Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227325168-227325455 | Common:6; Rare:101 | ||||
chr2:227717989-227718128 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
chr2:227871592-227871670 | Common:4; Rare:30 | ||||
chr2:229921291-229921430 | Common:2; Rare:37 | ||||
chr2:229921439-229921463 | Rare:1 | ||||
chr2:229921890-229922524 | Common:4; Rare:223 | ||||
chr2:229922881-229922997 | Rare:27 | ||||
chr2:229923167-229923258 | Rare:22 | ||||
chr2:230864574-230865038 | Common:8; Rare:115 | ||||
chr2:231198516-231198784 | Common:1; Rare:80 | ||||
chr2:231464152-231464222 | Rare:20 | ||||
chr2:231464376-231464769 | Common:3; Rare:134 | ||||
chr2:231706996-231707211 | Rare:53 | ||||
chr2:231707408-231707619 | Rare:60 | ||||
chr2:231707804-231707835 | Rare:11 |