chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 43670532 43670533 T TA 5 GENIC homozygous 768317083 14 43670599 43670600 A - 9 GENIC homozygous 768317084 14 43671816 43671817 G A 15 GENIC possibly homozygous 669014998 14 43671925 43671926 A G 6 GENIC homozygous 669014999 14 43672183 43672184 T TATAAA 3 GENIC homozygous 768317085 14 43672337 43672338 T C 25 GENIC possibly homozygous 669015000 14 43672956 43672957 A G 5 GENIC homozygous 669015001 14 43672974 43672975 C T 6 GENIC heterozygous 669015002 14 43673437 43673438 A T 22 GENIC possibly homozygous 669015003 14 43673802 43673803 G A 11 GENIC homozygous 669015004 14 43674375 43674376 T C 13 GENIC homozygous 669015005 14 43674426 43674427 G A 20 GENIC homozygous 669015006 14 43674549 43674550 C G 22 GENIC heterozygous 669015007 14 43674721 43674722 A AG 5 GENIC heterozygous 768317086 14 43675070 43675071 C CCCCG 4 GENIC heterozygous 768317087 14 43675119 43675120 A G 21 GENIC possibly homozygous 669015008 14 43675662 43675663 A G 18 GENIC possibly homozygous 669015009 14 43676242 43676243 T G 11 GENIC possibly homozygous 669015010 14 43676314 43676315 C T 7 GENIC heterozygous 669015011 14 43676331 43676332 C T 1 GENIC homozygous 669015012 14 43676394 43676395 G A 8 GENIC homozygous 669015013 14 43676497 43676498 G A 17 GENIC heterozygous 669015014 14 43676556 43676557 C T 18 GENIC homozygous 669015015 14 43676626 43676627 G GC 4 GENIC heterozygous 768317089 14 43676633 43676634 C T 7 GENIC homozygous 669015016 14 43676737 43676738 C T 8 GENIC possibly homozygous 669015017 14 43676928 43676929 G C 16 GENIC possibly homozygous 669015018