Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74458065-74458525 | Common:1; Rare:143 | ||||
chr2:74459095-74459346 | Common:1; Rare:54 | ||||
chr2:74465309-74465440 | Rare:36; Clinvar:1 | ||||
chr2:74482873-74483124 | Common:1; Rare:90 | ||||
chr2:74507276-74507428 | Rare:39 | ||||
chr2:74507669-74507823 | Rare:33 | ||||
chr2:74529596-74529779 | Rare:82; Clinvar:3 | ||||
chr2:74529786-74530202 | Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74548855-74549126 | Rare:77 | ||||
chr2:74549579-74549606 | Rare:10 | ||||
chr2:74553913-74554086 | Rare:27 | ||||
chr2:74554406-74554764 | Common:2; Rare:109 | ||||
chr2:74654092-74654367 | Common:1; Rare:92 | ||||
chr2:74833908-74834147 | Rare:72 | ||||
chr2:74835127-74835302 | Rare:45 |