chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 122206547 122206548 G T 28 GENIC possibly homozygous 118418333 7 122207651 122207652 T C 35 GENIC homozygous 118418334 7 122207899 122207900 T G 29 GENIC homozygous 115860320 7 122207900 122207901 C G 29 GENIC homozygous 115860322 7 122209496 122209497 G C 12 GENIC homozygous 115860332 7 122212538 122212539 G A 26 GENIC homozygous 116225930 7 122213905 122213906 C T 19 GENIC possibly homozygous 118418337 7 122214100 122214101 G A 22 GENIC possibly homozygous 118418338 7 122216161 122216162 T A 26 GENIC homozygous 116225931 7 122220891 122220892 G C 20 GENIC homozygous 118418339 7 122221714 122221715 A G 28 GENIC homozygous 118418340 7 122222709 122222710 G A 30 GENIC homozygous 118418342 7 122223634 122223635 C T 30 GENIC homozygous 118418343 7 122223933 122223934 T C 24 GENIC homozygous 116225932 7 122225715 122225716 T C 27 GENIC possibly homozygous 116225935 7 122227933 122227934 A G 24 GENIC possibly homozygous 118418344 7 122229412 122229413 T C 17 GENIC homozygous 116225938 7 122229684 122229685 A G 24 GENIC homozygous 116225939 7 122231302 122231303 T C 18 GENIC homozygous 116225940