Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:214603388-214603567 | Common:2; Rare:33 | ||||
chr1:215567022-215567247 | Common:2; Rare:58 | ||||
chr1:215567248-215567712 | Common:1; Rare:148 | ||||
chr1:215567725-215567974 | Rare:62 | ||||
chr1:216723318-216723651 | Rare:89 | ||||
chr1:217630997-217631465 | Common:4; Rare:141 | ||||
chr1:218284883-218284980 | Common:2; Rare:23 | ||||
chr1:218285031-218285350 | Common:4; Rare:121 | ||||
chr1:218345764-218345942 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
chr1:218345952-218346312 | Common:5; Rare:85; Clinvar:9; Clinvar (benign):3 | ||||
chr1:218346757-218346798 | Rare:7 | ||||
chr1:218347354-218347391 | Common:1; Rare:6 | ||||
chr1:219173740-219173942 | Common:2; Rare:110 | ||||
chr1:219174114-219174184 | Rare:13 | ||||
chr1:220046199-220046376 | Rare:43 |