Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212284972-212286000 | Common:40; Rare:1439 | ||||
chr1:212414751-212415251 | Common:15; Rare:484 | ||||
chr1:212432578-212433050 | Common:2; Rare:496 | ||||
chr1:212608006-212608412 | Common:11; Rare:196 | ||||
chr1:212608397-212609020 | Common:6; Rare:657 | ||||
chr1:212608942-212609806 | Common:13; Rare:417 | ||||
chr1:212699270-212699500 | Rare:53 | ||||
chr1:212699760-212700355 | Common:11; Rare:260 | ||||
chr1:212791350-212792321 | Common:38; Rare:1070 | ||||
chr1:212794541-212794941 | Common:1; Rare:85 | ||||
chr1:212858004-212858404 | Common:32; Rare:479; Clinvar:14; Clinvar (benign):2 | ||||
chr1:212950260-212950660 | Common:4; Rare:178 | ||||
chr1:213014704-213015653 | Common:2; Rare:444 | ||||
chr1:213015658-213016140 | Common:5; Rare:422 | ||||
chr1:213016131-213016531 | Common:1; Rare:82 |