chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 9304328 9304329 G T 44 GENIC homozygous 112489058 4 9304793 9304794 G A 45 GENIC homozygous 112489060 4 9305257 9305258 A G 40 GENIC homozygous 112489062 4 9305582 9305583 C T 29 GENIC homozygous 112489064 4 9306005 9306006 A G 30 GENIC homozygous 112489066 4 9306166 9306167 G A 27 GENIC homozygous 112489068 4 9306174 9306175 G C 26 GENIC homozygous 112489070 4 9306371 9306372 A G 27 GENIC homozygous 112489072 4 9306556 9306557 A G 43 GENIC possibly homozygous 112489074 4 9306970 9306971 T C 22 GENIC homozygous 112489076 4 9308165 9308166 C T 62 GENIC homozygous 112489084 4 9307156 9307157 C T 41 GENIC homozygous 112489078 4 9307728 9307729 G A 33 GENIC homozygous 112489080 4 9308043 9308044 T C 39 GENIC homozygous 112489082 4 9308243 9308244 G A 60 GENIC homozygous 112489086 4 9308414 9308415 T A 35 GENIC homozygous 112489088 4 9308833 9308834 T C 49 GENIC homozygous 112489090 4 9309166 9309167 T C 34 GENIC homozygous 112489092 4 9309878 9309879 T C 22 GENIC homozygous 112489098 4 9310507 9310508 A T 40 GENIC homozygous 112489100 4 9310978 9310979 G A 50 GENIC homozygous 112489102