geneid | 22938 |
---|---|
ensemblid | ENSG00000100603.14 |
hgncid | 16696 |
symbol | SNW1 |
name | SNW domain containing 1 |
refseq_nuc | NM_012245.3 |
refseq_prot | NP_036377.1 |
ensembl_nuc | ENST00000261531.12 |
ensembl_prot | ENSP00000261531.8 |
mane_status | MANE Select |
chr | chr14 |
start | 77717599 |
end | 77761156 |
strand | - |
ver | v1.2 |
region | chr14:77717599-77761156 |
region5000 | chr14:77712599-77766156 |
regionname0 | SNW1_chr14_77717599_77761156 |
regionname5000 | SNW1_chr14_77712599_77766156 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 536 | 365 | 94 | 62 | 153 | 18 | 36 | 119 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0002 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1611 | 220 | 57 | 36 | 90 | 9 | 28 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
c0002 | 1/0 | 1611 | 70 | 8 | 10 | 44 | 3 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
c0003 | 0/1 | 1611 | 69 | 24 | 15 | 19 | 6 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
c0004 | 0/0 | 1611 | 4 | 4 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
c0005 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
c0006 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
c0007 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 519 | 333 | 84 | 52 | 147 | 16 | 32 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
t0002 | 0/0 | 520 | 27 | 5 | 10 | 7 | 2 | 3 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
t0003 | 0/0 | 518 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
t0004 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
t0005 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
t0006 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0002 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1611 | 220 | 57 | 36 | 90 | 9 | 28 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0002 | 1/0 | 1611 | 70 | 8 | 10 | 44 | 3 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0003 | 0/1 | 1611 | 69 | 24 | 15 | 19 | 6 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0004 | 0/0 | 1611 | 4 | 4 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0006 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0007 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0002c0005 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2129 | 218 | 56 | 36 | 90 | 9 | 27 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0001t0004 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0001t0005 | 0/0 | 2129 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0002t0001 | 1/0 | 2129 | 69 | 7 | 10 | 44 | 3 | 4 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0002t0006 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0003t0001 | 0/1 | 2129 | 39 | 16 | 5 | 12 | 4 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0003t0002 | 0/0 | 2130 | 27 | 5 | 10 | 7 | 2 | 3 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0003t0003 | 0/0 | 2128 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0004t0001 | 0/0 | 2129 | 4 | 4 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0006t0001 | 0/0 | 2129 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0001c0007t0001 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
a0002c0005t0001 | 0/0 | 2105 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | copy fasta | chr14 | 77712599 | 77766156 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0006t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0001c0007t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
a0002c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0074 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0055 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0131 | EUR | FIN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0012 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0059 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01106 | hp2 | a0001 | c0006 | t0001 | g0096 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0143 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0127 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0137 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0012 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0123 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0133 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0005 | AMR | CLM | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0054 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0136 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01934 | hp1 | a0001 | c0003 | t0002 | g0126 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | KHV | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0321 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02165 | hp1 | a0001 | c0003 | t0002 | g0132 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02280 | hp2 | a0001 | c0002 | t0006 | g0104 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02293 | hp2 | a0001 | c0003 | t0002 | g0130 | AMR | PEL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0128 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02630 | hp1 | a0001 | c0003 | t0002 | g0142 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02630 | hp2 | a0001 | c0007 | t0001 | g0322 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02809 | hp2 | a0001 | c0003 | t0003 | g0122 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03195 | hp1 | a0001 | c0003 | t0002 | g0153 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0052 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0049 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03486 | hp1 | a0001 | c0003 | t0002 | g0135 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0050 | AFR | GWD | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0134 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0150 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0274 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0138 | SAS | STU | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18522 | hp2 | a0001 | c0003 | t0003 | g0120 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | CHB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18951 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18954 | hp2 | a0001 | c0003 | t0002 | g0139 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18961 | hp2 | a0001 | c0003 | t0002 | g0140 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18966 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18986 | hp2 | a0002 | c0005 | t0001 | g0285 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0141 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18995 | hp2 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19001 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19007 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ASW | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ASW | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0077 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0149 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0125 | EUR | TSI | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | GIH | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0121 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0051 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | USA | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0129 | AFR | LWK | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0053 | REF | REF | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0070 | REF | REF | SNW1_chr14_77712599_77766156 | SNW1 | chr14 | 77712599 | 77766156 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77755096
|
TAGCTGAG others(58): Show |
T | 1 | a0002 | 1 | NA18986.hp2 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.15-41_38delGAGTTTT others(58): Show |
p.Ser5_Leu13delinsAr others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/14 | 67/2129 | 15/1611 | 5/536 | chr14 | 77755096 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77718223
|
C | A | 5 | a0001c0001a0001c0003a0001c0004others(2): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
synonymous_variant | LOW | c.1476G>T | p.Val492Val | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 1505/2129 | 1476/1611 | 492/536 | chr14 | 77718223 | ||
chr14:77718447
|
G | C | 1 | a0001c0007 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1332C>G | p.Ala444Ala | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 13/14 | 1361/2129 | 1332/1611 | 444/536 | chr14 | 77718447 | ||
chr14:77731022
|
C | T | 3 | a0001c0001a0001c0004a0002c0005 | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
synonymous_variant | LOW | c.999G>A | p.Glu333Glu | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/14 | 1028/2129 | 999/1611 | 333/536 | chr14 | 77731022 | ||
chr14:77751355
|
A | G | 1 | a0001c0006 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.294T>C | p.Tyr98Tyr | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/14 | 323/2129 | 294/1611 | 98/536 | chr14 | 77751355 | ||
chr14:77755021
|
T | G | 1 | a0001c0004 | 4 | HG03195.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.114A>C | p.Arg38Arg | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/14 | 143/2129 | 114/1611 | 38/536 | chr14 | 77755021 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77717698
|
AT | A | 1 | a0001c0003t0003 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*389delA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 389 | chr14 | 77717698 | |||||
chr14:77717810
|
C | T | 1 | a0001c0001t0005 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 278 | chr14 | 77717810 | |||||
chr14:77717938
|
T | TC | 1 | a0001c0003t0002 | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*149dupG | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 149 | chr14 | 77717938 | |||||
chr14:77718038
|
C | T | 1 | a0001c0001t0004 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 50 | chr14 | 77718038 | |||||
chr14:77718067
|
T | A | 1 | a0001c0002t0006 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 14/14 | 21 | chr14 | 77718067 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:77718318
|
T | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1413-32A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 13/13 | chr14 | 77718318 | ||||||
chr14:77718613
|
T | C | 3 | a0001c0002t0001g0100a0001c0002t0001g0101a0001c0002t0001g0102 | 3 | NA18979.hp1 NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1249-83A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718613 | ||||||
chr14:77718639
|
A | G | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1249-109T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718639 | ||||||
chr14:77718713
|
C | CT | 7 | a0001c0001t0001g0209a0001c0001t0001g0265a0001c0001t0001g0319others(4): Show | 7 | HG01255.hp1 HG02071.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1249-184dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718713 | ||||||
chr14:77718854
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1249-324C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718854 | ||||||
chr14:77718972
|
A | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1249-442T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77718972 | ||||||
chr14:77719000
|
C | A | 23 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0013others(20): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1249-470G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719000 | ||||||
chr14:77719074
|
C | G | 1 | a0001c0003t0001g0155 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1249-544G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719074 | ||||||
chr14:77719085
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1249-555A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719085 | ||||||
chr14:77719118
|
G | A | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-588C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719118 | ||||||
chr14:77719167
|
T | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1249-637A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719167 | ||||||
chr14:77719232
|
T | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(115): Show | 133 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1249-702A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719232 | ||||||
chr14:77719380
|
G | A | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1249-850C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719380 | ||||||
chr14:77719420
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1249-890C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719420 | ||||||
chr14:77719498
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1249-968T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719498 | ||||||
chr14:77719554
|
T | A | 12 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0243others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1249-1024A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719554 | ||||||
chr14:77719556
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1249-1026G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719556 | ||||||
chr14:77719576
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 18 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1249-1046C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719576 | ||||||
chr14:77719649
|
A | AAAAC | 240 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(237): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1248+1058_1248+106 others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719649 | ||||||
chr14:77719659
|
A | AAC | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1248+1051_1248+105 others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719659 | ||||||
chr14:77719838
|
TAATA | T | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1248+869_1248+872d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719838 | ||||||
chr14:77719940
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1248+771A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719940 | ||||||
chr14:77719945
|
A | C | 1 | a0001c0001t0001g0309 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1248+766T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719945 | ||||||
chr14:77719946
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1248+765A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719946 | ||||||
chr14:77719948
|
C | T | 1 | a0001c0003t0002g0141 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1248+763G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719948 | ||||||
chr14:77719954
|
C | T | 4 | a0001c0002t0001g0004a0001c0002t0001g0103a0001c0002t0001g0105others(1): Show | 6 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248+757G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77719954 | ||||||
chr14:77720013
|
C | G | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1248+698G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720013 | ||||||
chr14:77720028
|
