geneid | 4678 |
---|---|
ensemblid | ENSG00000132780.17 |
hgncid | 7644 |
symbol | NASP |
name | nuclear autoantigenic sperm protein |
refseq_nuc | NM_002482.4 |
refseq_prot | NP_002473.2 |
ensembl_nuc | ENST00000350030.8 |
ensembl_prot | ENSP00000255120.5 |
mane_status | MANE Select |
chr | chr1 |
start | 45584041 |
end | 45618893 |
strand | + |
ver | v1.2 |
region | chr1:45584041-45618893 |
region5000 | chr1:45579041-45623893 |
regionname0 | NASP_chr1_45584041_45618893 |
regionname5000 | NASP_chr1_45579041_45623893 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 788 | 281 | 66 | 67 | 108 | 8 | 30 | 74 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0002 | 0/0 | 788 | 12 | 0 | 0 | 12 | 0 | 0 | 12 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0003 | 0/0 | 788 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0004 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0005 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0006 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0007 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0008 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2367 | 147 | 39 | 27 | 60 | 4 | 17 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0002 | 1/0 | 2367 | 102 | 21 | 29 | 42 | 1 | 8 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0003 | 0/1 | 2367 | 24 | 4 | 11 | 0 | 3 | 5 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0004 | 0/0 | 2367 | 12 | 0 | 0 | 12 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0005 | 0/0 | 2367 | 3 | 0 | 0 | 3 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0006 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0007 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0008 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0009 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0010 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0011 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0012 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0013 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
c0014 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 859 | 267 | 57 | 57 | 122 | 5 | 25 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
t0002 | 0/1 | 859 | 24 | 5 | 10 | 0 | 3 | 5 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
t0003 | 0/0 | 859 | 5 | 5 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
t0004 | 0/0 | 859 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
t0005 | 0/0 | 859 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
t0006 | 0/0 | 859 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2367 | 147 | 39 | 27 | 60 | 4 | 17 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0002 | 1/0 | 2367 | 102 | 21 | 29 | 42 | 1 | 8 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0003 | 0/1 | 2367 | 24 | 4 | 11 | 0 | 3 | 5 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0005 | 0/0 | 2367 | 3 | 0 | 0 | 3 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0007 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0008 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0010 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0002c0004 | 0/0 | 2367 | 12 | 0 | 0 | 12 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0003c0006 | 0/0 | 2367 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0004c0013 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0005c0011 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0006c0012 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0007c0009 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0008c0014 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3225 | 140 | 32 | 27 | 60 | 4 | 17 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0001t0003 | 0/0 | 3225 | 5 | 5 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0001t0004 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0002t0001 | 1/0 | 3225 | 100 | 20 | 28 | 42 | 1 | 8 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0002t0005 | 0/0 | 3225 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0002t0006 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0003t0001 | 0/0 | 3225 | 2 | 1 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0003t0002 | 0/1 | 3225 | 22 | 3 | 10 | 0 | 3 | 5 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0005t0001 | 0/0 | 3225 | 3 | 0 | 0 | 3 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0007t0001 | 0/0 | 3225 | 2 | 0 | 0 | 2 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0008t0002 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0001c0010t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0002c0004t0001 | 0/0 | 3225 | 12 | 0 | 0 | 12 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0003c0006t0001 | 0/0 | 3225 | 2 | 2 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0004c0013t0001 | 0/0 | 3225 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0005c0011t0001 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0006c0012t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0007c0009t0001 | 0/0 | 3225 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
a0008c0014t0001 | 0/0 | 3225 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | copy fasta | chr1 | 45579041 | 45623893 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0002t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0007t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0007t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0008t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0008t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0001c0010t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0002c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0003c0006t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0003c0006t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0004c0013t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0005c0011t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0006c0012t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0007c0009t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
a0008c0014t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | GBR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00280 | hp1 | a0001 | c0003 | t0002 | g0154 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0162 | EUR | FIN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00544 | hp1 | a0001 | c0007 | t0001 | g0285 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00673 | hp2 | a0001 | c0005 | t0001 | g0245 | EAS | CHS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00733 | hp2 | a0001 | c0003 | t0002 | g0152 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00735 | hp2 | a0001 | c0003 | t0002 | g0146 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0165 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01099 | hp1 | a0001 | c0003 | t0002 | g0145 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0195 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0166 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0153 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01257 | hp1 | a0001 | c0003 | t0002 | g0147 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01361 | hp1 | a0001 | c0003 | t0002 | g0150 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0286 | EUR | IBS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01943 | hp2 | a0001 | c0003 | t0002 | g0160 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0287 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02148 | hp2 | a0004 | c0013 | t0001 | g0233 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CDX | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02293 | hp2 | a0001 | c0002 | t0005 | g0288 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02602 | hp1 | a0001 | c0003 | t0002 | g0167 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0159 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02683 | hp2 | a0001 | c0003 | t0002 | g0158 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02717 | hp2 | a0003 | c0006 | t0001 | g0283 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02735 | hp2 | a0001 | c0003 | t0002 | g0161 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0149 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02922 | hp1 | a0001 | c0008 | t0002 | g0156 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0151 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0148 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03139 | hp1 | a0005 | c0011 | t0001 | g0173 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ESN | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0267 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03654 | hp1 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0278 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | STU | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18944 | hp1 | a0002 | c0004 | t0001 | g0182 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18959 | hp1 | a0007 | c0009 | t0001 | g0242 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18959 | hp2 | a0001 | c0007 | t0001 | g0284 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18968 | hp1 | a0002 | c0004 | t0001 | g0180 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0184 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18971 | hp2 | a0002 | c0004 | t0001 | g0181 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18974 | hp1 | a0002 | c0004 | t0001 | g0187 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18979 | hp2 | a0001 | c0005 | t0001 | g0272 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18984 | hp2 | a0002 | c0004 | t0001 | g0191 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18986 | hp2 | a0002 | c0004 | t0001 | g0186 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18987 | hp1 | a0001 | c0005 | t0001 | g0261 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19000 | hp2 | a0002 | c0004 | t0001 | g0185 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19002 | hp2 | a0006 | c0012 | t0001 | g0298 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19006 | hp1 | a0001 | c0010 | t0001 | g0139 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19006 | hp2 | a0002 | c0004 | t0001 | g0183 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19007 | hp1 | a0002 | c0004 | t0001 | g0188 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19043 | hp2 | a0008 | c0014 | t0001 | g0266 | AFR | LWK | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19067 | hp2 | a0002 | c0004 | t0001 | g0190 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19084 | hp1 | a0002 | c0004 | t0001 | g0189 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19240 | hp1 | a0003 | c0006 | t0001 | g0282 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ASW | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | CLM | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02486 | hp2 | a0001 | c0008 | t0002 | g0157 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | USA | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
HG06807 | hp2 | a0001 | c0002 | t0006 | g0268 | AFR | USA | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0155 | REF | REF | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0211 | REF | REF | NASP_chr1_45579041_45623893 | NASP | chr1 | 45579041 | 45623893 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:45584177
|
G | C | 1 | a0002 | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
missense_variant | MODERATE | c.31G>C | p.Val11Leu | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/15 | 137/3225 | 31/2367 | 11/788 | chr1 | 45584177 | ||
chr1:45607518
|
C | G | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.607C>G | p.Leu203Val | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 713/3225 | 607/2367 | 203/788 | chr1 | 45607518 | ||
chr1:45607814
|
C | A | 1 | a0007 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.903C>A | p.Asp301Glu | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1009/3225 | 903/2367 | 301/788 | chr1 | 45607814 | ||
chr1:45607845
|
G | A | 1 | a0006 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.934G>A | p.Asp312Asn | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1040/3225 | 934/2367 | 312/788 | chr1 | 45607845 | ||
chr1:45615137
|
C | G | 1 | a0004 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.1791C>G | p.Asn597Lys | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/15 | 1897/3225 | 1791/2367 | 597/788 | chr1 | 45615137 | ||
chr1:45616389
|
C | G | 1 | a0005 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2075C>G | p.Ser692Cys | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 12/15 | 2181/3225 | 2075/2367 | 692/788 | chr1 | 45616389 | ||
chr1:45617554
|
C | T | 1 | a0003 | 2 | HG02717.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.2249C>T | p.Pro750Leu | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/15 | 2355/3225 | 2249/2367 | 750/788 | chr1 | 45617554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:45607496
|
A | C | 1 | a0001c0008 | 2 | HG02486.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.585A>C | p.Pro195Pro | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 691/3225 | 585/2367 | 195/788 | chr1 | 45607496 | ||
chr1:45607817
|
G | A | 3 | a0001c0001a0001c0010a0005c0011 | 149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
