HVR sequences | Mutations | Comments |
1 | 16093C | this variant appeared in about 5% of most haplogroups, but most commonly in K |
| 16221T | indicates the H5 sub-clade of H |
| 16519C | corresponds to a hotspot; it appears in almost every haplogoup, in over half of them |
2 | 263G | determinates the H haplogroup |
| 309.1C | is one of the most recurrent mutation |
| 315.1C | most members of H also have this mutation |