C | T | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1248+683G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720028 | ||||||
chr14:77720083
|
T | G | 2 | a0001c0003t0001g0149a0001c0003t0001g0150 | 2 | HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1248+628A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720083 | ||||||
chr14:77720141
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1248+570C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720141 | ||||||
chr14:77720146
|
A | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1248+565T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720146 | ||||||
chr14:77720233
|
C | CATAAGCT others(1): Show |
267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1248+477_1248+478i others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720233 | ||||||
chr14:77720244
|
C | T | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1248+467G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720244 | ||||||
chr14:77720626
|
C | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1248+85G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720626 | ||||||
chr14:77720689
|
T | C | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1248+22A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 12/13 | chr14 | 77720689 | ||||||
chr14:77720970
|
CATA | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131-145_1131-143d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77720970 | ||||||
chr14:77720973
|
A | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(212): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1131-145T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77720973 | ||||||
chr14:77721108
|
C | A | 3 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055 | 3 | HG00280.hp1 HG01516.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1131-280G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721108 | ||||||
chr14:77721277
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1131-449C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721277 | ||||||
chr14:77721397
|
C | T | 23 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0013others(20): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1131-569G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721397 | ||||||
chr14:77721509
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0001t0005g0274 | 3 | HG03492.hp2 HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1131-681G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721509 | ||||||
chr14:77721654
|
CTT | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 10 | HG02055.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1131-828_1131-827d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721654 | ||||||
chr14:77721742
|
A | T | 10 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(7): Show | 10 | HG00408.hp1 HG01928.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.1131-914T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721742 | ||||||
chr14:77721746
|
T | A | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1131-918A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721746 | ||||||
chr14:77721910
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1131-1082C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721910 | ||||||
chr14:77721921
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1131-1093G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721921 | ||||||
chr14:77721949
|
T | C | 1 | a0001c0003t0002g0132 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1131-1121A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721949 | ||||||
chr14:77721961
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1131-1133A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77721961 | ||||||
chr14:77722023
|
C | A | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1130+1158G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722023 | ||||||
chr14:77722304
|
T | TA | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1130+876dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722304 | ||||||
chr14:77722535
|
T | C | 38 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(35): Show | 40 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1130+646A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722535 | ||||||
chr14:77722558
|
A | G | 5 | a0001c0001t0001g0170a0001c0001t0001g0250a0001c0001t0001g0314others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130+623T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722558 | ||||||
chr14:77722560
|
A | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0250 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1130+621T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722560 | ||||||
chr14:77722594
|
A | T | 2 | a0001c0003t0001g0053a0001c0003t0001g0054 | 2 | HG01516.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1130+587T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722594 | ||||||
chr14:77722769
|
C | A | 1 | a0001c0001t0001g0304 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1130+412G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722769 | ||||||
chr14:77722793
|
G | T | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1130+388C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722793 | ||||||
chr14:77722838
|
C | CT | 144 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(141): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1130+342dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722838 | ||||||
chr14:77722838
|
C | CTT | 61 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0174others(58): Show | 64 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1130+341_1130+342d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722838 | ||||||
chr14:77722838
|
C | CTTT | 8 | a0001c0001t0001g0288a0001c0001t0001g0294a0001c0001t0001g0300others(5): Show | 8 | HG00558.hp2 HG00621.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1130+340_1130+342d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722838 | ||||||
chr14:77722885
|
C | A | 2 | a0001c0002t0001g0097a0001c0002t0001g0099 | 2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1130+296G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722885 | ||||||
chr14:77722893
|
G | A | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+288C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722893 | ||||||
chr14:77722913
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1130+268G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722913 | ||||||
chr14:77722959
|
C | T | 2 | a0001c0003t0001g0057a0001c0003t0001g0065 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1130+222G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77722959 | ||||||
chr14:77723041
|
G | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(4): Show | 7 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1130+140C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77723041 | ||||||
chr14:77723057
|
C | G | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1130+124G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77723057 | ||||||
chr14:77723082
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1130+99G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 11/13 | chr14 | 77723082 | ||||||
chr14:77723354
|
T | C | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-77A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723354 | ||||||
chr14:77723559
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1034-282C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723559 | ||||||
chr14:77723614
|
T | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1034-337A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723614 | ||||||
chr14:77723662
|
T | C | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1034-385A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723662 | ||||||
chr14:77723706
|
A | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-429T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723706 | ||||||
chr14:77723940
|
T | C | 1 | a0001c0001t0004g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1034-663A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723940 | ||||||
chr14:77723995
|
TAA | T | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1034-720_1034-719d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77723995 | ||||||
chr14:77724053
|
C | T | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-776G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724053 | ||||||
chr14:77724088
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1034-811G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724088 | ||||||
chr14:77724101
|
T | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1034-824A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724101 | ||||||
chr14:77724155
|
T | C | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1034-878A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724155 | ||||||
chr14:77724181
|
A | G | 2 | a0001c0003t0001g0010a0001c0003t0001g0060 | 3 | HG01109.hp1 HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1034-904T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724181 | ||||||
chr14:77724222
|
A | G | 1 | a0001c0002t0001g0027 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1034-945T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724222 | ||||||
chr14:77724381
|
T | A | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1034-1104A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724381 | ||||||
chr14:77724419
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1034-1142G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724419 | ||||||
chr14:77724529
|
C | T | 1 | a0001c0001t0005g0274 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1034-1252G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724529 | ||||||
chr14:77724568
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1034-1291G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724568 | ||||||
chr14:77724765
|
T | C | 1 | a0001c0003t0002g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1034-1488A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77724765 | ||||||
chr14:77725072
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1034-1795A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725072 | ||||||
chr14:77725105
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1034-1828C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725105 | ||||||
chr14:77725169
|
A | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-1892T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725169 | ||||||
chr14:77725256
|
T | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1034-1979A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725256 | ||||||
chr14:77725460
|
G | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-2183C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725460 | ||||||
chr14:77725600
|
G | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0303a0001c0001t0001g0310others(2): Show | 6 | HG00558.hp2 HG00673.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-2323C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725600 | ||||||
chr14:77725668
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1034-2391G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725668 | ||||||
chr14:77725738
|
C | G | 1 | a0001c0002t0001g0074 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1034-2461G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725738 | ||||||
chr14:77725907
|
C | T | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1034-2630G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725907 | ||||||
chr14:77725935
|
T | C | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-2658A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725935 | ||||||
chr14:77725948
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1034-2671C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77725948 | ||||||
chr14:77726003
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1034-2726A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726003 | ||||||
chr14:77726280
|
T | C | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1034-3003A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726280 | ||||||
chr14:77726465
|
A | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1034-3188T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726465 | ||||||
chr14:77726470
|
T | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0180a0001c0001t0001g0181others(7): Show | 11 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1034-3193A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726470 | ||||||
chr14:77726470
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1034-3193A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726470 | ||||||
chr14:77726585
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1034-3308A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726585 | ||||||
chr14:77726629
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1034-3352C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726629 | ||||||
chr14:77726680
|
G | A | 1 | a0001c0001t0004g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1034-3403C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726680 | ||||||
chr14:77726825
|
A | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0045 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1034-3548T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77726825 | ||||||
chr14:77727046
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1034-3769A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727046 | ||||||
chr14:77727056
|
G | GT | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1034-3780dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727056 | ||||||
chr14:77727078
|
A | G | 326 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1034-3801T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727078 | ||||||
chr14:77727118
|
A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(114): Show | 132 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1034-3841T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727118 | ||||||
chr14:77727202
|
C | T | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1033+3786G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727202 | ||||||
chr14:77727555
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1033+3433A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727555 | ||||||
chr14:77727573
|
T | C | 21 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(18): Show | 25 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033+3415A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727573 | ||||||
chr14:77727664
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1033+3324C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727664 | ||||||
chr14:77727748
|
