Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrM:8428-8585 | |||||
chrM:8655-9547 | |||||
chrM:9727-10000 | |||||
chrM:10055-10110 | |||||
chrM:10160-10472 | |||||
chrM:13563-14222 | |||||
chrM:14273-14773 | |||||
chrM:14895-15187 | |||||
chrX:1391996-1392016 | Rare:7 | ||||
chrX:7927680-7927768 | Rare:14 | ||||
chrX:19887549-19887600 | Rare:2 | ||||
chrX:23782906-23783195 | Common:5; Rare:58 | ||||
chrX:24054375-24054678 | Common:4; Rare:45 | ||||
chrX:24054883-24055009 | Rare:47 | ||||
chrX:46545348-46545540 | Common:2; Rare:38; Clinvar (benign):2 |