chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 55954267 55954268 C T 26 GENIC homozygous 989637815 19 55954280 55954281 T C 26 GENIC homozygous 989637816 19 55954436 55954437 T G 21 GENIC homozygous 989637817 19 55955492 55955493 C T 23 GENIC homozygous 989637818 19 55955630 55955631 G A 21 GENIC homozygous 989637819 19 55956322 55956323 C T 31 GENIC homozygous 989637820 19 55956368 55956369 A G 40 GENIC homozygous 989637821 19 55956409 55956410 T C 39 GENIC homozygous 989637822 19 55956610 55956611 A G 29 GENIC homozygous 989637823 19 55957368 55957369 A G 32 GENIC homozygous 989637824 19 55959036 55959037 C A 33 GENIC homozygous 989637825 19 55970589 55970590 A T 35 GENIC homozygous 989637826 19 55970590 55970591 A G 36 GENIC homozygous 989637827 19 55970894 55970895 G A 26 GENIC homozygous 989637828 19 55971021 55971022 C T 25 GENIC homozygous 989637829 19 55971676 55971677 A G 44 GENIC homozygous 989637830 19 55972186 55972187 G C 24 GENIC homozygous 989637831 19 55974009 55974010 A G 37 GENIC homozygous 989637832 19 55977203 55977204 T C 27 GENIC homozygous 989637833