synonymous_variant | LOW | c.906G>A | p.Pro302Pro | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1012/3225 | 906/2367 | 302/788 | chr1 | 45607817 | ||
chr1:45607925
|
A | G | 2 | a0001c0007a0002c0004 | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
synonymous_variant | LOW | c.1014A>G | p.Val338Val | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1120/3225 | 1014/2367 | 338/788 | chr1 | 45607925 | ||
chr1:45608084
|
T | C | 1 | a0001c0010 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.1173T>C | p.Pro391Pro | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/15 | 1279/3225 | 1173/2367 | 391/788 | chr1 | 45608084 | ||
chr1:45613182
|
A | G | 5 | a0001c0001a0001c0003a0001c0008others(2): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
synonymous_variant | LOW | c.1440A>G | p.Ser480Ser | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/15 | 1546/3225 | 1440/2367 | 480/788 | chr1 | 45613182 | ||
chr1:45613212
|
C | T | 5 | a0001c0001a0001c0003a0001c0008others(2): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
synonymous_variant | LOW | c.1470C>T | p.Thr490Thr | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/15 | 1576/3225 | 1470/2367 | 490/788 | chr1 | 45613212 | ||
chr1:45614326
|
C | T | 1 | a0001c0005 | 3 | HG00673.hp2 NA18979.hp2 NA18987.hp1 |
synonymous_variant | LOW | c.1626C>T | p.Ala542Ala | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/15 | 1732/3225 | 1626/2367 | 542/788 | chr1 | 45614326 | ||
chr1:45616658
|
C | T | 1 | a0002c0004 | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
synonymous_variant | LOW | c.2112C>T | p.Ser704Ser | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/15 | 2218/3225 | 2112/2367 | 704/788 | chr1 | 45616658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:45584086
|
A | C | 1 | a0001c0002t0006 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/15 | 61 | chr1 | 45584086 | |||||
chr1:45618370
|
T | C | 1 | a0001c0002t0005 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*229T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 229 | chr1 | 45618370 | |||||
chr1:45618412
|
T | C | 1 | a0001c0001t0003 | 5 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*271T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 271 | chr1 | 45618412 | |||||
chr1:45618599
|
C | T | 1 | a0001c0001t0004 | 2 | HG03453.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*458C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 458 | chr1 | 45618599 | |||||
chr1:45618711
|
G | T | 2 | a0001c0003t0002a0001c0008t0002 | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 15/15 | 570 | chr1 | 45618711 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:45584229
|
A | C | 1 | a0001c0002t0001g0299 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.59+24A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584229 | ||||||
chr1:45584267
|
G | T | 1 | a0006c0012t0001g0298 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.59+62G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584267 | ||||||
chr1:45584332
|
TTCGG | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.59+128_59+131delTC others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584332 | ||||||
chr1:45584422
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59+217C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584422 | ||||||
chr1:45584462
|
T | A | 1 | a0001c0001t0003g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59+257T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584462 | ||||||
chr1:45584473
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.59+268C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584473 | ||||||
chr1:45584597
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | NA18963.hp1 NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.59+392C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584597 | ||||||
chr1:45584605
|
A | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG03490.hp1 HG03654.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+400A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584605 | ||||||
chr1:45584779
|
C | G | 9 | a0001c0002t0001g0287a0001c0002t0001g0289a0001c0002t0001g0290others(6): Show | 9 | HG01099.hp2 HG01109.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+574C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584779 | ||||||
chr1:45584795
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.59+590C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584795 | ||||||
chr1:45584889
|
G | T | 24 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0003t0002g0001others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.59+684G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584889 | ||||||
chr1:45584929
|
G | A | 2 | a0001c0001t0001g0174a0005c0011t0001g0173 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.59+724G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45584929 | ||||||
chr1:45585084
|
G | T | 1 | a0001c0002t0001g0286 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.59+879G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585084 | ||||||
chr1:45585159
|
T | C | 5 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0177others(2): Show | 5 | NA18962.hp2 NA18977.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+954T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585159 | ||||||
chr1:45585262
|
T | A | 1 | a0001c0001t0001g0006 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.59+1057T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585262 | ||||||
chr1:45585349
|
A | G | 1 | a0001c0003t0002g0167 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.59+1144A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585349 | ||||||
chr1:45585381
|
G | A | 3 | a0001c0003t0002g0145a0001c0003t0002g0146a0001c0003t0002g0147 | 3 | HG00735.hp2 HG01099.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.59+1176G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585381 | ||||||
chr1:45585474
|
A | G | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.59+1269A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585474 | ||||||
chr1:45585744
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01081.hp1 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.59+1539C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585744 | ||||||
chr1:45585803
|
T | C | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+1598T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585803 | ||||||
chr1:45585885
|
C | T | 4 | a0001c0001t0001g0174a0003c0006t0001g0282a0003c0006t0001g0283others(1): Show | 4 | HG02258.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+1680C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585885 | ||||||
chr1:45585947
|
T | G | 1 | a0001c0002t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59+1742T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45585947 | ||||||
chr1:45586043
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.59+1838G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586043 | ||||||
chr1:45586069
|
T | C | 2 | a0001c0002t0001g0193a0001c0002t0001g0194 | 2 | NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.59+1864T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586069 | ||||||
chr1:45586239
|
C | CGT | 19 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0227others(16): Show | 19 | HG01099.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.59+2078_59+2079dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGT | 16 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(13): Show | 16 | HG00408.hp1 HG00673.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.59+2076_59+2079dup others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGTGT | 6 | a0001c0002t0001g0254a0001c0002t0001g0255a0001c0002t0001g0256others(3): Show | 6 | HG00544.hp2 HG01346.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.59+2074_59+2079dup others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGTGTG others(1): Show |
5 | a0001c0002t0001g0260a0001c0002t0001g0262a0001c0002t0001g0263others(2): Show | 5 | HG02040.hp1 NA18522.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+2072_59+2079dup others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGTGTG others(3): Show |
1 | a0001c0002t0001g0265 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.59+2070_59+2079dup others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGTGTG others(7): Show |
2 | a0001c0002t0001g0267a0008c0014t0001g0266 | 2 | HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.59+2066_59+2079dup others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGTGTG others(9): Show |
1 | a0001c0002t0006g0268 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59+2064_59+2079dup others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
C | CGTGTGTG others(29): Show |
1 | a0003c0006t0001g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.59+2044_59+2079dup others(36): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
CGT | C | 10 | a0001c0002t0001g0193a0001c0002t0001g0203a0001c0002t0001g0204others(7): Show | 10 | HG01975.hp1 HG01975.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2078_59+2079del others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
CGTGT | C | 5 | a0001c0002t0001g0198a0001c0002t0001g0199a0001c0002t0001g0200others(2): Show | 5 | HG01891.hp1 HG01981.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+2076_59+2079del others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
CGTGTGTG others(9): Show |
C | 3 | a0001c0003t0002g0161a0001c0003t0002g0162a0001c0003t0002g0167 | 3 | HG00323.hp2 HG02602.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.59+2064_59+2079del others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586239
|
CGTGTGTG others(11): Show |
C | 12 | a0001c0003t0002g0001a0001c0003t0002g0145a0001c0003t0002g0148others(9): Show | 13 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+2062_59+2079del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586239 | |||||
chr1:45586261
|
TGTGTGTG others(16): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.59+2080_59+2102del others(23): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586261 | |||||
chr1:45586263
|
TGTGTGTG others(14): Show |
T | 1 | a0001c0001t0001g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59+2080_59+2100del others(21): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586263 | |||||
chr1:45586264
|
GTGTGTGT others(15): Show |
G | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011 | 3 | HG02486.hp1 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59+2060_59+2081del others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586264 | ||||||
chr1:45586264
|
GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0001g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.59+2060_59+2083del others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586264 | ||||||
chr1:45586266
|
GTGTGTGT others(25): Show |
G | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | NA18979.hp1 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.59+2062_59+2093del others(32): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586266 | ||||||
chr1:45586267
|
TGTGTGTG others(10): Show |
T | 1 | a0001c0003t0002g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.59+2080_59+2096del others(17): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586267 | |||||
chr1:45586268
|
GTGTGTGT others(11): Show |
G | 5 | a0001c0003t0002g0146a0001c0003t0002g0147a0001c0003t0002g0158others(2): Show | 5 | HG00735.hp2 HG01257.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+2064_59+2081del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586268 | ||||||
chr1:45586270
|
GTGTGTGT others(9): Show |
G | 2 | a0001c0003t0001g0015a0001c0003t0001g0016 | 2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.59+2066_59+2081del others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586270 | ||||||
chr1:45586271
|
TGTGTGTG others(6): Show |
T | 2 | a0001c0002t0001g0286a0001c0003t0002g0166 | 2 | HG01167.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.59+2080_59+2092del others(13): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586271 | |||||
chr1:45586272
|
GTGTGTGT others(7): Show |
G | 3 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0003t0002g0195 | 3 | HG01106.hp1 HG01192.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.59+2068_59+2081del others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586272 | ||||||
chr1:45586272
|
GTGTGTGT others(19): Show |
G | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG00280.hp2 NA18963.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+2068_59+2093del others(26): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586272 | ||||||
chr1:45586273
|
TGTGTGTG others(4): Show |
T | 7 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 7 | HG01109.hp1 HG01123.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.59+2080_59+2090del others(11): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586273 | |||||
chr1:45586274
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.59+2070_59+2087del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586274 | ||||||
chr1:45586275
|
TGTGTGTG others(2): Show |
T | 22 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(19): Show | 22 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.59+2080_59+2088del others(9): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586275 | |||||
chr1:45586276
