geneid | 27075 |
---|---|
ensemblid | ENSG00000106537.8 |
hgncid | 21643 |
symbol | TSPAN13 |
name | tetraspanin 13 |
refseq_nuc | NM_014399.4 |
refseq_prot | NP_055214.1 |
ensembl_nuc | ENST00000262067.5 |
ensembl_prot | ENSP00000262067.4 |
mane_status | MANE Select |
chr | chr7 |
start | 16753755 |
end | 16784536 |
strand | + |
ver | v1.2 |
region | chr7:16753755-16784536 |
region5000 | chr7:16748755-16789536 |
regionname0 | TSPAN13_chr7_16753755_16784536 |
regionname5000 | TSPAN13_chr7_16748755_16789536 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 204 | 439 | 96 | 82 | 197 | 14 | 48 | 149 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0002 | 0/0 | 204 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 615 | 203 | 32 | 28 | 120 | 5 | 17 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
c0002 | 0/1 | 615 | 118 | 21 | 31 | 41 | 2 | 22 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
c0003 | 0/0 | 615 | 60 | 29 | 9 | 19 | 3 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
c0004 | 0/0 | 615 | 58 | 14 | 14 | 17 | 4 | 9 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
c0005 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1260 | 202 | 15 | 44 | 106 | 5 | 31 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0002 | 0/0 | 1257 | 73 | 15 | 19 | 26 | 5 | 8 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0003 | 0/0 | 1259 | 39 | 7 | 1 | 29 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0004 | 1/0 | 1259 | 38 | 12 | 4 | 18 | 1 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0005 | 0/0 | 1260 | 18 | 5 | 3 | 6 | 0 | 4 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0006 | 0/0 | 1256 | 16 | 9 | 0 | 7 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0007 | 0/0 | 1260 | 9 | 4 | 3 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0008 | 0/0 | 1257 | 7 | 7 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0009 | 0/0 | 1260 | 6 | 5 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0010 | 0/0 | 1257 | 5 | 4 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0011 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0012 | 0/0 | 1256 | 3 | 1 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0013 | 0/0 | 1259 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0014 | 0/0 | 1260 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0015 | 0/0 | 1257 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0016 | 0/0 | 1259 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0017 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0018 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0019 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0020 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0021 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0022 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0023 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0024 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0025 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0026 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0027 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0028 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
t0029 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 2 | 3 | 5 | 1 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0002 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0004 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0006 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0009 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0016 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0045 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 615 | 203 | 32 | 28 | 120 | 5 | 17 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002 | 0/1 | 615 | 118 | 21 | 31 | 41 | 2 | 22 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003 | 0/0 | 615 | 60 | 29 | 9 | 19 | 3 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004 | 0/0 | 615 | 58 | 14 | 14 | 17 | 4 | 9 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0002c0005 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1874 | 108 | 5 | 16 | 71 | 4 | 12 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0002 | 0/0 | 1871 | 4 | 2 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0003 | 0/0 | 1873 | 39 | 7 | 1 | 29 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0004 | 1/0 | 1873 | 35 | 9 | 4 | 18 | 1 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0006 | 0/0 | 1870 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0007 | 0/0 | 1874 | 7 | 2 | 3 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0014 | 0/0 | 1874 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0016 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0019 | 0/0 | 1874 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0020 | 0/0 | 1874 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0001t0026 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0001 | 0/1 | 1874 | 85 | 7 | 25 | 33 | 1 | 18 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0002 | 0/0 | 1871 | 4 | 1 | 2 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0005 | 0/0 | 1874 | 15 | 4 | 1 | 6 | 0 | 4 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0008 | 0/0 | 1871 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0009 | 0/0 | 1874 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0010 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0013 | 0/0 | 1873 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0021 | 0/0 | 1874 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0002t0028 | 0/0 | 1871 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0001 | 0/0 | 1874 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0002 | 0/0 | 1871 | 22 | 6 | 5 | 10 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0004 | 0/0 | 1873 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0005 | 0/0 | 1874 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0006 | 0/0 | 1870 | 11 | 4 | 0 | 7 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0007 | 0/0 | 1874 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0010 | 0/0 | 1871 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0011 | 0/0 | 1874 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0012 | 0/0 | 1870 | 3 | 1 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0014 | 0/0 | 1874 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0015 | 0/0 | 1871 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0017 | 0/0 | 1874 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0018 | 0/0 | 1874 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0022 | 0/0 | 1871 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0024 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0025 | 0/0 | 1871 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0027 | 0/0 | 1871 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0003t0029 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0001 | 0/0 | 1874 | 6 | 2 | 2 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0002 | 0/0 | 1871 | 43 | 6 | 10 | 15 | 4 | 8 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0005 | 0/0 | 1874 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0008 | 0/0 | 1871 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0009 | 0/0 | 1874 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0010 | 0/0 | 1871 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0001c0004t0023 | 0/0 | 1871 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
a0002c0005t0001 | 0/0 | 1874 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | copy fasta | chr7 | 16748755 | 16789536 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0004g0313 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0007g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0016g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0020g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0001t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0002 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0009 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0016 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0009g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0009g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0013g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0021g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0002t0028g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0010g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0011g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0012g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0015g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0015g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0022g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0024g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0025g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0027g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0003t0029g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0001 | 0/0 | 11 | 2 | 3 | 4 | 1 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0010g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0010g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0001c0004t0023g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
a0002c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0002 | g0027 | EUR | GBR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00099 | hp2 | a0001 | c0004 | t0002 | g0330 | EUR | GBR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0230 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00280 | hp2 | a0001 | c0002 | t0021 | g0275 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00323 | hp2 | a0001 | c0004 | t0002 | g0027 | EUR | FIN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00408 | hp2 | a0001 | c0003 | t0006 | g0095 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00438 | hp2 | a0001 | c0004 | t0002 | g0109 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00544 | hp1 | a0001 | c0003 | t0006 | g0093 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00558 | hp2 | a0001 | c0004 | t0002 | g0097 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00639 | hp1 | a0001 | c0002 | t0009 | g0138 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00639 | hp2 | a0001 | c0003 | t0015 | g0301 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00642 | hp2 | a0001 | c0004 | t0002 | g0056 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00673 | hp1 | a0001 | c0004 | t0002 | g0102 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | CHS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00733 | hp1 | a0001 | c0004 | t0010 | g0323 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01070 | hp1 | a0001 | c0004 | t0002 | g0094 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01074 | hp2 | a0001 | c0001 | t0019 | g0136 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01109 | hp1 | a0001 | c0002 | t0005 | g0135 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01109 | hp2 | a0001 | c0004 | t0002 | g0333 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01168 | hp2 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01169 | hp1 | a0001 | c0004 | t0002 | g0001 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01169 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0108 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01243 | hp2 | a0001 | c0004 | t0005 | g0174 | AMR | PUR | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0173 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0050 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01257 | hp2 | a0001 | c0002 | t0013 | g0043 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01258 | hp1 | a0001 | c0002 | t0013 | g0043 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01258 | hp2 | a0001 | c0004 | t0001 | g0050 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01358 | hp1 | a0001 | c0004 | t0002 | g0334 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0020 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01433 | hp1 | a0001 | c0001 | t0020 | g0276 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0084 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01516 | hp1 | a0001 | c0003 | t0012 | g0025 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0195 