Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:232951037-232951302 | Common:2; Rare:43 | ||||
chr1:233295404-233295803 | Common:2; Rare:132 | ||||
chr1:233327226-233327853 | Common:5; Rare:113 | ||||
chr1:233613555-233614212 | Common:8; Rare:191 | ||||
chr1:233614225-233614484 | Rare:96 | ||||
chr1:233904504-233904941 | Common:5; Rare:112 | ||||
chr1:233905005-233905223 | Common:2; Rare:65 | ||||
chr1:234373047-234373792 | Common:5; Rare:268; Clinvar (benign):7 | ||||
chr1:234373837-234374094 | Rare:68; Clinvar (benign):1 | ||||
chr1:234478205-234479087 | Common:9; Rare:322 | ||||
chr1:234479090-234479261 | Common:5; Rare:66 | ||||
chr1:234607660-234607748 | Common:1; Rare:31 | ||||
chr1:234608046-234608432 | Common:2; Rare:137 | ||||
chr1:234608485-234608657 | Common:1; Rare:87; Clinvar (benign):1 | ||||
chr1:234608711-234609043 | Common:2; Rare:139 |