Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:137110901-137111196 | Common:1; Rare:94 | ||||
chrM:292-817 | |||||
chrM:1667-1765 | |||||
chrM:1844-1988 | |||||
chrM:1999-2067 | |||||
chrM:15250-15961 | |||||
chrM:16219-16284 | |||||
chrM:16286-16299 | |||||
chrX:15675619-15675735 | Common:1; Rare:23 | ||||
chrX:47214392-47214588 | Rare:42; Clinvar (benign):3 | ||||
chrX:47239145-47239388 | Common:1; Rare:45 | ||||
chrX:47566687-47567056 | Common:1; Rare:94 | ||||
chrX:48482402-48482698 | Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chrX:56564750-56564871 | Rare:20 | ||||
chrX:78113863-78114142 | Rare:74; Clinvar:2 |