chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 35625335 35625336 A C 25 GENIC homozygous 115064290 13 35625589 35625590 T C 23 GENIC homozygous 114313411 13 35626307 35626308 T C 31 GENIC homozygous 114313413 13 35628028 35628029 A T 18 GENIC homozygous 115064292 13 35629429 35629430 T C 23 GENIC homozygous 114313420 13 35629756 35629757 T G 18 GENIC homozygous 114313421 13 35630708 35630709 A G 32 GENIC homozygous 114313424 13 35630916 35630917 C T 20 GENIC homozygous 114662558 13 35632353 35632354 T C 26 GENIC homozygous 114313427 13 35632802 35632803 G A 28 GENIC homozygous 114313429 13 35633114 35633115 C T 28 GENIC homozygous 115064294 13 35634055 35634056 G A 32 GENIC homozygous 115064296 13 35640304 35640305 G C 21 GENIC homozygous 115064298 13 35640320 35640321 C T 25 GENIC homozygous 114313438 13 35636711 35636712 T G 25 GENIC possibly homozygous 114313435 13 35641065 35641066 C T 24 GENIC homozygous 114313440 13 35641662 35641663 G A 19 GENIC homozygous 115064300 13 35642336 35642337 G A 17 GENIC homozygous 115064302 13 35643696 35643697 G A 23 GENIC homozygous 114313443 13 35646034 35646035 T C 12 GENIC homozygous 114313445 13 35646245 35646246 T C 21 GENIC homozygous 114313446 13 35649768 35649769 C T 19 GENIC homozygous 114313450 13 35651122 35651123 T C 20 GENIC homozygous 115064304 13 35653134 35653135 T A 15 GENIC homozygous 115064306 13 35657272 35657273 T G 18 GENIC homozygous 115064308 13 35658153 35658154 A G 29 GENIC homozygous 115064310 13 35658559 35658560 T G 37 GENIC homozygous 114313459 13 35659576 35659577 T C 19 GENIC homozygous 115064312 13 35660352 35660353 T A 19 GENIC homozygous 114313461 13 35660535 35660536 T A 14 GENIC homozygous 114313462 13 35660990 35660991 T G 23 GENIC homozygous 114313463 13 35666110 35666111 C T 19 GENIC homozygous 115064314 13 35671296 35671297 G T 25 GENIC homozygous 115064316 13 35673185 35673186 T A 16 GENIC homozygous 114313473