chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 44011190 44011191 T G 36 GENIC possibly homozygous 115390198 12 44016186 44016187 A T 48 GENIC homozygous 115390200 12 44016887 44016888 A G 49 GENIC homozygous 115390202 12 44017080 44017081 C A 47 GENIC possibly homozygous 115390204 12 44017648 44017649 A G 42 GENIC homozygous 115390206 12 44020947 44020948 A G 30 GENIC homozygous 115390208 12 44021630 44021631 G A 42 GENIC homozygous 115390210 12 44022382 44022383 A T 51 GENIC homozygous 115390212 12 44011676 44011677 T C 40 GENIC homozygous 115336608 12 44012288 44012289 A G 38 GENIC homozygous 115336610 12 44029184 44029185 T C 15 GENIC homozygous 115336614 12 44022487 44022490 GCG 48 GENIC homozygous 128993922 12 44013979 44013981 AT 24 GENIC possibly homozygous 131119312 12 44018568 44018568 ATCAATCT 33 GENIC homozygous 131119313 12 44022390 44022391 A 50 GENIC homozygous 131119315 12 44029184 44029184 GGGCA 16 GENIC homozygous 128993923