Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:27450529-27450707 | Common:2; Rare:67 | ||||
chr13:27620440-27620799 | Common:2; Rare:120 | ||||
chr13:28138146-28138222 | Rare:20 | ||||
chr13:28659076-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
chr13:30617565-30618040 | Common:1; Rare:148 | ||||
chr13:30932605-30932709 | Rare:27 | ||||
chr13:32254100-32254329 | Common:3; Rare:57 | ||||
chr13:32315415-32315552 | Rare:42; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32428099-32428455 | Rare:67 | ||||
chr13:32586248-32586582 | Common:2; Rare:101 | ||||
chr13:33285670-33285880 | Rare:46 | ||||
chr13:36346301-36346441 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr13:37059596-37059738 | Common:1; Rare:49 | ||||
chr13:38349548-38349900 | Common:3; Rare:116; Clinvar (pathogenic):1 | ||||
chr13:38350217-38350284 | Rare:35 |