chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 42353840 42353841 C T 42 GENIC homozygous 143578403 13 42354470 42354472 AA 38 GENIC possibly homozygous 144924565 13 42354521 42354522 T C 43 GENIC homozygous 143578405 13 42354839 42354840 C T 44 GENIC homozygous 143578406 13 42355616 42355617 A G 35 GENIC homozygous 143578407 13 42355895 42355896 A G 32 GENIC homozygous 143578408 13 42356154 42356155 G A 37 GENIC homozygous 144929025 13 42356660 42356661 G A 31 GENIC homozygous 144929026 13 42356845 42356846 G A 43 GENIC homozygous 144929027 13 42356999 42357000 G C 47 GENIC homozygous 144929028 13 42357204 42357205 G A 36 GENIC homozygous 144929029 13 42357354 42357355 T C 25 GENIC homozygous 144929033 13 42357224 42357225 C T 35 GENIC homozygous 144929030 13 42357315 42357316 C T 26 GENIC homozygous 144929031 13 42357329 42357330 T C 28 GENIC homozygous 144929032 13 42357607 42357608 C A 24 GENIC homozygous 144929034 13 42357765 42357766 G A 36 GENIC homozygous 144929035 13 42357776 42357777 A G 37 GENIC homozygous 144929036 13 42357795 42357796 A G 38 GENIC homozygous 144929037 13 42357831 42357832 G A 32 GENIC homozygous 144929038 13 42358123 42358124 T C 35 GENIC homozygous 144929039 13 42358243 42358244 C T 50 GENIC homozygous 144929040 13 42358336 42358337 T C 49 GENIC homozygous 144929041 13 42358403 42358404 G A 44 GENIC homozygous 144929042