Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209805942-209806705 | Common:8; Rare:176; Clinvar:3; Clinvar (benign):2 | ||||
chr1:209827837-209828198 | Common:1; Rare:103 | ||||
chr1:211259075-211259395 | Common:1; Rare:102 | ||||
chr1:211259526-211259575 | Common:1; Rare:22 | ||||
chr1:211259735-211260038 | Rare:86 | ||||
chr1:211579034-211579175 | Rare:35 | ||||
chr1:211579179-211579503 | Rare:103 | ||||
chr1:211675615-211675767 | Rare:26 | ||||
chr1:212035494-212035803 | Common:2; Rare:87 | ||||
chr1:212285055-212285624 | Common:4; Rare:166 | ||||
chr1:212432778-212433117 | Rare:89 | ||||
chr1:212608473-212608791 | Common:1; Rare:82 | ||||
chr1:212615672-212616072 | Common:4; Rare:57 | ||||
chr1:212791723-212791930 | Common:5; Rare:93 | ||||
chr1:212858099-212858303 | Common:4; Rare:53; Clinvar:2 |