chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 93575784 93575785 G A 20 GENIC homozygous 109920560 2 93580702 93580703 T C 23 GENIC homozygous 109920576 2 93581833 93581834 G T 10 GENIC homozygous 109920578 2 93582369 93582370 A G 19 GENIC homozygous 109920580 2 93582428 93582429 A T 13 GENIC homozygous 109920582 2 93582488 93582489 T A 21 GENIC homozygous 109920584 2 93582671 93582672 C A 17 GENIC homozygous 109920586 2 93582820 93582821 A G 29 GENIC homozygous 109920588 2 93583025 93583026 C T 22 GENIC homozygous 109920590 2 93583988 93583989 A G 18 GENIC homozygous 109920592 2 93584652 93584653 T C 26 GENIC homozygous 109920594 2 93584856 93584857 A T 13 GENIC homozygous 109920596 2 93590413 93590414 C T 11 GENIC homozygous 109920598 2 93623510 93623511 T C 21 GENIC homozygous 109920608 2 93626187 93626188 T C 12 GENIC homozygous 109920610 2 93631250 93631251 A T 15 GENIC homozygous 109920614 2 93631251 93631252 G T 15 GENIC homozygous 109920616 2 93631718 93631719 G A 21 GENIC homozygous 109920618 2 93637458 93637459 T C 11 GENIC homozygous 109920627 2 93639259 93639260 C T 8 GENIC homozygous 109920633 2 93641282 93641283 T G 21 GENIC homozygous 109920635