Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:10689931-10689991 | Common:2; Rare:18 | ||||
chr2:11466135-11466213 | Common:2; Rare:20 | ||||
chr2:12716629-12717062 | Common:3; Rare:132 | ||||
chr2:12718177-12718248 | Common:1; Rare:15 | ||||
chr2:15561300-15561593 | Rare:81 | ||||
chr2:17753707-17754174 | Common:4; Rare:145; Clinvar (benign):1 | ||||
chr2:19901664-19901743 | Common:1; Rare:38 | ||||
chr2:19990084-19990188 | Rare:25 | ||||
chr2:20051612-20051843 | Common:1; Rare:58 | ||||
chr2:20350836-20351092 | Common:2; Rare:110 | ||||
chr2:20651067-20651200 | Rare:38 | ||||
chr2:20823055-20823171 | Rare:46 | ||||
chr2:23927066-23927301 | Common:3; Rare:85 | ||||
chr2:23940345-23940514 | Common:3; Rare:56 | ||||
chr2:24047355-24047459 | Rare:25 |