chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 32053963 32053964 A G 15 GENIC homozygous 139130574 12 32054165 32054166 A G 22 GENIC homozygous 139130575 12 32054169 32054170 A G 22 GENIC homozygous 144923002 12 32054447 32054448 G A 13 GENIC possibly homozygous 139130576 12 32054781 32054782 C T 23 GENIC homozygous 139130577 12 32055160 32055163 CCC 17 GENIC homozygous 139052327 12 32055476 32055476 T 7 GENIC homozygous 139052328 12 32055802 32055802 ACTG 7 GENIC homozygous 139052329 12 32056582 32056583 G C 20 GENIC homozygous 139130583 12 32055465 32055466 A T 7 GENIC homozygous 139130579 12 32055878 32055879 T C 8 GENIC homozygous 139130580 12 32055881 32055882 C G 8 GENIC homozygous 139130581 12 32056567 32056568 C T 19 GENIC homozygous 139130582 12 32056743 32056744 A G 19 GENIC homozygous 139130584 12 32057027 32057028 T C 14 GENIC homozygous 139130585 12 32057257 32057257 T 16 GENIC homozygous 139052330 12 32057374 32057375 T C 12 GENIC homozygous 139130586 12 32057637 32057638 C T 21 GENIC homozygous 139130588 12 32057686 32057687 T G 27 GENIC homozygous 139130589 12 32058041 32058042 G A 24 GENIC homozygous 139130590 12 32058063 32058064 A G 23 GENIC homozygous 139130591 12 32058175 32058176 A G 17 GENIC homozygous 139130592 12 32058607 32058608 A G 31 GENIC homozygous 139130593 12 32058934 32058935 C A 19 GENIC homozygous 139130594 12 32059341 32059342 G C 35 GENIC homozygous 139130595 12 32059397 32059398 C G 34 GENIC homozygous 139130596 12 32059711 32059712 C G 18 GENIC homozygous 139130597 12 32059905 32059905 C 20 GENIC homozygous 139052333 12 32059925 32059926 A G 16 GENIC homozygous 139130598