Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:17922606-17923018 | Common:5; Rare:162 | ||||
chr8:18084820-18084843 | Common:1; Rare:10; Clinvar (benign):1 | ||||
chr8:21919419-21919773 | Common:2; Rare:133 | ||||
chr8:22245020-22245452 | Common:2; Rare:154 | ||||
chr8:22367148-22367338 | Common:5; Rare:75 | ||||
chr8:22604542-22604826 | Common:1; Rare:106 | ||||
chr8:23068988-23069219 | Rare:94 | ||||
chr8:23164022-23164238 | Rare:45 | ||||
chr8:23224889-23225203 | Common:2; Rare:97 | ||||
chr8:23341162-23341239 | Common:1; Rare:25 | ||||
chr8:23457617-23457771 | Common:2; Rare:62 | ||||
chr8:23854489-23854580 | Rare:31 | ||||
chr8:25458393-25458743 | Common:3; Rare:105 | ||||
chr8:26293076-26293220 | Common:1; Rare:28 | ||||
chr8:26382922-26383133 | Common:3; Rare:93 |