chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 47893518 47893519 C A 21 GENIC homozygous 539130756 8 47893922 47893923 T C 16 GENIC heterozygous 541346922 8 47894033 47894034 T G 25 GENIC homozygous 539130757 8 47894347 47894348 A G 6 GENIC heterozygous 539130758 8 47894568 47894573 AAAAG ----- 13 GENIC homozygous 697519317 8 47894572 47894573 G GA 14 GENIC heterozygous 697519318 8 47895112 47895113 C A 40 GENIC homozygous 539130759 8 47896183 47896184 T A 31 GENIC homozygous 539130760 8 47896387 47896388 T C 17 GENIC heterozygous 541346923 8 47896404 47896405 C - 10 GENIC heterozygous 697519319 8 47896413 47896414 T TG 16 GENIC heterozygous 697519320 8 47896507 47896508 G T 36 GENIC homozygous 539130761 8 47897268 47897269 G C 43 GENIC homozygous 539130762 8 47897432 47897433 A G 36 GENIC homozygous 539130763 8 47897576 47897577 C T 5 GENIC heterozygous 541346924 8 47897586 47897587 C T 8 GENIC heterozygous 541346925 8 47897596 47897597 C T 7 GENIC possibly homozygous 541346926 8 47897614 47897615 C CT 5 GENIC homozygous 697519321 8 47897679 47897680 T C 7 GENIC heterozygous 539130764 8 47897775 47897776 C T 7 GENIC heterozygous 541346927 8 47898709 47898710 C T 21 GENIC homozygous 539130765 8 47898730 47898731 C T 19 GENIC homozygous 539130766 8 47898794 47898795 G A 19 GENIC homozygous 539130767 8 47898802 47898803 G A 18 GENIC homozygous 539130768 8 47898810 47898811 A G 21 GENIC heterozygous 539130769 8 47898818 47898819 A G 17 GENIC heterozygous 541346928