Item | Value |
---|---|
geneid | 116841 |
ensemblid | ENSG00000143740.15 |
hgncid | 30669 |
symbol | SNAP47 |
name | synaptosome associated protein 47 |
refseq_nuc | NM_053052.4 |
refseq_prot | NP_444280.3 |
ensembl_nuc | ENST00000617596.5 |
ensembl_prot | ENSP00000483253.1 |
mane_status | MANE Select |
chr | chr1 |
start | 227735435 |
end | 227781226 |
strand | + |
ver | v1.2 |
region | chr1:227735435-227781226 |
region5000 | chr1:227730435-227786226 |
regionname0 | SNAP47_chr1_227735435_227781226 |
regionname5000 | SNAP47_chr1_227730435_227786226 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 419 | 148 | 39 | 37 | 48 | 9 | 15 | 36 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002 | 1/1 | 419 | 118 | 35 | 21 | 39 | 5 | 16 | 30 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0003 | 0/0 | 419 | 87 | 12 | 13 | 51 | 1 | 10 | 38 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0004 | 0/0 | 419 | 23 | 0 | 0 | 21 | 2 | 0 | 19 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0005 | 0/0 | 419 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0006 | 0/0 | 419 | 8 | 0 | 5 | 0 | 1 | 2 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0007 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0008 | 0/0 | 419 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0009 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1260 | 146 | 39 | 36 | 47 | 9 | 15 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0002 | 1/1 | 1260 | 115 | 35 | 21 | 38 | 5 | 14 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0003 | 0/0 | 1260 | 78 | 12 | 13 | 42 | 1 | 10 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0004 | 0/0 | 1260 | 23 | 0 | 0 | 21 | 2 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0005 | 0/0 | 1260 | 9 | 9 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0006 | 0/0 | 1260 | 9 | 0 | 0 | 9 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0007 | 0/0 | 1260 | 8 | 0 | 5 | 0 | 1 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0008 | 0/0 | 1260 | 2 | 0 | 0 | 0 | 0 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0009 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0010 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0011 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0012 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0013 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
c0014 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 664 | 377 | 81 | 75 | 158 | 18 | 43 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
t0002 | 0/0 | 664 | 10 | 9 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
t0003 | 0/0 | 664 | 5 | 5 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
t0004 | 0/0 | 664 | 2 | 0 | 0 | 1 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
t0005 | 0/0 | 664 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
t0006 | 0/0 | 664 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0314 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1260 | 146 | 39 | 36 | 47 | 9 | 15 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0001c0013 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0001c0014 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0002 | 1/1 | 1260 | 115 | 35 | 21 | 38 | 5 | 14 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0008 | 0/0 | 1260 | 2 | 0 | 0 | 0 | 0 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0011 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0003c0003 | 0/0 | 1260 | 78 | 12 | 13 | 42 | 1 | 10 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0003c0006 | 0/0 | 1260 | 9 | 0 | 0 | 9 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0004c0004 | 0/0 | 1260 | 23 | 0 | 0 | 21 | 2 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0005c0005 | 0/0 | 1260 | 9 | 9 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0006c0007 | 0/0 | 1260 | 8 | 0 | 5 | 0 | 1 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0007c0010 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0008c0012 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0009c0009 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1923 | 136 | 30 | 35 | 47 | 9 | 15 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0001c0001t0002 | 0/0 | 1923 | 9 | 8 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0001c0001t0006 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0001c0013t0001 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0001c0014t0001 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0002t0001 | 1/1 | 1923 | 107 | 29 | 21 | 37 | 5 | 13 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0002t0002 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0002t0003 | 0/0 | 1923 | 5 | 5 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0002t0004 | 0/0 | 1923 | 2 | 0 | 0 | 1 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0008t0001 | 0/0 | 1923 | 2 | 0 | 0 | 0 | 0 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0002c0011t0001 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0003c0003t0001 | 0/0 | 1923 | 77 | 12 | 13 | 41 | 1 | 10 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0003c0003t0005 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0003c0006t0001 | 0/0 | 1923 | 9 | 0 | 0 | 9 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0004c0004t0001 | 0/0 | 1923 | 23 | 0 | 0 | 21 | 2 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0005c0005t0001 | 0/0 | 1923 | 9 | 9 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0006c0007t0001 | 0/0 | 1923 | 8 | 0 | 5 | 0 | 1 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0007c0010t0001 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0008c0012t0001 | 0/0 | 1923 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
a0009c0009t0001 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | copy fasta | chr1 | 227730435 | 227786226 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0013t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0001c0014t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0314 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0002t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0008t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0008t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0002c0011t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0003t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0003c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0005c0005t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0006c0007t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0007c0010t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0008c0012t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
a0009c0009t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | GBR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00140 | hp1 | a0006 | c0007 | t0001 | g0055 | EUR | GBR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0313 | EUR | GBR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0196 | EUR | FIN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0161 | EUR | FIN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0116 | EUR | FIN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00438 | hp2 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0102 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00639 | hp2 | a0006 | c0007 | t0001 | g0060 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00642 | hp2 | a0006 | c0007 | t0001 | g0014 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00733 | hp2 | a0001 | c0013 | t0001 | g0322 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00741 | hp1 | a0006 | c0007 | t0001 | g0061 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0097 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0270 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0034 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01169 | hp2 | a0003 | c0003 | t0001 | g0033 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0006 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | IBS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | IBS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01516 | hp2 | a0004 | c0004 | t0001 | g0062 | EUR | IBS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01517 | hp1 | a0004 | c0004 | t0001 | g0063 | EUR | IBS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | IBS | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01884 | hp2 | a0005 | c0005 | t0001 | g0348 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01934 | hp2 | a0003 | c0003 | t0001 | g0104 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01975 | hp1 | a0006 | c0007 | t0001 | g0053 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01993 | hp1 | a0006 | c0007 | t0001 | g0014 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02040 | hp2 | a0003 | c0003 | t0001 | g0094 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02055 | hp2 | a0005 | c0005 | t0001 | g0349 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0117 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02129 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0091 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02135 | hp2 | a0004 | c0004 | t0001 | g0013 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02165 | hp1 | a0003 | c0006 | t0001 | g0007 | EAS | CDX | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | CDX | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0044 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0018 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0089 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0340 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02523 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | KHV | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02683 | hp2 | a0003 | c0003 | t0001 | g0123 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0107 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0085 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02717 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0036 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02723 | hp2 | a0005 | c0005 | t0001 | g0346 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0311 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02735 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0041 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02895 | hp2 | a0005 | c0005 | t0001 | g0355 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02922 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0325 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0336 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0078 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0113 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0087 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0046 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03139 | hp2 | a0003 | c0003 | t0001 | g0131 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03195 | hp2 | a0005 | c0005 | t0001 | g0350 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03209 | hp2 | a0005 | c0005 | t0001 | g0347 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03239 | hp1 | a0002 | c0008 | t0001 | g0259 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0133 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03490 | hp2 | a0003 | c0003 | t0001 | g0105 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | ESN | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0351 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03654 | hp1 | a0002 | c0008 | t0001 | g0184 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0122 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0190 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03688 | hp2 | a0006 | c0007 | t0001 | g0056 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03704 | hp2 | a0003 | c0003 | t0001 | g0108 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | BEB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | BEB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03834 | hp2 | a0002 | c0002 | t0004 | g0150 | SAS | BEB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0257 | SAS | BEB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0140 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04204 | hp2 | a0006 | c0007 | t0001 | g0059 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04228 | hp1 | a0008 | c0012 | t0001 | g0265 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18522 | hp1 | a0005 | c0005 | t0001 | g0345 | AFR | YRI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0121 | AFR | YRI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18612 | hp2 | a0003 | c0006 | t0001 | g0007 | EAS | CHB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0120 | EAS | CHB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18747 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | CHB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | YRI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18940 | hp2 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18942 | hp2 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18945 | hp1 | a0004 | c0004 | t0001 | g0050 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18945 | hp2 | a0003 | c0006 | t0001 | g0007 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18953 | hp2 | a0009 | c0009 | t0001 | g0126 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18961 | hp1 | a0004 | c0004 | t0001 | g0049 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18962 | hp2 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18963 | hp1 | a0003 | c0006 | t0001 | g0144 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18966 | hp2 | a0004 | c0004 | t0001 | g0065 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0128 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18971 | hp1 | a0001 | c0014 | t0001 | g0031 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18973 | hp1 | a0003 | c0003 | t0001 | g0119 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18973 | hp2 | a0004 | c0004 | t0001 | g0010 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0096 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18980 | hp1 | a0004 | c0004 | t0001 | g0054 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18984 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18985 | hp1 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18989 | hp1 | a0004 | c0004 | t0001 | g0058 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18994 | hp1 | a0004 | c0004 | t0001 | g0010 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18997 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18999 | hp1 | a0003 | c0006 | t0001 | g0142 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19000 | hp1 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19000 | hp2 | a0004 | c0004 | t0001 | g0052 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19009 | hp2 | a0003 | c0006 | t0001 | g0145 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19010 | hp2 | a0003 | c0006 | t0001 | g0132 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19011 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19012 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19030 | hp1 | a0005 | c0005 | t0001 | g0352 | AFR | LWK | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | LWK | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | LWK | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19056 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19056 | hp2 | a0004 | c0004 | t0001 | g0051 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19057 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19058 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19060 | hp1 | a0004 | c0004 | t0001 | g0011 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19063 | hp2 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0100 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19068 | hp1 | a0004 | c0004 | t0001 | g0048 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19070 | hp2 | a0002 | c0002 | t0004 | g0148 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19077 | hp1 | a0003 | c0003 | t0005 | g0088 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19079 | hp2 | a0003 | c0006 | t0001 | g0134 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19080 | hp2 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0109 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19083 | hp1 | a0004 | c0004 | t0001 | g0057 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0095 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19085 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19088 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19090 | hp1 | a0002 | c0011 | t0001 | g0264 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19091 | hp1 | a0003 | c0006 | t0001 | g0146 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19091 | hp2 | a0004 | c0004 | t0001 | g0011 | EAS | JPT | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ASW | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0354 | AFR | ASW | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0185 | EUR | TSI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0020 | EUR | TSI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0106 | SAS | GIH | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | ACB | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03471 | hp1 | a0007 | c0010 | t0001 | g0039 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0344 | AFR | USA | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | USA | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20300 | hp1 | a0005 | c0005 | t0001 | g0353 | AFR | USA | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0112 | AFR | USA | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | LWK | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0273 | REF | REF | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0314 | REF | REF | SNAP47_chr1_227730435_227786226 | SNAP47 | chr1 | 227730435 | 227786226 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:227747743