G | A | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1033+3240C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727748 | ||||||
chr14:77727852
|
T | C | 5 | a0001c0001t0001g0158a0001c0001t0001g0173a0001c0001t0001g0182others(2): Show | 5 | HG01256.hp2 HG01433.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1033+3136A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727852 | ||||||
chr14:77727869
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1033+3119C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727869 | ||||||
chr14:77727903
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1033+3085A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727903 | ||||||
chr14:77727909
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1033+3079C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727909 | ||||||
chr14:77727949
|
G | A | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1033+3039C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77727949 | ||||||
chr14:77728051
|
T | TA | 180 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(177): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1033+2936dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728051 | ||||||
chr14:77728051
|
T | TAA | 26 | a0001c0001t0001g0007a0001c0001t0001g0171a0001c0001t0001g0319others(23): Show | 30 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1033+2935_1033+293 others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728051 | ||||||
chr14:77728098
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1033+2890C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728098 | ||||||
chr14:77728134
|
T | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1033+2854A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728134 | ||||||
chr14:77728392
|
A | C | 1 | a0001c0003t0002g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1033+2596T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728392 | ||||||
chr14:77728438
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 201 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1033+2550G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728438 | ||||||
chr14:77728512
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1033+2476A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728512 | ||||||
chr14:77728559
|
T | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0313 | 2 | HG00558.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1033+2429A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728559 | ||||||
chr14:77728729
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1033+2259G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728729 | ||||||
chr14:77728946
|
G | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1033+2042C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728946 | ||||||
chr14:77728975
|
A | G | 1 | a0001c0003t0002g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1033+2013T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728975 | ||||||
chr14:77728991
|
C | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0095a0001c0002t0001g0098 | 3 | HG02622.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1033+1997G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77728991 | ||||||
chr14:77729213
|
C | T | 8 | a0001c0001t0001g0284a0001c0001t0001g0287a0001c0001t0001g0288others(5): Show | 8 | HG00544.hp2 HG00621.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1033+1775G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729213 | ||||||
chr14:77729348
|
C | T | 20 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(17): Show | 22 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1033+1640G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729348 | ||||||
chr14:77729390
|
T | C | 65 | a0001c0002t0001g0083a0001c0003t0001g0009a0001c0003t0001g0010others(62): Show | 72 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1033+1598A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729390 | ||||||
chr14:77729439
|
T | C | 312 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(309): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1033+1549A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729439 | ||||||
chr14:77729469
|
T | C | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1033+1519A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729469 | ||||||
chr14:77729530
|
AAT | A | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1033+1456_1033+145 others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729530 | ||||||
chr14:77729744
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1033+1244C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729744 | ||||||
chr14:77729926
|
A | G | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.1033+1062T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729926 | ||||||
chr14:77729977
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+1011G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77729977 | ||||||
chr14:77730025
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1033+963C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730025 | ||||||
chr14:77730111
|
C | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+877G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730111 | ||||||
chr14:77730410
|
T | G | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1033+578A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730410 | ||||||
chr14:77730430
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0180a0001c0001t0001g0181others(7): Show | 11 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1033+558A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730430 | ||||||
chr14:77730504
|
C | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+484G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730504 | ||||||
chr14:77730520
|
T | C | 1 | a0001c0003t0002g0013 | 2 | NA18971.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1033+468A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730520 | ||||||
chr14:77730521
|
T | G | 1 | a0001c0003t0001g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1033+467A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730521 | ||||||
chr14:77730877
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1033+111A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730877 | ||||||
chr14:77730940
|
T | C | 23 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0013others(20): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1033+48A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 10/13 | chr14 | 77730940 | ||||||
chr14:77731197
|
T | C | 1 | a0001c0004t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892-68A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731197 | ||||||
chr14:77731428
|
C | G | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-299G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731428 | ||||||
chr14:77731457
|
T | C | 2 | a0001c0002t0001g0097a0001c0002t0001g0099 | 2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.892-328A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731457 | ||||||
chr14:77731563
|
T | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 7 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-434A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731563 | ||||||
chr14:77731613
|
T | G | 2 | a0001c0003t0002g0129a0001c0003t0002g0135 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.892-484A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731613 | ||||||
chr14:77731653
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.892-524A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731653 | ||||||
chr14:77731729
|
A | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.892-600T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731729 | ||||||
chr14:77731800
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 6 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-671C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731800 | ||||||
chr14:77731844
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+641A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731844 | ||||||
chr14:77731987
|
T | C | 1 | a0001c0002t0001g0081 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.891+498A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77731987 | ||||||
chr14:77732041
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.891+444G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732041 | ||||||
chr14:77732092
|
C | T | 1 | a0001c0003t0002g0137 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.891+393G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732092 | ||||||
chr14:77732106
|
C | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.891+379G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732106 | ||||||
chr14:77732217
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+268T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732217 | ||||||
chr14:77732443
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.891+42A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 9/13 | chr14 | 77732443 | ||||||
chr14:77732653
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.775-52C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732653 | ||||||
chr14:77732666
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0294 | 3 | NA18972.hp1 NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.775-65A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732666 | ||||||
chr14:77732676
|
T | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(115): Show | 133 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.775-75A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732676 | ||||||
chr14:77732767
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.775-166G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732767 | ||||||
chr14:77732789
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.775-188G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732789 | ||||||
chr14:77732853
|
G | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.775-252C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77732853 | ||||||
chr14:77733121
|
G | A | 1 | a0001c0003t0002g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.775-520C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733121 | ||||||
chr14:77733129
|
T | G | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.775-528A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733129 | ||||||
chr14:77733224
|
T | TCAGA | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.775-624_775-623ins others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733224 | ||||||
chr14:77733405
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-804A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733405 | ||||||
chr14:77733422
|
A | G | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.775-821T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733422 | ||||||
chr14:77733465
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.775-864G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733465 | ||||||
chr14:77733490
|
A | AT | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.775-890dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733490 | ||||||
chr14:77733732
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.775-1131C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733732 | ||||||
chr14:77733742
|
C | CA | 14 | a0001c0002t0001g0068a0001c0002t0001g0075a0001c0002t0001g0081others(11): Show | 14 | HG00544.hp1 HG01192.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.775-1142dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
C | CAA | 14 | a0001c0002t0001g0073a0001c0003t0001g0321a0001c0003t0002g0005others(11): Show | 16 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.775-1143_775-1142d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
C | CAAA | 10 | a0001c0003t0002g0012a0001c0003t0002g0127a0001c0003t0002g0128others(7): Show | 11 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.775-1144_775-1142d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
C | CAAAAAA | 7 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0125others(4): Show | 8 | HG01257.hp2 NA18946.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-1147_775-1142d others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
C | CAAAAAAA | 9 | a0001c0003t0001g0124a0001c0003t0001g0144a0001c0003t0001g0145others(6): Show | 9 | HG01258.hp1 HG03710.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-1148_775-1142d others(9): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
CA | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0016others(96): Show | 112 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.775-1142delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
CAA | C | 77 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0023others(74): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.775-1143_775-1142d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
CAAA | C | 17 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0031others(14): Show | 18 | HG01515.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.775-1144_775-1142d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733742
|
CAAAA | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0243others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-1145_775-1142d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733742 | ||||||
chr14:77733754
|
A | C | 1 | a0001c0002t0001g0088 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-1153T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733754 | ||||||
chr14:77733769
|
C | A | 1 | a0001c0001t0001g0263 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.775-1168G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733769 | ||||||
chr14:77733781
|
G | GA | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.774+1165dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77733781 | ||||||
chr14:77734049
|
G | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.774+898C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734049 | ||||||
chr14:77734056
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.774+891A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734056 | ||||||
chr14:77734242
|
C | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.774+705G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734242 | ||||||
chr14:77734277
|
G | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.774+670C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734277 | ||||||
chr14:77734549
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.774+398G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734549 | ||||||
chr14:77734566
|
C | T | 3 | a0001c0002t0001g0100a0001c0002t0001g0101a0001c0002t0001g0102 | 3 | NA18979.hp1 NA18985.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.774+381G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734566 | ||||||
chr14:77734594