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0023 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.59+2072_59+2093del others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586276 | ||||||
chr1:45586277
|
TGTGTGTG | T | 16 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(13): Show | 16 | HG01069.hp2 HG01167.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.59+2080_59+2086del others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586277 | |||||
chr1:45586278
|
GTGTGTGG others(13): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59+2074_59+2093del others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586278 | ||||||
chr1:45586279
|
T | TG | 3 | a0001c0002t0001g0297a0002c0004t0001g0180a0002c0004t0001g0181 | 3 | HG02922.hp2 NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.59+2075dupG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586279 | |||||
chr1:45586279
|
TGTGTG | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(12): Show | 15 | HG00408.hp2 HG00738.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.59+2080_59+2084del others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586279 | |||||
chr1:45586280
|
GTGTGGTG others(11): Show |
G | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01243.hp1 HG02647.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+2076_59+2093del others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586280 | ||||||
chr1:45586281
|
T | TGGTGTGT others(57): Show |
4 | a0002c0004t0001g0182a0002c0004t0001g0183a0002c0004t0001g0184others(1): Show | 4 | NA18944.hp1 NA18969.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2077_59+2078ins others(64): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586281 | |||||
chr1:45586281
|
TGTG | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0091a0001c0001t0001g0092others(7): Show | 10 | HG02071.hp2 HG02135.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2080_59+2082del others(3): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586281 | |||||
chr1:45586281
|
TGTGGTGT others(21): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.59+2080_59+2107del others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586281 | |||||
chr1:45586282
|
GTGGTGTG others(9): Show |
G | 6 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 6 | HG00642.hp1 HG00673.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.59+2078_59+2093del others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586282 | ||||||
chr1:45586283
|
TG | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0099others(17): Show | 20 | HG01074.hp2 HG01081.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.59+2080delG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586283 | |||||
chr1:45586284
|
G | GGT | 3 | a0001c0002t0001g0224a0001c0002t0001g0225a0001c0002t0001g0226 | 3 | HG01258.hp2 HG04204.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.59+2103_59+2104dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586284 | |||||
chr1:45586284
|
G | GGTGTGTG others(60): Show |
1 | a0002c0004t0001g0186 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.59+2091_59+2092ins others(67): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586284 | |||||
chr1:45586284
|
G | GT | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0112others(12): Show | 15 | HG00438.hp1 HG02004.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(1): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTCACCCA others(45): Show |
1 | a0001c0007t0001g0284 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(52): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGGTGTG others(62): Show |
3 | a0002c0004t0001g0187a0002c0004t0001g0188a0002c0004t0001g0189 | 3 | NA18974.hp1 NA19007.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(69): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGT | 9 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(6): Show | 9 | HG00642.hp2 HG00735.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(3): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTCACC others(47): Show |
1 | a0001c0007t0001g0285 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(54): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGT | 10 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG01928.hp1 HG02572.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGG others(66): Show |
1 | a0002c0004t0001g0190 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(73): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0296 | 3 | NA19043.hp1 NA19066.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(55): Show |
2 | a0002c0004t0001g0180a0002c0004t0001g0181 | 2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(62): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(2): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0003g0133 | 3 | HG00609.hp2 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(9): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(55): Show |
1 | a0002c0004t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(62): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(11): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(6): Show |
2 | a0001c0001t0003g0138a0001c0002t0001g0280 | 2 | HG00609.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.59+2079_59+2080ins others(13): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(8): Show |
1 | a0001c0002t0001g0281 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(15): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(10): Show |
1 | a0001c0010t0001g0139 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(17): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(14): Show |
1 | a0001c0001t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(21): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
G | GTGTGTGT others(24): Show |
1 | a0003c0006t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.59+2079_59+2080ins others(31): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586284 | ||||||
chr1:45586284
|
GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0001g0039a0001c0001t0003g0002 | 2 | HG02572.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.59+2091_59+2104del others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586284 | |||||
chr1:45586286
|
T | G | 1 | a0001c0002t0006g0268 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59+2081T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586286 | ||||||
chr1:45586297
|
GT | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.59+2093delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586297 | ||||||
chr1:45586298
|
T | TG | 24 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(21): Show | 24 | HG00735.hp1 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.59+2094dupG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586298 | |||||
chr1:45586306
|
T | G | 2 | a0001c0002t0001g0209a0001c0002t0001g0280 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.59+2101T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586306 | ||||||
chr1:45586308
|
TG | T | 3 | a0001c0001t0001g0174a0001c0002t0001g0253a0001c0002t0001g0276 | 3 | HG01433.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.59+2105delG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45586308 | |||||
chr1:45586518
|
G | A | 1 | a0001c0002t0001g0177 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.59+2313G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586518 | ||||||
chr1:45586548
|
C | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.59+2343C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586548 | ||||||
chr1:45586554
|
G | A | 1 | a0001c0002t0006g0268 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59+2349G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586554 | ||||||
chr1:45586568
|
C | T | 1 | a0001c0007t0001g0285 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.59+2363C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586568 | ||||||
chr1:45586920
|
A | C | 1 | a0001c0002t0001g0240 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.59+2715A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586920 | ||||||
chr1:45586924
|
C | G | 1 | a0001c0002t0001g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.59+2719C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45586924 | ||||||
chr1:45587089
|
C | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+2884C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587089 | ||||||
chr1:45587177
|
C | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+2972C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587177 | ||||||
chr1:45587185
|
G | GT | 16 | a0001c0001t0001g0111a0001c0001t0001g0296a0001c0002t0001g0222others(13): Show | 16 | NA18944.hp1 NA18955.hp2 NA18968.hp1 others(13): Show |
intron_variant | MODIFIER | c.59+2989dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587185 | |||||
chr1:45587291
|
A | G | 3 | a0001c0001t0001g0022a0001c0003t0001g0015a0001c0003t0001g0016 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.59+3086A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587291 | ||||||
chr1:45587425
|
C | T | 3 | a0001c0001t0001g0022a0001c0003t0001g0015a0001c0003t0001g0016 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.59+3220C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587425 | ||||||
chr1:45587487
|
C | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.59+3282C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587487 | ||||||
chr1:45587661
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59+3466_59+3483dup others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | |||||
chr1:45587661
|
C | CATATATA others(15): Show |
2 | a0001c0008t0002g0156a0001c0008t0002g0157 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.59+3462_59+3483dup others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | |||||
chr1:45587661
|
C | CATATATA others(19): Show |
1 | a0001c0002t0001g0290 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.59+3458_59+3483dup others(26): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | |||||
chr1:45587661
|
C | CATATATA others(21): Show |
1 | a0001c0002t0001g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | |||||
chr1:45587661
|
CAT | C | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0002t0001g0210others(1): Show | 4 | HG02074.hp1 HG02083.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3482_59+3483del others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | |||||
chr1:45587661
|
CATATATA others(1): Show |
C | 3 | a0001c0002t0001g0241a0001c0007t0001g0284a0001c0007t0001g0285 | 3 | HG00544.hp1 HG02300.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.59+3476_59+3483del others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587661 | |||||
chr1:45587685
|
T | A | 2 | a0001c0002t0001g0210a0001c0002t0001g0270 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.59+3480T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587685 | ||||||
chr1:45587687
|
T | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0098a0001c0001t0001g0099others(10): Show | 13 | HG01074.hp2 HG01934.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+3482T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587687 | ||||||
chr1:45587687
|
T | TAA | 3 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0122 | 3 | HG01928.hp1 HG03098.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.59+3483_59+3484dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATAA | 4 | a0001c0003t0002g0146a0001c0003t0002g0147a0001c0003t0002g0150others(1): Show | 4 | HG00735.hp2 HG01257.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(3): Show |
12 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0048others(9): Show | 12 | HG00438.hp2 HG00733.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(5): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 29 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(7): Show |
25 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0026others(22): Show | 25 | HG00609.hp2 HG00642.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(15): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(9): Show |
18 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(11): Show |
30 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0045others(27): Show | 30 | HG00323.hp2 HG00733.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(13): Show |
1 | a0001c0002t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(12): Show |
1 | a0001c0002t0001g0179 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(19): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(13): Show |
13 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0108others(10): Show | 13 | HG02040.hp2 HG02647.hp2 HG03486.hp2 others(10): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(15): Show |
30 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0062others(27): Show | 30 | HG00673.hp2 HG01106.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(17): Show |
21 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0064others(18): Show | 21 | HG00408.hp1 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(19): Show |
25 | a0001c0001t0001g0029a0001c0001t0001g0078a0001c0001t0001g0079others(22): Show | 25 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(26): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(21): Show |
22 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0022others(19): Show | 22 | HG00609.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(22): Show |
