chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 33176139 33176140 C T 12 GENIC homozygous 982121496 5 33177051 33177052 A C 10 GENIC homozygous 982121497 5 33177272 33177273 C T 13 GENIC heterozygous 982121498 5 33177642 33177643 G A 26 GENIC heterozygous 982121499 5 33177668 33177669 C A 29 GENIC heterozygous 982121500 5 33177751 33177752 G T 22 GENIC heterozygous 982121501 5 33177776 33177777 T C 28 GENIC heterozygous 982121502 5 33177853 33177854 A G 26 GENIC heterozygous 982121503 5 33177994 33177995 G A 11 GENIC heterozygous 982121504 5 33178007 33178008 G A 13 GENIC heterozygous 982121505 5 33178076 33178077 C A 22 GENIC heterozygous 982121506 5 33178080 33178081 G A 22 GENIC heterozygous 982121507 5 33178083 33178084 G A 22 GENIC heterozygous 982121508 5 33178112 33178113 G A 17 GENIC heterozygous 982121509 5 33178159 33178160 C T 22 GENIC heterozygous 982121510 5 33178210 33178211 C G 20 GENIC heterozygous 982121511 5 33178216 33178217 G A 20 GENIC heterozygous 982121512 5 33178221 33178222 A G 20 GENIC heterozygous 982121513 5 33178226 33178227 A G 19 GENIC heterozygous 982121514 5 33178231 33178232 G T 18 GENIC heterozygous 982121515 5 33179644 33179645 A G 8 GENIC homozygous 982121516 5 33180034 33180035 C T 10 GENIC homozygous 982121517 5 33180442 33180443 C T 6 GENIC homozygous 982121518 5 33180660 33180661 T C 9 GENIC homozygous 982121519