chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51022996 51022997 G A 5 GENIC homozygous 114672241 13 51023591 51023592 T C 17 GENIC homozygous 114672243 13 51024246 51024247 C T 24 GENIC homozygous 114672245 13 51024773 51024774 C T 23 GENIC homozygous 114890403 13 51023064 51023065 T G 5 GENIC homozygous 115100753 13 51023188 51023189 A 25 GENIC homozygous 131126449 13 51024772 51024773 A 23 GENIC homozygous 131126450 13 51023347 51023348 G A 5 GENIC homozygous 114890393 13 51023882 51023883 T G 15 GENIC homozygous 114890395 13 51024301 51024302 A G 24 GENIC homozygous 114890397 13 51024302 51024303 C T 24 GENIC homozygous 114890399 13 51024523 51024524 C T 17 GENIC homozygous 114890401 13 51023783 51023784 G T 21 GENIC homozygous 114342369 13 51024364 51024365 T C 21 GENIC homozygous 114342371 13 51025241 51025242 A T 29 GENIC homozygous 114342375 13 51025424 51025425 G C 25 GENIC homozygous 114890405 13 51026234 51026235 A G 12 GENIC homozygous 114890407 13 51026402 51026403 G A 20 GENIC homozygous 114342377 13 51026717 51026718 C 16 GENIC homozygous 131126451 13 51026928 51026929 T C 14 GENIC homozygous 114890409 13 51027012 51027013 T C 10 GENIC homozygous 114890411 13 51027431 51027432 G A 16 GENIC homozygous 114342379 13 51028237 51028238 A T 31 GENIC homozygous 114672249 13 51028446 51028447 C A 15 GENIC homozygous 114890413 13 51028743 51028744 C T 20 GENIC homozygous 114890415 13 51029139 51029140 C G 18 GENIC homozygous 114890417 13 51029367 51029368 A T 24 GENIC homozygous 114342381 13 51029598 51029599 G A 22 GENIC homozygous 114890419 13 51029669 51029670 A G 18 GENIC homozygous 114342383 13 51029870 51029871 A G 18 GENIC homozygous 114342387 13 51030147 51030148 C G 19 GENIC homozygous 114890421 13 51030402 51030403 C T 10 GENIC homozygous 114890423 13 51030556 51030557 T C 25 GENIC homozygous 114342389 13 51030613 51030613 AC 24 GENIC homozygous 131126452 13 51028085 51028086 G A 33 GENIC homozygous 114948043