|
A | G | 1 | a0001 | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
missense_variant | MODERATE | c.7A>G | p.Arg3Gly | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/5 | 117/1923 | 7/1260 | 3/419 | chr1 | 227747743 | ||
chr1:227747770
|
T | C | 1 | a0009 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.34T>C | p.Cys12Arg | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/5 | 144/1923 | 34/1260 | 12/419 | chr1 | 227747770 | ||
chr1:227747946
|
C | G | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.210C>G | p.Ile70Met | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/5 | 320/1923 | 210/1260 | 70/419 | chr1 | 227747946 | ||
chr1:227747956
|
G | C | 1 | a0005 | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
missense_variant | MODERATE | c.220G>C | p.Gly74Arg | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/5 | 330/1923 | 220/1260 | 74/419 | chr1 | 227747956 | ||
chr1:227748061
|
G | A | 2 | a0003a0009 | 88 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(85): Show |
missense_variant | MODERATE | c.325G>A | p.Val109Met | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/5 | 435/1923 | 325/1260 | 109/419 | chr1 | 227748061 | ||
chr1:227759473
|
G | T | 1 | a0007 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.976G>T | p.Val326Phe | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/5 | 1086/1923 | 976/1260 | 326/419 | chr1 | 227759473 | ||
chr1:227766976
|
C | T | 2 | a0004a0006 | 31 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
missense_variant | MODERATE | c.1006C>T | p.Arg336Cys | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/5 | 1116/1923 | 1006/1260 | 336/419 | chr1 | 227766976 | ||
chr1:227766988
|
C | T | 1 | a0004 | 23 | HG01516.hp2 HG01517.hp1 HG02135.hp2 others(20): Show |
missense_variant | MODERATE | c.1018C>T | p.Arg340Cys | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/5 | 1128/1923 | 1018/1260 | 340/419 | chr1 | 227766988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:227759106
|
C | T | 1 | a0002c0011 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.609C>T | p.Pro203Pro | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/5 | 719/1923 | 609/1260 | 203/419 | chr1 | 227759106 | ||
chr1:227759115
|
A | G | 1 | a0002c0008 | 2 | HG03239.hp1 HG03654.hp1 |
synonymous_variant | LOW | c.618A>G | p.Lys206Lys | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/5 | 728/1923 | 618/1260 | 206/419 | chr1 | 227759115 | ||
chr1:227759124
|
A | T | 1 | a0001c0014 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.627A>T | p.Ile209Ile | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/5 | 737/1923 | 627/1260 | 209/419 | chr1 | 227759124 | ||
chr1:227759454
|
C | T | 1 | a0003c0006 | 9 | HG02165.hp1 NA18612.hp2 NA18945.hp2 others(6): Show |
synonymous_variant | LOW | c.957C>T | p.Pro319Pro | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/5 | 1067/1923 | 957/1260 | 319/419 | chr1 | 227759454 | ||
chr1:227767041
|
C | T | 1 | a0001c0013 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.1071C>T | p.Ser357Ser | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/5 | 1181/1923 | 1071/1260 | 357/419 | chr1 | 227767041 | ||
chr1:227767068
|
C | G | 1 | a0008c0012 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1098C>G | p.Thr366Thr | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/5 | 1208/1923 | 1098/1260 | 366/419 | chr1 | 227767068 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:227735494
|
C | T | 1 | a0002c0002t0004 | 2 | HG03834.hp2 NA19070.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/5 | 12243 | chr1 | 227735494 | |||||
chr1:227735495
|
C | T | 1 | a0001c0001t0006 | 1 | HG03471.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/5 | 12242 | chr1 | 227735495 | |||||
chr1:227747716
|
C | T | 2 | a0001c0001t0002a0002c0002t0002 | 10 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-21C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/5 | 21 | chr1 | 227747716 | |||||
chr1:227780975
|
C | T | 1 | a0003c0003t0005 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 5/5 | 302 | chr1 | 227780975 | |||||
chr1:227781095
|
C | T | 1 | a0002c0002t0003 | 5 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 5/5 | 422 | chr1 | 227781095 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:227735525
|
G | A | 1 | a0002c0002t0001g0032 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-46+26G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227735525 | ||||||
chr1:227735742
|
A | G | 12 | a0002c0002t0001g0344a0002c0002t0001g0354a0003c0003t0001g0351others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46+243A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227735742 | ||||||
chr1:227735789
|
A | AGGGTCCT others(13): Show |
1 | a0001c0001t0001g0343 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-46+294_-46+313dup others(20): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227735789 | |||||
chr1:227735878
|
G | A | 6 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46+379G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227735878 | ||||||
chr1:227736058
|
G | C | 9 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(6): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46+559G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736058 | ||||||
chr1:227736163
|
G | A | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-46+664G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736163 | ||||||
chr1:227736291
|
G | A | 27 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(24): Show | 34 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-46+792G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736291 | ||||||
chr1:227736328
|
T | A | 1 | a0002c0002t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-46+829T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736328 | ||||||
chr1:227736355
|
G | A | 8 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0047others(5): Show | 11 | NA18945.hp1 NA18961.hp1 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.-46+856G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736355 | ||||||
chr1:227736398
|
G | A | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+899G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736398 | ||||||
chr1:227736477
|
C | T | 9 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46+978C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736477 | ||||||
chr1:227736502
|
G | GT | 8 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0002g0340others(5): Show | 9 | HG00099.hp2 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46+1038dupT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
G | GTT | 6 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0002g0342others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46+1037_-46+1038d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GT | G | 69 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(66): Show | 71 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.-46+1038delT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTT | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-46+1037_-46+1038d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTT | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0154a0001c0001t0001g0155others(19): Show | 24 | HG00323.hp1 HG00597.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-46+1036_-46+1038d others(5): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTT | G | 13 | a0001c0001t0001g0019a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 14 | HG01071.hp1 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46+1035_-46+1038d others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTT | G | 13 | a0001c0001t0001g0149a0002c0002t0004g0148a0004c0004t0001g0050others(10): Show | 13 | HG01516.hp2 HG01517.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-46+1034_-46+1038d others(7): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTT | G | 21 | a0003c0003t0001g0147a0003c0006t0001g0144a0003c0006t0001g0145others(18): Show | 28 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-46+1033_-46+1038d others(8): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT | G | 20 | a0003c0003t0001g0127a0003c0003t0001g0128a0003c0003t0001g0129others(17): Show | 22 | HG00438.hp2 HG01255.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.-46+1032_-46+1038d others(9): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT others(1): Show |
G | 50 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075others(47): Show | 61 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-46+1031_-46+1038d others(10): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT others(2): Show |
G | 11 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0071others(8): Show | 11 | HG01169.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-46+1030_-46+1038d others(11): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT others(5): Show |
G | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-46+1027_-46+1038d others(14): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT others(6): Show |
G | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-46+1026_-46+1038d others(15): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT others(9): Show |
G | 4 | a0002c0002t0001g0015a0002c0002t0001g0082a0002c0002t0001g0083others(1): Show | 5 | HG01074.hp2 HG01928.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+1023_-46+1038d others(18): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736502
|
GTTTTTTT others(14): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-46+1018_-46+1038d others(23): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736502 | |||||
chr1:227736510
|
T | G | 2 | a0001c0001t0001g0077a0002c0002t0001g0076 | 2 | HG01361.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-46+1011T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736510 | ||||||
chr1:227736511
|
T | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+1012T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736511 | ||||||
chr1:227736514
|
T | G | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-46+1015T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736514 | ||||||
chr1:227736520
|
T | G | 2 | a0002c0002t0001g0080a0002c0002t0001g0081 | 2 | NA18975.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-46+1021T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736520 | ||||||
chr1:227736563
|
C | T | 3 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0251 | 3 | HG02622.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-46+1064C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736563 | ||||||
chr1:227736565
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-46+1066G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736565 | ||||||
chr1:227736566
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-46+1067C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736566 | ||||||
chr1:227736636
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0250a0001c0001t0001g0310others(1): Show | 4 | NA18954.hp1 NA18959.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+1137A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736636 | ||||||
chr1:227736686
|
G | GT | 38 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0169others(35): Show | 41 | HG00438.hp1 HG00621.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.-46+1205dupT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736686 | |||||
chr1:227736686
|
GT | G | 106 | a0002c0002t0001g0003a0002c0002t0001g0040a0002c0002t0001g0042others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.-46+1205delT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736686 | |||||
chr1:227736686
|
GTT | G | 7 | a0001c0001t0001g0173a0001c0001t0001g0174a0002c0002t0001g0064others(4): Show | 7 | HG01891.hp1 HG03453.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46+1204_-46+1205d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227736686 | |||||
chr1:227736692
|
T | G | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0252others(1): Show | 4 | HG00738.hp2 HG01192.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+1193T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736692 | ||||||
chr1:227736693
|
T | G | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1194T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736693 | ||||||
chr1:227736718
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-46+1219C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736718 | ||||||
chr1:227736840
|
A | T | 1 | a0003c0003t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-46+1341A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736840 | ||||||
chr1:227736889
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-46+1390T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736889 | ||||||
chr1:227736964
|
A | T | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-46+1465A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227736964 | ||||||
chr1:227737054
|
G | A | 1 | a0006c0007t0001g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-46+1555G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737054 | ||||||
chr1:227737072
|
A | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-46+1573A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737072 | ||||||
chr1:227737302
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0296 | 2 | HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-46+1803A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737302 | ||||||
chr1:227737387
|
C | T | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-46+1888C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737387 | ||||||
chr1:227737402
|
T | C | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-46+1903T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737402 | ||||||
chr1:227737408
|
G | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0297others(2): Show | 6 | HG02109.hp2 HG02615.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46+1909G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737408 | ||||||
chr1:227737805
|
G | GTTGTTTT others(5): Show |
2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-46+2311_-46+2322d others(14): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227737805 | |||||
chr1:227737839
|
A | G | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+2340A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737839 | ||||||
chr1:227737934
|
G | A | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-46+2435G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737934 | ||||||
chr1:227737953
|
A | G | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-46+2454A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737953 | ||||||
chr1:227737974
|
C | T | 1 | a0002c0002t0001g0254 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46+2475C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227737974 | ||||||
