chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 79697969 79697970 A G 24 GENIC homozygous 114404221 13 79698634 79698635 C T 44 GENIC homozygous 114404223 13 79698784 79698785 T C 27 GENIC homozygous 114404225 13 79704619 79704620 G A 27 GENIC homozygous 114404253 13 79708373 79708374 T C 28 GENIC homozygous 114404304 13 79710419 79710420 A G 41 GENIC homozygous 114404319 13 79711540 79711541 G A 29 GENIC homozygous 114404326 13 79712670 79712671 C G 30 GENIC homozygous 114404338 13 79716813 79716814 C T 34 GENIC homozygous 114775565 13 79702877 79702878 G A 35 GENIC homozygous 114775557 13 79706164 79706165 C T 38 GENIC homozygous 114775559 13 79710962 79710963 G A 27 GENIC homozygous 114775561 13 79711758 79711759 G A 34 GENIC homozygous 114775563 13 79717033 79717034 C T 43 GENIC homozygous 114775567 13 79717289 79717290 G A 36 GENIC homozygous 114775569 13 79717441 79717442 C T 38 GENIC homozygous 114775571 13 79717460 79717461 T C 32 GENIC homozygous 114775573 13 79717539 79717540 C A 31 GENIC homozygous 114775575 13 79717566 79717567 A T 34 GENIC homozygous 114775577