Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73769112-73769324 | Rare:70 | ||||
chr10:73769834-73770302 | Common:1; Rare:129 | ||||
chr10:73775276-73775589 | Rare:86 | ||||
chr10:73776106-73776379 | Common:1; Rare:41 | ||||
chr10:73778732-73778929 | Common:1; Rare:34 | ||||
chr10:73844116-73844259 | Common:1; Rare:25 | ||||
chr10:73999138-73999249 | Rare:22 | ||||
chr10:73999324-73999608 | Common:1; Rare:48 | ||||
chr10:74000498-74000760 | Common:1; Rare:38 | ||||
chr10:74002912-74003091 | Common:1; Rare:32 | ||||
chr10:74003692-74003864 | Common:1; Rare:26 | ||||
chr10:74009681-74009911 | Common:2; Rare:49 | ||||
chr10:74021336-74021388 | Rare:6 | ||||
chr10:74045018-74045158 | Rare:28 | ||||
chr10:74070639-74071096 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):8 |