chr1:227738016
|
G | T | 79 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075others(76): Show | 92 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.-46+2517G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738016 | ||||||
chr1:227738320
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-46+2821G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738320 | ||||||
chr1:227738324
|
G | A | 1 | a0006c0007t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-46+2825G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738324 | ||||||
chr1:227738445
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(47): Show | 59 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-46+2946C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738445 | ||||||
chr1:227738467
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-46+2968C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738467 | ||||||
chr1:227738515
|
C | T | 16 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(13): Show | 17 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46+3016C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738515 | ||||||
chr1:227738713
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-46+3214A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738713 | ||||||
chr1:227738875
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-46+3376G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738875 | ||||||
chr1:227738939
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-46+3440C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738939 | ||||||
chr1:227738970
|
C | A | 4 | a0002c0002t0003g0009a0002c0002t0003g0041a0002c0002t0003g0044others(1): Show | 5 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+3471C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227738970 | ||||||
chr1:227739036
|
A | G | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-46+3537A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739036 | ||||||
chr1:227739077
|
G | C | 1 | a0003c0003t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46+3578G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739077 | ||||||
chr1:227739083
|
G | A | 1 | a0002c0002t0001g0175 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-46+3584G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739083 | ||||||
chr1:227739141
|
C | T | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+3642C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739141 | ||||||
chr1:227739145
|
A | G | 35 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(32): Show | 42 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-46+3646A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739145 | ||||||
chr1:227739186
|
G | T | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-46+3687G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739186 | ||||||
chr1:227739329
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-46+3830C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739329 | ||||||
chr1:227739541
|
A | G | 22 | a0001c0001t0001g0023a0001c0001t0001g0079a0001c0001t0001g0163others(19): Show | 23 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.-46+4042A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739541 | ||||||
chr1:227739822
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-46+4323G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739822 | ||||||
chr1:227739954
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46+4455A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739954 | ||||||
chr1:227739971
|
A | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-46+4472A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227739971 | ||||||
chr1:227740082
|
G | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-46+4583G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740082 | ||||||
chr1:227740118
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-46+4619G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740118 | ||||||
chr1:227740154
|
G | T | 1 | a0002c0002t0001g0216 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-46+4655G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740154 | ||||||
chr1:227740159
|
C | T | 24 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0011others(21): Show | 31 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46+4660C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740159 | ||||||
chr1:227740190
|
G | A | 3 | a0004c0004t0001g0011a0004c0004t0001g0057a0004c0004t0001g0058 | 4 | NA18989.hp1 NA19060.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+4691G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740190 | ||||||
chr1:227740202
|
A | G | 1 | a0002c0002t0001g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-46+4703A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740202 | ||||||
chr1:227740241
|
G | A | 1 | a0003c0003t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-46+4742G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740241 | ||||||
chr1:227740296
|
C | T | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-46+4797C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740296 | ||||||
chr1:227740478
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-46+4979C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740478 | ||||||
chr1:227740670
|
A | G | 1 | a0002c0002t0004g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-46+5171A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740670 | ||||||
chr1:227740733
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-46+5234A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740733 | ||||||
chr1:227740739
|
A | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0343 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-46+5240A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740739 | ||||||
chr1:227740755
|
G | C | 2 | a0003c0003t0001g0016a0003c0003t0001g0090 | 3 | NA18950.hp1 NA18964.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-46+5256G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740755 | ||||||
chr1:227740755
|
G | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-46+5256G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740755 | ||||||
chr1:227740789
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(69): Show | 82 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46+5290C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740789 | ||||||
chr1:227740793
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-46+5294G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227740793 | ||||||
chr1:227740933
|
GTGGGGGC others(115): Show |
G | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+5446_-46+5567d others(2): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227740933 | |||||
chr1:227740939
|
G | GCAGATGC others(53): Show |
1 | a0001c0001t0001g0329 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-46+5459_-46+5518d others(62): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227740939 | |||||
chr1:227741011
|
C | T | 1 | a0003c0003t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-46+5512C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741011 | ||||||
chr1:227741055
|
A | G | 1 | a0001c0001t0002g0342 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-46+5556A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741055 | ||||||
chr1:227741111
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-46+5612T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741111 | ||||||
chr1:227741166
|
T | A | 10 | a0003c0003t0001g0351a0005c0005t0001g0345a0005c0005t0001g0346others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46+5667T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741166 | ||||||
chr1:227741226
|
T | A | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-46+5727T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741226 | ||||||
chr1:227741268
|
G | A | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-46+5769G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741268 | ||||||
chr1:227741329
|
G | C | 9 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46+5830G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741329 | ||||||
chr1:227741346
|
T | G | 12 | a0001c0001t0001g0077a0001c0001t0001g0167a0001c0001t0001g0228others(9): Show | 12 | HG01358.hp2 HG02015.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46+5847T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741346 | ||||||
chr1:227741394
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-46+5895G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741394 | ||||||
chr1:227741430
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-46+5931G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741430 | ||||||
chr1:227741500
|
G | C | 1 | a0005c0005t0001g0349 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-46+6001G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741500 | ||||||
chr1:227741557
|
G | A | 2 | a0002c0002t0001g0179a0002c0002t0001g0180 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-46+6058G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741557 | ||||||
chr1:227741568
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-46+6069C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741568 | ||||||
chr1:227741569
|
G | A | 1 | a0002c0002t0004g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-46+6070G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741569 | ||||||
chr1:227741717
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02083.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-45-5975C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741717 | ||||||
chr1:227741740
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(124): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-45-5952C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741740 | ||||||
chr1:227741748
|
G | A | 1 | a0003c0003t0001g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-45-5944G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741748 | ||||||
chr1:227741752
|
C | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0328 | 2 | HG01258.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-45-5940C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227741752 | ||||||
chr1:227741897
|
GCTT | G | 80 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(77): Show | 91 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-45-5790_-45-5788d others(5): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227741897 | |||||
chr1:227741999
|
GTCTTTTT others(2): Show |
G | 18 | a0001c0001t0001g0022a0001c0001t0001g0203a0001c0001t0001g0204others(15): Show | 19 | HG00558.hp2 HG00621.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-45-5674_-45-5666d others(11): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227741999 | |||||
chr1:227742027
|
A | C | 1 | a0003c0003t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-45-5665A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742027 | ||||||
chr1:227742032
|
A | G | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45-5660A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742032 | ||||||
chr1:227742179
|
C | G | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-45-5513C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742179 | ||||||
chr1:227742276
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-5416C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742276 | ||||||
chr1:227742348
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-5344C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742348 | ||||||
chr1:227742542
|
G | A | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45-5150G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742542 | ||||||
chr1:227742894
|
G | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0305 | 2 | HG00621.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-45-4798G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227742894 | ||||||
chr1:227743134
|
C | T | 2 | a0003c0003t0001g0120a0003c0003t0001g0137 | 2 | NA18747.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-45-4558C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743134 | ||||||
chr1:227743156
|
G | GAGAT | 10 | a0003c0003t0001g0351a0005c0005t0001g0345a0005c0005t0001g0346others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45-4534_-45-4531d others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227743156 | |||||
chr1:227743194
|
T | G | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-45-4498T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743194 | ||||||
chr1:227743243
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-4449C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743243 | ||||||
chr1:227743244
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG01109.hp2 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-45-4448G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743244 | ||||||
chr1:227743244
|
G | C | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45-4448G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743244 | ||||||
chr1:227743362
|
G | C | 1 | a0006c0007t0001g0053 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-45-4330G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743362 | ||||||
chr1:227743463
|
G | A | 4 | a0001c0001t0001g0218a0003c0003t0001g0092a0003c0003t0001g0127others(1): Show | 4 | HG00735.hp2 NA18953.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45-4229G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743463 | ||||||
chr1:227743505
|
G | A | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45-4187G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743505 | ||||||
chr1:227743559
|
C | T | 1 | a0002c0002t0001g0202 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-45-4133C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743559 | ||||||
chr1:227743675
|
G | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-4017G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743675 | ||||||
chr1:227743677
|
C | T | 1 | a0002c0002t0001g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-45-4015C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743677 | ||||||
chr1:227743859
|
G | C | 143 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(140): Show | 164 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.-45-3833G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743859 | ||||||
chr1:227743868
|
G | A | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-45-3824G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743868 | ||||||
chr1:227743954
|
C | A | 3 | a0003c0003t0001g0092a0003c0003t0001g0127a0009c0009t0001g0126 | 3 | NA18953.hp2 NA18962.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-45-3738C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227743954 | ||||||
chr1:227744019
|
C | T | 27 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(24): Show | 34 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-45-3673C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744019 | ||||||
chr1:227744090
|
C | T | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45-3602C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744090 | ||||||
chr1:227744175
|
CT | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(334): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-45-3500delT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 227744175 | |||||
chr1:227744286
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-45-3406C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744286 | ||||||
chr1:227744525
|
A | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-3167A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744525 | ||||||
chr1:227744567
|
C | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-3125C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744567 | ||||||
chr1:227744571
|
C | T | 9 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(6): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45-3121C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744571 | ||||||
chr1:227744727
|
A | G | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45-2965A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744727 | ||||||
chr1:227744755
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-45-2937G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744755 | ||||||
chr1:227744790
|
T | C | 1 | a0003c0003t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-45-2902T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744790 | ||||||