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774+353G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734594 | ||||||
chr14:77734736
|
CA | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.774+210delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734736 | ||||||
chr14:77734811
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.774+136G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734811 | ||||||
chr14:77734918
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.774+29T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 8/13 | chr14 | 77734918 | ||||||
chr14:77735195
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.709-183T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735195 | ||||||
chr14:77735452
|
AT | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.709-441delA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735452 | ||||||
chr14:77735601
|
T | G | 1 | a0001c0003t0001g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.708+336A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735601 | ||||||
chr14:77735601
|
T | TGAAAAAT others(342): Show |
1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.708+335_708+336ins others(349): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735601 | ||||||
chr14:77735630
|
A | G | 1 | a0001c0001t0001g0007 | 3 | HG03471.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.708+307T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735630 | ||||||
chr14:77735732
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.708+205C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735732 | ||||||
chr14:77735789
|
T | C | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.708+148A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 7/13 | chr14 | 77735789 | ||||||
chr14:77736029
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0045 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.639-23C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736029 | ||||||
chr14:77736036
|
A | G | 5 | a0001c0003t0001g0056a0001c0003t0001g0063a0001c0003t0001g0321others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-30T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736036 | ||||||
chr14:77736068
|
A | C | 2 | a0001c0003t0001g0323a0001c0007t0001g0322 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.639-62T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736068 | ||||||
chr14:77736091
|
T | TA | 2 | a0001c0003t0001g0010a0001c0003t0001g0060 | 3 | HG01109.hp1 HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.639-86dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736091 | ||||||
chr14:77736104
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.639-98G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736104 | ||||||
chr14:77736135
|
TAC | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-131_639-130del others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736135 | ||||||
chr14:77736334
|
C | T | 32 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0279others(29): Show | 33 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.639-328G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736334 | ||||||
chr14:77736346
|
G | A | 1 | a0001c0003t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.639-340C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736346 | ||||||
chr14:77736394
|
A | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0180a0001c0001t0001g0181others(7): Show | 11 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.639-388T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736394 | ||||||
chr14:77736430
|
A | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.639-424T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736430 | ||||||
chr14:77736434
|
A | T | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.639-428T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736434 | ||||||
chr14:77736548
|
C | CA | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(149): Show | 169 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.638+422dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736548 | ||||||
chr14:77736548
|
C | CAAAAAAA | 37 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(34): Show | 40 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.638+422_638+423ins others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736548 | ||||||
chr14:77736549
|
A | AAAAAAAC | 28 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0157others(25): Show | 31 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.638+421_638+422ins others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736549 | ||||||
chr14:77736549
|
A | AAAAAAC | 8 | a0001c0002t0001g0116a0001c0003t0002g0005a0001c0003t0002g0012others(5): Show | 11 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.638+416_638+421dup others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736549 | ||||||
chr14:77736549
|
A | AAAAAACA others(5): Show |
16 | a0001c0003t0002g0013a0001c0003t0002g0025a0001c0003t0002g0128others(13): Show | 17 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.638+410_638+421dup others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736549 | ||||||
chr14:77736550
|
AAAAAC | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0276a0001c0001t0001g0291others(1): Show | 4 | HG02683.hp1 HG02698.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+416_638+420del others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736550 | ||||||
chr14:77736555
|
C | A | 1 | a0001c0004t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.638+416G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736555 | ||||||
chr14:77736585
|
A | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.638+386T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736585 | ||||||
chr14:77736906
|
A | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.638+65T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 6/13 | chr14 | 77736906 | ||||||
chr14:77737189
|
T | C | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.534-114A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737189 | ||||||
chr14:77737195
|
A | C | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.534-120T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737195 | ||||||
chr14:77737293
|
T | C | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.534-218A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737293 | ||||||
chr14:77737307
|
C | T | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.534-232G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737307 | ||||||
chr14:77737330
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.534-255T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737330 | ||||||
chr14:77737334
|
G | A | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.534-259C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737334 | ||||||
chr14:77737370
|
T | C | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.534-295A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737370 | ||||||
chr14:77737569
|
C | T | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.534-494G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737569 | ||||||
chr14:77737757
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.534-682C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737757 | ||||||
chr14:77737986
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.533+792G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737986 | ||||||
chr14:77737991
|
C | CA | 13 | a0001c0001t0001g0170a0001c0001t0001g0193a0001c0001t0001g0281others(10): Show | 13 | HG00558.hp1 HG01192.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.533+786dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | ||||||
chr14:77737991
|
C | CAA | 183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(180): Show | 204 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(201): Show |
intron_variant | MODIFIER | c.533+785_533+786dup others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | ||||||
chr14:77737991
|
C | CAAA | 52 | a0001c0001t0001g0020a0001c0001t0001g0183a0001c0001t0001g0216others(49): Show | 58 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.533+784_533+786dup others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | ||||||
chr14:77737991
|
C | CAAAA | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.533+783_533+786dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77737991 | ||||||
chr14:77738190
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.533+588G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738190 | ||||||
chr14:77738193
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.533+585C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738193 | ||||||
chr14:77738252
|
G | C | 1 | a0001c0002t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.533+526C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738252 | ||||||
chr14:77738320
|
A | G | 1 | a0001c0002t0001g0102 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.533+458T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738320 | ||||||
chr14:77738429
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+349G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738429 | ||||||
chr14:77738643
|
G | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.533+135C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 5/13 | chr14 | 77738643 | ||||||
chr14:77739173
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-112G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739173 | ||||||
chr14:77739351
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0268 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.331-290G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739351 | ||||||
chr14:77739357
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.331-296A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739357 | ||||||
chr14:77739461
|
T | G | 4 | a0001c0002t0001g0004a0001c0002t0001g0103a0001c0002t0001g0105others(1): Show | 6 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-400A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739461 | ||||||
chr14:77739487
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0218 | 3 | HG00408.hp2 NA18747.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.331-426A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739487 | ||||||
chr14:77739505
|
T | C | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-444A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739505 | ||||||
chr14:77739512
|
C | T | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-451G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739512 | ||||||
chr14:77739612
|
GAAAA | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-555_331-552del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739612 | ||||||
chr14:77739692
|
A | G | 1 | a0001c0003t0003g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.331-631T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739692 | ||||||
chr14:77739805
|
C | A | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.331-744G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739805 | ||||||
chr14:77739857
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.331-796C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739857 | ||||||
chr14:77739930
|
C | T | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-869G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739930 | ||||||
chr14:77739977
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.331-916T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77739977 | ||||||
chr14:77740026
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 7 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-965G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740026 | ||||||
chr14:77740135
|
T | TA | 7 | a0001c0002t0001g0068a0001c0002t0001g0082a0001c0003t0001g0152others(4): Show | 7 | HG01496.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-1075dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | ||||||
chr14:77740135
|
T | TAA | 31 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(28): Show | 33 | HG00323.hp2 HG01167.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.331-1076_331-1075d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | ||||||
chr14:77740135
|
T | TAAA | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-1077_331-1075d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | ||||||
chr14:77740135
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-1085_331-1075d others(13): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740135 | ||||||
chr14:77740156
|
AAAGAG | A | 12 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0243others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.331-1100_331-1096d others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740156 | ||||||
chr14:77740157
|
A | G | 1 | a0001c0002t0001g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.331-1096T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740157 | ||||||
chr14:77740157
|
AAG | A | 11 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0204others(8): Show | 11 | HG01257.hp1 HG01981.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-1098_331-1097d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740157 | ||||||
chr14:77740157
|
AAGAG | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0031others(25): Show | 30 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.331-1100_331-1097d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740157 | ||||||
chr14:77740158
|
AGAG | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 191 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.331-1100_331-1098d others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740158 | ||||||
chr14:77740161
|
G | A | 11 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0204others(8): Show | 11 | HG01257.hp1 HG01981.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-1100C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740161 | ||||||
chr14:77740287
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.331-1226A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740287 | ||||||
chr14:77740486
|
T | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-1425A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740486 | ||||||
chr14:77740835
|
G | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0024others(42): Show | 49 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.331-1774C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740835 | ||||||
chr14:77740862
|
C | T | 1 | a0001c0001t0005g0274 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.331-1801G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740862 | ||||||
chr14:77740925
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.331-1864G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77740925 | ||||||
chr14:77741005
|
G | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(4): Show | 7 | HG02280.hp1 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-1944C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741005 | ||||||
chr14:77741029
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0001g0219others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-1968C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741029 | ||||||
chr14:77741096
|
C | CA | 6 | a0001c0002t0001g0068a0001c0002t0001g0073a0001c0002t0001g0085others(3): Show | 6 | HG02027.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-2036dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | ||||||
chr14:77741096
|
CA | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.331-2036delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | ||||||
chr14:77741096
|
CAA | C | 42 | a0001c0001t0001g0211a0001c0001t0001g0221a0001c0001t0001g0257others(39): Show | 47 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.331-2037_331-2036d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | ||||||
chr14:77741096
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0003t0001g0156 | 3 | NA18943.hp2 NA18947.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.331-2047_331-2036d others(14): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741096 | ||||||
chr14:77741137
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.331-2076T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741137 | ||||||
chr14:77741155
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-2094A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741155 | ||||||
chr14:77741312
|
G | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-2251C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741312 | ||||||
chr14:77741365
|
G | A | 2 | a0001c0003t0002g0129a0001c0003t0002g0135 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.331-2304C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741365 | ||||||
chr14:77741382
|
A | G | 1 | a0001c0003t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331-2321T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741382 | ||||||
chr14:77741486
|
G | A | 1 | a0001c0002t0001g0195 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.331-2425C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741486 | ||||||
chr14:77741550
|
T | TA | 2 | a0001c0001t0001g0016a0001c0001t0001g0218 | 3 | HG00408.hp2 NA18747.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.331-2490dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741550 | ||||||
chr14:77741736
|
A | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.331-2675T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741736 | ||||||
chr14:77741742
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.331-2681C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741742 | ||||||
chr14:77741742
|
GA | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0171a0001c0001t0001g0178others(5): Show | 9 | HG00642.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-2682delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741742 | ||||||
chr14:77741778
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.331-2717C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741778 | ||||||
chr14:77741951
|
A | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-2890T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741951 | ||||||
chr14:77741962
|
G | A | 5 | a0001c0001t0001g0284a0001c0001t0001g0288a0001c0001t0001g0306others(2): Show | 5 | HG00544.hp2 HG00621.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-2901C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77741962 | ||||||
chr14:77742035
|
A | AT | 7 | a0001c0001t0001g0246a0001c0001t0001g0309a0001c0003t0002g0005others(4): Show | 10 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-2975dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742035 | ||||||
chr14:77742085
|
G | C | 7 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0056others(4): Show | 9 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.331-3024C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742085 | ||||||
chr14:77742093
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.331-3032C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742093 | ||||||
chr14:77742125
|
G | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-3064C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742125 | ||||||
chr14:77742225
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.331-3164C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742225 | ||||||
chr14:77742413
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.331-3352G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742413 | ||||||
chr14:77742571
|
C | T | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.331-3510G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742571 | ||||||
chr14:77742723
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.331-3662G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742723 | ||||||
chr14:77742761
|
A | G | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-3700T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742761 | ||||||
chr14:77742793
|
G | A | 1 | a0001c0002t0001g0195 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.331-3732C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742793 | ||||||
chr14:77742862
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0289 | 3 | HG01175.hp1 HG01978.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.331-3801C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742862 | ||||||
chr14:77742991
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(116): Show | 134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.331-3930G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77742991 | ||||||
chr14:77743014
|
T | C | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-3953A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743014 | ||||||
chr14:77743218
|
T | C | 8 | a0001c0003t0002g0128a0001c0003t0002g0130a0001c0003t0002g0131others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-4157A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743218 | ||||||
chr14:77743261
|
GA | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-4201delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743261 | ||||||
chr14:77743307
|
T | C | 1 | a0001c0003t0001g0155 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.331-4246A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743307 | ||||||
chr14:77743500
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.331-4439G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743500 | ||||||
chr14:77743525
|
C | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.331-4464G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743525 | ||||||
chr14:77743526
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-4465C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743526 | ||||||
chr14:77743842
|
C | A | 1 | a0001c0003t0001g0156 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.331-4781G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743842 | ||||||
chr14:77743910
|
T | A | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.331-4849A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77743910 | ||||||
chr14:77744095
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331-5034G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744095 | ||||||
chr14:77744135
|
CA | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.331-5075delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744135 | ||||||
chr14:77744135
|
CAA | C | 13 | a0001c0001t0001g0174a0001c0001t0001g0281a0001c0003t0001g0060others(10): Show | 14 | HG01069.hp2 HG01167.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.331-5076_331-5075d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744135 | ||||||
chr14:77744191
|
G | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.331-5130C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744191 | ||||||
chr14:77744446
|
C | CA | 7 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0002t0001g0003others(4): Show | 9 | HG00099.hp1 HG01099.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-5386dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744446 | ||||||
chr14:77744446
|
CA | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(174): Show | 195 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.331-5386delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744446 | ||||||
chr14:77744446
|
CAA | C | 43 | a0001c0001t0001g0168a0001c0001t0001g0188a0001c0001t0001g0196others(40): Show | 48 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.331-5387_331-5386d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744446 | ||||||
chr14:77744615
|
C | T | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.331-5554G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744615 | ||||||
chr14:77744644
|
A | G | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.331-5583T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744644 | ||||||
chr14:77744691
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.331-5630G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744691 | ||||||
chr14:77744882
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.331-5821T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744882 | ||||||
chr14:77744934
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.331-5873G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744934 | ||||||
chr14:77744947
|
C | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.331-5886G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77744947 | ||||||
chr14:77745242
|
T | C | 4 | a0001c0004t0001g0049a0001c0004t0001g0050a0001c0004t0001g0051others(1): Show | 4 | HG03195.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+6077A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745242 | ||||||
chr14:77745320
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+5999C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745320 | ||||||
chr14:77745404
|
T | A | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+5915A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745404 | ||||||
chr14:77745435
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.330+5884G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745435 | ||||||
chr14:77745568
|
A | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.330+5751T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745568 | ||||||
chr14:77745681
|
T | G | 2 | a0001c0003t0001g0149a0001c0003t0001g0150 | 2 | HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.330+5638A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745681 | ||||||
chr14:77745891
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.330+5428C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745891 | ||||||
chr14:77745904
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.330+5415C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77745904 | ||||||
chr14:77746000
|
G | T | 1 | a0001c0006t0001g0096 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.330+5319C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746000 | ||||||
chr14:77746119
|
G | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.330+5200C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746119 | ||||||
chr14:77746173
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.330+5146A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746173 | ||||||
chr14:77746176
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0040 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.330+5143G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746176 | ||||||
chr14:77746201
|
A | G | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.330+5118T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746201 | ||||||
chr14:77746234
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+5085G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746234 | ||||||
chr14:77746314
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.330+5005C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746314 | ||||||
chr14:77746423
|
G | A | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+4896C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746423 | ||||||
chr14:77746429
|
TCA | T | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+4888_330+4889d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746429 | ||||||
chr14:77746519
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.330+4800A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746519 | ||||||
chr14:77746757
|
T | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.330+4562A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746757 | ||||||
chr14:77746901
|
C | T | 1 | a0001c0003t0002g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.330+4418G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746901 | ||||||
chr14:77746922
|
GTCTCCCT others(5): Show |
G | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.330+4385_330+4396d others(14): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77746922 | ||||||
chr14:77747004
|
T | G | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.330+4315A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747004 | ||||||
chr14:77747041
|
C | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.330+4278G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747041 | ||||||
chr14:77747065
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0299 | 2 | HG02293.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.330+4254G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747065 | ||||||
chr14:77747073
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0045 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.330+4246G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747073 | ||||||
chr14:77747179
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.330+4140C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747179 | ||||||
chr14:77747315
|
C | T | 79 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(76): Show | 87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.330+4004G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747315 | ||||||
chr14:77747514
|
C | T | 2 | a0001c0001t0001g0275a0001c0004t0001g0049 | 2 | HG00609.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.330+3805G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747514 | ||||||
chr14:77747525
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+3794G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747525 | ||||||
chr14:77747533
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330+3786C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747533 | ||||||
chr14:77747601
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.330+3718G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747601 | ||||||
chr14:77747607
|
C | A | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.330+3712G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747607 | ||||||
