Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12001633-12001857 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
chr1:12137195-12137454 | Common:2; Rare:47 | ||||
chr1:12143696-12143907 | Common:3; Rare:47 | ||||
chr1:12230940-12231104 | Common:1; Rare:36 | ||||
chr1:12231352-12231423 | Rare:10 | ||||
chr1:12618355-12618542 | Common:1; Rare:38 | ||||
chr1:12618560-12618692 | Common:1; Rare:29 | ||||
chr1:12619037-12619228 | Rare:37 | ||||
chr1:12619296-12619339 | Rare:11 | ||||
chr1:12745360-12745592 | Rare:30 | ||||
chr1:12851755-12851877 | Common:2; Rare:21 | ||||
chr1:13587365-13587598 | Common:2; Rare:40 | ||||
chr1:13593604-13593790 | Common:2; Rare:37 | ||||
chr1:13593950-13594154 | Rare:32 | ||||
chr1:13599886-13600029 | Common:2; Rare:17 |