1 | a0001c0002t0001g0197 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(29): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(23): Show |
20 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0080others(17): Show | 20 | HG00408.hp2 HG01517.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(30): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(25): Show |
7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0089others(4): Show | 7 | HG01975.hp2 HG02080.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(32): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(27): Show |
4 | a0001c0001t0001g0163a0001c0002t0001g0221a0001c0002t0001g0226others(1): Show | 4 | HG01069.hp1 HG01361.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(34): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(28): Show |
1 | a0001c0002t0001g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(35): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(29): Show |
2 | a0001c0001t0001g0090a0002c0004t0001g0185 | 2 | NA18947.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.59+3483_59+3484ins others(36): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(30): Show |
1 | a0001c0001t0001g0047 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(37): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(31): Show |
1 | a0001c0002t0001g0275 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(38): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587687
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.59+3483_59+3484ins others(42): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45587687 | |||||
chr1:45587709
|
G | A | 1 | a0001c0002t0001g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59+3504G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587709 | ||||||
chr1:45587840
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.60-3383C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587840 | ||||||
chr1:45587841
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.60-3382C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587841 | ||||||
chr1:45587855
|
A | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-3368A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587855 | ||||||
chr1:45587869
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.60-3354G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587869 | ||||||
chr1:45587877
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.60-3346C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587877 | ||||||
chr1:45587902
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.60-3321C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587902 | ||||||
chr1:45587979
|
G | A | 1 | a0001c0003t0002g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.60-3244G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45587979 | ||||||
chr1:45588011
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.60-3212G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588011 | ||||||
chr1:45588076
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.60-3147C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588076 | ||||||
chr1:45588357
|
C | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-2866C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588357 | ||||||
chr1:45588383
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.60-2840C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588383 | ||||||
chr1:45588463
|
T | A | 1 | a0001c0001t0003g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60-2760T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588463 | ||||||
chr1:45588466
|
C | T | 2 | a0001c0001t0001g0174a0005c0011t0001g0173 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.60-2757C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588466 | ||||||
chr1:45588665
|
C | T | 1 | a0001c0002t0001g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.60-2558C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588665 | ||||||
chr1:45588668
|
G | A | 1 | a0001c0003t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60-2555G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588668 | ||||||
chr1:45588814
|
A | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.60-2409A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45588814 | ||||||
chr1:45588957
|
G | GTGTT | 15 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0198others(12): Show | 15 | HG00733.hp1 HG01106.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.60-2242_60-2239dup others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | |||||
chr1:45588957
|
G | GTGTTTGT others(5): Show |
4 | a0001c0002t0001g0205a0001c0002t0001g0217a0001c0002t0001g0235others(1): Show | 4 | HG00738.hp2 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-2250_60-2239dup others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | |||||
chr1:45588957
|
G | GTGTTTGT others(9): Show |
1 | a0001c0002t0001g0201 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.60-2254_60-2239dup others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | |||||
chr1:45588957
|
GTGTT | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.60-2242_60-2239del others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | |||||
chr1:45588957
|
GTGTTTGT others(1): Show |
G | 5 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0002t0001g0260others(2): Show | 5 | HG00544.hp1 HG02040.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-2246_60-2239del others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45588957 | |||||
chr1:45589064
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.60-2159A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589064 | ||||||
chr1:45589105
|
G | A | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-2118G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589105 | ||||||
chr1:45589320
|
C | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1903C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589320 | ||||||
chr1:45589444
|
G | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1779G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589444 | ||||||
chr1:45589514
|
A | G | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1709A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589514 | ||||||
chr1:45589629
|
G | T | 1 | a0001c0003t0002g0147 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.60-1594G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589629 | ||||||
chr1:45589889
|
G | A | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-1334G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589889 | ||||||
chr1:45589928
|
C | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.60-1295C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589928 | ||||||
chr1:45589957
|
A | G | 2 | a0001c0003t0002g0148a0001c0003t0002g0149 | 2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.60-1266A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589957 | ||||||
chr1:45589998
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0069 | 3 | HG01081.hp2 HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.60-1225G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45589998 | ||||||
chr1:45590015
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.60-1208T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590015 | ||||||
chr1:45590022
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.60-1201C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590022 | ||||||
chr1:45590099
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.60-1124T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590099 | ||||||
chr1:45590180
|
C | A | 1 | a0001c0002t0001g0222 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.60-1043C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590180 | ||||||
chr1:45590186
|
A | G | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.60-1037A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590186 | ||||||
chr1:45590318
|
G | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.60-905G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590318 | ||||||
chr1:45590338
|
A | AT | 298 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.60-885_60-884insT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590338 | ||||||
chr1:45590359
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.60-864C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590359 | ||||||
chr1:45590371
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.60-852G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590371 | ||||||
chr1:45590405
|
A | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-818A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590405 | ||||||
chr1:45590460
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-763A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590460 | ||||||
chr1:45590473
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-750C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590473 | ||||||
chr1:45590480
|
C | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.60-743C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590480 | ||||||
chr1:45590504
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0082a0001c0001t0001g0103others(2): Show | 5 | HG01943.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-719C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590504 | ||||||
chr1:45590528
|
C | T | 3 | a0001c0001t0001g0022a0001c0003t0001g0015a0001c0003t0001g0016 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.60-695C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590528 | ||||||
chr1:45590549
|
C | CA | 14 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0040others(11): Show | 14 | HG00738.hp2 HG01346.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.60-656dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590549 | |||||
chr1:45590682
|
C | CT | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 35 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.60-520dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | |||||
chr1:45590682
|
C | CTT | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.60-521_60-520dupTT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | |||||
chr1:45590682
|
C | CTTT | 12 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0035others(9): Show | 12 | HG00673.hp1 HG00738.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.60-522_60-520dupTT others(1): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | |||||
chr1:45590682
|
CT | C | 42 | a0001c0001t0001g0022a0001c0001t0001g0296a0001c0002t0001g0192others(39): Show | 42 | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.60-520delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590682 | |||||
chr1:45590709
|
G | A | 3 | a0001c0002t0001g0232a0001c0002t0001g0243a0001c0002t0001g0297 | 3 | HG02280.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.60-514G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590709 | ||||||
chr1:45590744
|
T | TA | 5 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0039others(2): Show | 5 | HG00673.hp1 NA18945.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-472dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 45590744 | |||||
chr1:45590866
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02486.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-357A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | chr1 | 45590866 | ||||||
chr1:45591386
|
G | A | 3 | a0001c0002t0001g0232a0001c0002t0001g0243a0001c0002t0001g0297 | 3 | HG02280.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.107+116G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591386 | ||||||
chr1:45591470
|
C | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.107+200C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591470 | ||||||
chr1:45591472
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.107+202A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591472 | ||||||
chr1:45591554
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02486.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+284A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591554 | ||||||
chr1:45591613
|
T | G | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.107+343T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591613 | ||||||
chr1:45591730
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+460G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591730 | ||||||
chr1:45591881
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+611T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45591881 | ||||||
chr1:45592048
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+778C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592048 | ||||||
chr1:45592054
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.107+784C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592054 | ||||||
chr1:45592137
|
A | C | 1 | a0001c0002t0001g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.107+867A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592137 | ||||||
chr1:45592145
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+875C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592145 | ||||||
chr1:45592181
|
C | T | 1 | a0005c0011t0001g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.107+911C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592181 | ||||||
