chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 57623010 57623011 G A 26 GENIC homozygous 116785619 10 57624345 57624346 C T 21 GENIC homozygous 116785621 10 57625189 57625190 A T 23 GENIC homozygous 116604077 10 57625717 57625718 A C 23 GENIC homozygous 116604083 10 57627104 57627105 A C 22 GENIC homozygous 116785623 10 57627375 57627376 C G 22 GENIC homozygous 116785625 10 57627395 57627401 AGACAG 20 GENIC homozygous 131094810 10 57627658 57627659 C T 25 GENIC homozygous 117011627 10 57628415 57628416 T G 30 GENIC homozygous 116604095 10 57628638 57628642 TGCT 24 GENIC homozygous 128819814 10 57629218 57629219 T C 33 GENIC homozygous 116604097 10 57629811 57629812 A G 18 GENIC homozygous 116604099 10 57629837 57629838 T C 27 GENIC homozygous 116604101 10 57630497 57630498 G A 28 GENIC homozygous 116785627 10 57630760 57630761 T C 16 GENIC homozygous 116604103 10 57631729 57631730 C T 30 GENIC homozygous 116785629 10 57632395 57632396 G A 6 GENIC homozygous 116604107 10 57632568 57632569 A T 15 GENIC homozygous 116604111 10 57632632 57632633 C A 14 GENIC homozygous 116785633 10 57632975 57632976 T C 23 GENIC homozygous 116604115 10 57633085 57633086 C T 29 GENIC homozygous 116785635 10 57633511 57633512 C T 30 GENIC homozygous 116785637 10 57633723 57633724 T A 26 GENIC homozygous 123364479 10 57634311 57634312 G A 32 GENIC homozygous 116604119 10 57635350 57635351 C T 21 GENIC homozygous 116785639 10 57636025 57636026 C T 24 GENIC homozygous 116785641 10 57636248 57636249 G C 18 GENIC homozygous 116604123 10 57636912 57636913 T G 23 GENIC homozygous 116785643 10 57638040 57638041 T C 32 GENIC homozygous 116604125 10 57633719 57633720 T A 26 GENIC possibly homozygous 128869703 10 57633721 57633722 T A 27 GENIC possibly homozygous 128869704