Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93879143-93879293 | Common:2; Rare:52 | ||||
chr1:94418185-94418470 | Common:2; Rare:103 | ||||
chr1:95072876-95073008 | Rare:52 | ||||
chr1:95234034-95234251 | Common:3; Rare:76 | ||||
chr1:96721690-96721844 | Common:1; Rare:63 | ||||
chr1:97920991-97921128 | Rare:60; Clinvar:3 | ||||
chr1:99849997-99850123 | Common:1; Rare:47 | ||||
chr1:99969762-99970062 | Common:1; Rare:61 | ||||
chr1:100037988-100038122 | Common:1; Rare:55 | ||||
chr1:100132881-100133214 | Common:3; Rare:121 | ||||
chr1:100249802-100250031 | Common:4; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266107-100266301 | Common:3; Rare:72 | ||||
chr1:100894822-100894890 | Rare:12 | ||||
chr1:100895958-100896155 | Rare:54 | ||||
chr1:101025754-101025920 | Common:1; Rare:51 |