Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:40745083-40745405 | Rare:82 | ||||
chr15:40755212-40755370 | Common:1; Rare:52 | ||||
chr15:40763734-40764131 | Common:3; Rare:96 | ||||
chr15:40806997-40807125 | Rare:26 | ||||
chr15:40807376-40807771 | Common:4; Rare:127 | ||||
chr15:40828515-40828850 | Rare:76 | ||||
chr15:40843832-40844108 | Common:2; Rare:87 | ||||
chr15:40844128-40844194 | Common:1; Rare:20 | ||||
chr15:40853276-40853578 | Rare:78 | ||||
chr15:40855921-40856333 | Common:4; Rare:113 | ||||
chr15:40894361-40894477 | Rare:41 | ||||
chr15:40929132-40929343 | Common:1; Rare:52 | ||||
chr15:40953203-40953484 | Common:2; Rare:77 | ||||
chr15:41115987-41116037 | Rare:19 | ||||
chr15:41231039-41231446 | Rare:126; Clinvar (pathogenic):1 |