Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27450119-27450215 | Common:3; Rare:29 | ||||
chr13:28659049-28659180 | Rare:58; Clinvar (pathogenic):1 | ||||
chr13:32538748-32538978 | Common:1; Rare:54 | ||||
chr13:33285697-33285880 | Rare:40 | ||||
chr13:36432342-36432504 | Common:1; Rare:52 | ||||
chr13:36999303-36999457 | Rare:58 | ||||
chr13:37000601-37000805 | Rare:70 | ||||
chr13:40771138-40771421 | Common:3; Rare:84 | ||||
chr13:41019306-41019488 | Rare:29 | ||||
chr13:41061203-41061590 | Common:3; Rare:133 | ||||
chr13:43879684-43879881 | Common:18; Rare:60 | ||||
chr13:44436760-44437038 | Common:2; Rare:86 | ||||
chr13:44989437-44989634 | Rare:77 | ||||
chr13:45120231-45120561 | Common:2; Rare:83 | ||||
chr13:45341109-45341570 | Common:4; Rare:220 |