Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111755512-111755744 | Common:3; Rare:80 | ||||
chr1:112619075-112619242 | Rare:63 | ||||
chr1:112619643-112619883 | Common:2; Rare:85 | ||||
chr1:112956144-112956437 | Common:4; Rare:126; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073095-113073250 | Common:1; Rare:61 | ||||
chr1:113759466-113759616 | Common:1; Rare:49 | ||||
chr1:113812251-113812591 | Common:2; Rare:134 | ||||
chr1:113904824-113905425 | Common:7; Rare:178; Clinvar (benign):1 | ||||
chr1:113979416-113979582 | Rare:52 | ||||
chr1:114510784-114511153 | Common:2; Rare:139 | ||||
chr1:114581579-114581829 | Common:1; Rare:112 | ||||
chr1:115089435-115089622 | Common:3; Rare:76 | ||||
chr1:116399200-116399510 | Rare:53 | ||||
chr1:116570937-116571180 | Common:2; Rare:72 | ||||
chr1:116667672-116667869 | Common:1; Rare:69 |