Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrM:9182-9735 | |||||
chrM:10224-10494 | |||||
chrM:12029-12138 | |||||
chrM:12303-12582 | |||||
chrM:14533-14834 | |||||
chrX:2751921-2752148 | Common:1; Rare:49 | ||||
chrX:11111199-11111368 | Common:3; Rare:34 | ||||
chrX:11759440-11759657 | Rare:27 | ||||
chrX:13734551-13734849 | Common:3; Rare:90; Clinvar (benign):1 | ||||
chrX:14029800-14030024 | Common:2; Rare:66 | ||||
chrX:14873027-14873474 | Common:1; Rare:85 | ||||
chrX:16719382-16719690 | Rare:78 | ||||
chrX:19670869-19670990 | Rare:24 | ||||
chrX:23667280-23667573 | Common:3; Rare:89 | ||||
chrX:23907872-23908157 | Rare:63 |