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01517 | hp1 | a0001 | c0003 | t0012 | g0025 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0302 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01891 | hp1 | a0001 | c0004 | t0002 | g0001 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01928 | hp1 | a0001 | c0004 | t0002 | g0337 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0335 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01981 | hp1 | a0001 | c0004 | t0002 | g0026 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01993 | hp1 | a0001 | c0004 | t0002 | g0096 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02004 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02004 | hp2 | a0001 | c0003 | t0005 | g0176 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02027 | hp1 | a0001 | c0003 | t0002 | g0090 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02055 | hp1 | a0001 | c0003 | t0002 | g0303 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02055 | hp2 | a0001 | c0003 | t0011 | g0005 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02083 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02132 | hp1 | a0001 | c0004 | t0001 | g0219 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0324 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02145 | hp2 | a0001 | c0003 | t0007 | g0126 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02165 | hp1 | a0001 | c0003 | t0002 | g0098 | EAS | CDX | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02165 | hp2 | a0001 | c0002 | t0005 | g0066 | EAS | CDX | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0115 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0336 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02280 | hp1 | a0001 | c0004 | t0001 | g0116 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02280 | hp2 | a0001 | c0002 | t0008 | g0329 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02300 | hp2 | a0001 | c0003 | t0022 | g0026 | AMR | PEL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02451 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02451 | hp2 | a0001 | c0002 | t0008 | g0311 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0099 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02572 | hp2 | a0001 | c0002 | t0009 | g0051 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02630 | hp1 | a0001 | c0003 | t0010 | g0054 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02630 | hp2 | a0001 | c0003 | t0024 | g0106 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02647 | hp2 | a0001 | c0002 | t0008 | g0328 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02683 | hp2 | a0001 | c0002 | t0005 | g0024 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0216 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02717 | hp2 | a0001 | c0002 | t0009 | g0274 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02723 | hp1 | a0001 | c0004 | t0009 | g0120 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02723 | hp2 | a0001 | c0003 | t0006 | g0307 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02818 | hp1 | a0001 | c0003 | t0017 | g0177 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02818 | hp2 | a0001 | c0003 | t0004 | g0128 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02896 | hp1 | a0001 | c0004 | t0002 | g0322 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02897 | hp1 | a0001 | c0002 | t0005 | g0170 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02922 | hp1 | a0001 | c0003 | t0006 | g0022 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02922 | hp2 | a0001 | c0003 | t0011 | g0005 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02970 | hp1 | a0001 | c0003 | t0004 | g0121 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02976 | hp1 | a0001 | c0002 | t0005 | g0277 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02976 | hp2 | a0001 | c0003 | t0006 | g0022 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03041 | hp1 | a0001 | c0004 | t0005 | g0175 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03041 | hp2 | a0001 | c0004 | t0009 | g0222 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03098 | hp1 | a0001 | c0003 | t0010 | g0054 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03098 | hp2 | a0001 | c0002 | t0005 | g0256 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03130 | hp2 | a0001 | c0004 | t0008 | g0031 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03139 | hp2 | a0001 | c0001 | t0014 | g0122 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0318 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03195 | hp2 | a0001 | c0004 | t0008 | g0031 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0310 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03209 | hp2 | a0001 | c0002 | t0009 | g0051 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03225 | hp1 | a0001 | c0003 | t0014 | g0218 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03486 | hp1 | a0001 | c0002 | t0005 | g0124 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0316 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03490 | hp1 | a0001 | c0004 | t0002 | g0056 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03491 | hp1 | a0001 | c0004 | t0002 | g0030 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03492 | hp1 | a0001 | c0004 | t0002 | g0030 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03516 | hp2 | a0001 | c0003 | t0011 | g0005 | AFR | ESN | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03540 | hp1 | a0001 | c0003 | t0018 | g0268 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03540 | hp2 | a0001 | c0003 | t0029 | g0105 | AFR | GWD | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03579 | hp2 | a0001 | c0003 | t0006 | g0022 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03654 | hp1 | a0001 | c0004 | t0002 | g0083 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03669 | hp1 | a0001 | c0002 | t0005 | g0070 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03688 | hp1 | a0001 | c0002 | t0005 | g0024 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0281 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03704 | hp2 | a0001 | c0001 | t0016 | g0197 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03710 | hp1 | a0001 | c0004 | t0002 | g0332 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03831 | hp2 | a0001 | c0004 | t0002 | g0104 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03834 | hp2 | a0001 | c0002 | t0005 | g0062 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04115 | hp1 | a0001 | c0004 | t0002 | g0001 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04199 | hp2 | a0001 | c0004 | t0002 | g0085 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | STU | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0331 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18747 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18747 | hp2 | a0001 | c0004 | t0023 | g0001 | EAS | CHB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0315 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18906 | hp2 | a0001 | c0003 | t0004 | g0272 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18940 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0078 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18950 | hp2 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18952 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18953 | hp1 | a0001 | c0004 | t0002 | g0089 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18956 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18957 | hp2 | a0001 | c0003 | t0002 | g0092 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18959 | hp1 | a0001 | c0002 | t0005 | g0023 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18962 | hp1 | a0001 | c0004 | t0002 | g0032 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18966 | hp1 | a0001 | c0004 | t0002 | g0107 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18969 | hp1 | a0001 | c0003 | t0027 | g0080 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18971 | hp2 | a0001 | c0004 | t0002 | g0075 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18973 | hp1 | a0001 | c0002 | t0028 | g0082 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18975 | hp2 | a0001 | c0002 | t0005 | g0068 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0291 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18979 | hp2 | a0001 | c0003 | t0006 | g0100 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18988 | hp2 | a0001 | c0003 | t0002 | g0086 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18989 | hp2 | a0001 | c0003 | t0025 | g0113 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18990 | hp2 | a0001 | c0003 | t0006 | g0091 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18994 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19004 | hp2 | a0001 | c0002 | t0005 | g0261 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19006 | hp1 | a0001 | c0003 | t0006 | g0029 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19030 | hp1 | a0001 | c0001 | t0026 | g0110 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19043 | hp1 | a0001 | c0002 | t0008 | g0327 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19043 | hp2 | a0001 | c0004 | t0002 | g0314 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19055 | hp1 | a0001 | c0004 | t0002 | g0079 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19057 | hp2 | a0001 | c0003 | t0006 | g0029 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19058 | hp1 | a0001 | c0003 | t0002 | g0112 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19062 | hp2 | a0001 | c0004 | t0002 | g0032 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19064 | hp2 | a0001 | c0003 | t0006 | g0081 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19077 | hp1 | a0001 | c0004 | t0002 | g0077 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19078 | hp1 | a0001 | c0002 | t0005 | g0071 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19079 | hp1 | a0001 | c0004 | t0002 | g0111 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19086 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19089 | hp2 | a0002 | c0005 | t0001 | g0189 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19240 | hp1 | a0001 | c0003 | t0012 | g0309 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA19240 | hp2 | a0001 | c0003 | t0015 | g0306 | AFR | YRI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20129 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | ASW | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20129 | hp2 | a0001 | c0004 | t0010 | g0321 | AFR | ASW | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20752 | hp1 | a0001 | c0004 | t0002 | g0001 | EUR | TSI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | GIH | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | GIH | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG01123 | hp2 | a0001 | c0004 | t0002 | g0001 | AMR | CLM | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0325 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02486 | hp2 | a0001 | c0003 | t0011 | g0005 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0312 | AFR | ACB | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03471 | hp1 | a0001 | c0004 | t0002 | g0308 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG03471 | hp2 | a0001 | c0002 | t0008 | g0305 | AFR | MSL | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
HG06807 | hp2 | a0001 | c0003 | t0007 | g0127 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA18955 | hp2 | a0001 | c0002 | t0005 | g0023 | EAS | JPT | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20300 | hp1 | a0001 | c0002 | t0010 | g0319 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | USA | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
NA21309 | hp2 | a0001 | c0004 | t0002 | g0001 | AFR | LWK | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0016 | REF | REF | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0313 | REF | REF | TSPAN13_chr7_16748755_16789536 | TSPAN13 | chr7 | 16748755 | 16789536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16779091
|
