Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27254875-27255128 | Common:2; Rare:71 | ||||
chr13:27449964-27450278 | Common:3; Rare:99 | ||||
chr13:27450526-27450752 | Common:2; Rare:84 | ||||
chr13:27620602-27620812 | Common:1; Rare:58 | ||||
chr13:28658966-28659191 | Rare:102; Clinvar (pathogenic):1 | ||||
chr13:30306846-30307161 | Common:5; Rare:80 | ||||
chr13:30463963-30464194 | Common:2; Rare:57 | ||||
chr13:30616953-30617107 | Rare:28 | ||||
chr13:30617605-30618000 | Common:1; Rare:123 | ||||
chr13:32428140-32428505 | Rare:65 | ||||
chr13:33818013-33818106 | Common:1; Rare:25 | ||||
chr13:36346346-36346439 | Common:1; Rare:19; Clinvar (benign):1 | ||||
chr13:36999322-36999484 | Rare:50 | ||||
chr13:37000501-37000809 | Common:3; Rare:96 | ||||
chr13:37059617-37059747 | Common:1; Rare:41 |