Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:149402-149553 | Common:4; Rare:65 | ||||
chr7:601925-602072 | Common:1; Rare:31 | ||||
chr7:1532804-1533042 | Common:1; Rare:59 | ||||
chr7:1742249-1742326 | Common:1; Rare:25 | ||||
chr7:5421918-5422192 | Common:2; Rare:92 | ||||
chr7:5823010-5823171 | Common:3; Rare:62 | ||||
chr7:15685901-15686287 | Common:1; Rare:165 | ||||
chr7:15688007-15688420 | Common:2; Rare:112 | ||||
chr7:24979553-24979557 | Rare:2 | ||||
chr7:26193313-26193696 | Rare:139; Clinvar (benign):2 | ||||
chr7:32728737-32728849 | Common:4; Rare:37 | ||||
chr7:44467783-44467881 | Common:3; Rare:24 | ||||
chr7:44986597-44986742 | Common:2; Rare:74 | ||||
chr7:45768931-45769141 | Common:1; Rare:61 | ||||
chr7:47328226-47328325 | Rare:24 |