T | A | 1 | a0002 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.515T>A | p.Ile172Asn | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/6 | 728/1873 | 515/615 | 172/204 | chr7 | 16779091 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16776375
|
T | C | 2 | a0001c0003a0001c0004 | 118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
synonymous_variant | LOW | c.228T>C | p.Phe76Phe | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/6 | 441/1873 | 228/615 | 76/204 | chr7 | 16776375 | ||
chr7:16783470
|
G | A | 3 | a0001c0002a0001c0004a0002c0005 | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(174): Show |
synonymous_variant | LOW | c.594G>A | p.Ala198Ala | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 807/1873 | 594/615 | 198/204 | chr7 | 16783470 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16753796
|
AGCC | A | 21 | a0001c0001t0002a0001c0001t0006a0001c0001t0026others(18): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
5_prime_UTR_variant | MODIFIER | c.-163_-161delCGC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 161 | INFO_REALIGN_3_PRIME | chr7 | 16753796 | ||||
chr7:16753801
|
C | T | 1 | a0001c0003t0029 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-167C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 167 | chr7 | 16753801 | |||||
chr7:16753846
|
C | A | 1 | a0001c0003t0022 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-122C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 122 | chr7 | 16753846 | |||||
chr7:16753874
|
G | A | 1 | a0001c0004t0023 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 94 | chr7 | 16753874 | |||||
chr7:16753879
|
A | G | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0020others(20): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-89A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 89 | chr7 | 16753879 | |||||
chr7:16753930
|
G | C | 1 | a0001c0003t0024 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/6 | 38 | chr7 | 16753930 | |||||
chr7:16783492
|
T | G | 4 | a0001c0001t0003a0001c0001t0016a0001c0003t0012others(1): Show | 44 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 1 | chr7 | 16783492 | |||||
chr7:16783544
|
A | C | 8 | a0001c0001t0003a0001c0001t0007a0001c0002t0028others(5): Show | 56 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*53A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 53 | chr7 | 16783544 | |||||
chr7:16783552
|
G | A | 1 | a0001c0003t0025 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*61G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 61 | chr7 | 16783552 | |||||
chr7:16783693
|
C | T | 1 | a0001c0001t0019 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 202 | chr7 | 16783693 | |||||
chr7:16783703
|
C | T | 10 | a0001c0001t0014a0001c0002t0005a0001c0002t0010others(7): Show | 27 | HG00280.hp2 HG00733.hp1 HG01109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*212C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 212 | chr7 | 16783703 | |||||
chr7:16783861
|
T | C | 1 | a0001c0003t0011 | 4 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*370T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 370 | chr7 | 16783861 | |||||
chr7:16783928
|
G | C | 2 | a0001c0001t0026a0001c0003t0018 | 2 | HG03540.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 437 | chr7 | 16783928 | |||||
chr7:16783982
|
T | TG | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(35): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*491_*492insG | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 492 | chr7 | 16783982 | |||||
chr7:16784251
|
T | C | 1 | a0001c0003t0027 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 760 | chr7 | 16784251 | |||||
chr7:16784288
|
G | A | 2 | a0001c0001t0014a0001c0003t0014 | 2 | HG03139.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*797G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 797 | chr7 | 16784288 | |||||
chr7:16784353
|
T | G | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(19): Show | 300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*862T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 6/6 | 862 | chr7 | 16784353 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16754043
|
A | G | 9 | a0001c0002t0002g0336a0001c0003t0002g0331a0001c0003t0002g0335others(6): Show | 10 | HG00099.hp2 HG00642.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+13A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754043 | ||||||
chr7:16754052
|
C | T | 16 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(13): Show | 16 | HG00733.hp1 HG01081.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+22C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754052 | ||||||
chr7:16754154
|
G | GC | 338 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(335): Show | 439 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(436): Show |
intron_variant | MODIFIER | c.63+124_63+125insC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754154 | ||||||
chr7:16754389
|
C | T | 16 | a0001c0001t0006g0304a0001c0001t0006g0310a0001c0001t0006g0312others(13): Show | 21 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+359C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754389 | ||||||
chr7:16754473
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0004g0057 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.63+443G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754473 | ||||||
chr7:16754509
|
G | C | 109 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0002g0088others(106): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.63+479G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754509 | ||||||
chr7:16754632
|
A | C | 79 | a0001c0001t0001g0300a0001c0001t0002g0088a0001c0001t0006g0304others(76): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.63+602A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754632 | ||||||
chr7:16754639
|
G | C | 2 | a0001c0001t0001g0033a0001c0002t0001g0114 | 3 | HG01255.hp1 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.63+609G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754639 | ||||||
chr7:16754691
|
A | T | 78 | a0001c0001t0002g0088a0001c0001t0006g0304a0001c0001t0006g0310others(75): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.63+661A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754691 | ||||||
chr7:16754860
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.63+830A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754860 | ||||||
chr7:16754895
|
C | A | 2 | a0001c0004t0001g0115a0001c0004t0001g0116 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.63+865C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754895 | ||||||
chr7:16754928
|
A | G | 1 | a0001c0002t0001g0052 | 2 | NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.63+898A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754928 | ||||||
chr7:16754957
|
G | C | 19 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(16): Show | 19 | HG00733.hp1 HG01081.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+927G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754957 | ||||||
chr7:16754972
|
A | C | 18 | a0001c0001t0001g0021a0001c0001t0001g0286a0001c0001t0001g0287others(15): Show | 22 | HG00609.hp1 HG01256.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+942A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16754972 | ||||||
chr7:16755037
|
TTCCACAG others(5828): Show |
T | 3 | a0001c0003t0002g0112a0001c0003t0025g0113a0001c0004t0002g0111 | 3 | NA18989.hp2 NA19058.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.63+1011_63+6845del | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755037 | |||||
chr7:16755045
|
G | A | 1 | a0001c0004t0002g0075 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.63+1015G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755045 | ||||||
chr7:16755115
|
A | G | 4 | a0001c0002t0002g0336a0001c0003t0002g0335a0001c0004t0002g0334others(1): Show | 4 | HG01358.hp1 HG01928.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1085A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755115 | ||||||
chr7:16755489
|
T | C | 106 | a0001c0001t0001g0058a0001c0001t0001g0117a0001c0001t0001g0118others(103): Show | 132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+1459T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755489 | ||||||
chr7:16755541
|
G | GT | 6 | a0001c0001t0001g0282a0001c0001t0001g0298a0001c0003t0002g0078others(3): Show | 6 | HG00639.hp2 NA18941.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+1528dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | |||||
chr7:16755541
|
G | GTT | 82 | a0001c0001t0001g0300a0001c0001t0002g0088a0001c0001t0002g0317others(79): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.63+1527_63+1528dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | |||||
chr7:16755541
|
G | GTTT | 7 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0326others(4): Show | 7 | HG00438.hp2 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+1526_63+1528dup others(3): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | |||||
chr7:16755541
|
GT | G | 84 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(81): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+1528delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16755541 | |||||
chr7:16755578
|
G | T | 1 | a0001c0002t0001g0281 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.63+1548G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755578 | ||||||
chr7:16755636
|
A | G | 3 | a0001c0003t0002g0078a0001c0004t0002g0032a0001c0004t0002g0107 | 4 | NA18941.hp1 NA18962.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1606A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755636 | ||||||
chr7:16755658
|
C | G | 2 | a0001c0001t0001g0280a0001c0002t0001g0195 | 2 | HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.63+1628C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755658 | ||||||
chr7:16755701
|
C | T | 8 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0014g0122others(5): Show | 8 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+1671C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755701 | ||||||
chr7:16755745
|
C | A | 99 | a0001c0001t0002g0088a0001c0001t0002g0317a0001c0001t0002g0320others(96): Show | 125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.63+1715C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755745 | ||||||
chr7:16755797
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+1767T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755797 | ||||||
chr7:16755837
|
C | T | 1 | a0001c0002t0001g0279 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.63+1807C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755837 | ||||||
chr7:16755939
|
A | G | 35 | a0001c0001t0002g0326a0001c0001t0003g0125a0001c0001t0004g0123others(32): Show | 44 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.63+1909A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755939 | ||||||
chr7:16755961
|
A | G | 33 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0194others(30): Show | 47 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+1931A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16755961 | ||||||
chr7:16756246
|
A | T | 18 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(15): Show | 20 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+2216A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756246 | ||||||
chr7:16756267
|
T | G | 1 | a0001c0001t0004g0061 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.63+2237T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756267 | ||||||
chr7:16756412
|
G | T | 7 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0001t0020g0276others(4): Show | 8 | HG00280.hp2 HG01433.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+2382G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756412 | ||||||
chr7:16756658
|
G | A | 32 | a0001c0001t0002g0326a0001c0001t0003g0125a0001c0001t0004g0123others(29): Show | 38 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.63+2628G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756658 | ||||||
chr7:16756867
|
T | C | 1 | a0001c0003t0002g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+2837T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756867 | ||||||
chr7:16756907
|
