Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161045878-161046057 | Common:1; Rare:46 | ||||
chr1:161118012-161118129 | Rare:52 | ||||
chr1:161132431-161132703 | Common:1; Rare:95 | ||||
chr1:161199040-161199226 | Rare:33 | ||||
chr1:161225768-161226069 | Common:10; Rare:44 | ||||
chr1:161309838-161310266 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
chr1:161314262-161314414 | Common:3; Rare:57; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766080-161766364 | Common:3; Rare:75 | ||||
chr1:162023622-162023956 | Common:1; Rare:93 | ||||
chr1:162632253-162632576 | Rare:63 | ||||
chr1:162790481-162790789 | Common:4; Rare:84 | ||||
chr1:163321713-163322000 | Common:1; Rare:78 | ||||
chr1:165445097-165445259 | Common:1; Rare:35 | ||||
chr1:165768738-165768933 | Common:1; Rare:76 | ||||
chr1:166839322-166839522 | Rare:57 |