Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrM:12669-12809 | |||||
chrM:14274-14316 | |||||
chrM:14514-14749 | |||||
chrM:14750-15005 | |||||
chrX:38220805-38221017 | Rare:47 | ||||
chrX:57121497-57121596 | Common:1; Rare:21 | ||||
chrX:103356215-103356535 | Common:1; Rare:50 | ||||
chrX:108091480-108091788 | Rare:82 | ||||
chrX:119468215-119468506 | Common:3; Rare:98 | ||||
chrX:152830717-152831094 | Common:2; Rare:66 | ||||
chrX:153794334-153794667 | Common:1; Rare:108; Clinvar (benign):2 | ||||
chrX:154428471-154428698 | Common:2; Rare:40 | ||||
chrX:154547550-154547640 | Common:1; Rare:24; Clinvar (benign):1 |