Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:180502529-180502711 | Rare:77 | ||||
chr1:180631861-180632039 | Common:3; Rare:52 | ||||
chr1:182391782-182392022 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):3 | ||||
chr1:182604381-182604519 | Rare:30 | ||||
chr1:182789620-182789778 | Common:2; Rare:51 | ||||
chr1:182839194-182839428 | Common:1; Rare:99 | ||||
chr1:182839542-182839752 | Common:2; Rare:91 | ||||
chr1:183472321-183472515 | Common:2; Rare:68 | ||||
chr1:183635666-183636110 | Common:5; Rare:126 | ||||
chr1:184051615-184051768 | Common:3; Rare:58 | ||||
chr1:184386725-184387087 | Common:3; Rare:113 | ||||
chr1:184754812-184755156 | Common:1; Rare:84 | ||||
chr1:185156923-185157303 | Common:1; Rare:105 | ||||
chr1:185317214-185317468 | Common:1; Rare:76 | ||||
chr1:186375087-186375450 | Rare:102 |