chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 71124519 71124520 C T 25 GENIC possibly homozygous 117965383 8 71125452 71125453 A C 34 GENIC homozygous 117965384 8 71125837 71125838 T C 27 GENIC homozygous 117965385 8 71126100 71126101 T C 37 GENIC homozygous 117965386 8 71126104 71126105 C G 37 GENIC homozygous 117965387 8 71126174 71126175 C A 35 GENIC homozygous 117965388 8 71126295 71126296 T C 17 GENIC homozygous 117965389 8 71126327 71126328 A G 18 GENIC homozygous 117965390 8 71126413 71126414 G C 27 GENIC homozygous 117965391 8 71126475 71126476 T G 29 GENIC homozygous 117965392 8 71126710 71126711 C T 32 GENIC homozygous 117965393 8 71126722 71126723 C T 30 GENIC homozygous 117965394 8 71126876 71126877 C T 25 GENIC homozygous 118149675 8 71126966 71126967 G T 32 GENIC homozygous 117965395 8 71127261 71127262 T C 42 GENIC homozygous 117965396 8 71127327 71127328 C T 34 GENIC homozygous 117965397 8 71127383 71127384 A T 35 GENIC homozygous 117965398 8 71128367 71128367 T 17 GENIC homozygous 132993605 8 71128824 71128825 T C 17 GENIC homozygous 122993274 8 71128780 71128781 T C 20 GENIC homozygous 122993272 8 71128823 71128824 A G 17 GENIC homozygous 122993273 8 71129030 71129031 C A 22 GENIC homozygous 117965399 8 71129179 71129180 A C 34 GENIC homozygous 117965400 8 71129782 71129783 C T 28 GENIC homozygous 117965401 8 71130355 71130356 T A 23 GENIC homozygous 117965402 8 71130516 71130517 A G 31 GENIC homozygous 117965403 8 71131297 71131297 AATA 36 GENIC homozygous 132993606 8 71131529 71131530 C 18 GENIC homozygous 132993607 8 71131530 71131531 C T 18 GENIC homozygous 117965404 8 71131604 71131605 T C 25 GENIC homozygous 117965405 8 71131611 71131612 A T 26 GENIC homozygous 117965406 8 71131840 71131850 CTGCACCCGT 26 GENIC homozygous 132993608 8 71131967 71131969 TC 30 GENIC homozygous 132993609 8 71132113 71132115 AC 33 GENIC homozygous 132993610 8 71132116 71132116 GATGAGGCCATC 33 GENIC homozygous 132993611 8 71133346 71133347 G A 29 GENIC homozygous 117965407