chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 150508868 150508869 G A 37 GENIC homozygous 118983832 5 150509081 150509082 T C 17 GENIC homozygous 114539690 5 150509412 150509413 G A 21 GENIC homozygous 118983833 5 150510136 150510137 C T 29 GENIC homozygous 114539692 5 150511952 150511953 T C 31 GENIC homozygous 114539712 5 150516480 150516481 C T 24 GENIC homozygous 118983834 5 150516481 150516482 C G 24 GENIC homozygous 118983835 5 150518710 150518711 T C 30 GENIC homozygous 114539806 5 150518888 150518889 C A 31 GENIC homozygous 118983836 5 150521135 150521136 G A 9 GENIC homozygous 118983837 5 150522913 150522914 G A 31 GENIC homozygous 118983838 5 150523305 150523306 T C 17 GENIC homozygous 114539830 5 150524537 150524538 C T 43 GENIC homozygous 118983839 5 150524716 150524717 A T 45 GENIC homozygous 118983840 5 150524848 150524849 A C 35 GENIC homozygous 118983841 5 150530813 150530814 A G 15 GENIC homozygous 118983842 5 150530954 150530955 A G 17 GENIC homozygous 118983843 5 150531056 150531057 T G 22 GENIC homozygous 114539834