G | T | 318 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(315): Show | 416 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(413): Show |
intron_variant | MODIFIER | c.63+2877G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756907 | ||||||
chr7:16756971
|
A | G | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0003t0011g0005 | 6 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2941A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16756971 | ||||||
chr7:16757246
|
T | G | 1 | a0001c0004t0009g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+3216T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757246 | ||||||
chr7:16757371
|
A | T | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0003t0011g0005 | 6 | HG02055.hp2 HG02486.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3341A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757371 | ||||||
chr7:16757491
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+3461A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757491 | ||||||
chr7:16757507
|
CA | C | 58 | a0001c0001t0002g0088a0001c0002t0002g0087a0001c0002t0002g0336others(55): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.63+3485delA | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16757507 | |||||
chr7:16757578
|
AC | A | 3 | a0001c0003t0002g0103a0001c0004t0002g0102a0001c0004t0002g0104 | 3 | HG00673.hp1 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.63+3549delC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757578 | ||||||
chr7:16757651
|
T | C | 1 | a0001c0002t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.63+3621T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757651 | ||||||
chr7:16757765
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.63+3735T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757765 | ||||||
chr7:16757815
|
G | A | 11 | a0001c0001t0002g0326a0001c0001t0003g0125a0001c0001t0004g0123others(8): Show | 11 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+3785G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757815 | ||||||
chr7:16757850
|
T | C | 1 | a0001c0003t0002g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+3820T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757850 | ||||||
chr7:16757982
|
C | T | 1 | a0001c0001t0003g0273 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.63+3952C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16757982 | ||||||
chr7:16758054
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.63+4024T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758054 | ||||||
chr7:16758087
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+4057G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758087 | ||||||
chr7:16758236
|
T | A | 8 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0001t0020g0276others(5): Show | 9 | HG00280.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+4206T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758236 | ||||||
chr7:16758390
|
T | A | 8 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0001t0020g0276others(5): Show | 9 | HG00280.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+4360T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758390 | ||||||
chr7:16758731
|
C | A | 1 | a0001c0003t0002g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+4701C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758731 | ||||||
chr7:16758751
|
C | CT | 85 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(82): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.63+4733dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16758751 | |||||
chr7:16758861
|
G | T | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+4831G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16758861 | ||||||
chr7:16759009
|
G | C | 1 | a0001c0001t0001g0298 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.63+4979G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759009 | ||||||
chr7:16759014
|
C | G | 3 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0003t0011g0005 | 6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+4984C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759014 | ||||||
chr7:16759085
|
C | T | 3 | a0001c0001t0004g0074a0001c0002t0001g0072a0001c0002t0001g0073 | 3 | HG01074.hp1 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.63+5055C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759085 | ||||||
chr7:16759149
|
C | T | 1 | a0001c0003t0002g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+5119C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759149 | ||||||
chr7:16759177
|
G | T | 5 | a0001c0003t0001g0173a0001c0003t0005g0176a0001c0003t0017g0177others(2): Show | 5 | HG01243.hp2 HG01255.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+5147G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759177 | ||||||
chr7:16759292
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.63+5262T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759292 | ||||||
chr7:16759397
|
C | T | 4 | a0001c0001t0004g0206a0001c0002t0001g0013a0001c0002t0001g0207others(1): Show | 6 | HG00741.hp1 HG01192.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5367C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759397 | ||||||
chr7:16759429
|
A | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5399A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759429 | ||||||
chr7:16759487
|
C | T | 1 | a0001c0002t0008g0311 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63+5457C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759487 | ||||||
chr7:16759506
|
T | A | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5476T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759506 | ||||||
chr7:16759510
|
G | T | 3 | a0001c0003t0002g0103a0001c0004t0002g0102a0001c0004t0002g0104 | 3 | HG00673.hp1 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.63+5480G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759510 | ||||||
chr7:16759513
|
C | G | 3 | a0001c0003t0024g0106a0001c0003t0029g0105a0001c0004t0008g0031 | 4 | HG02630.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5483C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759513 | ||||||
chr7:16759607
|
G | A | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5577G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759607 | ||||||
chr7:16759641
|
C | G | 227 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0035others(224): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.63+5611C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759641 | ||||||
chr7:16759677
|
C | CT | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5655dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759677 | |||||
chr7:16759695
|
CTTTCTTT others(3): Show |
C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+5669_63+5678del others(10): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759695 | |||||
chr7:16759699
|
C | CT | 17 | a0001c0001t0001g0171a0001c0001t0001g0260a0001c0001t0003g0269others(14): Show | 18 | HG00280.hp2 HG00738.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+5686dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759699 | |||||
chr7:16759699
|
CT | C | 9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0019g0136others(6): Show | 9 | HG01074.hp2 HG01243.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+5686delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759699 | |||||
chr7:16759699
|
CTT | C | 70 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(67): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+5685_63+5686del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16759699 | |||||
chr7:16759745
|
G | C | 91 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(88): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+5715G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759745 | ||||||
chr7:16759780
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+5750C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759780 | ||||||
chr7:16759979
|
G | C | 91 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(88): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+5949G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16759979 | ||||||
chr7:16760023
|
A | G | 4 | a0001c0001t0004g0190a0001c0001t0004g0191a0001c0002t0001g0193others(1): Show | 4 | NA18953.hp2 NA19065.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5993A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760023 | ||||||
chr7:16760074
|
G | T | 16 | a0001c0001t0006g0310a0001c0001t0026g0110a0001c0002t0008g0311others(13): Show | 21 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+6044G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760074 | ||||||
chr7:16760151
|
A | G | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6121A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760151 | ||||||
chr7:16760183
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+6153C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760183 | ||||||
chr7:16760183
|
C | T | 1 | a0001c0001t0026g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+6153C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760183 | ||||||
chr7:16760207
|
T | A | 92 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(89): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.63+6177T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760207 | ||||||
chr7:16760408
|
A | G | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6378A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760408 | ||||||
chr7:16760418
|
G | C | 1 | a0001c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.63+6388G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760418 | ||||||
chr7:16760580
|
T | C | 103 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(100): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+6550T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760580 | ||||||
chr7:16760581
|
A | T | 94 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(91): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+6551A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760581 | ||||||
chr7:16760623
|
G | A | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6593G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760623 | ||||||
chr7:16760633
|
A | G | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6603A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760633 | ||||||
chr7:16760654
|
G | T | 1 | a0001c0004t0009g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+6624G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760654 | ||||||
chr7:16760688
|
G | A | 1 | a0001c0003t0029g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+6658G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760688 | ||||||
chr7:16760689
|
G | T | 1 | a0001c0003t0029g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+6659G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760689 | ||||||
chr7:16760760
|
C | G | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+6730C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760760 | ||||||
chr7:16760771
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0004g0057 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.63+6741A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760771 | ||||||
chr7:16760808
|
G | T | 59 | a0001c0001t0002g0088a0001c0002t0002g0087a0001c0002t0002g0336others(56): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.63+6778G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760808 | ||||||
chr7:16760836
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0035others(223): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.63+6806G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760836 | ||||||
chr7:16760898
|
G | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6868G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760898 | ||||||
chr7:16760900
|
A | C | 1 | a0001c0001t0001g0258 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+6870A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760900 | ||||||
chr7:16760907
|
C | G | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6877C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16760907 | ||||||
chr7:16761007
|
