chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 23962971 23962972 A G 30 GENIC homozygous 929370086 7 23963009 23963010 A C 33 GENIC homozygous 929370087 7 23963041 23963042 G T 34 GENIC homozygous 929370088 7 23968083 23968084 T A 61 GENIC homozygous 929370089 7 23968093 23968094 A C 66 GENIC homozygous 929370090 7 23968094 23968095 T G 66 GENIC homozygous 929370091 7 23968096 23968097 G T 65 GENIC homozygous 929370092 7 23968467 23968468 A T 36 GENIC homozygous 929370093 7 23968822 23968823 T C 27 GENIC homozygous 929370094 7 23972977 23972978 A G 20 GENIC homozygous 929370095 7 23973551 23973552 A G 32 GENIC homozygous 929370096 7 23974442 23974443 A G 21 GENIC homozygous 929370097 7 23974631 23974632 G A 33 GENIC homozygous 929370098 7 23976387 23976388 T C 53 GENIC homozygous 929370099 7 23981209 23981210 T C 50 GENIC homozygous 929370100 7 23982800 23982801 G A 30 GENIC homozygous 929370101 7 23984875 23984876 T C 48 GENIC homozygous 929370102 7 23984996 23984997 T C 59 GENIC homozygous 929370103 7 23985223 23985224 T C 38 GENIC homozygous 929370104