Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:175181654-175181740 | Common:3; Rare:44 | ||||
chr2:176002232-176002398 | Common:2; Rare:69 | ||||
chr2:176129586-176129727 | Rare:83 | ||||
chr2:177212416-177212817 | Common:4; Rare:162 | ||||
chr2:177263427-177263651 | Common:1; Rare:51 | ||||
chr2:177264630-177264860 | Common:2; Rare:74 | ||||
chr2:177392672-177392876 | Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
chr2:178451083-178451378 | Common:6; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
chr2:180980287-180980545 | Common:1; Rare:85 | ||||
chr2:181891664-181892058 | Common:4; Rare:163 | ||||
chr2:183078679-183078765 | Rare:10 | ||||
chr2:183124273-183124452 | Common:1; Rare:62 | ||||
chr2:186485976-186486354 | Common:3; Rare:107 | ||||
chr2:186589881-186590029 | Rare:43 | ||||
chr2:188974218-188974329 | Rare:27 |