Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:17758935-17759225 | Common:1; Rare:52 | ||||
chr2:19021140-19021346 | Rare:33 | ||||
chr2:19355297-19355461 | Common:1; Rare:28 | ||||
chr2:19962961-19962986 | Rare:1 | ||||
chr2:20035970-20036109 | Rare:22 | ||||
chr2:20037483-20037598 | Rare:24 | ||||
chr2:20258405-20258498 | Rare:22 | ||||
chr2:20277865-20278171 | Rare:58 | ||||
chr2:20283166-20283353 | Rare:54 | ||||
chr2:20425089-20425163 | Common:1; Rare:11 | ||||
chr2:20448343-20448659 | Common:2; Rare:87 | ||||
chr2:20448664-20449071 | Common:3; Rare:103 | ||||
chr2:20687970-20688132 | Rare:30 | ||||
chr2:25242612-25242741 | Rare:20 | ||||
chr2:26285415-26285699 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |