Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:31148430-31148566 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr13:31204632-31204844 | Rare:24 | ||||
chr13:31281300-31281365 | Rare:12 | ||||
chr13:32264375-32264788 | Common:1; Rare:62 | ||||
chr13:32268151-32268265 | Common:2; Rare:14 | ||||
chr13:32278675-32278811 | Rare:18 | ||||
chr13:32286793-32287093 | Rare:57 | ||||
chr13:32439562-32439851 | Common:1; Rare:42 | ||||
chr13:32500608-32500857 | Common:1; Rare:50 | ||||
chr13:32526732-32526794 | Common:1; Rare:10 | ||||
chr13:32528629-32528829 | Common:1; Rare:32 | ||||
chr13:32530734-32530883 | Common:1; Rare:30 | ||||
chr13:32768822-32769014 | Common:2; Rare:27 | ||||
chr13:32771973-32772285 | Rare:67 | ||||
chr13:33092683-33092907 | Common:1; Rare:44 |