890836 | Common:2; Rare:102 | ||||
chr7:75358962-75359246 | Common:1; Rare:9 |