C | A | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+6977C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761007 | ||||||
chr7:16761062
|
G | T | 1 | a0001c0004t0002g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.63+7032G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761062 | ||||||
chr7:16761187
|
A | G | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7157A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761187 | ||||||
chr7:16761254
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0213others(2): Show | 6 | HG01975.hp2 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+7224T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761254 | ||||||
chr7:16761334
|
G | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7304G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761334 | ||||||
chr7:16761358
|
A | G | 20 | a0001c0001t0006g0310a0001c0001t0026g0110a0001c0002t0002g0324others(17): Show | 26 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.63+7328A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761358 | ||||||
chr7:16761381
|
C | T | 94 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(91): Show | 118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+7351C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761381 | ||||||
chr7:16761391
|
T | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7361T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761391 | ||||||
chr7:16761454
|
T | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7424T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761454 | ||||||
chr7:16761536
|
A | T | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7506A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761536 | ||||||
chr7:16761550
|
A | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7520A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761550 | ||||||
chr7:16761560
|
T | C | 108 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(105): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.63+7530T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761560 | ||||||
chr7:16761565
|
C | G | 1 | a0001c0001t0004g0257 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+7535C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761565 | ||||||
chr7:16761573
|
C | T | 1 | a0001c0003t0002g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.63+7543C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761573 | ||||||
chr7:16761589
|
C | T | 1 | a0001c0003t0029g0105 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+7559C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761589 | ||||||
chr7:16761602
|
T | C | 29 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0310others(26): Show | 35 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.63+7572T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761602 | ||||||
chr7:16761603
|
G | A | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7573G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761603 | ||||||
chr7:16761690
|
A | AT | 74 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0069others(71): Show | 98 | HG00597.hp1 HG00609.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.63+7684dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761690
|
A | ATT | 38 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(35): Show | 49 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.63+7683_63+7684dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761690
|
A | ATTT | 7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0297others(4): Show | 7 | HG02027.hp2 HG02647.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+7682_63+7684dup others(3): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761690
|
AT | A | 82 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(79): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.63+7684delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761690
|
ATT | A | 7 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(4): Show | 10 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+7683_63+7684del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761690
|
ATTTTTT | A | 11 | a0001c0001t0001g0060a0001c0001t0003g0125a0001c0001t0004g0123others(8): Show | 11 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+7679_63+7684del others(6): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761690
|
ATTTTTTT others(3): Show |
A | 11 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0067others(8): Show | 12 | HG00423.hp2 HG02165.hp2 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+7675_63+7684del others(10): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16761690 | |||||
chr7:16761711
|
T | C | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7681T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761711 | ||||||
chr7:16761810
|
C | G | 3 | a0001c0001t0006g0310a0001c0002t0008g0311a0001c0002t0009g0274 | 3 | HG02451.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.63+7780C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761810 | ||||||
chr7:16761955
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+7925C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761955 | ||||||
chr7:16761985
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+7955T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16761985 | ||||||
chr7:16762067
|
G | A | 6 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8037G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762067 | ||||||
chr7:16762070
|
C | G | 6 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8040C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762070 | ||||||
chr7:16762164
|
A | C | 1 | a0001c0001t0001g0251 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.63+8134A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762164 | ||||||
chr7:16762197
|
G | C | 1 | a0001c0002t0005g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+8167G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762197 | ||||||
chr7:16762243
|
G | A | 10 | a0001c0003t0002g0053a0001c0003t0002g0055a0001c0003t0002g0303others(7): Show | 15 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+8213G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762243 | ||||||
chr7:16762436
|
G | A | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+8406G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762436 | ||||||
chr7:16762452
|
C | T | 2 | a0001c0001t0002g0326a0001c0001t0006g0325 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.63+8422C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762452 | ||||||
chr7:16762474
|
C | A | 6 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8444C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762474 | ||||||
chr7:16762511
|
T | A | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8481T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762511 | ||||||
chr7:16762523
|
G | C | 9 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8493G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762523 | ||||||
chr7:16762553
|
C | T | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+8523C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762553 | ||||||
chr7:16762575
|
C | A | 107 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(104): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.63+8545C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762575 | ||||||
chr7:16762622
|
C | G | 1 | a0001c0004t0010g0323 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+8592C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762622 | ||||||
chr7:16762623
|
C | T | 2 | a0001c0001t0001g0280a0001c0002t0001g0195 | 2 | HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.63+8593C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762623 | ||||||
chr7:16762755
|
A | C | 2 | a0001c0002t0005g0062a0001c0002t0005g0070 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.63+8725A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762755 | ||||||
chr7:16762796
|
G | T | 5 | a0001c0001t0007g0034a0001c0002t0001g0142a0001c0002t0001g0163others(2): Show | 6 | HG00639.hp1 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8766G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762796 | ||||||
chr7:16762867
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+8837G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762867 | ||||||
chr7:16762870
|
G | A | 1 | a0001c0002t0021g0275 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+8840G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762870 | ||||||
chr7:16762964
|
A | G | 97 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(94): Show | 121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.63+8934A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16762964 | ||||||
chr7:16763036
|
C | G | 1 | a0001c0004t0009g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+9006C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763036 | ||||||
chr7:16763066
|
C | T | 6 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9036C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763066 | ||||||
chr7:16763166
|
T | G | 2 | a0001c0002t0005g0062a0001c0002t0005g0070 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.63+9136T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763166 | ||||||
chr7:16763232
|
T | C | 7 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9202T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763232 | ||||||
chr7:16763284
|
G | A | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+9254G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763284 | ||||||
chr7:16763285
|
A | G | 7 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9255A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763285 | ||||||
chr7:16763319
|
T | A | 7 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9289T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763319 | ||||||
chr7:16763321
|
T | C | 1 | a0001c0004t0009g0120 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+9291T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763321 | ||||||
chr7:16763365
|
G | A | 114 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(111): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.63+9335G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763365 | ||||||
chr7:16763421
|
A | G | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+9391A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763421 | ||||||
chr7:16763436
|
A | T | 15 | a0001c0001t0006g0310a0001c0002t0008g0311a0001c0002t0009g0274others(12): Show | 20 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+9406A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763436 | ||||||
chr7:16763475
|
G | C | 98 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(95): Show | 122 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.63+9445G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763475 | ||||||
chr7:16763497
|
C | T | 6 | a0001c0003t0001g0173a0001c0003t0005g0176a0001c0003t0017g0177others(3): Show | 6 | HG01243.hp2 HG01255.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9467C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763497 | ||||||
chr7:16763536
|
C | T | 1 | a0001c0002t0005g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.63+9506C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763536 | ||||||
chr7:16763572
|
C | G | 9 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0006g0318others(6): Show | 9 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+9542C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763572 | ||||||
chr7:16763580
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0004g0049a0001c0001t0004g0257 | 4 | NA18966.hp2 NA18979.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+9550A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763580 | ||||||
chr7:16763645
|
C | T | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.63+9615C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763645 | ||||||
chr7:16763654
|
A | G | 58 | a0001c0001t0001g0300a0001c0001t0002g0088a0001c0002t0002g0087others(55): Show | 76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.63+9624A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763654 | ||||||
chr7:16763690
