chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 87114213 87114214 G A 33 GENIC homozygous 51029715 11 87114458 87114459 A G 30 GENIC homozygous 51029716 11 87114510 87114511 A G 23 GENIC homozygous 51029717 11 87114819 87114820 T C 16 GENIC homozygous 51029718 11 87114835 87114836 A ACGCT 16 GENIC homozygous 51192282 11 87114841 87114843 AT -- 14 GENIC homozygous 51192283 11 87114859 87114860 T TCACA 3 GENIC homozygous 51192285 11 87115431 87115432 C T 22 GENIC homozygous 51029721 11 87115439 87115440 C T 18 GENIC homozygous 51029722 11 87116384 87116385 G A 20 GENIC homozygous 51029724 11 87116482 87116483 G C 31 GENIC homozygous 51029725 11 87116483 87116484 G C 31 GENIC homozygous 51029726 11 87116514 87116515 C G 31 GENIC homozygous 51029727 11 87117246 87117247 T A 22 GENIC homozygous 51029728 11 87117424 87117425 G C 25 GENIC homozygous 51029729 11 87117695 87117696 A T 15 GENIC homozygous 50857413 11 87118349 87118350 A G 34 GENIC homozygous 51029730 11 87118495 87118496 T G 24 GENIC homozygous 51029731 11 87118799 87118800 C T 34 GENIC homozygous 51029732 11 87118991 87118992 A - 9 GENIC homozygous 50857414 11 87119025 87119035 AAAAATATAT ---------- 6 GENIC homozygous 51192286 11 87119136 87119137 T TTGG 4 GENIC homozygous 50857416 11 87119703 87119704 C T 21 GENIC homozygous 51029734 11 87119720 87119721 C G 22 GENIC homozygous 51029735