Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168225943-168226050 | Common:1; Rare:37 | ||||
chr1:173477050-173477440 | Common:5; Rare:140 | ||||
chr1:173824402-173824684 | Rare:49 | ||||
chr1:174999648-175000088 | Common:1; Rare:125 | ||||
chr1:186375212-186375545 | Rare:75 | ||||
chr1:186375692-186375878 | Common:1; Rare:46 | ||||
chr1:193059308-193059653 | Rare:158 | ||||
chr1:193186567-193186636 | Rare:12 | ||||
chr1:212791777-212791916 | Common:2; Rare:51 | ||||
chr1:217631051-217631323 | Common:2; Rare:62 | ||||
chr1:218346127-218346393 | Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr1:225999316-225999616 | Common:2; Rare:100 | ||||
chr1:231241112-231241231 | Rare:61 | ||||
chr1:231528583-231528689 | Common:1; Rare:31 | ||||
chr1:243255755-243256067 | Rare:85; Clinvar:3 |