chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
219362681
219362682
T
C
74
GENIC
homozygous
108993895
1
219363005
219363005
CCAGTG
87
GENIC
homozygous
131782396
1
219363175
219363176
G
A
69
GENIC
homozygous
108993896
1
219363698
219363699
G
A
65
GENIC
homozygous
108993897
1
219364768
219364769
G
T
81
GENIC
possibly homozygous
108993898
1
219365601
219365602
T
C
67
GENIC
homozygous
108993899
1
219366370
219366493
GAGACAGCTCATTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCCC
21
GENIC
heterozygous
131782397
1
219366837
219366838
C
T
75
GENIC
homozygous
108993900
1
219367263
219367264
G
A
40
GENIC
homozygous
108993901
1
219367916
219367917
C
T
62
GENIC
homozygous
108993902
1
219367943
219367944
T
C
69
GENIC
homozygous
108993903
1
219368875
219368895
CAACACACACACACACACAC
25
GENIC
possibly homozygous
131782398
1
219368944
219368945
A
C
28
GENIC
homozygous
108993904
1
219370871
219370872
A
G
53
GENIC
homozygous
108540625
1
219371516
219371517
T
C
65
GENIC
homozygous
108540629
1
219372326
219372327
G
A
51
GENIC
homozygous
108993905
1
219373001
219373002
A
G
56
GENIC
possibly homozygous
108540631
1
219373680
219373681
G
C
42
GENIC
homozygous
108993906
