Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:90289931-90290144 | Common:4; Rare:40 | ||||
chr1:91007297-91007334 | Rare:2 | ||||
chr1:91518574-91518764 | Rare:22 | ||||
chr1:92841460-92841802 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93083133-93083240 | Rare:22 | ||||
chr1:93090344-93090460 | Common:3; Rare:20 | ||||
chr1:93133729-93134198 | Rare:135 | ||||
chr1:93154679-93155038 | Common:3; Rare:108 | ||||
chr1:93338514-93338590 | Rare:14 | ||||
chr1:93834347-93834638 | Common:1; Rare:56 | ||||
chr1:93835917-93836158 | Common:4; Rare:56 | ||||
chr1:96623420-96623667 | Common:1; Rare:49 | ||||
chr1:96722420-96722554 | Common:2; Rare:45 | ||||
chr1:96796741-96797090 | Rare:66 | ||||
chr1:96805676-96805945 | Rare:41 |