chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 43473470 43473471 C T 33 GENIC homozygous 977370085 17 43478538 43478539 C A 18 GENIC homozygous 977370086 17 43479459 43479460 T A 22 GENIC homozygous 977370087 17 43482505 43482506 A G 19 GENIC homozygous 977370088 17 43482535 43482536 T C 27 GENIC homozygous 977370089 17 43484390 43484391 C G 32 GENIC homozygous 977370090 17 43489046 43489047 A G 27 GENIC homozygous 977370091 17 43490998 43490999 T C 18 GENIC homozygous 977370092 17 43493277 43493278 G A 39 GENIC homozygous 977370093 17 43494230 43494231 G A 38 GENIC homozygous 977370094 17 43496269 43496270 G T 20 GENIC homozygous 977370095 17 43496408 43496409 C T 33 GENIC homozygous 977370096 17 43497333 43497334 C T 33 GENIC homozygous 977370097 17 43498415 43498416 A C 4 GENIC homozygous 977370098 17 43503310 43503311 C T 21 GENIC homozygous 977370099 17 43503943 43503944 A G 25 GENIC homozygous 977370100 17 43504050 43504051 T C 32 GENIC homozygous 977370101 17 43504507 43504508 C T 29 GENIC homozygous 977370102