Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:37420300-37420780 | Common:2; Rare:122 | ||||
chr18:37448345-37448745 | Common:5; Rare:156 | ||||
chr18:37450640-37451100 | Common:4; Rare:153 | ||||
chr18:37452890-37453400 | Common:5; Rare:148 | ||||
chr18:39800242-39800348 | Rare:42 | ||||
chr18:45324371-45325155 | Common:13; Rare:329 | ||||
chr18:46089630-46089882 | Common:3; Rare:114; Clinvar (benign):3 | ||||
chr18:46293747-46294033 | Rare:37 | ||||
chr18:46294401-46294561 | Rare:34 | ||||
chr18:46321940-46322270 | Common:5; Rare:118 | ||||
chr18:46322420-46322692 | Common:2; Rare:91 | ||||
chr18:46335520-46335860 | Rare:106 | ||||
chr18:47157467-47157851 | Rare:158; Clinvar (benign):4 | ||||
chr18:47945408-47945853 | Common:2; Rare:109 | ||||
chr18:47967980-47968360 | Common:3; Rare:122 |