Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:29409426-29409606 | Common:1; Rare:51 | ||||
chr10:38356227-38356428 | Common:3; Rare:49 | ||||
chr10:47553478-47553569 | Rare:7 | ||||
chr10:73247208-73247362 | Rare:83 | ||||
chr10:73730476-73730713 | Rare:47 | ||||
chr10:78248760-78248881 | Common:1; Rare:25 | ||||
chr10:87342283-87342708 | Common:5; Rare:136 | ||||
chr10:88939608-88939817 | Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
chr10:103668723-103668836 | Rare:32 | ||||
chr11:319540-319756 | Common:1; Rare:55 | ||||
chr11:7906252-7906458 | Common:3; Rare:31 | ||||
chr11:9759528-9759662 | Common:1; Rare:18 | ||||
chr11:12086326-12086604 | Common:2; Rare:49 | ||||
chr11:12086692-12086871 | Common:2; Rare:31 | ||||
chr11:65455120-65455293 | Rare:81 |