Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228088957-228089127 | Rare:34 | ||||
chr1:228275993-228276240 | Common:1; Rare:72 | ||||
chr1:228457043-228457174 | Common:1; Rare:34 | ||||
chr1:229333156-229333428 | Common:11; Rare:142 | ||||
chr1:229486811-229486896 | Rare:13 | ||||
chr1:229498260-229498572 | Rare:81 | ||||
chr1:229930901-229931183 | Common:1; Rare:37 | ||||
chr1:230186334-230186481 | Common:2; Rare:24 | ||||
chr1:231025881-231026067 | Common:1; Rare:25 | ||||
chr1:231269702-231269741 | Common:1; Rare:7 | ||||
chr1:231270337-231270572 | Common:1; Rare:51 | ||||
chr1:231336255-231336459 | Rare:58 | ||||
chr1:231350468-231350943 | Common:4; Rare:72 | ||||
chr1:231359945-231360227 | Common:3; Rare:50 | ||||
chr1:231366440-231366555 | Common:7; Rare:35; Clinvar (benign):1 |