Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373636-234373775 | Rare:53; Clinvar (benign):3 | ||||
chr1:234608183-234608318 | Rare:45 | ||||
chr1:235128768-235129048 | Rare:114 | ||||
chr1:236064991-236065353 | Common:3; Rare:131; Clinvar (pathogenic):1 | ||||
chr1:236523508-236523786 | Common:3; Rare:61 | ||||
chr1:236541385-236541692 | Common:13; Rare:72 | ||||
chr1:236604486-236604633 | Common:4; Rare:41 | ||||
chr1:243255045-243255127 | Rare:22 | ||||
chr1:243255136-243255359 | Common:1; Rare:45 | ||||
chr1:243255772-243256124 | Rare:101; Clinvar:4 | ||||
chr1:244835160-244835333 | Rare:67 | ||||
chr1:244835616-244835736 | Common:1; Rare:56; Clinvar (benign):4 | ||||
chr1:244863994-244864581 | Common:1; Rare:194; Clinvar:3; Clinvar (benign):5 | ||||
chr1:244969596-244969798 | Rare:53 | ||||
chr1:244969979-244970145 | Rare:58 |