chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 39435020 39435020 C 33 GENIC homozygous 129531486 18 39436216 39436217 C G 58 GENIC homozygous 110328233 18 39437231 39437232 T C 43 GENIC homozygous 110328237 18 39437446 39437447 G 32 GENIC homozygous 129531487 18 39437580 39437581 C 20 GENIC homozygous 129531488 18 39437730 39437731 C 20 GENIC homozygous 129531489 18 39437733 39437734 C A 21 GENIC homozygous 110463273 18 39437734 39437735 A C 21 GENIC homozygous 110463274 18 39437759 39437760 G 32 GENIC homozygous 129531490 18 39437837 39437838 T 31 GENIC homozygous 129531491 18 39437850 39437851 C 31 GENIC homozygous 129531492 18 39437972 39437973 C 17 GENIC homozygous 129531493 18 39437995 39437996 C 16 GENIC homozygous 129531494 18 39437999 39438000 T C 16 GENIC homozygous 110463275 18 39438000 39438001 C T 16 GENIC homozygous 110463276 18 39437510 39437511 T 20 GENIC heterozygous 133446471