chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 143595239 143595240 T A 18 GENIC homozygous 826778578 4 143595754 143595755 A G 11 GENIC homozygous 826778579 4 143598221 143598222 C A 18 GENIC homozygous 826778580 4 143599736 143599737 A G 16 GENIC homozygous 826778581 4 143599907 143599908 T C 12 GENIC homozygous 826778582 4 143604440 143604441 C - 23 GENIC homozygous 826778583 4 143604674 143604675 C T 10 GENIC homozygous 826778584 4 143604748 143604754 ACACCC ------ 15 GENIC homozygous 826778585 4 143605173 143605174 G A 22 GENIC homozygous 826778586 4 143605468 143605469 G T 20 GENIC homozygous 826778587 4 143605475 143605476 T A 19 GENIC homozygous 826778588 4 143606027 143606028 A C 18 GENIC homozygous 826778589 4 143606162 143606163 C T 17 GENIC homozygous 826778590 4 143607052 143607053 T - 14 GENIC homozygous 826778591 4 143607735 143607736 T G 21 GENIC homozygous 826778592 4 143608290 143608291 G A 23 GENIC homozygous 826778593 4 143609090 143609091 A AAAAG 11 GENIC homozygous 826778594 4 143610355 143610356 A G 13 GENIC homozygous 826778595 4 143611152 143611153 A T 8 GENIC homozygous 826778596 4 143611331 143611332 T TCGGA 8 GENIC homozygous 826778597 4 143611780 143611781 T C 10 GENIC homozygous 826778598