Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954185-122954484 | Rare:110 | ||||
chr10:122980365-122980478 | Common:1; Rare:34 | ||||
chr10:123008791-123009026 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124093483-124093659 | Common:2; Rare:33 | ||||
chr10:124418875-124419075 | Common:4; Rare:94; Clinvar:4; Clinvar (benign):1 | ||||
chr10:124791785-124791938 | Common:1; Rare:80 | ||||
chr10:124801733-124801835 | Rare:35 | ||||
chr10:125719440-125719805 | Common:1; Rare:137 | ||||
chr10:125823248-125823594 | Rare:115 | ||||
chr10:125896300-125896628 | Common:5; Rare:28 | ||||
chr10:126905277-126905473 | Rare:75 | ||||
chr10:131981842-131982154 | Common:4; Rare:116 | ||||
chr10:132331786-132332216 | Common:17; Rare:146 | ||||
chr10:132942558-132942764 | Common:3; Rare:54 | ||||
chr10:133308835-133308989 | Rare:72 |