chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 124339161 124339162 G C 21 GENIC homozygous 958404592 7 124339853 124339854 C T 17 GENIC homozygous 958404593 7 124340150 124340151 T C 22 GENIC homozygous 958404594 7 124341609 124341610 C A 29 GENIC homozygous 958404595 7 124344290 124344291 C A 29 GENIC possibly homozygous 958404596 7 124344725 124344726 A G 21 GENIC homozygous 958404597 7 124346017 124346018 A G 19 GENIC homozygous 958404598 7 124351259 124351260 T G 25 GENIC homozygous 958404599 7 124351260 124351261 G C 25 GENIC homozygous 958404600 7 124351265 124351266 A G 27 GENIC homozygous 958404601 7 124354543 124354544 T C 28 GENIC homozygous 958404602 7 124356107 124356108 G A 30 GENIC homozygous 958404603 7 124357590 124357591 C T 30 GENIC homozygous 958404604 7 124359860 124359861 A C 3 GENIC homozygous 958404605 7 124360113 124360114 C T 23 GENIC homozygous 958404606 7 124361076 124361077 A G 20 GENIC homozygous 958404607 7 124361238 124361239 C T 15 GENIC homozygous 958404608 7 124361846 124361847 G A 33 GENIC homozygous 958404609 7 124366145 124366146 T C 20 GENIC homozygous 958404610