chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 50111996 50111997 C T 43 GENIC homozygous 47672581 16 50112006 50112007 T C 44 GENIC homozygous 47672582 16 50112187 50112189 AA -- 62 GENIC homozygous 47672583 16 50112437 50112438 A G 78 GENIC homozygous 47444633 16 50113809 50113810 C A 66 GENIC homozygous 47672584 16 50114684 50114685 C T 65 GENIC homozygous 47672585 16 50119989 50119990 T C 50 GENIC homozygous 47444649 16 50122688 50122689 G A 64 GENIC possibly homozygous 47444651 16 50125528 50125529 C T 57 GENIC possibly homozygous 47672586 16 50125552 50125553 A - 51 GENIC homozygous 47444665 16 50125797 50125798 C A 80 GENIC homozygous 47672587 16 50126038 50126039 G A 50 GENIC possibly homozygous 47672588 16 50127275 50127276 T C 47 GENIC homozygous 47444670 16 50128473 50128474 G T 58 GENIC homozygous 47444678 16 50128557 50128558 C T 67 GENIC possibly homozygous 47672589 16 50128760 50128761 C CCATGTGGA 24 GENIC homozygous 47444680 16 50129862 50129863 T C 75 GENIC possibly homozygous 47444685 16 50130726 50130727 C T 59 GENIC homozygous 47444689 16 50130985 50130986 T C 54 GENIC homozygous 47444691 16 50132329 50132330 C T 70 GENIC homozygous 47672590 16 50133083 50133084 A C 69 GENIC homozygous 47444693 16 50133216 50133217 T C 72 GENIC homozygous 47672591 16 50133330 50133331 T TGA 24 GENIC heterozygous 47444695 16 50133332 50133333 A T 38 GENIC heterozygous 47444697 16 50133348 50133350 AA -- 33 GENIC possibly homozygous 47444699 16 50133355 50133356 G C 38 GENIC heterozygous 47672592 16 50133367 50133368 G C 33 GENIC heterozygous 47672593 16 50133377 50133378 C G 29 GENIC homozygous 47444703 16 50133749 50133750 C T 67 GENIC homozygous 47672594 16 50134101 50134102 C T 50 GENIC homozygous 47672595 16 50134583 50134584 A G 61 GENIC homozygous 47444705 16 50135094 50135095 A G 58 GENIC homozygous 47444707 16 50135907 50135908 A G 68 GENIC homozygous 47444711 16 50136149 50136150 G A 57 GENIC homozygous 47444713 16 50136435 50136436 C CT 29 GENIC homozygous 47672596