Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161159389-161159520 | Common:1; Rare:34 | ||||
chr1:161166257-161166511 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197206-161197416 | Common:2; Rare:37 | ||||
chr1:161198945-161199326 | Rare:61 | ||||
chr1:161199711-161200025 | Common:3; Rare:42 | ||||
chr1:161201874-161202025 | Common:1; Rare:23 | ||||
chr1:161215118-161215367 | Common:2; Rare:79 | ||||
chr1:161225768-161226085 | Common:10; Rare:46 | ||||
chr1:161307424-161307621 | Rare:44 | ||||
chr1:161314262-161314412 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161524254-161524546 | Common:5; Rare:91 | ||||
chr1:161549789-161549898 | Rare:39 | ||||
chr1:161631108-161631375 | Common:8; Rare:99 | ||||
chr1:161749739-161749822 | Rare:32 | ||||
chr1:161750257-161750351 | Rare:23 |