Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:125822999-125823041 | Common:1; Rare:8; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125823051-125823081 | Rare:4 | ||||
chr10:125823170-125823620 | Common:2; Rare:163; Clinvar:1; Clinvar (benign):2 | ||||
chr10:125895723-125896062 | Common:1; Rare:20 | ||||
chr10:125896228-125896656 | Common:5; Rare:41 | ||||
chr10:126388045-126388150 | Rare:22 | ||||
chr10:126388386-126388505 | Common:1; Rare:29 | ||||
chr10:126388617-126388778 | Rare:43 | ||||
chr10:126904951-126905038 | Common:1; Rare:20 | ||||
chr10:126905253-126905553 | Rare:115 | ||||
chr10:126905595-126905718 | Rare:37 | ||||
chr10:126905907-126906074 | Common:1; Rare:53 | ||||
chr10:127196379-127196504 | Common:1; Rare:25 | ||||
chr10:127906888-127907385 | Common:6; Rare:131 | ||||
chr10:128047376-128047686 | Common:4; Rare:109 |