chr1:227744815
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-45-2877C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744815 | ||||||
chr1:227744927
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-45-2765G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744927 | ||||||
chr1:227744930
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-45-2762C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227744930 | ||||||
chr1:227745035
|
G | C | 10 | a0003c0003t0001g0351a0005c0005t0001g0345a0005c0005t0001g0346others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45-2657G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745035 | ||||||
chr1:227745038
|
G | A | 6 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45-2654G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745038 | ||||||
chr1:227745274
|
G | T | 1 | a0002c0002t0001g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-45-2418G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745274 | ||||||
chr1:227745455
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45-2237G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745455 | ||||||
chr1:227745607
|
G | C | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-45-2085G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745607 | ||||||
chr1:227745635
|
T | A | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45-2057T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745635 | ||||||
chr1:227745638
|
G | A | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-45-2054G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745638 | ||||||
chr1:227745846
|
A | C | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45-1846A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745846 | ||||||
chr1:227745849
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-45-1843C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745849 | ||||||
chr1:227745919
|
A | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-45-1773A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745919 | ||||||
chr1:227745929
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-45-1763G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745929 | ||||||
chr1:227745997
|
G | C | 2 | a0004c0004t0001g0062a0004c0004t0001g0063 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-45-1695G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227745997 | ||||||
chr1:227746104
|
A | G | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-1588A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227746104 | ||||||
chr1:227746203
|
C | T | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-1489C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227746203 | ||||||
chr1:227746582
|
G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0306others(3): Show | 7 | HG01516.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-45-1110G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227746582 | ||||||
chr1:227746847
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-45-845C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227746847 | ||||||
chr1:227746905
|
T | G | 58 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(55): Show | 66 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-45-787T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227746905 | ||||||
chr1:227747035
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-45-657G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747035 | ||||||
chr1:227747049
|
T | C | 81 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(78): Show | 92 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.-45-643T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747049 | ||||||
chr1:227747068
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-45-624C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747068 | ||||||
chr1:227747073
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-619G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747073 | ||||||
chr1:227747117
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-45-575G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747117 | ||||||
chr1:227747120
|
C | T | 1 | a0003c0003t0001g0118 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-45-572C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747120 | ||||||
chr1:227747328
|
A | C | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45-364A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747328 | ||||||
chr1:227747357
|
A | G | 24 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0011others(21): Show | 31 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-45-335A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747357 | ||||||
chr1:227747400
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-45-292G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747400 | ||||||
chr1:227747538
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-45-154G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747538 | ||||||
chr1:227747539
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-45-153G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747539 | ||||||
chr1:227747579
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(268): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-45-113C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747579 | ||||||
chr1:227747608
|
G | A | 9 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(6): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45-84G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747608 | ||||||
chr1:227747654
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(268): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-45-38T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 1/4 | chr1 | 227747654 | ||||||
chr1:227748283
|
A | G | 1 | a0003c0003t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497+50A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748283 | ||||||
chr1:227748316
|
A | G | 1 | a0004c0004t0001g0058 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.497+83A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748316 | ||||||
chr1:227748341
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(5): Show | 9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+108G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748341 | ||||||
chr1:227748376
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+143T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748376 | ||||||
chr1:227748454
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+221C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748454 | ||||||
chr1:227748458
|
G | A | 3 | a0003c0003t0001g0093a0003c0003t0001g0094a0003c0003t0001g0128 | 3 | HG02040.hp2 HG02056.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.497+225G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748458 | ||||||
chr1:227748658
|
C | T | 1 | a0002c0002t0001g0313 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.497+425C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748658 | ||||||
chr1:227748759
|
T | C | 80 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075others(77): Show | 93 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.497+526T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748759 | ||||||
chr1:227748826
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(131): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.497+593G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227748826 | ||||||
chr1:227749226
|
GGT | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01361.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.497+1001_497+1002d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227749226 | |||||
chr1:227749283
|
C | T | 9 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+1050C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749283 | ||||||
chr1:227749544
|
C | A | 1 | a0005c0005t0001g0352 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.497+1311C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749544 | ||||||
chr1:227749644
|
G | T | 1 | a0003c0003t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497+1411G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749644 | ||||||
chr1:227749687
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.497+1454G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749687 | ||||||
chr1:227749750
|
CTGTGTGT others(62): Show |
C | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.497+1528_497+1596d others(71): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227749750 | |||||
chr1:227749830
|
A | G | 4 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+1597A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749830 | ||||||
chr1:227749905
|
A | G | 6 | a0001c0001t0001g0162a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.497+1672A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749905 | ||||||
chr1:227749931
|
G | A | 8 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(5): Show | 8 | HG01884.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.497+1698G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749931 | ||||||
chr1:227749979
|
A | G | 1 | a0002c0002t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497+1746A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227749979 | ||||||
chr1:227750004
|
T | A | 1 | a0003c0003t0001g0095 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.497+1771T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750004 | ||||||
chr1:227750112
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.497+1879T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750112 | ||||||
chr1:227750141
|
A | T | 10 | a0003c0003t0001g0351a0005c0005t0001g0345a0005c0005t0001g0346others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.497+1908A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750141 | ||||||
chr1:227750272
|
C | T | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+2039C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750272 | ||||||
chr1:227750288
|
G | A | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497+2055G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750288 | ||||||
chr1:227750581
|
C | T | 1 | a0003c0003t0001g0135 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.497+2348C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750581 | ||||||
chr1:227750621
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.497+2388C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750621 | ||||||
chr1:227750713
|
C | T | 8 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(5): Show | 9 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+2480C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750713 | ||||||
chr1:227750714
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(131): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.497+2481G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750714 | ||||||
chr1:227750819
|
G | T | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+2586G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750819 | ||||||
chr1:227750849
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+2616G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750849 | ||||||
chr1:227750872
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.497+2639A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750872 | ||||||
chr1:227750888
|
G | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(268): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.497+2655G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750888 | ||||||
chr1:227750941
|
C | T | 1 | a0002c0002t0001g0064 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.497+2708C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750941 | ||||||
chr1:227750942
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.497+2709G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227750942 | ||||||
chr1:227751079
|
A | G | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.497+2846A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751079 | ||||||
chr1:227751130
|
T | G | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.497+2897T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751130 | ||||||
chr1:227751148
|
T | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0280a0001c0001t0001g0343 | 3 | HG02615.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.497+2915T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751148 | ||||||
chr1:227751276
|
A | T | 27 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(24): Show | 34 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.497+3043A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751276 | ||||||
chr1:227751297
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.497+3064G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751297 | ||||||
chr1:227751351
|
C | T | 1 | a0002c0002t0001g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.497+3118C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751351 | ||||||
chr1:227751383
|
C | G | 4 | a0002c0002t0003g0009a0002c0002t0003g0041a0002c0002t0003g0044others(1): Show | 5 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+3150C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751383 | ||||||
chr1:227751384
|
C | A | 2 | a0002c0002t0001g0156a0002c0002t0001g0255 | 2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.497+3151C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751384 | ||||||
chr1:227751478
|
C | T | 2 | a0003c0006t0001g0134a0003c0006t0001g0142 | 2 | NA18999.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.497+3245C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751478 | ||||||
chr1:227751627
|
C | G | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.497+3394C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751627 | ||||||
chr1:227751704
|
A | G | 1 | a0005c0005t0001g0348 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.497+3471A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751704 | ||||||
chr1:227751744
|
G | GT | 28 | a0002c0002t0001g0015a0002c0002t0001g0021a0002c0002t0001g0069others(25): Show | 30 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.497+3548dupT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
G | GTT | 27 | a0002c0002t0001g0026a0002c0002t0001g0072a0002c0002t0001g0076others(24): Show | 28 | HG01106.hp1 HG01346.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.497+3547_497+3548d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
G | GTTT | 17 | a0002c0002t0001g0084a0002c0002t0001g0172a0002c0002t0001g0191others(14): Show | 17 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.497+3546_497+3548d others(5): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
G | GTTTTTTT others(7): Show |
1 | a0002c0002t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.497+3535_497+3548d others(16): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTT | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0208others(5): Show | 10 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.497+3546_497+3548d others(5): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTT | G | 17 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0207others(14): Show | 17 | HG00621.hp2 HG01106.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.497+3545_497+3548d others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTT | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0028others(46): Show | 52 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.497+3544_497+3548d others(7): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTT | G | 27 | a0001c0001t0001g0306a0001c0001t0001g0321a0002c0002t0001g0045others(24): Show | 29 | HG01261.hp1 HG01433.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.497+3543_497+3548d others(8): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT | G | 61 | a0001c0001t0001g0320a0002c0002t0001g0040a0002c0002t0001g0042others(58): Show | 71 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.497+3542_497+3548d others(9): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT others(4): Show |
G | 8 | a0002c0002t0001g0064a0002c0002t0002g0078a0004c0004t0001g0010others(5): Show | 9 | HG00639.hp2 HG00741.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.497+3538_497+3548d others(13): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT others(5): Show |
