Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:36346301-36346454 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
chr13:37000744-37000815 | Rare:31; Clinvar (pathogenic):1 | ||||
chr13:37059600-37059726 | Common:1; Rare:45 | ||||
chr13:39038113-39038439 | Common:1; Rare:79 | ||||
chr13:40789393-40789621 | Common:2; Rare:77; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41060915-41061068 | Common:13; Rare:83 | ||||
chr13:41061415-41061645 | Common:2; Rare:67 | ||||
chr13:41263552-41263610 | Rare:13 | ||||
chr13:43879492-43879602 | Rare:33 | ||||
chr13:43879691-43879867 | Common:18; Rare:56 | ||||
chr13:44989432-44989610 | Rare:67 | ||||
chr13:45341040-45341525 | Common:4; Rare:233 | ||||
chr13:48001246-48001405 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):4 | ||||
chr13:48976420-48976662 | Common:3; Rare:87 | ||||
chr13:49247830-49247982 | Rare:47 |