Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28138133-28138229 | Common:1; Rare:30 | ||||
chr13:28658948-28659032 | Rare:28 | ||||
chr13:28659049-28659194 | Rare:63; Clinvar (pathogenic):1 | ||||
chr13:28659533-28659818 | Common:1; Rare:74 | ||||
chr13:28718797-28719123 | Common:1; Rare:82 | ||||
chr13:29595697-29595855 | Common:2; Rare:70 | ||||
chr13:29849829-29850225 | Common:1; Rare:114 | ||||
chr13:29850319-29850435 | Common:2; Rare:35 | ||||
chr13:30306832-30307175 | Common:5; Rare:92 | ||||
chr13:30307383-30307613 | Common:3; Rare:76 | ||||
chr13:30463529-30463864 | Common:2; Rare:83 | ||||
chr13:30465754-30466134 | Common:1; Rare:118 | ||||
chr13:30616970-30617162 | Rare:33 | ||||
chr13:30617235-30617366 | Rare:25 | ||||
chr13:30617474-30618046 | Common:1; Rare:184 |