Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111739356-111739414 | Rare:18 | ||||
chr1:111755622-111755948 | Common:2; Rare:111 | ||||
chr1:112396009-112396267 | Common:1; Rare:81 | ||||
chr1:112619101-112619236 | Rare:49 | ||||
chr1:112619642-112619880 | Common:2; Rare:86 | ||||
chr1:112674261-112674504 | Common:1; Rare:58 | ||||
chr1:112707085-112707220 | Rare:45 | ||||
chr1:112956178-112956473 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073074-113073250 | Common:1; Rare:67 | ||||
chr1:113812260-113812608 | Common:2; Rare:135 | ||||
chr1:113904824-113905468 | Common:7; Rare:185; Clinvar (benign):1 | ||||
chr1:114581592-114581726 | Rare:66 | ||||
chr1:114670005-114670255 | Common:1; Rare:77 | ||||
chr1:115089462-115089566 | Rare:42 | ||||
chr1:115338224-115338285 | Rare:15 |