chr14:77747638
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.330+3681G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747638 | ||||||
chr14:77747651
|
A | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.330+3668T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747651 | ||||||
chr14:77747669
|
G | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.330+3650C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747669 | ||||||
chr14:77747675
|
GCCCGGCA others(39): Show |
G | 1 | a0001c0002t0001g0085 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.330+3598_330+3643d others(48): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747675 | ||||||
chr14:77747678
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(96): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.330+3641G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747678 | ||||||
chr14:77747695
|
AGGAGGGA others(39): Show |
A | 4 | a0001c0001t0001g0007a0001c0001t0001g0159a0001c0001t0001g0319others(1): Show | 6 | HG02818.hp2 HG02922.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+3578_330+3623d others(48): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747695 | ||||||
chr14:77747725
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0186 | 2 | NA19082.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.330+3594C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747725 | ||||||
chr14:77747736
|
CGTCT | C | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+3579_330+3582d others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747736 | ||||||
chr14:77747740
|
T | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(238): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.330+3579A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747740 | ||||||
chr14:77747767
|
C | G | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+3552G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747767 | ||||||
chr14:77747786
|
C | T | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+3533G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747786 | ||||||
chr14:77747818
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+3501C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747818 | ||||||
chr14:77747826
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.330+3493G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747826 | ||||||
chr14:77747854
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.330+3465G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747854 | ||||||
chr14:77747912
|
T | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+3407A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747912 | ||||||
chr14:77747946
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.330+3373G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747946 | ||||||
chr14:77747947
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(114): Show | 132 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.330+3372C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747947 | ||||||
chr14:77747962
|
G | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.330+3357C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77747962 | ||||||
chr14:77748239
|
CCTAATCT | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.330+3073_330+3079d others(9): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748239 | ||||||
chr14:77748382
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.330+2937G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748382 | ||||||
chr14:77748447
|
GA | G | 18 | a0001c0003t0002g0013a0001c0003t0002g0025a0001c0003t0002g0128others(15): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.330+2871delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748447 | ||||||
chr14:77748532
|
A | G | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.330+2787T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748532 | ||||||
chr14:77748900
|
T | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.330+2419A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748900 | ||||||
chr14:77748905
|
T | A | 45 | a0001c0002t0001g0083a0001c0003t0001g0014a0001c0003t0001g0123others(42): Show | 50 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.330+2414A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748905 | ||||||
chr14:77748956
|
A | G | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+2363T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748956 | ||||||
chr14:77748971
|
T | C | 2 | a0001c0002t0001g0108a0001c0002t0001g0109 | 2 | HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.330+2348A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77748971 | ||||||
chr14:77749184
|
C | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+2135G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749184 | ||||||
chr14:77749262
|
G | A | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.330+2057C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749262 | ||||||
chr14:77749305
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.330+2014G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749305 | ||||||
chr14:77749444
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330+1875G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749444 | ||||||
chr14:77749537
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.330+1782A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749537 | ||||||
chr14:77749628
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.330+1691T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749628 | ||||||
chr14:77749663
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.330+1656C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749663 | ||||||
chr14:77749671
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.330+1648T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749671 | ||||||
chr14:77749704
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.330+1615A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749704 | ||||||
chr14:77749763
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.330+1556A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749763 | ||||||
chr14:77749827
|
G | T | 1 | a0001c0003t0001g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.330+1492C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749827 | ||||||
chr14:77749948
|
C | A | 3 | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0001g0312 | 3 | HG02486.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.330+1371G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77749948 | ||||||
chr14:77750044
|
A | G | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.330+1275T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750044 | ||||||
chr14:77750176
|
G | A | 10 | a0001c0003t0001g0053a0001c0003t0001g0054a0001c0003t0001g0055others(7): Show | 10 | HG00280.hp1 HG01516.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.330+1143C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750176 | ||||||
chr14:77750260
|
C | T | 23 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0013others(20): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.330+1059G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750260 | ||||||
chr14:77750261
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.330+1058C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750261 | ||||||
chr14:77750502
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.330+817C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750502 | ||||||
chr14:77750510
|
A | G | 1 | a0001c0002t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.330+809T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750510 | ||||||
chr14:77750629
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.330+690C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750629 | ||||||
chr14:77750667
|
GA | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.330+651delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750667 | ||||||
chr14:77750674
|
A | G | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.330+645T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750674 | ||||||
chr14:77750949
|
T | C | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.330+370A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77750949 | ||||||
chr14:77751254
|
G | A | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+65C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 3/13 | chr14 | 77751254 | ||||||
chr14:77751532
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-52T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751532 | ||||||
chr14:77751567
|
TCCTTAGT others(3): Show |
T | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.169-97_169-88delCA others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751567 | ||||||
chr14:77751733
|
G | C | 1 | a0001c0002t0001g0102 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.169-253C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751733 | ||||||
chr14:77751805
|
G | GAC | 9 | a0001c0001t0001g0038a0001c0002t0001g0011a0001c0002t0001g0084others(6): Show | 10 | HG01167.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-327_169-326dup others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
G | GACAC | 6 | a0001c0002t0001g0028a0001c0002t0001g0077a0001c0002t0001g0085others(3): Show | 6 | HG01109.hp2 HG01928.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-329_169-326dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
G | GACACAC | 26 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0027others(23): Show | 34 | HG00099.hp1 HG00423.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.169-331_169-326dup others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
G | GACACACA others(1): Show |
6 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0002t0001g0095others(3): Show | 6 | HG01891.hp2 HG02809.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-333_169-326dup others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
G | GACACACA others(3): Show |
4 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0099others(1): Show | 4 | HG00544.hp1 HG01106.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-335_169-326dup others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
GAC | G | 46 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0040others(43): Show | 48 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.169-327_169-326del others(2): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
GACACACA others(3): Show |
G | 28 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0014others(25): Show | 31 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.169-335_169-326del others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
GACACACA others(5): Show |
G | 1 | a0001c0003t0001g0053 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.169-337_169-326del others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
GACACACA others(9): Show |
G | 2 | a0001c0001t0001g0308a0001c0003t0001g0058 | 2 | HG01891.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.169-341_169-326del others(16): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751805
|
GACACACA others(13): Show |
G | 3 | a0001c0003t0001g0057a0001c0003t0001g0064a0001c0003t0001g0065 | 3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.169-345_169-326del others(20): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751805 | ||||||
chr14:77751807
|
C | G | 1 | a0001c0003t0002g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.169-327G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751807 | ||||||
chr14:77751814
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.169-334T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751814 | ||||||
chr14:77751821
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.169-341G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751821 | ||||||
chr14:77751837
|
CACACA | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0159a0001c0001t0001g0319others(1): Show | 6 | HG02818.hp2 HG02922.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-362_169-358del others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751837 | ||||||
chr14:77751838
|
A | ACACACAC | 3 | a0001c0002t0001g0004a0001c0002t0001g0103a0001c0002t0006g0104 | 5 | HG00099.hp2 HG00733.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-365_169-359dup others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751838 | ||||||
chr14:77751839
|
CACA | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 9 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-362_169-360del others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751839 | ||||||
chr14:77751841
|
CA | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0004g0241 | 3 | HG02486.hp2 HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.169-362delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751841 | ||||||
chr14:77751843
|
CACCACA | C | 11 | a0001c0001t0001g0165a0001c0001t0001g0176a0001c0001t0001g0177others(8): Show | 11 | HG00673.hp2 HG02165.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-369_169-364del others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751843 | ||||||
chr14:77751844
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.169-364T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751844 | ||||||
chr14:77751844
|
AC | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.169-365delG | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751844 | ||||||
chr14:77751845
|
C | A | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.169-365G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751845
|
C | CA | 13 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(10): Show | 13 | HG01106.hp1 HG03492.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751845
|
C | CACACACA others(3): Show |
6 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0002t0001g0076others(3): Show | 6 | HG02615.hp1 NA18945.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751845
|
C | CACACACC others(1): Show |
4 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0244others(1): Show | 4 | HG02280.hp1 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751845
|
C | CACACCA | 4 | a0001c0001t0001g0243a0001c0001t0001g0272a0001c0002t0001g0118others(1): Show | 4 | HG02258.hp1 NA18906.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751845
|
C | CACCA | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0271others(1): Show | 4 | HG03654.hp2 HG04199.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-366_169-365ins others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751845
|
CCACA | C | 11 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0196others(8): Show | 11 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-369_169-366del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751845 | ||||||
chr14:77751848
|
