Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrM:9262-9429 | |||||
chrM:10227-10542 | |||||
chrM:14743-15254 | |||||
chrX:2929289-2929513 | Common:2; Rare:63 | ||||
chrX:7927697-7927778 | Rare:17 | ||||
chrX:10620489-10620699 | Common:1; Rare:27 | ||||
chrX:11111136-11111371 | Common:3; Rare:50 | ||||
chrX:12791302-12791439 | Rare:22 | ||||
chrX:13734557-13734823 | Common:3; Rare:84; Clinvar (benign):1 | ||||
chrX:14029801-14030024 | Common:2; Rare:66 | ||||
chrX:14873035-14873470 | Common:1; Rare:81 | ||||
chrX:15790450-15790516 | Rare:21 | ||||
chrX:16719444-16719722 | Rare:82 | ||||
chrX:19343728-19343985 | Common:5; Rare:69 | ||||
chrX:19670876-19670990 | Rare:24 |