chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51023554 51023555 T C 13 GENIC homozygous 114342367 13 51023783 51023784 G T 20 GENIC homozygous 114342369 13 51024364 51024365 T C 24 GENIC homozygous 114342371 13 51024592 51024593 T C 25 GENIC homozygous 114342373 13 51025241 51025242 A T 15 GENIC homozygous 114342375 13 51026402 51026403 G A 26 GENIC homozygous 114342377 13 51027431 51027432 G A 18 GENIC homozygous 114342379 13 51028237 51028238 A T 35 GENIC homozygous 114672249 13 51029367 51029368 A T 10 GENIC homozygous 114342381 13 51029669 51029670 A G 36 GENIC homozygous 114342383 13 51029671 51029672 G A 38 GENIC homozygous 114342385 13 51029870 51029871 A G 30 GENIC homozygous 114342387 13 51030556 51030557 T C 20 GENIC homozygous 114342389