Furthermore, the specific subtype T1 tends to be found further east and is common in Central Asian and modern Turkic populations (Lalueza-Fox 2004), who inhabit much of the same territory as the ancient Saka, Sarmatian, Andronovo, and other putative Iranian peoples of the 2nd and 1st millennia BC.
Within subhaplogroup T2e, a very rare motif is identified among Sephardic Jews of Turkey and Bulgaria and suspected conversos from the New World (Bedford 2012).
Apart from a peak in Cyprus, T2c1 is most common in the Persian Gulf region but is also found in the Levant and in Mediterranean Europe, with a more far-flung distribution at very low levels.
[8] Additionally, haplogroup T has been observed among ancient Egyptian mummies excavated at the Abusir el-Meleq archaeological site in Middle Egypt, which date from the Pre-Ptolemaic/late New Kingdom (T1, T2), Ptolemaic (T1, T2), and Roman (undifferentiated T, T1) periods.
[9] Fossils excavated at the Late Neolithic site of Kelif el Boroud in Morocco, which have been dated to around 3,000 BCE, have also been observed to carry the T2 subclade.
[10] Additionally, haplogroup T has been observed in ancient Guanche fossils excavated in Gran Canaria and Tenerife on the Canary Islands, which have been radiocarbon-dated to between the 7th and 11th centuries CE.
[12] This phylogenetic tree of haplogroup I subclades is based on the paper (van Oven 2008) and subsequent published research (Behar 2012b).
[14] Certain medical studies had shown mitochondrial Haplogroup T to be associated with reduced sperm motility in males, although these results have been challenged (Mishmar 2002).
Assuming all relevant pedigrees are correct, this includes all female-line descendants of his female line ancestor Barbara of Celje (1390–1451), wife of Sigismund, Holy Roman Emperor.