chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 12071850 12071851 T TA 20 GENIC homozygous 698196391 20 12072354 12072355 C T 33 GENIC homozygous 539062180 20 12072589 12072590 C G 33 GENIC homozygous 539062181 20 12072655 12072656 G A 28 GENIC homozygous 539062182 20 12072708 12072709 C A 31 GENIC homozygous 539062183 20 12072847 12072848 T C 30 GENIC homozygous 539062184 20 12072900 12072901 C T 30 GENIC homozygous 539062185 20 12072929 12072930 C T 22 GENIC homozygous 539062186 20 12072942 12072943 A G 23 GENIC homozygous 539062187 20 12073350 12073351 C - 18 GENIC homozygous 698196392 20 12073365 12073366 C T 19 GENIC homozygous 539062188 20 12073378 12073379 T C 14 GENIC homozygous 539880772 20 12073381 12073382 A - 12 GENIC homozygous 698196393 20 12073417 12073418 A ACTGGCACT 14 GENIC homozygous 698196394 20 12074484 12074485 G A 16 GENIC heterozygous 539880773 20 12074488 12074489 G A 14 GENIC heterozygous 539880774 20 12074489 12074490 A - 10 GENIC possibly homozygous 698196395 20 12075331 12075332 T C 30 GENIC homozygous 539062189 20 12075380 12075381 T C 27 GENIC homozygous 539062190 20 12075390 12075391 C G 27 GENIC homozygous 539062191