Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619112-112619205 | Rare:31 | ||||
chr1:112619744-112619842 | Common:1; Rare:39 | ||||
chr1:112707091-112707220 | Rare:43 | ||||
chr1:112956175-112956422 | Common:4; Rare:109; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073089-113073221 | Common:1; Rare:45 | ||||
chr1:113759120-113759167 | Rare:14 | ||||
chr1:113812216-113812579 | Common:2; Rare:148 | ||||
chr1:113905022-113905392 | Common:5; Rare:103 | ||||
chr1:113979297-113979468 | Rare:34 | ||||
chr1:114152914-114153052 | Common:2; Rare:39 | ||||
chr1:114581577-114581858 | Common:1; Rare:123 | ||||
chr1:114716713-114716862 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
chr1:114757947-114758118 | Common:3; Rare:52 | ||||
chr1:114780549-114780743 | Rare:76 | ||||
chr1:115089461-115089623 | Common:3; Rare:62 |