| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:8942-9433 | |||||
| chrM:9485-9586 | |||||
| chrM:9755-10098 | |||||
| chrM:10256-11166 | |||||
| chrM:12793-13157 | |||||
| chrM:13288-14223 | |||||
| chrM:14273-14821 | |||||
| chrM:14978-15894 | |||||
| chrX:1392049-1392421 | Common:6; Rare:168 | ||||
| chrX:7927365-7927498 | Common:1; Rare:36 | ||||
| chrX:11111139-11111299 | Common:1; Rare:28 | ||||
| chrX:13734584-13734789 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chrX:19887529-19887599 | Rare:2 | ||||
| chrX:31266905-31267070 | Common:1; Rare:46 | ||||
| chrX:38220831-38221023 | Rare:45 |