chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 123900994 123900995 A G 41 GENIC homozygous 796771499 X 123901333 123901334 T C 51 GENIC possibly homozygous 796771500 X 123901666 123901667 C A 39 GENIC homozygous 796771501 X 123901786 123901787 C G 42 GENIC homozygous 796771502 X 123902364 123902365 T C 21 GENIC homozygous 796771503 X 123902771 123902772 C T 37 GENIC homozygous 796771504 X 123903040 123903041 C T 46 GENIC homozygous 796771505 X 123903719 123903720 T A 39 GENIC homozygous 796771506 X 123904966 123904967 G A 36 GENIC homozygous 796771507 X 123905627 123905628 A G 39 GENIC homozygous 796771508 X 123906352 123906353 G T 28 GENIC homozygous 796771509 X 123906808 123906809 A G 48 GENIC homozygous 796771510 X 123906932 123906933 T A 49 GENIC homozygous 796771511 X 123907599 123907600 C T 34 GENIC homozygous 796771512 X 123907796 123907797 C T 26 GENIC homozygous 796771513 X 123907829 123907830 T C 17 GENIC homozygous 796771514 X 123908139 123908140 A G 53 GENIC heterozygous 796771515 X 123909136 123909137 C G 33 GENIC homozygous 796771516 X 123910070 123910071 T G 33 GENIC homozygous 796771517 X 123910074 123910075 G A 33 GENIC homozygous 796771518 X 123910082 123910083 A G 33 GENIC homozygous 796771519 X 123910759 123910760 A C 15 GENIC homozygous 796771520 X 123910765 123910766 T G 18 GENIC homozygous 796771521 X 123910855 123910856 C T 23 GENIC homozygous 796771522 X 123910914 123910915 T A 28 GENIC possibly homozygous 796771523 X 123911112 123911113 G T 21 GENIC homozygous 796771524 X 123911193 123911194 A T 22 GENIC homozygous 796771525 X 123911321 123911322 T C 34 GENIC homozygous 796771526 X 123911461 123911462 G T 43 GENIC homozygous 796771527 X 123912197 123912198 T C 37 GENIC homozygous 796771528 X 123914613 123914614 A G 62 GENIC homozygous 796771529 X 123916196 123916197 A G 46 GENIC homozygous 796771530 X 123916552 123916553 G A 37 GENIC possibly homozygous 796771531 X 123916936 123916937 A G 34 GENIC homozygous 796771532