Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:136728141-136728371 | Common:7; Rare:97 | ||||
chrM:302-816 | |||||
chrM:979-1017 | |||||
chrM:1843-2281 | |||||
chrM:5071-5119 | |||||
chrM:6525-6688 | |||||
chrM:13638-13718 | |||||
chrM:15424-15800 | |||||
chrX:24076600-24076892 | Common:1; Rare:28 | ||||
chrX:48482412-48482665 | Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
chrX:49173138-49173405 | Rare:56 | ||||
chrX:56564854-56564871 | Rare:3 | ||||
chrX:78113862-78114142 | Rare:74; Clinvar:2 |