chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 47893518 47893519 C A 33 GENIC homozygous 525791049 8 47893922 47893923 T C 19 GENIC heterozygous 528329878 8 47894033 47894034 T G 15 GENIC homozygous 525791050 8 47894336 47894337 C T 21 GENIC heterozygous 525791051 8 47894340 47894341 C T 22 GENIC heterozygous 528329879 8 47894347 47894348 A G 22 GENIC possibly homozygous 525791052 8 47894568 47894573 AAAAG ----- 19 GENIC homozygous 692604727 8 47894572 47894573 G GA 19 GENIC heterozygous 692604728 8 47895112 47895113 C A 29 GENIC homozygous 525791053 8 47896183 47896184 T A 32 GENIC homozygous 525791054 8 47896366 47896370 GTTC ---- 28 GENIC heterozygous 692604729 8 47896387 47896388 T C 33 GENIC heterozygous 528329880 8 47896398 47896402 GTTC ---- 26 GENIC heterozygous 692604730 8 47896404 47896405 C - 22 GENIC possibly homozygous 692604731 8 47896406 47896409 TTC --- 26 GENIC heterozygous 692604732 8 47896413 47896414 T TG 26 GENIC heterozygous 692604733 8 47896507 47896508 G T 44 GENIC homozygous 525791055 8 47897268 47897269 G C 27 GENIC homozygous 525791056 8 47897432 47897433 A G 45 GENIC homozygous 525791057 8 47897576 47897577 C T 7 GENIC homozygous 528329881 8 47897586 47897587 C T 11 GENIC heterozygous 528329882 8 47897596 47897597 C T 11 GENIC heterozygous 528329883 8 47897614 47897615 C CT 9 GENIC homozygous 692604734 8 47897679 47897680 T C 14 GENIC possibly homozygous 525791058 8 47897750 47897751 T - 10 GENIC heterozygous 692604735 8 47897775 47897776 C T 17 GENIC heterozygous 528329884 8 47898709 47898710 C T 28 GENIC homozygous 525791059 8 47898730 47898731 C T 30 GENIC homozygous 525791060 8 47898794 47898795 G A 22 GENIC possibly homozygous 525791061 8 47898802 47898803 G A 20 GENIC homozygous 525791062 8 47898810 47898811 A G 22 GENIC heterozygous 525791063 8 47898818 47898819 A G 18 GENIC heterozygous 528329885