Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100346451-100346663 | Common:3; Rare:47 | ||||
chr10:100346946-100347475 | Common:3; Rare:125 | ||||
chr10:100529831-100530018 | Common:1; Rare:50 | ||||
chr10:100535904-100536028 | Rare:61 | ||||
chr10:100912654-100912979 | Common:1; Rare:94 | ||||
chr10:100913317-100913415 | Rare:30 | ||||
chr10:100987176-100987954 | Common:2; Rare:217; Clinvar:3; Clinvar (benign):4 | ||||
chr10:100996969-100997144 | Common:2; Rare:47 | ||||
chr10:101031093-101031295 | Common:1; Rare:48 | ||||
chr10:101588107-101588357 | Rare:108; Clinvar:1 | ||||
chr10:101694748-101695165 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
chr10:101695173-101695284 | Rare:23 | ||||
chr10:101783362-101783479 | Rare:54 | ||||
chr10:101788171-101788415 | Rare:39 | ||||
chr10:101792921-101792962 | Rare:11 |