chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 15099176 15099177 T C 38 GENIC heterozygous 117074909 10 15099997 15099998 C T 34 GENIC heterozygous 116497711 10 15100001 15100002 C T 37 GENIC heterozygous 116497713 10 15100064 15100065 G A 41 GENIC heterozygous 116497715 10 15100573 15100574 T C 45 GENIC heterozygous 116497721 10 15100983 15100984 C T 30 GENIC heterozygous 118062992 10 15100991 15100992 C T 29 GENIC heterozygous 117982590 10 15101972 15101973 T C 33 GENIC heterozygous 116497725 10 15101980 15101981 T C 35 GENIC heterozygous 116497727 10 15101985 15101986 G A 31 GENIC heterozygous 116497729 10 15102034 15102035 C T 33 GENIC heterozygous 116497731 10 15102050 15102051 G A 27 GENIC heterozygous 116497733 10 15102102 15102103 C T 34 GENIC heterozygous 116497735 10 15102120 15102121 C A 32 GENIC heterozygous 116497737 10 15102144 15102145 A G 31 GENIC heterozygous 116497739 10 15102149 15102150 C T 33 GENIC heterozygous 116497741 10 15102150 15102151 A G 31 GENIC heterozygous 116497743 10 15102162 15102163 C T 28 GENIC heterozygous 116497745 10 15102212 15102213 A G 33 GENIC heterozygous 116497747 10 15102251 15102252 A G 31 GENIC heterozygous 116497749 10 15102273 15102274 A G 30 GENIC heterozygous 116497751 10 15102301 15102302 A G 32 GENIC heterozygous 116497753 10 15102513 15102514 T C 34 GENIC heterozygous 116859931 10 15102531 15102532 C T 36 GENIC heterozygous 116859933 10 15102551 15102552 T G 27 GENIC heterozygous 116859935