Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:22933770-22933912 | Common:1; Rare:57 | ||||
chr18:23453169-23453356 | Rare:65 | ||||
chr18:23503298-23503576 | Common:2; Rare:103 | ||||
chr18:23586360-23586573 | Common:4; Rare:92; Clinvar:6; Clinvar (benign):3 | ||||
chr18:24397788-24398019 | Common:2; Rare:97 | ||||
chr18:24426562-24426765 | Common:4; Rare:88 | ||||
chr18:26090508-26090981 | Common:5; Rare:182 | ||||
chr18:26657380-26657476 | Rare:25 | ||||
chr18:28176968-28177219 | Common:3; Rare:123 | ||||
chr18:31102403-31102457 | Rare:14 | ||||
chr18:31498050-31498303 | Common:1; Rare:87; Clinvar:7; Clinvar (benign):6 | ||||
chr18:32018802-32018837 | Rare:11 | ||||
chr18:32092390-32092727 | Common:5; Rare:150 | ||||
chr18:35041250-35041428 | Common:1; Rare:62 | ||||
chr18:35240914-35241100 | Common:2; Rare:71 |