CA | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0015others(84): Show | 102 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.169-369delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751848 | ||||||
chr14:77751865
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0276 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-385T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77751865 | ||||||
chr14:77752065
|
T | C | 18 | a0001c0003t0002g0013a0001c0003t0002g0025a0001c0003t0002g0128others(15): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-585A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752065 | ||||||
chr14:77752096
|
C | G | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.169-616G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752096 | ||||||
chr14:77752413
|
G | A | 4 | a0001c0002t0001g0004a0001c0002t0001g0103a0001c0002t0001g0105others(1): Show | 6 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-933C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752413 | ||||||
chr14:77752499
|
C | G | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.169-1019G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752499 | ||||||
chr14:77752800
|
C | T | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-1320G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752800 | ||||||
chr14:77752801
|
G | A | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-1321C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752801 | ||||||
chr14:77752817
|
A | T | 1 | a0001c0001t0001g0273 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.169-1337T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752817 | ||||||
chr14:77752841
|
T | C | 1 | a0001c0003t0001g0321 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.169-1361A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752841 | ||||||
chr14:77752942
|
T | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 202 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.169-1462A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752942 | ||||||
chr14:77752988
|
TAG | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.169-1510_169-1509d others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77752988 | ||||||
chr14:77753066
|
T | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 50 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-1586A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753066 | ||||||
chr14:77753112
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.169-1632G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753112 | ||||||
chr14:77753207
|
A | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0196 | 2 | NA19065.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.169-1727T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753207 | ||||||
chr14:77753464
|
T | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.168+1503A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753464 | ||||||
chr14:77753469
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.168+1498T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753469 | ||||||
chr14:77753812
|
A | G | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.168+1155T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753812 | ||||||
chr14:77753823
|
C | T | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.168+1144G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753823 | ||||||
chr14:77753825
|
T | C | 4 | a0001c0004t0001g0049a0001c0004t0001g0050a0001c0004t0001g0051others(1): Show | 4 | HG03195.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+1142A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77753825 | ||||||
chr14:77754040
|
A | C | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.168+927T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754040 | ||||||
chr14:77754046
|
A | C | 1 | a0001c0003t0002g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.168+921T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754046 | ||||||
chr14:77754194
|
G | A | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.168+773C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754194 | ||||||
chr14:77754232
|
C | T | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.168+735G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754232 | ||||||
chr14:77754271
|
T | G | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.168+696A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754271 | ||||||
chr14:77754529
|
C | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.168+438G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754529 | ||||||
chr14:77754597
|
C | T | 1 | a0001c0004t0001g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.168+370G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754597 | ||||||
chr14:77754635
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.168+332T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754635 | ||||||
chr14:77754683
|
T | A | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.168+284A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 2/13 | chr14 | 77754683 | ||||||
chr14:77755159
|
C | CAA | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-40_15-39insTT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755159 | ||||||
chr14:77755160
|
T | G | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-40A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755160 | ||||||
chr14:77755161
|
C | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-41G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755161 | ||||||
chr14:77755166
|
G | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-46C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755166 | ||||||
chr14:77755167
|
T | TTCTTTCT others(90): Show |
1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-48_15-47insGAAA others(93): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755167 | ||||||
chr14:77755170
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-50T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755170 | ||||||
chr14:77755171
|
A | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-51T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755171 | ||||||
chr14:77755175
|
G | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-55C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755175 | ||||||
chr14:77755179
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-59T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755179 | ||||||
chr14:77755180
|
C | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-60G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755180 | ||||||
chr14:77755182
|
G | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-62C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755182 | ||||||
chr14:77755184
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-64T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755184 | ||||||
chr14:77755186
|
C | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-66G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755186 | ||||||
chr14:77755188
|
TGGCCACA others(4): Show |
T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-79_15-69delTCTC others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755188 | ||||||
chr14:77755201
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-81T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755201 | ||||||
chr14:77755202
|
A | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-82T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755202 | ||||||
chr14:77755211
|
A | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-91T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755211 | ||||||
chr14:77755213
|
G | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-93C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755213 | ||||||
chr14:77755214
|
A | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-94T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755214 | ||||||
chr14:77755216
|
G | A | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-96C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755216 | ||||||
chr14:77755222
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-102T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755222 | ||||||
chr14:77755225
|
T | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-105A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755225 | ||||||
chr14:77755228
|
CAGAAAAA others(7): Show |
C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-122_15-109delTC others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755228 | ||||||
chr14:77755244
|
T | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-124A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755244 | ||||||
chr14:77755257
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-137T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755257 | ||||||
chr14:77755260
|
G | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-140C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755260 | ||||||
chr14:77755261
|
T | C | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-141A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755261 | ||||||
chr14:77755262
|
A | T | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-142T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755262 | ||||||
chr14:77755272
|
A | G | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-152T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755272 | ||||||
chr14:77755273
|
C | A | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-153G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755273 | ||||||
chr14:77755274
|
T | G | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-154A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755274 | ||||||
chr14:77755277
|
C | A | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-157G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755277 | ||||||
chr14:77755278
|
C | G | 1 | a0002c0005t0001g0285 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.15-158G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755278 | ||||||
chr14:77755386
|
A | G | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-266T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755386 | ||||||
chr14:77755487
|
C | T | 5 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0126others(2): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-367G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755487 | ||||||
chr14:77755725
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.15-605C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755725 | ||||||
chr14:77755744
|
C | CT | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.15-625dupA | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755744 | ||||||
chr14:77755808
|
A | G | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.15-688T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755808 | ||||||
chr14:77755893
|
C | T | 2 | a0001c0002t0001g0106a0001c0002t0001g0107 | 2 | HG02155.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.15-773G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755893 | ||||||
chr14:77755958
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.15-838G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77755958 | ||||||
chr14:77756131
|
T | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-1011A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756131 | ||||||
chr14:77756455
|
T | C | 16 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(13): Show | 17 | HG01257.hp2 HG01258.hp1 HG03710.hp1 others(14): Show |
intron_variant | MODIFIER | c.15-1335A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756455 | ||||||
chr14:77756563
|
T | C | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-1443A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756563 | ||||||
chr14:77756613
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.15-1493C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756613 | ||||||
chr14:77756653
|
G | A | 2 | a0001c0004t0001g0049a0001c0004t0001g0050 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.15-1533C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756653 | ||||||
chr14:77756804
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15-1684C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756804 | ||||||
chr14:77756840
|
T | C | 1 | a0001c0003t0002g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.15-1720A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756840 | ||||||
chr14:77756939
|
G | A | 2 | a0001c0004t0001g0051a0001c0004t0001g0052 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.15-1819C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77756939 | ||||||
chr14:77757224
|
C | CA | 8 | a0001c0001t0001g0265a0001c0001t0001g0315a0001c0002t0001g0077others(5): Show | 11 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-2105dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757224 | ||||||
chr14:77757224
|
CA | C | 68 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0280others(65): Show | 72 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.15-2105delT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757224 | ||||||
chr14:77757307
|
A | C | 2 | a0001c0003t0001g0056a0001c0003t0001g0063 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.15-2187T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757307 | ||||||
chr14:77757862
|
C | T | 23 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0013others(20): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.15-2742G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757862 | ||||||
chr14:77757890
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.15-2770A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757890 | ||||||
chr14:77757919
|
C | CATCT | 55 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0016others(52): Show | 61 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.15-2803_15-2800dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | ||||||
chr14:77757919
|
C | CATCTATC others(1): Show |
21 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(18): Show | 21 | HG00558.hp1 HG00621.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-2807_15-2800dup others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | ||||||
chr14:77757919
|
C | CATCTATC others(5): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0159others(3): Show | 6 | HG00544.hp2 HG02559.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-2811_15-2800dup others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | ||||||
chr14:77757919
|
CATCT | C | 89 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0048others(86): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.15-2803_15-2800del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | ||||||
chr14:77757919
|
CATCTATC others(1): Show |
C | 12 | a0001c0001t0001g0020a0001c0001t0001g0236a0001c0001t0001g0237others(9): Show | 13 | HG01168.hp2 HG02109.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-2807_15-2800del others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | ||||||
