chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 13346453 13346454 C T 13 GENIC homozygous 115362625 12 13347401 13347402 A C 18 GENIC homozygous 115260521 12 13350583 13350584 C T 27 GENIC homozygous 115416916 12 13352412 13352413 T C 21 GENIC homozygous 115260535 12 13353851 13353852 A G 21 GENIC homozygous 115260541 12 13355080 13355081 T C 8 GENIC homozygous 115416918 12 13355086 13355087 C T 9 GENIC homozygous 115416920 12 13355930 13355931 C A 19 GENIC homozygous 115416922 12 13356270 13356271 A G 32 GENIC homozygous 115260549 12 13356301 13356302 G A 30 GENIC homozygous 115416924 12 13357440 13357441 T C 19 GENIC homozygous 115362637 12 13358151 13358152 T G 23 GENIC homozygous 115362638 12 13358757 13358758 A G 18 GENIC homozygous 115362639 12 13358926 13358927 C T 20 GENIC homozygous 115260553 12 13359105 13359106 C T 32 GENIC homozygous 115362640 12 13359311 13359312 G A 14 GENIC homozygous 115362641 12 13359672 13359673 C A 16 GENIC homozygous 115362642 12 13359758 13359759 A G 17 GENIC homozygous 115362643 12 13359794 13359795 T C 17 GENIC homozygous 115362644 12 13359868 13359869 G T 18 GENIC homozygous 115362645 12 13359947 13359948 G A 19 GENIC homozygous 115362646 12 13359951 13359952 A G 20 GENIC homozygous 115362647 12 13359969 13359970 G A 16 GENIC homozygous 115416926 12 13360505 13360506 T C 14 GENIC homozygous 115260557 12 13361695 13361696 T C 19 GENIC homozygous 115362648 12 13361762 13361763 A C 12 GENIC homozygous 115362649 12 13362430 13362431 C T 8 GENIC homozygous 115416928 12 13367214 13367215 G A 26 GENIC homozygous 115260571