Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109283100-109283305 | Common:1; Rare:49 | ||||
chr1:109548462-109548693 | Common:4; Rare:88 | ||||
chr1:109619777-109619864 | Rare:19 | ||||
chr1:109656023-109656132 | Common:2; Rare:38 | ||||
chr1:110407625-110407795 | Common:2; Rare:79 | ||||
chr1:111140041-111140259 | Common:1; Rare:76 | ||||
chr1:112396055-112396257 | Common:1; Rare:63 | ||||
chr1:112619106-112619173 | Rare:28 | ||||
chr1:112619643-112619860 | Common:1; Rare:77 | ||||
chr1:112707091-112707287 | Rare:68 | ||||
chr1:112956169-112956473 | Common:5; Rare:132; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113905010-113905392 | Common:5; Rare:111 | ||||
chr1:113979297-113979502 | Rare:51 | ||||
chr1:114152920-114153056 | Common:2; Rare:38 | ||||
chr1:115089470-115089556 | Rare:34 |