Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40691590-40691863 | Common:1; Rare:120 | ||||
chr1:40692026-40692296 | Common:2; Rare:86 | ||||
chr1:42035892-42036128 | Common:1; Rare:59 | ||||
chr1:42335163-42335375 | Common:5; Rare:101 | ||||
chr1:42456219-42456590 | Common:1; Rare:116 | ||||
chr1:42682154-42682494 | Common:2; Rare:97 | ||||
chr1:42682569-42682724 | Common:1; Rare:64 | ||||
chr1:42766975-42767314 | Common:5; Rare:116; Clinvar (benign):1 | ||||
chr1:42816961-42817158 | Common:1; Rare:61 | ||||
chr1:42817185-42817625 | Rare:132 | ||||
chr1:42846392-42846657 | Common:1; Rare:76 | ||||
chr1:42958644-42959078 | Common:4; Rare:112; Clinvar:6; Clinvar (benign):8 | ||||
chr1:42959160-42959532 | Common:2; Rare:81 | ||||
chr1:43171873-43172359 | Common:4; Rare:176 | ||||
chr1:43172493-43172730 | Common:6; Rare:60 |