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+9660A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763690 | ||||||
chr7:16763691
|
TC | T | 6 | a0001c0003t0001g0173a0001c0003t0005g0176a0001c0003t0017g0177others(3): Show | 6 | HG01243.hp2 HG01255.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9664delC | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16763691 | |||||
chr7:16763837
|
T | C | 113 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(110): Show | 137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.63+9807T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16763837 | ||||||
chr7:16764050
|
G | A | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10020G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764050 | ||||||
chr7:16764092
|
A | G | 12 | a0001c0003t0001g0173a0001c0003t0002g0053a0001c0003t0002g0055others(9): Show | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+10062A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764092 | ||||||
chr7:16764095
|
G | A | 1 | a0001c0002t0005g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+10065G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764095 | ||||||
chr7:16764111
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0143 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.63+10081G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764111 | ||||||
chr7:16764184
|
A | AT | 6 | a0001c0001t0020g0276a0001c0002t0001g0167a0001c0002t0001g0172others(3): Show | 6 | HG01433.hp1 HG02738.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10170dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16764184 | |||||
chr7:16764184
|
ATTT | A | 115 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(112): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.63+10168_63+10170d others(5): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16764184 | |||||
chr7:16764317
|
G | A | 1 | a0001c0001t0003g0014 | 3 | NA18959.hp2 NA19055.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.63+10287G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764317 | ||||||
chr7:16764365
|
T | C | 199 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0035others(196): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.63+10335T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764365 | ||||||
chr7:16764384
|
T | C | 116 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(113): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.63+10354T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764384 | ||||||
chr7:16764452
|
G | A | 10 | a0001c0003t0002g0053a0001c0003t0002g0055a0001c0003t0002g0303others(7): Show | 15 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+10422G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764452 | ||||||
chr7:16764455
|
G | C | 1 | a0001c0001t0004g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+10425G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764455 | ||||||
chr7:16764495
|
T | C | 10 | a0001c0003t0002g0053a0001c0003t0002g0055a0001c0003t0002g0303others(7): Show | 15 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+10465T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764495 | ||||||
chr7:16764541
|
A | G | 1 | a0001c0004t0002g0030 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.63+10511A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764541 | ||||||
chr7:16764934
|
G | GT | 119 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0171others(116): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.63+10914dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16764934 | |||||
chr7:16764953
|
G | A | 108 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(105): Show | 132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+10923G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16764953 | ||||||
chr7:16765047
|
C | G | 1 | a0001c0001t0004g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+11017C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765047 | ||||||
chr7:16765062
|
G | T | 1 | a0001c0002t0009g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.63+11032G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765062 | ||||||
chr7:16765107
|
C | A | 2 | a0001c0001t0001g0221a0001c0002t0005g0256 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.63+11077C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765107 | ||||||
chr7:16765167
|
A | C | 1 | a0001c0001t0004g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-11044A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765167 | ||||||
chr7:16765266
|
AT | A | 116 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(113): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-10937delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16765266 | |||||
chr7:16765363
|
C | G | 22 | a0001c0001t0006g0310a0001c0001t0026g0110a0001c0002t0008g0311others(19): Show | 28 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-10848C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765363 | ||||||
chr7:16765369
|
G | A | 1 | a0001c0001t0004g0061 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-10842G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765369 | ||||||
chr7:16765451
|
C | A | 8 | a0001c0001t0001g0038a0001c0001t0003g0012a0001c0001t0004g0179others(5): Show | 18 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-10760C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765451 | ||||||
chr7:16765515
|
G | A | 1 | a0001c0001t0004g0182 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-10696G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765515 | ||||||
chr7:16765610
|
T | C | 1 | a0001c0004t0009g0222 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64-10601T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765610 | ||||||
chr7:16765707
|
A | G | 1 | a0001c0002t0001g0278 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.64-10504A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765707 | ||||||
chr7:16765912
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-10299C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765912 | ||||||
chr7:16765963
|
C | T | 18 | a0001c0001t0001g0137a0001c0001t0001g0153a0001c0001t0001g0154others(15): Show | 22 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-10248C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765963 | ||||||
chr7:16765978
|
A | G | 23 | a0001c0001t0006g0310a0001c0001t0026g0110a0001c0002t0008g0311others(20): Show | 29 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.64-10233A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16765978 | ||||||
chr7:16766071
|
A | G | 2 | a0001c0001t0019g0136a0001c0002t0001g0146 | 2 | HG01074.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.64-10140A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766071 | ||||||
chr7:16766136
|
T | A | 1 | a0001c0001t0001g0286 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64-10075T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766136 | ||||||
chr7:16766201
|
C | G | 4 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0271others(1): Show | 4 | HG03130.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-10010C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766201 | ||||||
chr7:16766346
|
T | A | 111 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0088others(108): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.64-9865T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766346 | ||||||
chr7:16766348
|
C | G | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9863C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766348 | ||||||
chr7:16766403
|
G | T | 17 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 19 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-9808G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766403 | ||||||
chr7:16766436
|
T | C | 4 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175others(1): Show | 4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-9775T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766436 | ||||||
chr7:16766517
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.64-9694T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766517 | ||||||
chr7:16766655
|
A | T | 1 | a0001c0002t0001g0152 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64-9556A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766655 | ||||||
chr7:16766676
|
C | T | 42 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(39): Show | 48 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.64-9535C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766676 | ||||||
chr7:16766726
|
A | G | 4 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175others(1): Show | 4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-9485A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766726 | ||||||
chr7:16766849
|
A | G | 4 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0271others(1): Show | 4 | HG03130.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9362A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766849 | ||||||
chr7:16766918
|
A | T | 1 | a0001c0003t0015g0306 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64-9293A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766918 | ||||||
chr7:16766973
|
C | A | 1 | a0001c0002t0002g0324 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-9238C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16766973 | ||||||
chr7:16767049
|
C | T | 1 | a0001c0003t0018g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64-9162C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767049 | ||||||
chr7:16767055
|
C | T | 5 | a0001c0003t0004g0128a0001c0003t0007g0126a0001c0003t0007g0127others(2): Show | 6 | HG02145.hp2 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9156C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767055 | ||||||
chr7:16767087
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0021others(83): Show | 115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.64-9124A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767087 | ||||||
chr7:16767438
|
G | C | 1 | a0001c0002t0009g0051 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.64-8773G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767438 | ||||||
chr7:16767541
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0263 | 2 | NA18942.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.64-8670T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767541 | ||||||
chr7:16767600
|
A | G | 1 | a0001c0004t0002g0337 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64-8611A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767600 | ||||||
chr7:16767640
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0004g0246 | 4 | NA18978.hp1 NA18994.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-8571C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767640 | ||||||
chr7:16767661
|
C | T | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0088others(66): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-8550C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767661 | ||||||
chr7:16767666
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0003t0011g0005 | 6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8545A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767666 | ||||||
chr7:16767671
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0003t0011g0005 | 6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8540A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767671 | ||||||
chr7:16767729
|
A | G | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0088others(66): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-8482A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767729 | ||||||
chr7:16767813
|
T | C | 1 | a0001c0002t0002g0324 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-8398T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767813 | ||||||
chr7:16767943
|
G | A | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0088others(66): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-8268G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767943 | ||||||
chr7:16767974
|
A | G | 1 | a0001c0004t0002g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.64-8237A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16767974 | ||||||
