Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219498670-219498919 | Common:2; Rare:50 | ||||
chr2:227325209-227325311 | Common:2; Rare:36 | ||||
chr2:230416054-230416254 | Common:1; Rare:56 | ||||
chr2:231961637-231961739 | Rare:28; Clinvar:1 | ||||
chr2:232550545-232550716 | Rare:65 | ||||
chr2:233854509-233854779 | Common:4; Rare:71 | ||||
chr2:241315150-241315285 | Rare:50 | ||||
chr2:241315655-241315990 | Common:5; Rare:130 | ||||
chr20:2652438-2652635 | Common:6; Rare:63 | ||||
chr20:2840672-2840759 | Common:1; Rare:38 | ||||
chr20:3209446-3209508 | Rare:15 | ||||
chr20:4686274-4686483 | Common:1; Rare:48; Clinvar (benign):1 | ||||
chr20:13784893-13785053 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr20:17968784-17969117 | Common:3; Rare:120 | ||||
chr20:21303252-21303368 | Rare:46 |