chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 12071850 12071851 T TA 28 GENIC homozygous 696584986 20 12072354 12072355 C T 48 GENIC possibly homozygous 534619948 20 12072589 12072590 C G 45 GENIC homozygous 534619949 20 12072655 12072656 G A 54 GENIC homozygous 534619950 20 12072708 12072709 C A 57 GENIC homozygous 534619951 20 12072847 12072848 T C 62 GENIC homozygous 534619952 20 12072900 12072901 C T 43 GENIC homozygous 534619953 20 12072929 12072930 C T 43 GENIC possibly homozygous 534619954 20 12072942 12072943 A G 46 GENIC homozygous 534619955 20 12073350 12073351 C - 31 GENIC homozygous 696584987 20 12073365 12073366 C T 30 GENIC homozygous 534619956 20 12073378 12073379 T C 32 GENIC homozygous 535484588 20 12073381 12073382 A - 26 GENIC homozygous 696584988 20 12073417 12073418 A ACTGGCACT 21 GENIC homozygous 696584989 20 12073990 12073991 A T 24 GENIC heterozygous 535484589 20 12074418 12074419 A G 25 GENIC heterozygous 535484590 20 12074484 12074485 G A 38 GENIC heterozygous 535484591 20 12074488 12074489 G A 39 GENIC heterozygous 535484592 20 12074489 12074490 A - 20 GENIC possibly homozygous 696584990 20 12075331 12075332 T C 46 GENIC homozygous 534619957 20 12075380 12075381 T C 41 GENIC homozygous 534619958 20 12075390 12075391 C G 37 GENIC homozygous 534619959