chr7:16768015
|
C | T | 4 | a0001c0001t0002g0320a0001c0001t0002g0326a0001c0001t0006g0325others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-8196C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768015 | ||||||
chr7:16768033
|
C | T | 1 | a0001c0003t0002g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-8178C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768033 | ||||||
chr7:16768036
|
C | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(44): Show | 65 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-8175C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768036 | ||||||
chr7:16768156
|
C | T | 17 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(14): Show | 17 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-8055C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768156 | ||||||
chr7:16768157
|
G | A | 1 | a0001c0002t0001g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64-8054G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768157 | ||||||
chr7:16768180
|
C | T | 1 | a0001c0001t0004g0245 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.64-8031C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768180 | ||||||
chr7:16768198
|
G | A | 1 | a0001c0004t0002g0330 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.64-8013G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768198 | ||||||
chr7:16768259
|
C | T | 3 | a0001c0003t0002g0092a0001c0003t0006g0091a0001c0003t0006g0093 | 3 | HG00544.hp1 NA18957.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.64-7952C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768259 | ||||||
chr7:16768265
|
T | C | 188 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(185): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.64-7946T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768265 | ||||||
chr7:16768397
|
C | A | 3 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175 | 3 | HG02004.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-7814C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768397 | ||||||
chr7:16768486
|
A | G | 1 | a0001c0002t0005g0261 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.64-7725A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768486 | ||||||
chr7:16768689
|
G | A | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0088others(66): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-7522G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768689 | ||||||
chr7:16768746
|
A | T | 1 | a0001c0004t0002g0079 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.64-7465A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768746 | ||||||
chr7:16768752
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.64-7459G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768752 | ||||||
chr7:16768842
|
C | T | 1 | a0001c0001t0004g0133 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.64-7369C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768842 | ||||||
chr7:16768847
|
G | A | 22 | a0001c0001t0006g0310a0001c0001t0026g0110a0001c0002t0008g0311others(19): Show | 28 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-7364G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768847 | ||||||
chr7:16768878
|
CTTATT | C | 4 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175others(1): Show | 4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-7325_64-7321del others(5): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16768878 | |||||
chr7:16768937
|
C | T | 1 | a0001c0002t0008g0329 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-7274C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768937 | ||||||
chr7:16768938
|
G | A | 2 | a0001c0004t0005g0174a0001c0004t0010g0321 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-7273G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16768938 | ||||||
chr7:16769015
|
A | G | 338 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(335): Show | 439 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(436): Show |
intron_variant | MODIFIER | c.64-7196A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769015 | ||||||
chr7:16769228
|
A | G | 4 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175others(1): Show | 4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-6983A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769228 | ||||||
chr7:16769280
|
A | G | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6931A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769280 | ||||||
chr7:16769286
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0004g0057a0001c0001t0004g0129others(4): Show | 10 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-6925G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769286 | ||||||
chr7:16769447
|
T | G | 4 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175others(1): Show | 4 | HG02004.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-6764T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769447 | ||||||
chr7:16769537
|
T | TGG | 71 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(68): Show | 89 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.64-6670_64-6669dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16769537 | |||||
chr7:16769545
|
T | A | 20 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(17): Show | 20 | HG01081.hp1 HG01109.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-6666T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769545 | ||||||
chr7:16769571
|
T | C | 232 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0035others(229): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.64-6640T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769571 | ||||||
chr7:16769572
|
G | A | 20 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(17): Show | 20 | HG01081.hp1 HG01109.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-6639G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769572 | ||||||
chr7:16769807
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.64-6404T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16769807 | ||||||
chr7:16770066
|
C | T | 2 | a0001c0001t0007g0034a0001c0002t0009g0138 | 3 | HG00639.hp1 HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.64-6145C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770066 | ||||||
chr7:16770123
|
T | A | 1 | a0001c0001t0004g0179 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.64-6088T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770123 | ||||||
chr7:16770124
|
A | T | 3 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175 | 3 | HG02004.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-6087A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770124 | ||||||
chr7:16770191
|
TTA | T | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6018_64-6017del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16770191 | |||||
chr7:16770198
|
A | T | 139 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(136): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.64-6013A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770198 | ||||||
chr7:16770457
|
G | C | 52 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(49): Show | 70 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-5754G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770457 | ||||||
chr7:16770510
|
C | G | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-5701C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770510 | ||||||
chr7:16770697
|
G | A | 16 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(13): Show | 16 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-5514G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770697 | ||||||
chr7:16770902
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-5309G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770902 | ||||||
chr7:16770980
|
C | G | 1 | a0001c0003t0015g0301 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64-5231C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770980 | ||||||
chr7:16770994
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.64-5217A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16770994 | ||||||
chr7:16771062
|
T | C | 131 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(128): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-5149T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771062 | ||||||
chr7:16771252
|
C | G | 57 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(54): Show | 78 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.64-4959C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771252 | ||||||
chr7:16771294
|
G | A | 11 | a0001c0003t0001g0173a0001c0003t0002g0053a0001c0003t0002g0055others(8): Show | 16 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-4917G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771294 | ||||||
chr7:16771366
|
C | A | 3 | a0001c0004t0002g0314a0001c0004t0002g0322a0001c0004t0009g0222 | 3 | HG02896.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.64-4845C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771366 | ||||||
chr7:16771459
|
G | C | 9 | a0001c0003t0002g0053a0001c0003t0002g0055a0001c0003t0002g0303others(6): Show | 14 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-4752G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771459 | ||||||
chr7:16771514
|
G | A | 13 | a0001c0001t0001g0060a0001c0001t0001g0221a0001c0001t0003g0269others(10): Show | 14 | HG00280.hp2 HG01433.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-4697G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771514 | ||||||
chr7:16771542
|
T | C | 131 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(128): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-4669T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771542 | ||||||
chr7:16771685
|
T | C | 3 | a0001c0003t0004g0128a0001c0003t0007g0126a0001c0003t0007g0127 | 3 | HG02145.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.64-4526T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771685 | ||||||
chr7:16771767
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.64-4444A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771767 | ||||||
chr7:16771775
|
C | G | 1 | a0001c0004t0002g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64-4436C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771775 | ||||||
chr7:16771887
|
G | C | 1 | a0001c0001t0003g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64-4324G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771887 | ||||||
chr7:16771928
|
C | T | 69 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(66): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-4283C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771928 | ||||||
chr7:16771948
|
A | C | 16 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(13): Show | 16 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-4263A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16771948 | ||||||
chr7:16772040
|
T | G | 1 | a0001c0001t0001g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.64-4171T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772040 | ||||||
chr7:16772113
|
G | T | 25 | a0001c0001t0001g0017a0001c0001t0001g0205a0001c0001t0001g0210others(22): Show | 35 | HG02015.hp2 HG02056.hp1 HG02135.hp1 others(32): Show |
intron_variant | MODIFIER | c.64-4098G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772113 | ||||||
chr7:16772139
|
C | T | 2 | a0001c0001t0001g0069a0001c0002t0005g0024 | 3 | HG02683.hp2 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.64-4072C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772139 | ||||||
chr7:16772151
|
G | A | 122 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0058others(119): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.64-4060G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772151 | ||||||
chr7:16772161
|
T | C | 1 | a0001c0003t0014g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-4050T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772161 | ||||||
chr7:16772183
|
C | T | 54 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0058others(51): Show | 71 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.64-4028C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772183 | ||||||
