Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112396046-112396285 | Common:1; Rare:72 | ||||
chr1:112619101-112619236 | Rare:49 | ||||
chr1:112619642-112619870 | Common:1; Rare:82 | ||||
chr1:112707076-112707248 | Rare:60 | ||||
chr1:112956117-112956510 | Common:5; Rare:154; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073081-113073261 | Common:1; Rare:73 | ||||
chr1:113390187-113390573 | Common:1; Rare:101 | ||||
chr1:113390724-113391193 | Common:3; Rare:126 | ||||
chr1:113391206-113391349 | Rare:32 | ||||
chr1:113904781-113905402 | Common:7; Rare:180; Clinvar (benign):2 | ||||
chr1:114511201-114511330 | Common:3; Rare:45 | ||||
chr1:114581565-114581775 | Common:1; Rare:105 | ||||
chr1:114757925-114758078 | Common:2; Rare:51 | ||||
chr1:114780539-114780805 | Common:1; Rare:102 | ||||
chr1:115089455-115089612 | Common:2; Rare:59 |