chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 4108567 4108568 C A 78 GENIC homozygous 782658986 17 4108679 4108680 C T 64 GENIC homozygous 782658987 17 4108683 4108684 T G 63 GENIC homozygous 782658988 17 4108733 4108734 C T 54 GENIC homozygous 782658989 17 4108849 4108850 T C 80 GENIC homozygous 782658990 17 4109002 4109003 T C 64 GENIC homozygous 782658991 17 4109201 4109202 A C 42 GENIC homozygous 782658992 17 4109301 4109302 C G 56 GENIC possibly homozygous 782658993 17 4109332 4109333 A G 50 GENIC homozygous 782658994 17 4109334 4109335 T C 52 GENIC possibly homozygous 782658995 17 4109410 4109411 T G 49 GENIC possibly homozygous 782658996 17 4109526 4109527 A G 49 GENIC homozygous 782658997 17 4109586 4109587 A G 56 GENIC homozygous 782658998 17 4109606 4109607 A G 53 GENIC homozygous 782658999