Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:21427809-21428249 | Common:6; Rare:172 | ||||
chr7:21945861-21946196 | Common:3; Rare:96 | ||||
chr7:22193682-22193965 | Rare:91 | ||||
chr7:22822704-22822985 | Common:3; Rare:106 | ||||
chr7:23105642-23106009 | Common:4; Rare:164; Clinvar:4; Clinvar (benign):3 | ||||
chr7:23106156-23106398 | Common:2; Rare:61 | ||||
chr7:23106412-23106672 | Common:2; Rare:45 | ||||
chr7:23181891-23182117 | Rare:92 | ||||
chr7:23299193-23299431 | Common:2; Rare:124 | ||||
chr7:23470294-23470572 | Rare:85 | ||||
chr7:23470609-23470746 | Rare:32 | ||||
chr7:23531948-23532141 | Common:2; Rare:77 | ||||
chr7:23597246-23597476 | Common:1; Rare:77 | ||||
chr7:24757374-24757490 | Common:3; Rare:35 | ||||
chr7:24757749-24757857 | Rare:30 |