chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 12071850 12071851 T TA 26 GENIC homozygous 725367130 20 12072354 12072355 C T 24 GENIC homozygous 593522210 20 12072589 12072590 C G 28 GENIC homozygous 593522211 20 12072655 12072656 G A 30 GENIC homozygous 593522212 20 12072708 12072709 C A 39 GENIC homozygous 593522213 20 12072847 12072848 T C 34 GENIC homozygous 593522214 20 12072900 12072901 C T 26 GENIC homozygous 593522215 20 12072929 12072930 C T 30 GENIC homozygous 593522216 20 12072942 12072943 A G 33 GENIC homozygous 593522217 20 12073350 12073351 C - 23 GENIC homozygous 725367131 20 12073365 12073366 C T 23 GENIC homozygous 593522218 20 12073378 12073379 T C 23 GENIC homozygous 594185128 20 12073381 12073382 A - 24 GENIC homozygous 725367132 20 12073417 12073418 A ACTGGCACT 27 GENIC homozygous 725367133 20 12074465 12074466 G GAAAAAA 5 GENIC homozygous 725367134 20 12074489 12074490 A - 2 GENIC homozygous 725367135 20 12075331 12075332 T C 32 GENIC homozygous 593522219 20 12075380 12075381 T C 31 GENIC homozygous 593522220 20 12075390 12075391 C G 34 GENIC homozygous 593522221