chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
129795360
129795361
T
C
12
GENIC
homozygous
54109587
7
129795406
129795407
A
-
30
GENIC
homozygous
54241221
7
129795959
129795960
T
TTGGG
18
GENIC
homozygous
55010199
7
129795961
129795962
A
ATTTAGCTCAGTGGTAGAGCGCTTGCCTAG
18
GENIC
homozygous
55010201
7
129796093
129796094
A
T
31
GENIC
homozygous
54109589
7
129796801
129796803
CC
--
17
GENIC
possibly homozygous
54109590
7
129796802
129796803
C
-
17
GENIC
heterozygous
55010203
7
129797073
129797074
G
A
23
GENIC
homozygous
54109591
7
129798576
129798577
A
AAAGC
12
GENIC
homozygous
54109592
7
129798798
129798802
GAAG
----
11
GENIC
homozygous
55010205
7
129800366
129800367
T
-
20
GENIC
homozygous
54754231
7
129800826
129800827
C
CAT
24
GENIC
possibly homozygous
54109594
7
129801567
129801568
G
-
15
GENIC
possibly homozygous
54109596
7
129802532
129802533
T
C
28
GENIC
homozygous
54109597
7
129803707
129803708
T
A
26
GENIC
homozygous
54109598
7
129803754
129803755
A
C
33
GENIC
homozygous
54109599
7
129804462
129804465
CAC
---
27
GENIC
homozygous
54109600