G | 20 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0168others(17): Show | 26 | HG00140.hp1 HG00642.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.497+3537_497+3548d others(14): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT others(6): Show |
G | 1 | a0004c0004t0001g0047 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.497+3536_497+3548d others(15): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT others(8): Show |
G | 12 | a0001c0001t0001g0153a0001c0001t0001g0237a0001c0001t0001g0279others(9): Show | 12 | HG00733.hp1 HG00735.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.497+3534_497+3548d others(17): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT others(9): Show |
G | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(47): Show | 59 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.497+3533_497+3548d others(18): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751744
|
GTTTTTTT others(12): Show |
G | 4 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075others(1): Show | 6 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.497+3530_497+3548d others(21): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227751744 | |||||
chr1:227751763
|
T | G | 1 | a0002c0002t0001g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497+3530T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751763 | ||||||
chr1:227751764
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+3531T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751764 | ||||||
chr1:227751764
|
T | G | 3 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.497+3531T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751764 | ||||||
chr1:227751823
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.497+3590G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751823 | ||||||
chr1:227751924
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+3691T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227751924 | ||||||
chr1:227752054
|
C | T | 1 | a0002c0002t0001g0081 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.497+3821C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752054 | ||||||
chr1:227752118
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.497+3885G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752118 | ||||||
chr1:227752158
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.497+3925G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752158 | ||||||
chr1:227752350
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.497+4117G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752350 | ||||||
chr1:227752415
|
C | T | 16 | a0002c0002t0001g0015a0002c0002t0001g0032a0002c0002t0001g0080others(13): Show | 17 | HG00438.hp1 HG01074.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.497+4182C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752415 | ||||||
chr1:227752418
|
G | A | 76 | a0003c0003t0001g0004a0003c0003t0001g0005a0003c0003t0001g0006others(73): Show | 87 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.497+4185G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752418 | ||||||
chr1:227752426
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.497+4193C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752426 | ||||||
chr1:227752636
|
C | T | 2 | a0002c0002t0001g0080a0002c0002t0001g0081 | 2 | NA18975.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.497+4403C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752636 | ||||||
chr1:227752752
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.497+4519T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227752752 | ||||||
chr1:227752831
|
CAG | C | 24 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0011others(21): Show | 31 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.497+4601_497+4602d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227752831 | |||||
chr1:227753037
|
C | T | 67 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(64): Show | 72 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.497+4804C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753037 | ||||||
chr1:227753119
|
G | C | 1 | a0002c0002t0004g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.497+4886G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753119 | ||||||
chr1:227753200
|
G | T | 1 | a0001c0001t0001g0332 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.497+4967G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753200 | ||||||
chr1:227753315
|
A | T | 3 | a0001c0001t0001g0284a0002c0002t0004g0148a0002c0002t0004g0150 | 3 | HG02080.hp2 HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.497+5082A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753315 | ||||||
chr1:227753350
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.497+5117T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753350 | ||||||
chr1:227753632
|
A | G | 1 | a0003c0003t0001g0351 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498-5363A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753632 | ||||||
chr1:227753968
|
C | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.498-5027C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227753968 | ||||||
chr1:227754021
|
G | C | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-4974G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754021 | ||||||
chr1:227754101
|
A | T | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.498-4894A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754101 | ||||||
chr1:227754232
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.498-4763G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754232 | ||||||
chr1:227754407
|
A | G | 5 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0071others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.498-4588A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754407 | ||||||
chr1:227754453
|
G | A | 1 | a0001c0013t0001g0322 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.498-4542G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754453 | ||||||
chr1:227754487
|
C | T | 1 | a0002c0002t0001g0304 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.498-4508C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754487 | ||||||
chr1:227754676
|
C | T | 2 | a0002c0002t0001g0187a0002c0002t0001g0300 | 2 | HG01981.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.498-4319C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227754676 | ||||||
chr1:227755113
|
A | G | 4 | a0003c0003t0001g0109a0003c0003t0001g0110a0003c0003t0001g0114others(1): Show | 4 | NA19012.hp2 NA19066.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-3882A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755113 | ||||||
chr1:227755116
|
T | C | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.498-3879T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755116 | ||||||
chr1:227755141
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(261): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.498-3854T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755141 | ||||||
chr1:227755227
|
AG | A | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.498-3766delG | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227755227 | |||||
chr1:227755264
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.498-3731C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755264 | ||||||
chr1:227755266
|
C | T | 9 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-3729C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755266 | ||||||
chr1:227755282
|
C | T | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-3713C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755282 | ||||||
chr1:227755287
|
T | G | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.498-3708T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755287 | ||||||
chr1:227755374
|
GTTTTCTT others(2): Show |
G | 8 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(5): Show | 9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-3608_498-3600d others(11): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227755374 | |||||
chr1:227755456
|
G | A | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-3539G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755456 | ||||||
chr1:227755532
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.498-3463G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755532 | ||||||
chr1:227755596
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.498-3399G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755596 | ||||||
chr1:227755615
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-3380G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755615 | ||||||
chr1:227755693
|
T | A | 1 | a0003c0003t0001g0096 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.498-3302T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755693 | ||||||
chr1:227755923
|
C | T | 1 | a0002c0002t0001g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.498-3072C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755923 | ||||||
chr1:227755961
|
A | G | 80 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(77): Show | 91 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.498-3034A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755961 | ||||||
chr1:227755980
|
G | A | 83 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(80): Show | 96 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.498-3015G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755980 | ||||||
chr1:227755990
|
T | C | 53 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(50): Show | 60 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.498-3005T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755990 | ||||||
chr1:227755993
|
G | A | 40 | a0003c0003t0001g0004a0003c0003t0001g0006a0003c0003t0001g0016others(37): Show | 47 | HG00438.hp2 HG00609.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.498-3002G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227755993 | ||||||
chr1:227756052
|
A | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-2943A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756052 | ||||||
chr1:227756077
|
A | G | 9 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-2918A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756077 | ||||||
chr1:227756096
|
C | T | 1 | a0002c0002t0001g0313 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.498-2899C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756096 | ||||||
chr1:227756097
|
G | A | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.498-2898G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756097 | ||||||
chr1:227756170
|
T | C | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-2825T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756170 | ||||||
chr1:227756258
|
G | A | 79 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075others(76): Show | 92 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.498-2737G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756258 | ||||||
chr1:227756495
|
T | C | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.498-2500T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756495 | ||||||
chr1:227756600
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-2395G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756600 | ||||||
chr1:227756694
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-2301T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756694 | ||||||
chr1:227756739
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.498-2256G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756739 | ||||||
chr1:227756933
|
C | A | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-2062C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227756933 | ||||||
chr1:227757057
|
T | TG | 35 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(32): Show | 42 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.498-1938_498-1937i others(3): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757057 | ||||||
chr1:227757096
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.498-1899C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757096 | ||||||
chr1:227757443
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.498-1552C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757443 | ||||||
chr1:227757539
|
G | A | 7 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0047others(4): Show | 10 | NA18945.hp1 NA18961.hp1 NA18973.hp2 others(7): Show |
intron_variant | MODIFIER | c.498-1456G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757539 | ||||||
chr1:227757590
|
A | G | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.498-1405A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757590 | ||||||
chr1:227757619
|
G | A | 1 | a0003c0003t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.498-1376G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757619 | ||||||
chr1:227757665
|
T | C | 80 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(77): Show | 91 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.498-1330T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757665 | ||||||
chr1:227757727
|
A | G | 1 | a0002c0002t0001g0263 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.498-1268A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757727 | ||||||
chr1:227757823
|
T | G | 9 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.498-1172T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757823 | ||||||
chr1:227757895
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0027others(5): Show | 12 | HG00597.hp1 HG00621.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.498-1100C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757895 | ||||||
chr1:227757914
|
C | T | 6 | a0002c0002t0001g0186a0002c0002t0001g0261a0002c0002t0001g0262others(3): Show | 6 | NA18953.hp1 NA18967.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-1081C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757914 | ||||||
chr1:227757943
|
A | AT | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.498-1050dupT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227757943 | |||||
chr1:227757974
|
G | A | 27 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(24): Show | 34 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.498-1021G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227757974 | ||||||
chr1:227758208
|
C | G | 1 | a0003c0003t0001g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.498-787C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758208 | ||||||
chr1:227758219
|
C | T | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.498-776C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758219 | ||||||
chr1:227758248
|
A | T | 4 | a0001c0001t0001g0235a0001c0001t0001g0294a0001c0001t0001g0295others(1): Show | 4 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-747A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758248 | ||||||
chr1:227758249
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.498-746C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758249 | ||||||
chr1:227758279
|
C | T | 2 | a0001c0001t0002g0340a0001c0001t0002g0342 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.498-716C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758279 | ||||||
chr1:227758298
|
C | T | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.498-697C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758298 | ||||||
chr1:227758359
|
C | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.498-636C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758359 | ||||||
chr1:227758512
|
AG | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(50): Show | 62 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.498-482delG | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758512 | ||||||
chr1:227758574
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0328 | 2 | HG01258.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.498-421G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758574 | ||||||
chr1:227758591
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.498-404C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | chr1 | 227758591 | ||||||
chr1:227758800
|
G | GCC | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(269): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.498-194_498-193ins others(2): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227758800 | |||||
chr1:227758927
|
C | CA | 6 | a0001c0001t0001g0162a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-59dupA | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 227758927 | |||||