chr1:45592291
|
T | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+1021T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592291 | ||||||
chr1:45592571
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.107+1301A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592571 | ||||||
chr1:45592605
|
C | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.107+1335C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592605 | ||||||
chr1:45592748
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+1478C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592748 | ||||||
chr1:45592753
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.107+1483G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592753 | ||||||
chr1:45592754
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.107+1484A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592754 | ||||||
chr1:45592853
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02486.hp1 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+1583T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592853 | ||||||
chr1:45592883
|
G | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+1613G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592883 | ||||||
chr1:45592915
|
A | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+1645A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45592915 | ||||||
chr1:45593086
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+1816T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593086 | ||||||
chr1:45593218
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+1948G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593218 | ||||||
chr1:45593252
|
G | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+1982G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593252 | ||||||
chr1:45593462
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0057a0001c0001t0001g0142others(2): Show | 5 | HG01081.hp1 HG01168.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+2192G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593462 | ||||||
chr1:45593510
|
G | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0075others(8): Show | 11 | HG02083.hp1 HG02602.hp2 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+2240G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593510 | ||||||
chr1:45593533
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.107+2263C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593533 | ||||||
chr1:45593535
|
C | CA | 43 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(40): Show | 43 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.107+2285dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593535 | |||||
chr1:45593535
|
C | CAA | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0007t0001g0285others(10): Show | 13 | HG00544.hp1 HG02486.hp1 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+2284_107+2285d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593535 | |||||
chr1:45593535
|
CA | C | 17 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0091others(14): Show | 17 | HG00408.hp2 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.107+2285delA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593535 | |||||
chr1:45593663
|
CT | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+2405delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593663 | |||||
chr1:45593684
|
C | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+2414C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593684 | ||||||
chr1:45593710
|
T | C | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2440T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593710 | ||||||
chr1:45593855
|
CA | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.107+2597delA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45593855 | |||||
chr1:45593866
|
AAT | A | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+2597_107+2598d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593866 | ||||||
chr1:45593868
|
T | A | 1 | a0001c0002t0001g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+2598T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593868 | ||||||
chr1:45593941
|
A | G | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+2671A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593941 | ||||||
chr1:45593996
|
T | C | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2726T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45593996 | ||||||
chr1:45594064
|
C | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+2794C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594064 | ||||||
chr1:45594163
|
T | TA | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.107+2899dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45594163 | |||||
chr1:45594174
|
C | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2904C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594174 | ||||||
chr1:45594190
|
G | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.107+2920G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594190 | ||||||
chr1:45594201
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+2931C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594201 | ||||||
chr1:45594258
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+2988G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594258 | ||||||
chr1:45594265
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030 | 3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107+2995G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594265 | ||||||
chr1:45594323
|
C | CA | 7 | a0001c0002t0001g0194a0001c0002t0001g0227a0001c0002t0001g0235others(4): Show | 7 | HG00544.hp1 HG01175.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+3065dupA | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45594323 | |||||
chr1:45594568
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+3298G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594568 | ||||||
chr1:45594936
|
A | G | 1 | a0001c0002t0001g0279 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.107+3666A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594936 | ||||||
chr1:45594991
|
C | T | 2 | a0001c0001t0001g0174a0005c0011t0001g0173 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.107+3721C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45594991 | ||||||
chr1:45595002
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.107+3732T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595002 | ||||||
chr1:45595090
|
A | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+3820A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595090 | ||||||
chr1:45595127
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0110 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.107+3858_107+3859i others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | |||||
chr1:45595127
|
TTTTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.107+3859_107+3868d others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | |||||
chr1:45595127
|
TTTTGTGT others(11): Show |
T | 1 | a0003c0006t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.107+3859_107+3876d others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | |||||
chr1:45595127
|
TTTTGTGT others(15): Show |
T | 1 | a0003c0006t0001g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107+3859_107+3880d others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595127 | |||||
chr1:45595128
|
TTTGTG | T | 3 | a0001c0001t0001g0004a0001c0002t0001g0199a0001c0002t0001g0240 | 3 | HG02055.hp2 NA19002.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.107+3860_107+3864d others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595128 | |||||
chr1:45595129
|
T | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0090a0001c0001t0001g0110others(4): Show | 7 | HG00280.hp1 HG02132.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+3859T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595129 | ||||||
chr1:45595129
|
T | TTG | 21 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0061others(18): Show | 22 | HG00099.hp2 HG00408.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.107+3917_107+3918d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTG | 12 | a0001c0001t0001g0020a0001c0001t0001g0044a0001c0001t0001g0060others(9): Show | 12 | HG00438.hp1 HG01099.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+3915_107+3918d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTGTG | 14 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0055others(11): Show | 14 | HG00323.hp1 HG01346.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+3913_107+3918d others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTGTGT others(1): Show |
11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0035others(8): Show | 11 | HG00673.hp1 HG02083.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+3911_107+3918d others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTGTGT others(3): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0043others(4): Show | 7 | HG01109.hp1 HG03486.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+3909_107+3918d others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0001g0068a0001c0002t0001g0257 | 2 | HG00544.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.107+3907_107+3918d others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0009 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.107+3905_107+3918d others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.107+3903_107+3918d others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTG | T | 41 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.107+3917_107+3918d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTG | T | 32 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0065others(29): Show | 32 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.107+3915_107+3918d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTG | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0045others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.107+3913_107+3918d others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(1): Show |
T | 22 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0062others(19): Show | 22 | HG00609.hp2 HG00733.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.107+3911_107+3918d others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(3): Show |
T | 20 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0066others(17): Show | 20 | HG00642.hp1 HG01891.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.107+3909_107+3918d others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0001g0080a0001c0007t0001g0284a0002c0004t0001g0180 | 3 | HG03239.hp1 NA18959.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.107+3907_107+3918d others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(7): Show |
T | 4 | a0001c0001t0001g0107a0001c0001t0001g0125a0001c0002t0001g0232others(1): Show | 4 | HG02280.hp1 HG03942.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+3905_107+3918d others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(9): Show |
T | 3 | a0001c0001t0001g0027a0001c0003t0002g0153a0004c0013t0001g0233 | 3 | HG01192.hp1 HG02148.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.107+3903_107+3918d others(18): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(11): Show |
T | 3 | a0001c0001t0001g0076a0001c0001t0001g0174a0001c0002t0001g0263 | 3 | HG02258.hp2 HG02735.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.107+3901_107+3918d others(20): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0001g0040a0001c0002t0001g0244 | 2 | HG03710.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.107+3899_107+3918d others(22): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(15): Show |
T | 3 | a0001c0002t0001g0220a0001c0002t0001g0226a0001c0002t0001g0246 | 3 | HG02451.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.107+3897_107+3918d others(24): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(19): Show |
T | 1 | a0001c0002t0001g0203 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107+3893_107+3918d others(28): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595129
|
TTGTGTGT others(31): Show |
T | 3 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030 | 3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107+3881_107+3918d others(40): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45595129 | |||||
chr1:45595234
|
T | C | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.107+3964T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595234 | ||||||
chr1:45595434
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.107+4164T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595434 | ||||||
chr1:45595452
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.107+4182A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595452 | ||||||
chr1:45595639
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+4369T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595639 | ||||||
chr1:45595650
|
A | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4380A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595650 | ||||||
chr1:45595850
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4580C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595850 | ||||||
chr1:45595944
|
T | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+4674T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45595944 | ||||||
chr1:45596155
|
G | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+4885G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596155 | ||||||
chr1:45596206
|
G | C | 2 | a0001c0001t0001g0174a0005c0011t0001g0173 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.107+4936G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596206 | ||||||
chr1:45596304
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.107+5034C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596304 | ||||||
chr1:45596376
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+5106T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596376 | ||||||
chr1:45596590
|
C | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.107+5320C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596590 | ||||||
chr1:45596741
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.107+5471C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596741 | ||||||
chr1:45596745
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.107+5475A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596745 | ||||||
chr1:45596771
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.108-5484C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596771 | ||||||
chr1:45596847
|
T | TG | 3 | a0001c0001t0001g0022a0001c0003t0001g0015a0001c0003t0001g0016 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.108-5406dupG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45596847 | |||||
chr1:45596907
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-5348T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45596907 | ||||||
chr1:45597237
|
G | A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-5018G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597237 | ||||||
chr1:45597281
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.108-4974T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597281 | ||||||
chr1:45597285
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0107 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.108-4970C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597285 | ||||||
chr1:45597298
|
C | CTT | 111 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(108): Show | 111 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.108-4934_108-4933d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | |||||
chr1:45597298
|
C | CTTT | 98 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.108-4935_108-4933d others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | |||||
chr1:45597298
|
C | CTTTT | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(33): Show | 36 | HG01346.hp2 HG01943.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.108-4936_108-4933d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | |||||
chr1:45597298
|
C | CTTTTT | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG02486.hp1 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-4937_108-4933d others(7): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | |||||
chr1:45597298
|
CT | C | 9 | a0002c0004t0001g0181a0002c0004t0001g0182a0002c0004t0001g0183others(6): Show | 9 | NA18944.hp1 NA18969.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-4933delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | |||||
chr1:45597298
|
CTTTTTTT others(1): Show |
C | 23 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0003t0002g0001others(20): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.108-4940_108-4933d others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45597298 | |||||
chr1:45597786
|
A | G | 1 | a0001c0003t0001g0016 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-4469A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45597786 | ||||||
chr1:45598026
|
T | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.108-4229T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598026 | ||||||
chr1:45598058
|
A | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-4197A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598058 | ||||||
chr1:45598163
|
C | T | 3 | a0001c0002t0001g0175a0001c0002t0001g0176a0001c0002t0001g0178 | 3 | NA18977.hp2 NA18988.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.108-4092C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598163 | ||||||
chr1:45598172
|
C | CT | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.108-4067dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45598172 | |||||
chr1:45598172
|
C | CTT | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.108-4068_108-4067d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45598172 | |||||
chr1:45598470
|
T | C | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-3785T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598470 | ||||||
chr1:45598490
|
G | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-3765G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45598490 | ||||||
chr1:45599000
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108-3255G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599000 | ||||||
chr1:45599081
|
G | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-3174G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599081 | ||||||
chr1:45599090
|
C | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-3165C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599090 | ||||||
chr1:45599224
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0069 | 2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.108-3031G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599224 | ||||||
chr1:45599280
|
C | T | 1 | a0001c0002t0001g0259 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.108-2975C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599280 | ||||||
chr1:45599307
|
C | G | 1 | a0001c0002t0001g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.108-2948C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599307 | ||||||
chr1:45599379
|
C | T | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-2876C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599379 | ||||||
chr1:45599568
|
C | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.108-2687C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599568 | ||||||
chr1:45599610
|
A | T | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.108-2645A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599610 | ||||||
chr1:45599619
|
GGGTTTCA others(16): Show |
G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-2629_108-2607d others(25): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599619 | |||||
chr1:45599803
|
C | T | 2 | a0003c0006t0001g0282a0003c0006t0001g0283 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2452C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599803 | ||||||
chr1:45599820
|
A | C | 3 | a0002c0004t0001g0183a0002c0004t0001g0187a0002c0004t0001g0188 | 3 | NA18974.hp1 NA19006.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.108-2435A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599820 | ||||||
chr1:45599881
|
A | G | 2 | a0001c0001t0001g0174a0005c0011t0001g0173 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.108-2374A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599881 | ||||||
chr1:45599951
|
G | GTTTTTTT others(7): Show |
1 | a0005c0011t0001g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108-2303_108-2302i others(16): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599951 | |||||
chr1:45599953
|
A | AT | 43 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0029others(40): Show | 43 | HG00408.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.108-2280dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | |||||
chr1:45599953
|
A | ATT | 8 | a0001c0002t0001g0222a0001c0002t0001g0234a0001c0002t0001g0257others(5): Show | 8 | HG00544.hp2 HG00673.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-2281_108-2280d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | |||||
chr1:45599953
|
A | T | 5 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0112others(2): Show | 5 | HG02083.hp1 HG02258.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-2302A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45599953 | ||||||
chr1:45599953
|
AT | A | 128 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.108-2280delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | |||||
chr1:45599953
|
ATT | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(4): Show | 7 | HG00642.hp1 HG01069.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-2281_108-2280d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | |||||
chr1:45599953
|
ATTTT | A | 9 | a0002c0004t0001g0182a0002c0004t0001g0183a0002c0004t0001g0184others(6): Show | 9 | NA18944.hp1 NA18969.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-2283_108-2280d others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45599953 | |||||
chr1:45600087
|
A | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-2168A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600087 | ||||||
chr1:45600203
|
A | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-2052A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600203 | ||||||
chr1:45600271
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030 | 3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.108-1984T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600271 | ||||||
chr1:45600281
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.108-1974C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600281 | ||||||
chr1:45600326
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.108-1929T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600326 | ||||||
chr1:45600369
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-1886T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600369 | ||||||
chr1:45600618
|
T | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-1637T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600618 | ||||||
chr1:45600659
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.108-1596A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600659 | ||||||
chr1:45600737
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.108-1518T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600737 | ||||||
chr1:45600936
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.108-1319A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45600936 | ||||||
chr1:45601013
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | NA18979.hp1 NA18986.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.108-1242C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601013 | ||||||
chr1:45601049
|
A | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030 | 3 | HG01891.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.108-1206A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601049 | ||||||
chr1:45601189
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.108-1066T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601189 | ||||||
chr1:45601356
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.108-899A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601356 | ||||||
chr1:45601514
|
A | G | 1 | a0001c0002t0001g0193 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.108-741A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601514 | ||||||
chr1:45601591
|
C | G | 3 | a0001c0002t0001g0192a0001c0002t0001g0210a0001c0002t0001g0270 | 3 | HG02015.hp2 HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.108-664C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601591 | ||||||
chr1:45601597
|
G | A | 26 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0004g0129others(23): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.108-658G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601597 | ||||||
chr1:45601678
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.108-577G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601678 | ||||||
chr1:45601745
|
A | AT | 124 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.108-482dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
A | ATT | 73 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0021others(70): Show | 73 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.108-483_108-482dup others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
A | ATTT | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01074.hp2 HG01109.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-484_108-482dup others(3): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
A | ATTTT | 16 | a0001c0001t0004g0130a0001c0002t0001g0198a0001c0002t0001g0199others(13): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.108-485_108-482dup others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
A | ATTTTT | 7 | a0001c0001t0004g0129a0001c0003t0002g0146a0001c0003t0002g0153others(4): Show | 7 | HG00735.hp2 HG01167.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.108-486_108-482dup others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.108-491_108-482dup others(10): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
AT | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0083others(3): Show | 6 | HG02083.hp1 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-482delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601745
|
ATTTTTTT others(4): Show |
A | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-492_108-482del others(11): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 45601745 | |||||
