chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 95288449 95288450 A G 40 GENIC homozygous 118318636 7 95288760 95288761 A G 51 GENIC homozygous 116054272 7 95293409 95293410 C T 49 GENIC homozygous 118354197 7 95293429 95293430 G A 44 GENIC homozygous 118354199 7 95295528 95295529 C T 80 GENIC homozygous 118318659 7 95296203 95296204 A G 60 GENIC homozygous 118354200 7 95299608 95299609 A T 41 GENIC homozygous 118354202 7 95301700 95301701 A T 57 GENIC homozygous 118354204 7 95303399 95303400 C T 70 GENIC homozygous 118354206 7 95305873 95305874 T C 27 GENIC homozygous 118318679 7 95306272 95306273 A G 23 GENIC homozygous 118354207 7 95306530 95306531 T C 50 GENIC homozygous 118318687 7 95307060 95307061 A G 48 GENIC homozygous 116054280 7 95295925 95295926 A G 54 GENIC homozygous 118415287 7 95298211 95298212 T C 37 GENIC homozygous 131691181 7 95306387 95306388 C T 29 GENIC homozygous 131691182 7 95298959 95298959 T 48 GENIC homozygous 131681361 7 95306628 95306628 G 42 GENIC homozygous 131681362