chr1:227759570
|
A | G | 6 | a0002c0002t0001g0068a0002c0002t0001g0069a0002c0002t0001g0070others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.988+85A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759570 | ||||||
chr1:227759600
|
C | T | 1 | a0003c0003t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.988+115C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759600 | ||||||
chr1:227759670
|
A | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.988+185A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759670 | ||||||
chr1:227759732
|
C | T | 2 | a0003c0003t0001g0086a0003c0003t0001g0111 | 2 | NA19002.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.988+247C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759732 | ||||||
chr1:227759733
|
G | A | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.988+248G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759733 | ||||||
chr1:227759852
|
A | G | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+367A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759852 | ||||||
chr1:227759915
|
G | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.988+430G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759915 | ||||||
chr1:227759985
|
G | A | 9 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(6): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.988+500G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759985 | ||||||
chr1:227759993
|
C | G | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.988+508C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227759993 | ||||||
chr1:227760126
|
A | T | 1 | a0006c0007t0001g0059 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.988+641A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760126 | ||||||
chr1:227760213
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.988+728C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760213 | ||||||
chr1:227760248
|
C | G | 1 | a0001c0001t0002g0339 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.988+763C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760248 | ||||||
chr1:227760368
|
A | C | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.988+883A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760368 | ||||||
chr1:227760376
|
A | C | 1 | a0002c0002t0001g0202 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.988+891A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760376 | ||||||
chr1:227760454
|
G | A | 9 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.988+969G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760454 | ||||||
chr1:227760548
|
G | A | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.988+1063G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760548 | ||||||
chr1:227760634
|
A | G | 1 | a0003c0003t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.988+1149A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227760634 | ||||||
chr1:227761092
|
C | T | 10 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(7): Show | 10 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.988+1607C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761092 | ||||||
chr1:227761183
|
G | A | 2 | a0003c0003t0001g0092a0003c0003t0001g0127 | 2 | NA18962.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.988+1698G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761183 | ||||||
chr1:227761285
|
G | A | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.988+1800G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761285 | ||||||
chr1:227761319
|
A | G | 9 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.988+1834A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761319 | ||||||
chr1:227761382
|
G | A | 1 | a0002c0002t0001g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.988+1897G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761382 | ||||||
chr1:227761491
|
T | C | 9 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.988+2006T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761491 | ||||||
chr1:227761518
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.988+2033A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761518 | ||||||
chr1:227761573
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.988+2088T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761573 | ||||||
chr1:227761641
|
G | A | 1 | a0003c0003t0001g0017 | 2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.988+2156G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761641 | ||||||
chr1:227761713
|
G | T | 83 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(80): Show | 96 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.988+2228G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761713 | ||||||
chr1:227761749
|
G | C | 33 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(30): Show | 40 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.988+2264G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761749 | ||||||
chr1:227761754
|
A | T | 1 | a0001c0001t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.988+2269A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761754 | ||||||
chr1:227761911
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(259): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.988+2426C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227761911 | ||||||
chr1:227762253
|
C | G | 2 | a0003c0003t0001g0123a0003c0003t0001g0140 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.988+2768C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762253 | ||||||
chr1:227762372
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0331 | 3 | NA18954.hp2 NA18963.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.988+2887G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762372 | ||||||
chr1:227762387
|
A | C | 3 | a0003c0003t0001g0096a0003c0003t0001g0104a0003c0003t0001g0117 | 3 | HG01934.hp2 HG02083.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.988+2902A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762387 | ||||||
chr1:227762410
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(259): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.988+2925T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762410 | ||||||
chr1:227762457
|
A | G | 34 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(31): Show | 41 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.988+2972A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762457 | ||||||
chr1:227762576
|
C | T | 1 | a0002c0002t0003g0041 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.988+3091C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762576 | ||||||
chr1:227762614
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.988+3129C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762614 | ||||||
chr1:227762641
|
G | C | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.988+3156G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762641 | ||||||
chr1:227762651
|
C | T | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+3166C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762651 | ||||||
chr1:227762726
|
G | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.988+3241G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762726 | ||||||
chr1:227762861
|
C | T | 1 | a0003c0003t0001g0107 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.988+3376C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227762861 | ||||||
chr1:227763873
|
G | A | 1 | a0002c0002t0001g0191 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.989-3086G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227763873 | ||||||
chr1:227763882
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0152a0001c0001t0001g0153 | 4 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3077C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227763882 | ||||||
chr1:227764238
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.989-2721C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764238 | ||||||
chr1:227764328
|
G | A | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.989-2631G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764328 | ||||||
chr1:227764373
|
T | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.989-2586T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764373 | ||||||
chr1:227764393
|
C | G | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.989-2566C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764393 | ||||||
chr1:227764425
|
T | C | 1 | a0002c0002t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.989-2534T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764425 | ||||||
chr1:227764548
|
A | G | 1 | a0002c0002t0001g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.989-2411A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764548 | ||||||
chr1:227764605
|
TA | T | 45 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(42): Show | 52 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.989-2347delA | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 227764605 | |||||
chr1:227764690
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.989-2269G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764690 | ||||||
chr1:227764904
|
AAAAC | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(5): Show | 9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-2047_989-2044d others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 227764904 | |||||
chr1:227764986
|
G | C | 1 | a0002c0002t0001g0266 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.989-1973G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227764986 | ||||||
chr1:227765047
|
A | AGTT | 46 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(43): Show | 53 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.989-1905_989-1903d others(5): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 227765047 | |||||
chr1:227765057
|
T | G | 57 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028others(54): Show | 61 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.989-1902T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765057 | ||||||
chr1:227765121
|
C | T | 1 | a0002c0002t0001g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.989-1838C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765121 | ||||||
chr1:227765224
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.989-1735G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765224 | ||||||
chr1:227765295
|
G | T | 1 | a0003c0003t0001g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.989-1664G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765295 | ||||||
chr1:227765308
|
C | T | 84 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(81): Show | 97 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.989-1651C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765308 | ||||||
chr1:227765412
|
G | T | 24 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0011others(21): Show | 31 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.989-1547G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765412 | ||||||
chr1:227765546
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.989-1413G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765546 | ||||||
chr1:227765580
|
G | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.989-1379G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765580 | ||||||
chr1:227765686
|
A | G | 68 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(65): Show | 73 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.989-1273A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765686 | ||||||
chr1:227765839
|
C | G | 34 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(31): Show | 41 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.989-1120C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765839 | ||||||
chr1:227765889
|
T | G | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.989-1070T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765889 | ||||||
chr1:227765996
|
G | A | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-963G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227765996 | ||||||
chr1:227766066
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0275 | 2 | HG00558.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.989-893G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766066 | ||||||
chr1:227766114
|
G | A | 9 | a0005c0005t0001g0345a0005c0005t0001g0346a0005c0005t0001g0347others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-845G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766114 | ||||||
chr1:227766254
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(267): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.989-705C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766254 | ||||||
chr1:227766319
|
G | C | 84 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(81): Show | 97 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.989-640G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766319 | ||||||
chr1:227766504
|
C | A | 1 | a0003c0003t0001g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.989-455C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766504 | ||||||
chr1:227766516
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.989-443C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766516 | ||||||
chr1:227766728
|
G | A | 6 | a0003c0003t0001g0033a0003c0003t0001g0034a0003c0003t0001g0035others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.989-231G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766728 | ||||||
chr1:227766748
|
A | G | 2 | a0002c0002t0001g0179a0002c0002t0001g0180 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.989-211A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766748 | ||||||
chr1:227766827
|
G | A | 17 | a0004c0004t0001g0002a0004c0004t0001g0010a0004c0004t0001g0011others(14): Show | 23 | HG01516.hp2 HG01517.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.989-132G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766827 | ||||||
chr1:227766868
|
C | G | 1 | a0002c0002t0001g0158 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.989-91C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 3/4 | chr1 | 227766868 | ||||||
chr1:227767335
|
C | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0249 | 2 | NA18966.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1113+252C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767335 | ||||||
chr1:227767445
|
CACATTGT others(151): Show |
C | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+363_1113+520d others(2): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767445 | ||||||
chr1:227767488
|
T | G | 3 | a0002c0002t0001g0003a0002c0002t0001g0074a0002c0002t0001g0075 | 5 | HG02258.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+405T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767488 | ||||||
chr1:227767535
|
A | G | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+452A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767535 | ||||||
chr1:227767558
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(267): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1113+475G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767558 | ||||||
chr1:227767559
|
T | A | 1 | a0001c0001t0001g0231 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1113+476T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767559 | ||||||
chr1:227767565
|
T | C | 100 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(97): Show | 119 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.1113+482T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767565 | ||||||
chr1:227767565
|
TTG | T | 5 | a0002c0002t0001g0168a0002c0002t0001g0175a0002c0002t0001g0176others(2): Show | 5 | HG00738.hp2 HG01192.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+490_1113+491d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227767565 | |||||
chr1:227767567
|
G | A | 1 | a0003c0003t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1113+484G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767567 | ||||||
chr1:227767575
|
A | G | 23 | a0001c0001t0001g0023a0001c0001t0001g0079a0001c0001t0001g0163others(20): Show | 24 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1113+492A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767575 | ||||||
chr1:227767617
|
T | C | 57 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028others(54): Show | 61 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1113+534T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767617 | ||||||
