Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10472415-10472730 | Rare:78 | ||||
chr1:10474857-10474996 | Rare:43; Clinvar:3 | ||||
chr1:10693431-10693490 | Common:2; Rare:3 | ||||
chr1:10694422-10694579 | Rare:46 | ||||
chr1:11012273-11012452 | Rare:43 | ||||
chr1:11013037-11013175 | Rare:47 | ||||
chr1:11016891-11017193 | Common:1; Rare:70 | ||||
chr1:11059923-11060283 | Common:2; Rare:111 | ||||
chr1:11071954-11072168 | Common:1; Rare:69 | ||||
chr1:11080494-11080839 | Common:16; Rare:112 | ||||
chr1:11099329-11099486 | Rare:39 | ||||
chr1:11099722-11099939 | Common:3; Rare:84 | ||||
chr1:11262490-11262839 | Common:2; Rare:104 | ||||
chr1:11272906-11273250 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273429-11273555 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 |