Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343171-160343432 | Rare:106 | ||||
chr1:161045866-161046057 | Common:1; Rare:49 | ||||
chr1:161117953-161118141 | Rare:92 | ||||
chr1:161132412-161132872 | Common:2; Rare:139 | ||||
chr1:161197274-161197448 | Common:3; Rare:34 | ||||
chr1:161314285-161314405 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161766198-161766367 | Common:3; Rare:56 | ||||
chr1:163321706-163322134 | Common:1; Rare:112 | ||||
chr1:165698482-165698742 | Common:4; Rare:108 | ||||
chr1:165768756-165769019 | Common:2; Rare:104 | ||||
chr1:167722075-167722179 | Rare:19 | ||||
chr1:167935882-167936266 | Common:1; Rare:105 | ||||
chr1:167936556-167936955 | Common:1; Rare:141 | ||||
chr1:169367728-169368254 | Common:3; Rare:113 | ||||
chr1:169485936-169486158 | Rare:55; Clinvar:1 |