chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 40587089 40587090 T G 51 GENIC possibly homozygous 110329492 18 40587163 40587164 C T 53 GENIC homozygous 110329494 18 40587872 40587873 G A 32 GENIC homozygous 110589678 18 40588612 40588613 C A 41 GENIC homozygous 110329496 18 40590194 40590195 G A 36 GENIC homozygous 110329498 18 40591689 40591690 G C 35 GENIC homozygous 110329500 18 40593229 40593230 C T 14 GENIC homozygous 119490608 18 40593255 40593256 G A 8 GENIC homozygous 119490609 18 40593259 40593260 A G 8 GENIC homozygous 119490610 18 40594201 40594202 C T 14 GENIC homozygous 110329502 18 40594215 40594216 C G 15 GENIC homozygous 110329504 18 40595450 40595451 G A 65 GENIC possibly homozygous 110329506 18 40595725 40595726 A G 42 GENIC possibly homozygous 110463648 18 40596004 40596005 A G 47 GENIC homozygous 110329508 18 40597461 40597462 T G 10 GENIC homozygous 110329510 18 40597836 40597837 A G 10 GENIC homozygous 110329512