chr1:45601778
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.108-477T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601778 | ||||||
chr1:45601878
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-377C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601878 | ||||||
chr1:45601879
|
C | T | 1 | a0001c0002t0001g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.108-376C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601879 | ||||||
chr1:45601975
|
A | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-280A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45601975 | ||||||
chr1:45602030
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.108-225G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45602030 | ||||||
chr1:45602208
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-47A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 2/14 | chr1 | 45602208 | ||||||
chr1:45602643
|
C | A | 1 | a0001c0002t0001g0271 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.218+278C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602643 | ||||||
chr1:45602725
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.218+360G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602725 | ||||||
chr1:45602748
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.218+383G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602748 | ||||||
chr1:45602872
|
C | T | 1 | a0002c0004t0001g0185 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.218+507C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602872 | ||||||
chr1:45602947
|
T | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.218+582T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45602947 | ||||||
chr1:45603070
|
C | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218+705C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603070 | ||||||
chr1:45603205
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.218+840C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603205 | ||||||
chr1:45603423
|
G | A | 1 | a0001c0002t0001g0217 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.218+1058G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603423 | ||||||
chr1:45603605
|
A | AT | 18 | a0001c0001t0001g0011a0001c0001t0001g0136a0001c0001t0001g0142others(15): Show | 18 | HG00544.hp1 HG00642.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+1260dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 45603605 | |||||
chr1:45603605
|
A | ATT | 132 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.218+1259_218+1260d others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 45603605 | |||||
chr1:45603605
|
A | ATTT | 39 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(36): Show | 39 | HG02083.hp1 HG02109.hp1 HG02148.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+1258_218+1260d others(5): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 45603605 | |||||
chr1:45603640
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218+1275G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603640 | ||||||
chr1:45603720
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-1216C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603720 | ||||||
chr1:45603860
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-1076C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603860 | ||||||
chr1:45603940
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.219-996G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45603940 | ||||||
chr1:45604282
|
C | T | 2 | a0003c0006t0001g0282a0003c0006t0001g0283 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-654C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604282 | ||||||
chr1:45604534
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.219-402G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604534 | ||||||
chr1:45604565
|
A | T | 1 | a0001c0002t0001g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.219-371A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604565 | ||||||
chr1:45604575
|
A | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-361A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604575 | ||||||
chr1:45604748
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.219-188A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604748 | ||||||
chr1:45604898
|
A | G | 2 | a0001c0002t0001g0204a0001c0003t0002g0150 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.219-38A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 3/14 | chr1 | 45604898 | ||||||
chr1:45605166
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.299+150C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605166 | ||||||
chr1:45605525
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.299+509C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605525 | ||||||
chr1:45605651
|
A | G | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.299+635A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605651 | ||||||
chr1:45605749
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.299+733A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605749 | ||||||
chr1:45605774
|
G | GT | 16 | a0001c0002t0001g0179a0001c0002t0001g0194a0001c0002t0001g0222others(13): Show | 16 | NA18944.hp1 NA18966.hp2 NA18968.hp1 others(13): Show |
intron_variant | MODIFIER | c.300-689dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 45605774 | |||||
chr1:45605774
|
GT | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.300-689delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 45605774 | |||||
chr1:45605791
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01167.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.300-691T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605791 | ||||||
chr1:45605793
|
T | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.300-689T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605793 | ||||||
chr1:45605833
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.300-649A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605833 | ||||||
chr1:45605883
|
T | C | 31 | a0001c0002t0001g0179a0001c0002t0001g0192a0001c0002t0001g0204others(28): Show | 31 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.300-599T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605883 | ||||||
chr1:45605912
|
G | A | 1 | a0001c0002t0001g0240 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.300-570G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45605912 | ||||||
chr1:45606007
|
C | T | 26 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0004g0129others(23): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.300-475C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606007 | ||||||
chr1:45606055
|
C | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.300-427C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606055 | ||||||
chr1:45606136
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.300-346T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606136 | ||||||
chr1:45606168
|
C | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-314C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606168 | ||||||
chr1:45606339
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300-143C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 4/14 | chr1 | 45606339 | ||||||
chr1:45606712
|
G | T | 3 | a0001c0002t0001g0220a0001c0002t0001g0226a0001c0002t0001g0246 | 3 | HG02451.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.409+121G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606712 | ||||||
chr1:45606713
|
C | T | 3 | a0001c0002t0001g0220a0001c0002t0001g0226a0001c0002t0001g0246 | 3 | HG02451.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.409+122C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606713 | ||||||
chr1:45606718
|
A | C | 1 | a0001c0002t0001g0225 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.409+127A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606718 | ||||||
chr1:45606818
|
T | C | 1 | a0002c0004t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.409+227T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606818 | ||||||
chr1:45606890
|
G | A | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.409+299G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606890 | ||||||
chr1:45606936
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.409+345T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606936 | ||||||
chr1:45606965
|
T | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.410-356T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45606965 | ||||||
chr1:45607047
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01069.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.410-274T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607047 | ||||||
chr1:45607098
|
A | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-223A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607098 | ||||||
chr1:45607106
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.410-215T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607106 | ||||||
chr1:45607215
|
G | C | 4 | a0001c0002t0001g0207a0001c0002t0001g0209a0001c0002t0001g0219others(1): Show | 4 | HG00438.hp2 HG00609.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-106G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607215 | ||||||
chr1:45607283
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.410-38G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 5/14 | chr1 | 45607283 | ||||||
chr1:45608381
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1426+44G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608381 | ||||||
chr1:45608457
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1426+120G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608457 | ||||||
chr1:45608961
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1426+624C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608961 | ||||||
chr1:45608995
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1426+658A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45608995 | ||||||
chr1:45609218
|
T | C | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+881T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609218 | ||||||
chr1:45609435
|
T | C | 1 | a0001c0003t0002g0001 | 2 | HG00099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1426+1098T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609435 | ||||||
chr1:45609499
|
A | AAAAC | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1426+1174_1426+117 others(8): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45609499 | |||||
chr1:45609511
|
C | CAAACAAA others(1): Show |
14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+1177_1426+117 others(12): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45609511 | |||||
chr1:45609628
|
C | G | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+1291C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609628 | ||||||
chr1:45609732
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0001g0082a0001c0001t0001g0103others(2): Show | 5 | HG01943.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426+1395A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609732 | ||||||
chr1:45609875
|
T | G | 1 | a0001c0003t0002g0150 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1426+1538T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609875 | ||||||
chr1:45609892
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1426+1555C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609892 | ||||||
chr1:45609937
|
C | T | 35 | a0001c0002t0001g0179a0001c0002t0001g0203a0001c0002t0001g0204others(32): Show | 35 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1426+1600C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609937 | ||||||
chr1:45609966
|
C | T | 36 | a0001c0002t0001g0179a0001c0002t0001g0203a0001c0002t0001g0204others(33): Show | 36 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1426+1629C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45609966 | ||||||
chr1:45610060
|
G | A | 14 | a0001c0007t0001g0284a0001c0007t0001g0285a0002c0004t0001g0180others(11): Show | 14 | HG00544.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.1426+1723G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610060 | ||||||
chr1:45610111
|
A | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1426+1774A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610111 | ||||||
chr1:45610124
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1426+1787G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610124 | ||||||
chr1:45610127
|
A | G | 25 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0003t0002g0001others(22): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1426+1790A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610127 | ||||||
chr1:45610190
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1426+1853C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610190 | ||||||
chr1:45610349
|
G | T | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1426+2012G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610349 | ||||||
chr1:45610386
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1426+2049C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610386 | ||||||
chr1:45610619
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1426+2282A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610619 | ||||||
