Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156054660-156054910 | Common:3; Rare:69 | ||||
chr1:156061027-156061215 | Common:1; Rare:47 | ||||
chr1:156135032-156135312 | Common:2; Rare:63; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr1:156136040-156136436 | Common:4; Rare:126; Clinvar:22; Clinvar (benign):19; Clinvar (pathogenic):8 | ||||
chr1:156212952-156213049 | Rare:30 | ||||
chr1:156282605-156282948 | Common:3; Rare:117 | ||||
chr1:156284186-156284371 | Rare:41 | ||||
chr1:156338153-156338570 | Common:2; Rare:152 | ||||
chr1:156500762-156500992 | Common:1; Rare:85 | ||||
chr1:156591678-156591855 | Common:4; Rare:93 | ||||
chr1:156601410-156601678 | Common:2; Rare:79 | ||||
chr1:156728396-156728489 | Common:1; Rare:20 | ||||
chr1:156741029-156741272 | Rare:71 | ||||
chr1:156767383-156767574 | Common:1; Rare:63 | ||||
chr1:157138316-157138642 | Common:3; Rare:97 |