chr1:227767621
|
A | C | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+538A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767621 | ||||||
chr1:227767624
|
C | T | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+541C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767624 | ||||||
chr1:227767629
|
A | G | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+546A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767629 | ||||||
chr1:227767631
|
A | G | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+548A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767631 | ||||||
chr1:227767632
|
T | C | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+549T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767632 | ||||||
chr1:227767633
|
G | A | 1 | a0003c0003t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+550G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767633 | ||||||
chr1:227767662
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1113+579G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767662 | ||||||
chr1:227767665
|
T | G | 1 | a0003c0003t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1113+582T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767665 | ||||||
chr1:227767688
|
CTT | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(126): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1113+606_1113+607d others(4): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767688 | ||||||
chr1:227767702
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0343 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1113+619G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767702 | ||||||
chr1:227767793
|
G | A | 8 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(5): Show | 9 | HG02280.hp2 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+710G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767793 | ||||||
chr1:227767800
|
G | A | 1 | a0003c0003t0001g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1113+717G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227767800 | ||||||
chr1:227768044
|
C | T | 1 | a0003c0003t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1113+961C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768044 | ||||||
chr1:227768116
|
G | C | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1113+1033G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768116 | ||||||
chr1:227768320
|
C | T | 16 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(13): Show | 17 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+1237C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768320 | ||||||
chr1:227768376
|
G | A | 1 | a0003c0003t0001g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1113+1293G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768376 | ||||||
chr1:227768376
|
G | T | 1 | a0001c0013t0001g0322 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1113+1293G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768376 | ||||||
chr1:227768389
|
C | T | 1 | a0003c0003t0001g0351 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1113+1306C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768389 | ||||||
chr1:227768503
|
G | A | 19 | a0002c0002t0001g0344a0002c0002t0001g0354a0004c0004t0001g0002others(16): Show | 25 | HG01516.hp2 HG01517.hp1 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+1420G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768503 | ||||||
chr1:227768661
|
G | C | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+1578G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768661 | ||||||
chr1:227768826
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1113+1743C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768826 | ||||||
chr1:227768895
|
C | T | 17 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(14): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+1812C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768895 | ||||||
chr1:227768930
|
C | T | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1113+1847C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227768930 | ||||||
chr1:227769037
|
T | A | 1 | a0004c0004t0001g0011 | 2 | NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1113+1954T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227769037 | ||||||
chr1:227769225
|
C | A | 1 | a0002c0002t0001g0257 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1113+2142C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227769225 | ||||||
chr1:227769311
|
A | G | 98 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(95): Show | 115 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.1113+2228A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227769311 | ||||||
chr1:227769499
|
A | C | 17 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(14): Show | 18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+2416A>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227769499 | ||||||
chr1:227769621
|
G | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1113+2538G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227769621 | ||||||
chr1:227769890
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(127): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1113+2807C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227769890 | ||||||
chr1:227770248
|
G | A | 40 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(37): Show | 42 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1113+3165G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770248 | ||||||
chr1:227770284
|
G | A | 1 | a0003c0003t0001g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1113+3201G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770284 | ||||||
chr1:227770435
|
A | G | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+3352A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770435 | ||||||
chr1:227770514
|
A | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1113+3431A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770514 | ||||||
chr1:227770524
|
T | C | 20 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(17): Show | 21 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+3441T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770524 | ||||||
chr1:227770609
|
G | A | 4 | a0002c0002t0003g0009a0002c0002t0003g0041a0002c0002t0003g0044others(1): Show | 5 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+3526G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770609 | ||||||
chr1:227770653
|
A | G | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+3570A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770653 | ||||||
chr1:227770950
|
T | G | 101 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(98): Show | 120 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.1113+3867T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227770950 | ||||||
chr1:227771067
|
C | T | 1 | a0005c0005t0001g0353 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1113+3984C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771067 | ||||||
chr1:227771152
|
G | A | 1 | a0001c0001t0002g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1113+4069G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771152 | ||||||
chr1:227771291
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1113+4208G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771291 | ||||||
chr1:227771505
|
A | G | 148 | a0001c0001t0001g0025a0001c0001t0001g0149a0001c0001t0001g0151others(145): Show | 170 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.1113+4422A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771505 | ||||||
chr1:227771593
|
A | G | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+4510A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771593 | ||||||
chr1:227771596
|
C | T | 4 | a0001c0001t0001g0235a0001c0001t0001g0294a0001c0001t0001g0295others(1): Show | 4 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+4513C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771596 | ||||||
chr1:227771635
|
A | G | 39 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(36): Show | 43 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1113+4552A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771635 | ||||||
chr1:227771653
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1113+4570C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771653 | ||||||
chr1:227771716
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(113): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1113+4633C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771716 | ||||||
chr1:227771803
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1113+4720C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771803 | ||||||
chr1:227771811
|
C | T | 2 | a0002c0002t0001g0197a0002c0002t0001g0272 | 2 | HG02015.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1113+4728C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771811 | ||||||
chr1:227771839
|
G | A | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+4756G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771839 | ||||||
chr1:227771953
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1113+4870C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227771953 | ||||||
chr1:227772017
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1113+4934G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772017 | ||||||
chr1:227772164
|
T | A | 3 | a0002c0002t0001g0244a0002c0002t0001g0267a0002c0002t0001g0325 | 3 | HG02145.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1113+5081T>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772164 | ||||||
chr1:227772167
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1113+5084C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772167 | ||||||
chr1:227772176
|
G | A | 3 | a0001c0001t0001g0328a0002c0002t0001g0344a0002c0002t0001g0354 | 3 | HG02055.hp1 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+5093G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772176 | ||||||
chr1:227772208
|
T | C | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1113+5125T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772208 | ||||||
chr1:227772276
|
A | G | 1 | a0002c0002t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+5193A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772276 | ||||||
chr1:227772285
|
A | G | 5 | a0001c0001t0001g0234a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | NA18942.hp2 NA18975.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+5202A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772285 | ||||||
chr1:227772321
|
C | T | 1 | a0003c0003t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1113+5238C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772321 | ||||||
chr1:227772349
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1113+5266G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772349 | ||||||
chr1:227772435
|
C | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0149a0001c0001t0001g0151others(37): Show | 42 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1113+5352C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772435 | ||||||
chr1:227772459
|
G | A | 3 | a0002c0002t0004g0148a0002c0002t0004g0150a0003c0003t0001g0108 | 3 | HG03704.hp2 HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1113+5376G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772459 | ||||||
chr1:227772551
|
C | T | 13 | a0001c0001t0001g0226a0003c0003t0001g0004a0003c0003t0001g0006others(10): Show | 17 | HG00438.hp2 HG00609.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+5468C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772551 | ||||||
chr1:227772641
|
C | T | 2 | a0002c0002t0001g0020a0002c0002t0001g0198 | 3 | HG01167.hp2 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1113+5558C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772641 | ||||||
chr1:227772642
|
C | T | 3 | a0001c0001t0001g0079a0003c0003t0001g0102a0003c0003t0001g0125 | 3 | HG00609.hp2 HG02129.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1113+5559C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772642 | ||||||
chr1:227772860
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG01099.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1113+5777C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772860 | ||||||
chr1:227772953
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(269): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1113+5870A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227772953 | ||||||
chr1:227773047
|
G | A | 1 | a0002c0002t0001g0175 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1113+5964G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773047 | ||||||
chr1:227773075
|
C | T | 83 | a0001c0001t0001g0282a0002c0002t0001g0187a0003c0003t0001g0004others(80): Show | 99 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1113+5992C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773075 | ||||||
chr1:227773127
|
A | AT | 87 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(84): Show | 101 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1113+6068dupT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227773127 | |||||
chr1:227773127
|
A | ATT | 21 | a0001c0001t0001g0077a0001c0001t0001g0166a0001c0001t0001g0167others(18): Show | 21 | HG01175.hp2 HG01358.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+6067_1113+606 others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227773127 | |||||
chr1:227773127
|
AT | A | 13 | a0001c0001t0001g0214a0001c0001t0001g0280a0002c0002t0001g0040others(10): Show | 13 | HG02572.hp1 HG02615.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113+6068delT | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227773127 | |||||
chr1:227773127
|
ATT | A | 21 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(18): Show | 23 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+6067_1113+606 others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227773127 | |||||
chr1:227773127
|
ATTTTTTT | A | 8 | a0002c0002t0001g0068a0003c0003t0001g0004a0003c0003t0001g0006others(5): Show | 12 | HG01081.hp2 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+6062_1113+606 others(11): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227773127 | |||||
chr1:227773154
|
A | G | 1 | a0003c0003t0001g0137 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1113+6071A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773154 | ||||||
chr1:227773420
|
G | A | 15 | a0002c0002t0001g0015a0002c0002t0001g0032a0002c0002t0001g0080others(12): Show | 16 | HG00438.hp1 HG01074.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1113+6337G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773420 | ||||||
chr1:227773528
|
C | A | 17 | a0002c0002t0001g0003a0002c0002t0001g0068a0002c0002t0001g0069others(14): Show | 20 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+6445C>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773528 | ||||||
chr1:227773680
|
G | A | 1 | a0007c0010t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1113+6597G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773680 | ||||||
chr1:227773702
|
C | T | 57 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028others(54): Show | 61 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1113+6619C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773702 | ||||||
chr1:227773703
|
G | A | 1 | a0003c0003t0001g0096 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1113+6620G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773703 | ||||||
chr1:227773724
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1113+6641C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773724 | ||||||
chr1:227773803
|
C | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1113+6720C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773803 | ||||||
chr1:227773845
|
C | T | 9 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0336others(6): Show | 9 | HG01261.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-6682C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773845 | ||||||
chr1:227773914
|
A | G | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1114-6613A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227773914 | ||||||
chr1:227774095
|
C | T | 1 | a0003c0003t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1114-6432C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774095 | ||||||
chr1:227774145
|