chr1:45610826
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1427-2343C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610826 | ||||||
chr1:45610850
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1427-2319G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45610850 | ||||||
chr1:45611063
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-2106C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611063 | ||||||
chr1:45611232
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1427-1937T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611232 | ||||||
chr1:45611456
|
C | CT | 38 | a0001c0001t0001g0111a0001c0002t0001g0178a0001c0002t0001g0179others(35): Show | 38 | HG00544.hp1 HG00609.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1427-1685dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611456
|
C | CTT | 12 | a0001c0001t0001g0040a0001c0002t0001g0202a0001c0002t0001g0207others(9): Show | 12 | HG00438.hp2 HG00733.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-1686_1427-168 others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611456
|
CT | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 44 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1427-1685delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611456
|
CTT | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1427-1686_1427-168 others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611456
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1427-1693_1427-168 others(13): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611456
|
CTTTTTTT others(3): Show |
C | 10 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(7): Show | 10 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.1427-1694_1427-168 others(14): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611456
|
CTTTTTTT others(393): Show |
C | 1 | a0001c0002t0001g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1427-1691_1427-129 others(4): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611456 | |||||
chr1:45611555
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031 | 3 | HG01243.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1427-1614C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611555 | ||||||
chr1:45611581
|
C | T | 2 | a0001c0002t0001g0254a0008c0014t0001g0266 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1427-1588C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611581 | ||||||
chr1:45611591
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1427-1578C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611591 | ||||||
chr1:45611666
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1427-1503C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611666 | ||||||
chr1:45611756
|
G | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1427-1413G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611756 | ||||||
chr1:45611855
|
C | CT | 24 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(21): Show | 24 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1427-1292dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611855 | |||||
chr1:45611855
|
CT | C | 6 | a0001c0001t0001g0057a0001c0001t0001g0076a0001c0003t0002g0151others(3): Show | 6 | HG01168.hp2 HG01192.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1427-1292delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611855 | |||||
chr1:45611855
|
CTT | C | 12 | a0001c0001t0001g0174a0002c0004t0001g0180a0002c0004t0001g0181others(9): Show | 12 | HG02258.hp2 NA18944.hp1 NA18968.hp1 others(9): Show |
intron_variant | MODIFIER | c.1427-1293_1427-129 others(6): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45611855 | |||||
chr1:45611877
|
TG | T | 4 | a0001c0002t0001g0236a0001c0002t0001g0237a0003c0006t0001g0282others(1): Show | 4 | HG02280.hp2 HG02717.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1427-1291delG | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611877 | ||||||
chr1:45611878
|
G | T | 105 | a0001c0002t0001g0102a0001c0002t0001g0106a0001c0002t0001g0175others(102): Show | 105 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1427-1291G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611878 | ||||||
chr1:45611883
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1427-1286G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45611883 | ||||||
chr1:45612043
|
G | GT | 20 | a0001c0001t0001g0118a0001c0001t0001g0136a0001c0002t0001g0212others(17): Show | 20 | HG00544.hp1 HG01074.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.1427-1115dupT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 45612043 | |||||
chr1:45612054
|
T | A | 1 | a0001c0002t0001g0260 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1427-1115T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612054 | ||||||
chr1:45612061
|
G | A | 1 | a0002c0004t0001g0190 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1427-1108G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612061 | ||||||
chr1:45612427
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1427-742C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612427 | ||||||
chr1:45612519
|
T | A | 11 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0201others(8): Show | 11 | HG00733.hp1 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1427-650T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612519 | ||||||
chr1:45612770
|
A | G | 1 | a0001c0002t0001g0256 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1427-399A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612770 | ||||||
chr1:45612858
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1427-311A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612858 | ||||||
chr1:45612892
|
T | C | 2 | a0003c0006t0001g0282a0003c0006t0001g0283 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1427-277T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612892 | ||||||
chr1:45612958
|
A | G | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1427-211A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45612958 | ||||||
chr1:45613013
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1427-156A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45613013 | ||||||
chr1:45613125
|
C | T | 3 | a0001c0001t0001g0022a0001c0003t0001g0015a0001c0003t0001g0016 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1427-44C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 6/14 | chr1 | 45613125 | ||||||
chr1:45613443
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031 | 3 | HG01243.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1506+195C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45613443 | ||||||
chr1:45613719
|
T | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1507-377T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45613719 | ||||||
chr1:45613821
|
A | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1507-275A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45613821 | ||||||
chr1:45613908
|
AT | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1507-185delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 45613908 | |||||
chr1:45614068
|
A | G | 2 | a0001c0001t0001g0174a0005c0011t0001g0173 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1507-28A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 7/14 | chr1 | 45614068 | ||||||
chr1:45614388
|
ACT | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0096 | 3 | HG02015.hp1 HG02135.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1666+26_1666+27del others(2): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 45614388 | |||||
chr1:45614475
|
C | T | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.1666+109C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614475 | ||||||
chr1:45614548
|
GT | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1666+190delT | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 45614548 | |||||
chr1:45614595
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1666+229A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614595 | ||||||
chr1:45614628
|
A | T | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1666+262A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614628 | ||||||
chr1:45614639
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0031 | 3 | HG01243.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1666+273A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614639 | ||||||
chr1:45614694
|
A | G | 1 | a0001c0005t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1667-319A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614694 | ||||||
chr1:45614696
|
G | A | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1667-317G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614696 | ||||||
chr1:45614696
|
G | C | 1 | a0001c0005t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1667-317G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614696 | ||||||
chr1:45614843
|
G | T | 1 | a0001c0005t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1667-170G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614843 | ||||||
chr1:45614858
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1667-155T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 9/14 | chr1 | 45614858 | ||||||
chr1:45615216
|
G | A | 1 | a0001c0002t0001g0239 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1855+15G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/14 | chr1 | 45615216 | ||||||
chr1:45615275
|
A | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1856-30A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/14 | chr1 | 45615275 | ||||||
chr1:45615289
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1856-16A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 10/14 | chr1 | 45615289 | ||||||
chr1:45615492
|
G | C | 2 | a0001c0007t0001g0284a0001c0007t0001g0285 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2022+21G>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615492 | ||||||
chr1:45615551
|
A | T | 2 | a0001c0002t0001g0209a0001c0002t0001g0280 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.2022+80A>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615551 | ||||||
chr1:45615610
|
T | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2022+139T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615610 | ||||||
chr1:45615750
|
C | G | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.2022+279C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615750 | ||||||
chr1:45615808
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2022+337A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615808 | ||||||
chr1:45615811
|
C | T | 5 | a0001c0002t0001g0207a0001c0002t0001g0209a0001c0002t0001g0219others(2): Show | 5 | HG00438.hp2 HG00609.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2022+340C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615811 | ||||||
chr1:45615926
|
G | A | 1 | a0001c0003t0002g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2023-411G>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45615926 | ||||||
chr1:45616018
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2023-319G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616018 | ||||||
chr1:45616059
|
A | G | 12 | a0002c0004t0001g0180a0002c0004t0001g0181a0002c0004t0001g0182others(9): Show | 12 | NA18944.hp1 NA18968.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.2023-278A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616059 | ||||||
chr1:45616109
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2023-228G>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616109 | ||||||
chr1:45616268
|
T | A | 296 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.2023-69T>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616268 | ||||||
chr1:45616288
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2023-49C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 11/14 | chr1 | 45616288 | ||||||
chr1:45616605
|
A | C | 1 | a0001c0001t0001g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2080-21A>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 12/14 | chr1 | 45616605 | ||||||
chr1:45616759
|
C | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2157+56C>A | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45616759 | ||||||
chr1:45617284
|
A | G | 1 | a0001c0002t0005g0288 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2158-179A>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45617284 | ||||||
chr1:45617293
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.2158-170C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45617293 | ||||||
chr1:45617352
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2158-111T>C | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 13/14 | chr1 | 45617352 | ||||||
chr1:45617654
|
C | T | 1 | a0001c0003t0002g0152 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2286+63C>T | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/14 | chr1 | 45617654 | ||||||
chr1:45617872
|
T | G | 1 | a0001c0003t0002g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2287-189T>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/14 | chr1 | 45617872 | ||||||
chr1:45618034
|
C | G | 23 | a0001c0003t0002g0001a0001c0003t0002g0145a0001c0003t0002g0146others(20): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.2287-27C>G | NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 14/14 | chr1 | 45618034 |