chr14:77757919
|
CATCTATC others(5): Show |
C | 6 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-2811_15-2800del others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757919 | ||||||
chr14:77757942
|
CTATCTAT others(9): Show |
C | 1 | a0001c0003t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15-2838_15-2823del others(16): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757942 | ||||||
chr14:77757946
|
CTATCTAT others(5): Show |
C | 19 | a0001c0003t0001g0014a0001c0003t0001g0144a0001c0003t0001g0145others(16): Show | 21 | HG02630.hp1 HG03710.hp1 NA18943.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-2838_15-2827del others(12): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757946 | ||||||
chr14:77757950
|
CTATCGCA others(1): Show |
C | 9 | a0001c0003t0001g0125a0001c0003t0002g0131a0001c0003t0002g0132others(6): Show | 9 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-2838_15-2831del others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757950 | ||||||
chr14:77757954
|
C | T | 12 | a0001c0001t0001g0157a0001c0001t0001g0169a0001c0001t0001g0243others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.15-2834G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757954 | ||||||
chr14:77757955
|
G | T | 2 | a0001c0003t0002g0126a0001c0003t0002g0128 | 2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2835C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757955 | ||||||
chr14:77757955
|
GCAAT | G | 8 | a0001c0003t0001g0123a0001c0003t0001g0124a0001c0003t0002g0005others(5): Show | 11 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-2839_15-2836del others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757955 | ||||||
chr14:77757956
|
C | A | 2 | a0001c0003t0002g0126a0001c0003t0002g0128 | 2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2836G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757956 | ||||||
chr14:77757957
|
A | T | 2 | a0001c0003t0002g0126a0001c0003t0002g0128 | 2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2837T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757957 | ||||||
chr14:77757958
|
A | C | 2 | a0001c0003t0002g0126a0001c0003t0002g0128 | 2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.15-2838T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757958 | ||||||
chr14:77757959
|
T | G | 31 | a0001c0003t0001g0014a0001c0003t0001g0125a0001c0003t0001g0144others(28): Show | 33 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.15-2839A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757959 | ||||||
chr14:77757978
|
C | CTCTA | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(265): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.15-2862_15-2859dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77757978 | ||||||
chr14:77758021
|
T | C | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.15-2901A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758021 | ||||||
chr14:77758027
|
G | GCAAT | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.15-2911_15-2908dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758027 | ||||||
chr14:77758059
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-2939C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758059 | ||||||
chr14:77758098
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15-2978C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758098 | ||||||
chr14:77758189
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.14+2925C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758189 | ||||||
chr14:77758193
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14+2921C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758193 | ||||||
chr14:77758203
|
G | A | 18 | a0001c0003t0002g0013a0001c0003t0002g0025a0001c0003t0002g0128others(15): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+2911C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758203 | ||||||
chr14:77758295
|
G | A | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+2819C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758295 | ||||||
chr14:77758315
|
C | CA | 7 | a0001c0002t0001g0110a0001c0002t0001g0111a0001c0002t0001g0112others(4): Show | 7 | HG02055.hp1 NA18948.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+2798dupT | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAA | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 6 | HG00280.hp1 HG01516.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+2796_14+2798dup others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAA | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(105): Show | 125 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.14+2795_14+2798dup others(4): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAA | 59 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0039others(56): Show | 61 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.14+2794_14+2798dup others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAA | 38 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0024others(35): Show | 42 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.14+2793_14+2798dup others(6): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAAA | 13 | a0001c0001t0001g0275a0001c0001t0001g0305a0001c0001t0001g0306others(10): Show | 13 | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+2792_14+2798dup others(7): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAAA others(3): Show |
2 | a0001c0003t0001g0321a0001c0007t0001g0322 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.14+2789_14+2798dup others(10): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAAA others(4): Show |
1 | a0001c0003t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+2788_14+2798dup others(11): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAAA others(7): Show |
5 | a0001c0003t0001g0123a0001c0003t0001g0124a0001c0003t0001g0125others(2): Show | 5 | HG01257.hp2 HG01258.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+2785_14+2798dup others(14): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAAA others(8): Show |
6 | a0001c0003t0001g0014a0001c0003t0001g0146a0001c0003t0001g0147others(3): Show | 7 | HG03710.hp1 NA18960.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+2784_14+2798dup others(15): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
C | CAAAAAAA others(9): Show |
5 | a0001c0003t0001g0151a0001c0003t0001g0152a0001c0003t0001g0154others(2): Show | 5 | NA18943.hp2 NA18946.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+2783_14+2798dup others(16): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758315
|
CAAA | C | 22 | a0001c0003t0002g0005a0001c0003t0002g0012a0001c0003t0002g0013others(19): Show | 26 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.14+2796_14+2798del others(3): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758315 | ||||||
chr14:77758562
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.14+2552G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758562 | ||||||
chr14:77758610
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0159a0001c0001t0001g0160others(5): Show | 10 | HG02055.hp2 HG02647.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.14+2504G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758610 | ||||||
chr14:77758790
|
C | T | 3 | a0001c0003t0003g0120a0001c0003t0003g0121a0001c0003t0003g0122 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.14+2324G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758790 | ||||||
chr14:77758868
|
A | AAGTGT | 3 | a0001c0003t0001g0123a0001c0003t0001g0124a0001c0003t0001g0125 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.14+2241_14+2245dup others(5): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758868 | ||||||
chr14:77758888
|
C | G | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.14+2226G>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758888 | ||||||
chr14:77758914
|
T | C | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.14+2200A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77758914 | ||||||
chr14:77759156
|
TC | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 202 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.14+1957delG | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759156 | ||||||
chr14:77759226
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.14+1888G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759226 | ||||||
chr14:77759385
|
G | A | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.14+1729C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759385 | ||||||
chr14:77759405
|
T | G | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.14+1709A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759405 | ||||||
chr14:77759413
|
T | C | 1 | a0001c0003t0002g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.14+1701A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759413 | ||||||
chr14:77759414
|
G | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+1700C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759414 | ||||||
chr14:77759515
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.14+1599T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759515 | ||||||
chr14:77759566
|
T | C | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.14+1548A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759566 | ||||||
chr14:77759768
|
G | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.14+1346C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759768 | ||||||
chr14:77759820
|
T | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0280others(33): Show | 38 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.14+1294A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759820 | ||||||
chr14:77759820
|
T | TA | 17 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(14): Show | 19 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+1293_14+1294ins others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759820 | ||||||
chr14:77759821
|
T | A | 99 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(96): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.14+1293A>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759821 | ||||||
chr14:77759822
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+1292T>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759822 | ||||||
chr14:77759827
|
A | AG | 6 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 7 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+1286_14+1287ins others(1): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759827 | ||||||
chr14:77759827
|
A | G | 13 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 13 | HG02257.hp1 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+1287T>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759827 | ||||||
chr14:77759846
|
G | A | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG02738.hp2 HG04228.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.14+1268C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759846 | ||||||
chr14:77759963
|
T | C | 3 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0003t0001g0156 | 3 | NA18943.hp2 NA18947.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.14+1151A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759963 | ||||||
chr14:77759996
|
G | C | 21 | a0001c0003t0001g0009a0001c0003t0001g0010a0001c0003t0001g0053others(18): Show | 23 | HG00280.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+1118C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77759996 | ||||||
chr14:77760173
|
G | A | 1 | a0001c0001t0001g0024 | 2 | NA18959.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.14+941C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760173 | ||||||
chr14:77760310
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.14+804C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760310 | ||||||
chr14:77760349
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.14+765G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760349 | ||||||
chr14:77760369
|
T | G | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG00597.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.14+745A>C | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760369 | ||||||
chr14:77760371
|
G | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(219): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.14+743C>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760371 | ||||||
chr14:77760384
|
C | A | 39 | a0001c0003t0001g0014a0001c0003t0001g0123a0001c0003t0001g0124others(36): Show | 44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+730G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760384 | ||||||
chr14:77760507
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 202 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.14+607C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760507 | ||||||
chr14:77760616
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0319a0001c0001t0001g0320 | 5 | HG02818.hp2 HG02922.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+498A>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760616 | ||||||
chr14:77760631
|
A | C | 4 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(1): Show | 4 | HG01928.hp2 NA18747.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+483T>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760631 | ||||||
chr14:77760668
|
G | A | 3 | a0001c0003t0001g0321a0001c0003t0001g0323a0001c0007t0001g0322 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.14+446C>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760668 | ||||||
chr14:77760702
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.14+412G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760702 | ||||||
chr14:77760718
|
G | C | 1 | a0001c0001t0001g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.14+396C>G | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760718 | ||||||
chr14:77760804
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.14+310G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760804 | ||||||
chr14:77760875
|
C | T | 1 | a0001c0003t0002g0025 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.14+239G>A | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760875 | ||||||
chr14:77760917
|
C | A | 1 | a0001c0001t0001g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.14+197G>T | SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760917 | ||||||
chr14:77760999
|
CCCACGTC others(8): Show |
C | 1 | a0001c0001t0001g0326 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.14+100_14+114delCA others(13): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77760999 | ||||||
chr14:77761093
|
G | GGACCCCA others(6): Show |
1 | a0001c0001t0001g0327 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.14+8_14+20dupGTTGA others(8): Show |
SNW1 | ENSG00000100603.14 | transcript | ENST00000261531.12 | protein_coding | 1/13 | chr14 | 77761093 |