Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111204345-111204654 | Rare:78 | ||||
chr1:111503599-111503797 | Rare:36 | ||||
chr1:111619542-111619942 | Common:2; Rare:122 | ||||
chr1:111739339-111739560 | Common:2; Rare:57 | ||||
chr1:111755672-111755771 | Common:1; Rare:39 | ||||
chr1:112395987-112396281 | Common:1; Rare:90 | ||||
chr1:112619091-112619236 | Rare:54 | ||||
chr1:112619634-112619877 | Common:2; Rare:86 | ||||
chr1:112956137-112956514 | Common:5; Rare:153; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073095-113073250 | Common:1; Rare:61 | ||||
chr1:113390176-113390531 | Common:1; Rare:90 | ||||
chr1:113812251-113812576 | Common:2; Rare:131 | ||||
chr1:113904742-113905414 | Common:7; Rare:200; Clinvar (benign):2 | ||||
chr1:114669982-114670181 | Rare:63 | ||||
chr1:114757925-114758144 | Common:3; Rare:70 |