Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:21704742-21704991 | Rare:71 | ||||
chr18:22933257-22933395 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr18:22933789-22933867 | Common:1; Rare:31 | ||||
chr18:23453172-23453339 | Rare:58 | ||||
chr18:23503308-23503603 | Common:4; Rare:120 | ||||
chr18:23586402-23586563 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
chr18:24397784-24397979 | Common:2; Rare:82 | ||||
chr18:24426613-24426786 | Common:3; Rare:65 | ||||
chr18:25350983-25351169 | Rare:62 | ||||
chr18:25352003-25352412 | Common:2; Rare:156 | ||||
chr18:26546834-26547310 | Rare:140 | ||||
chr18:28176968-28177295 | Common:3; Rare:158 | ||||
chr18:31101255-31101647 | Common:11; Rare:107 | ||||
chr18:31101914-31101999 | Common:1; Rare:21; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr18:31943098-31943423 | Common:7; Rare:109 |