G | A | 6 | a0001c0001t0002g0334a0001c0001t0002g0335a0001c0001t0002g0339others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-6382G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774145 | ||||||
chr1:227774184
|
G | C | 8 | a0002c0002t0001g0003a0002c0002t0001g0069a0002c0002t0001g0070others(5): Show | 10 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-6343G>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774184 | ||||||
chr1:227774278
|
G | A | 81 | a0003c0003t0001g0004a0003c0003t0001g0005a0003c0003t0001g0006others(78): Show | 97 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.1114-6249G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774278 | ||||||
chr1:227774323
|
G | A | 1 | a0004c0004t0001g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1114-6204G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774323 | ||||||
chr1:227774417
|
A | ACCCACCG others(11): Show |
1 | a0002c0002t0001g0080 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1114-6108_1114-609 others(22): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227774417 | |||||
chr1:227774422
|
C | T | 5 | a0001c0001t0001g0214a0001c0001t0001g0280a0001c0001t0001g0343others(2): Show | 5 | HG02615.hp2 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-6105C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774422 | ||||||
chr1:227774586
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1114-5941C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774586 | ||||||
chr1:227774843
|
C | G | 1 | a0002c0002t0001g0200 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1114-5684C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774843 | ||||||
chr1:227774931
|
C | T | 7 | a0006c0007t0001g0014a0006c0007t0001g0053a0006c0007t0001g0055others(4): Show | 8 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-5596C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774931 | ||||||
chr1:227774977
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1114-5550C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774977 | ||||||
chr1:227774988
|
C | T | 3 | a0002c0002t0001g0196a0002c0002t0001g0266a0002c0002t0001g0270 | 3 | HG00280.hp2 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1114-5539C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227774988 | ||||||
chr1:227775090
|
C | T | 3 | a0002c0002t0001g0196a0002c0002t0001g0266a0002c0002t0001g0270 | 3 | HG00280.hp2 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1114-5437C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775090 | ||||||
chr1:227775116
|
C | T | 2 | a0003c0003t0001g0100a0003c0003t0001g0136 | 2 | NA19058.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1114-5411C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775116 | ||||||
chr1:227775187
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1114-5340G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775187 | ||||||
chr1:227775377
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(113): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1114-5150C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775377 | ||||||
chr1:227775423
|
G | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(113): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1114-5104G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775423 | ||||||
chr1:227775435
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1114-5092C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775435 | ||||||
chr1:227775452
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(130): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1114-5075C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775452 | ||||||
chr1:227775463
|
C | T | 92 | a0001c0001t0001g0167a0001c0001t0001g0248a0001c0001t0001g0287others(89): Show | 109 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.1114-5064C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775463 | ||||||
chr1:227775520
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1114-5007C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775520 | ||||||
chr1:227775705
|
G | A | 2 | a0003c0003t0001g0099a0003c0003t0001g0119 | 2 | NA18973.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1114-4822G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775705 | ||||||
chr1:227775790
|
G | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(44): Show | 56 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1114-4737G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775790 | ||||||
chr1:227775893
|
G | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0152a0001c0001t0001g0153 | 4 | HG01071.hp1 HG01175.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-4634G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775893 | ||||||
chr1:227775956
|
C | T | 1 | a0006c0007t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1114-4571C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227775956 | ||||||
chr1:227776252
|
C | T | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1114-4275C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776252 | ||||||
chr1:227776383
|
G | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0279 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1114-4144G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776383 | ||||||
chr1:227776449
|
G | T | 1 | a0002c0002t0001g0194 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1114-4078G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776449 | ||||||
chr1:227776465
|
G | A | 5 | a0001c0001t0001g0214a0001c0001t0001g0280a0001c0001t0001g0343others(2): Show | 5 | HG02615.hp2 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-4062G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776465 | ||||||
chr1:227776504
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01361.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1114-4023C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776504 | ||||||
chr1:227776558
|
C | T | 1 | a0003c0003t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1114-3969C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776558 | ||||||
chr1:227776641
|
GCACACGA others(13): Show |
G | 1 | a0003c0003t0001g0130 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1114-3884_1114-386 others(24): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227776641 | |||||
chr1:227776646
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(14): Show | 18 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1114-3881C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776646 | ||||||
chr1:227776698
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(264): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1114-3829T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776698 | ||||||
chr1:227776841
|
A | G | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1114-3686A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776841 | ||||||
chr1:227776880
|
C | T | 1 | a0006c0007t0001g0055 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1114-3647C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776880 | ||||||
chr1:227776963
|
T | C | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1114-3564T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227776963 | ||||||
chr1:227777109
|
T | TAA | 136 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(133): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1114-3409_1114-340 others(6): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227777109 | |||||
chr1:227777109
|
TA | T | 91 | a0001c0001t0001g0167a0001c0001t0001g0287a0002c0002t0001g0258others(88): Show | 108 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1114-3408delA | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227777109 | |||||
chr1:227777225
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1114-3302C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777225 | ||||||
chr1:227777226
|
A | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1114-3301A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777226 | ||||||
chr1:227777266
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0294 | 2 | HG00735.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1114-3261C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777266 | ||||||
chr1:227777289
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(269): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1114-3238A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777289 | ||||||
chr1:227777305
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1114-3222G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777305 | ||||||
chr1:227777315
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(137): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1114-3212C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777315 | ||||||
chr1:227777319
|
C | G | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1114-3208C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777319 | ||||||
chr1:227777328
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(14): Show | 18 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1114-3199C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777328 | ||||||
chr1:227777440
|
C | T | 25 | a0001c0001t0001g0167a0001c0001t0001g0248a0001c0001t0001g0287others(22): Show | 29 | HG00642.hp1 HG02074.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.1114-3087C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777440 | ||||||
chr1:227777454
|
C | T | 13 | a0002c0002t0001g0021a0002c0002t0001g0026a0002c0002t0001g0158others(10): Show | 15 | HG00609.hp1 HG01346.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114-3073C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777454 | ||||||
chr1:227777456
|
C | T | 10 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(7): Show | 10 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1114-3071C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777456 | ||||||
chr1:227777575
|
T | G | 1 | a0003c0003t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1114-2952T>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777575 | ||||||
chr1:227777633
|
A | G | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-2894A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777633 | ||||||
chr1:227777664
|
C | T | 2 | a0003c0003t0001g0105a0003c0003t0001g0112 | 2 | HG03490.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1114-2863C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777664 | ||||||
chr1:227777692
|
G | A | 92 | a0001c0001t0001g0167a0001c0001t0001g0248a0001c0001t0001g0287others(89): Show | 109 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.1114-2835G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777692 | ||||||
chr1:227777726
|
A | G | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-2801A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777726 | ||||||
chr1:227777730
|
A | G | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1114-2797A>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777730 | ||||||
chr1:227777755
|
C | G | 127 | a0001c0001t0001g0025a0001c0001t0001g0167a0001c0001t0001g0169others(124): Show | 146 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1114-2772C>G | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227777755 | ||||||
chr1:227778212
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0305 | 2 | HG00621.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1114-2315C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227778212 | ||||||
chr1:227778627
|
C | T | 1 | a0003c0003t0001g0106 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1114-1900C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227778627 | ||||||
chr1:227778743
|
G | A | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-1784G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227778743 | ||||||
chr1:227778778
|
G | A | 2 | a0002c0002t0004g0148a0002c0002t0004g0150 | 2 | HG03834.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1114-1749G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227778778 | ||||||
chr1:227778880
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(142): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1114-1647T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227778880 | ||||||
chr1:227779091
|
TGGCAGCC others(13): Show |
T | 15 | a0001c0001t0001g0022a0001c0001t0001g0203a0001c0001t0001g0204others(12): Show | 16 | HG00558.hp2 HG00621.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1114-1435_1114-141 others(24): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779091 | ||||||
chr1:227779118
|
C | T | 4 | a0002c0002t0003g0009a0002c0002t0003g0041a0002c0002t0003g0044others(1): Show | 5 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-1409C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779118 | ||||||
chr1:227779150
|
C | T | 3 | a0002c0002t0001g0161a0002c0002t0001g0179a0002c0002t0001g0180 | 3 | HG00323.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1114-1377C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779150 | ||||||
chr1:227779152
|
T | C | 1 | a0002c0002t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1114-1375T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779152 | ||||||
chr1:227779293
|
GCATGTGT others(2): Show |
G | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG01891.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1114-1231_1114-122 others(13): Show |
SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 227779293 | |||||
chr1:227779410
|
G | A | 1 | a0002c0002t0001g0354 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1114-1117G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779410 | ||||||
chr1:227779428
|
A | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(264): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1114-1099A>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779428 | ||||||
chr1:227779437
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1114-1090C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779437 | ||||||
chr1:227779466
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-1061C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779466 | ||||||
chr1:227779495
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(142): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1114-1032T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779495 | ||||||
chr1:227779502
|
G | T | 2 | a0004c0004t0001g0062a0004c0004t0001g0063 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1114-1025G>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779502 | ||||||
chr1:227779941
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1114-586C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227779941 | ||||||
chr1:227780148
|
C | T | 4 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0001g0043others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-379C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780148 | ||||||
chr1:227780236
|
C | T | 2 | a0002c0002t0001g0344a0002c0002t0001g0354 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-291C>T | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780236 | ||||||
chr1:227780237
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(141): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1114-290G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780237 | ||||||
chr1:227780262
|
T | C | 3 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG01109.hp2 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1114-265T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780262 | ||||||
chr1:227780290
|
G | A | 18 | a0003c0003t0001g0131a0004c0004t0001g0002a0004c0004t0001g0010others(15): Show | 24 | HG01516.hp2 HG01517.hp1 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.1114-237G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780290 | ||||||
chr1:227780332
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(269): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1114-195T>C | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780332 | ||||||
chr1:227780406
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(140): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1114-121G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780406 | ||||||
chr1:227780446
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0246others(5): Show | 9 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-81G>A | SNAP47 | ENSG00000143740.15 | transcript | ENST00000617596.5 | protein_coding | 4/4 | chr1 | 227780446 |