Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:75410266-75410362 | Rare:3 | ||||
chr7:88218925-88219109 | Rare:46 | ||||
chr7:91267701-91267777 | Rare:10 | ||||
chr7:96321307-96321540 | Common:2; Rare:59 | ||||
chr7:98386579-98386879 | Common:1; Rare:54 | ||||
chr7:99403398-99403668 | Rare:66 | ||||
chr7:100094255-100094514 | Rare:92 | ||||
chr7:100335859-100336160 | Common:1; Rare:101 | ||||
chr7:100678043-100678159 | Rare:46 | ||||
chr7:102822436-102822735 | Common:4; Rare:42 | ||||
chr7:105013031-105013199 | Rare:60 | ||||
chr7:105013581-105013620 | Rare:14 | ||||
chr7:105013628-105013646 | Rare:6 | ||||
chr7:105110066-105110308 | Common:1; Rare:58 | ||||
chr7:107926268-107926584 | Common:1; Rare:89; Clinvar (benign):2 |