chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 9303657 9303658 C T 26 GENIC homozygous 113328542 4 9304328 9304329 G T 20 GENIC homozygous 112489058 4 9304793 9304794 G A 23 GENIC homozygous 112489060 4 9304803 9304804 G A 21 GENIC homozygous 113328544 4 9305257 9305258 A G 24 GENIC homozygous 112489062 4 9305813 9305814 G A 40 GENIC homozygous 113328546 4 9306005 9306006 A G 27 GENIC homozygous 112489066 4 9306166 9306167 G A 18 GENIC homozygous 112489068 4 9306174 9306175 G C 19 GENIC homozygous 112489070 4 9306371 9306372 A G 14 GENIC homozygous 112489072 4 9306556 9306557 A G 35 GENIC homozygous 112489074 4 9306967 9306968 C G 21 GENIC homozygous 113328548 4 9306970 9306971 T C 22 GENIC homozygous 112489076 4 9307156 9307157 C T 34 GENIC homozygous 112489078 4 9308043 9308044 T C 32 GENIC homozygous 112489082 4 9308243 9308244 G A 32 GENIC homozygous 112489086 4 9308414 9308415 T A 21 GENIC homozygous 112489088 4 9308629 9308630 C G 31 GENIC homozygous 113077581 4 9308833 9308834 T C 29 GENIC homozygous 112489090 4 9309166 9309167 T C 34 GENIC homozygous 112489092 4 9309878 9309879 T C 6 GENIC homozygous 112489098 4 9310978 9310979 G A 38 GENIC homozygous 112489102