chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56771729 56771730 G GAAA 38 GENIC homozygous 730410996 19 56771975 56771976 C CTTTT 8 GENIC homozygous 730410997 19 56772001 56772002 T C 24 GENIC homozygous 602369147 19 56772187 56772188 A G 26 GENIC homozygous 602369148 19 56772906 56772907 G A 37 GENIC homozygous 602369149 19 56772944 56772945 C T 30 GENIC homozygous 602369150 19 56773115 56773116 A G 23 GENIC homozygous 602369151 19 56773406 56773407 C T 28 GENIC homozygous 602369152 19 56774043 56774044 A - 28 GENIC homozygous 730410998 19 56774127 56774128 T TG 33 GENIC homozygous 730410999 19 56776273 56776274 G GCACA 12 GENIC heterozygous 730411001 19 56776273 56776274 G GCACACA 12 GENIC heterozygous 730411002 19 56777283 56777284 C G 22 GENIC homozygous 601053552 19 56778175 56778176 C CT 17 GENIC homozygous 730411003 19 56778187 56778188 A T 27 GENIC homozygous 602369153 19 56778940 56778942 AT -- 22 GENIC homozygous 730411004 19 56779221 56779222 T C 25 GENIC homozygous 601053553 19 56779358 56779359 A G 23 GENIC homozygous 601053554 19 56779461 56779462 T C 41 GENIC homozygous 601053555 19 56779802 56779803 A G 32 GENIC homozygous 602369154 19 56779960 56779961 T G 31 GENIC homozygous 602369155 19 56780876 56780877 T C 13 GENIC homozygous 601053556 19 56780916 56780917 T C 14 GENIC homozygous 602369156