Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102643210-102643420 | Common:3; Rare:44 | ||||
chr10:119908386-119908547 | Common:1; Rare:32 | ||||
chr10:124943094-124943160 | Rare:24 | ||||
chr10:132065860-132066016 | Common:1; Rare:33 | ||||
chr11:310015-310059 | Rare:10 | ||||
chr11:2138235-2138452 | Common:1; Rare:47 | ||||
chr11:3018460-3018651 | Common:1; Rare:59 | ||||
chr11:7906251-7906284 | Rare:9 | ||||
chr11:9437947-9438108 | Common:13; Rare:74 | ||||
chr11:9808047-9808320 | Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
chr11:11920248-11920455 | Common:1; Rare:46 | ||||
chr11:12676578-12676843 | Common:1; Rare:45 | ||||
chr11:14476985-14477048 | Rare:12 | ||||
chr11:27499305-27499386 | Rare:23 | ||||
chr11:34062650-34062674 | Rare:3 |