chr7:16772304
|
C | A | 6 | a0001c0003t0004g0128a0001c0003t0007g0126a0001c0003t0007g0127others(3): Show | 7 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-3907C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772304 | ||||||
chr7:16772369
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.64-3842G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772369 | ||||||
chr7:16772457
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.64-3754G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772457 | ||||||
chr7:16772482
|
G | A | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(1): Show | 7 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3729G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772482 | ||||||
chr7:16772508
|
C | G | 1 | a0001c0001t0001g0251 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.64-3703C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772508 | ||||||
chr7:16772604
|
G | C | 17 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(14): Show | 19 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-3607G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772604 | ||||||
chr7:16772610
|
C | A | 2 | a0001c0001t0007g0034a0001c0002t0009g0138 | 3 | HG00639.hp1 HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.64-3601C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772610 | ||||||
chr7:16772678
|
T | G | 1 | a0001c0003t0002g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64-3533T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772678 | ||||||
chr7:16772717
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0003g0289others(3): Show | 8 | HG01256.hp1 HG01361.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3494C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772717 | ||||||
chr7:16772722
|
G | A | 2 | a0001c0001t0002g0317a0001c0001t0006g0318 | 2 | HG01081.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-3489G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772722 | ||||||
chr7:16772724
|
G | A | 5 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3487G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772724 | ||||||
chr7:16772824
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.64-3387C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772824 | ||||||
chr7:16772857
|
G | C | 1 | a0001c0002t0009g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.64-3354G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772857 | ||||||
chr7:16772921
|
G | C | 1 | a0001c0003t0015g0301 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64-3290G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772921 | ||||||
chr7:16772952
|
C | T | 1 | a0001c0002t0002g0324 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-3259C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772952 | ||||||
chr7:16772994
|
T | C | 16 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0002g0326others(13): Show | 16 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-3217T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772994 | ||||||
chr7:16772995
|
C | A | 7 | a0001c0003t0002g0053a0001c0003t0002g0055a0001c0003t0002g0303others(4): Show | 12 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-3216C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16772995 | ||||||
chr7:16773075
|
G | T | 6 | a0001c0003t0004g0128a0001c0003t0007g0126a0001c0003t0007g0127others(3): Show | 7 | HG02145.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-3136G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773075 | ||||||
chr7:16773087
|
A | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0253 | 2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.64-3124A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773087 | ||||||
chr7:16773116
|
CA | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0209a0001c0001t0001g0288 | 4 | HG02080.hp1 NA18986.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-3094delA | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773116 | ||||||
chr7:16773152
|
T | C | 5 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0312others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3059T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773152 | ||||||
chr7:16773164
|
T | TG | 40 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0117others(37): Show | 51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-3038dupG | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773164 | |||||
chr7:16773168
|
G | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0143 | 3 | HG01515.hp1 HG01517.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.64-3043G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773168 | ||||||
chr7:16773206
|
G | T | 1 | a0001c0001t0004g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.64-3005G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773206 | ||||||
chr7:16773239
|
G | A | 1 | a0001c0001t0004g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64-2972G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773239 | ||||||
chr7:16773290
|
T | G | 67 | a0001c0001t0001g0300a0001c0002t0028g0082a0001c0003t0002g0028others(64): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.64-2921T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773290 | ||||||
chr7:16773337
|
T | TA | 53 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0036others(50): Show | 65 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-2859dupA | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773337 | |||||
chr7:16773337
|
TAA | T | 66 | a0001c0001t0001g0300a0001c0002t0028g0082a0001c0003t0002g0028others(63): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.64-2860_64-2859del others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773337 | |||||
chr7:16773351
|
AAGG | A | 5 | a0001c0001t0003g0064a0001c0001t0004g0061a0001c0002t0001g0063others(2): Show | 6 | NA18955.hp2 NA18959.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-2855_64-2853del others(3): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16773351 | |||||
chr7:16773552
|
G | C | 1 | a0001c0001t0026g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-2659G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773552 | ||||||
chr7:16773665
|
A | T | 18 | a0001c0001t0003g0125a0001c0001t0004g0123a0001c0001t0006g0310others(15): Show | 20 | HG01255.hp2 HG01884.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-2546A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773665 | ||||||
chr7:16773733
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0007g0159 | 2 | NA18963.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.64-2478A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773733 | ||||||
chr7:16773802
|
T | C | 185 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(182): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.64-2409T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773802 | ||||||
chr7:16773820
|
T | C | 1 | a0001c0001t0003g0010 | 3 | HG02257.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.64-2391T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773820 | ||||||
chr7:16773863
|
T | C | 99 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(96): Show | 119 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.64-2348T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773863 | ||||||
chr7:16773892
|
C | G | 2 | a0001c0001t0001g0280a0001c0002t0001g0195 | 2 | HG01433.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.64-2319C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773892 | ||||||
chr7:16773902
|
A | G | 1 | a0001c0002t0005g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64-2309A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773902 | ||||||
chr7:16773951
|
G | T | 1 | a0001c0003t0017g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-2260G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773951 | ||||||
chr7:16773970
|
T | G | 97 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(94): Show | 117 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.64-2241T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16773970 | ||||||
chr7:16774011
|
T | A | 97 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(94): Show | 117 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.64-2200T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774011 | ||||||
chr7:16774166
|
G | A | 3 | a0001c0003t0002g0103a0001c0004t0002g0102a0001c0004t0002g0104 | 3 | HG00673.hp1 HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.64-2045G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774166 | ||||||
chr7:16774421
|
C | T | 89 | a0001c0002t0028g0082a0001c0003t0001g0173a0001c0003t0001g0267others(86): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.64-1790C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774421 | ||||||
chr7:16774449
|
G | A | 3 | a0001c0001t0004g0123a0001c0001t0014g0122a0001c0002t0005g0124 | 3 | HG02965.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-1762G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774449 | ||||||
chr7:16774647
|
A | T | 1 | a0001c0002t0001g0158 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64-1564A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774647 | ||||||
chr7:16774663
|
A | G | 2 | a0001c0002t0008g0305a0001c0002t0008g0328 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-1548A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774663 | ||||||
chr7:16774709
|
C | T | 90 | a0001c0002t0028g0082a0001c0003t0001g0173a0001c0003t0001g0267others(87): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.64-1502C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774709 | ||||||
chr7:16774774
|
T | C | 327 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(324): Show | 425 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(422): Show |
intron_variant | MODIFIER | c.64-1437T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774774 | ||||||
chr7:16774778
|
A | G | 1 | a0001c0002t0005g0277 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-1433A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774778 | ||||||
chr7:16774831
|
GT | G | 12 | a0001c0001t0001g0060a0001c0001t0001g0117a0001c0001t0001g0118others(9): Show | 13 | HG00280.hp2 HG01433.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-1376delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16774831 | |||||
chr7:16774857
|
A | C | 1 | a0001c0003t0025g0113 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-1354A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774857 | ||||||
chr7:16774865
|
A | G | 1 | a0001c0003t0025g0113 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-1346A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774865 | ||||||
chr7:16774881
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64-1330A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774881 | ||||||
chr7:16774982
|
G | A | 7 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304others(4): Show | 7 | HG02280.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1229G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16774982 | ||||||
chr7:16775185
|
G | T | 1 | a0001c0003t0002g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-1026G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775185 | ||||||
chr7:16775477
|
A | ATGATCTC others(15): Show |
1 | a0002c0005t0001g0189 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.64-732_64-711dupGA others(20): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 16775477 | |||||
chr7:16775495
|
A | G | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.64-716A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775495 | ||||||
chr7:16775502
|
A | G | 1 | a0001c0002t0001g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64-709A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775502 | ||||||
chr7:16775505
|
A | C | 1 | a0001c0002t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.64-706A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775505 | ||||||
chr7:16775585
|
C | T | 2 | a0001c0002t0001g0046a0001c0002t0001g0235 | 3 | HG01081.hp2 HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.64-626C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775585 | ||||||
chr7:16775720
|
T | G | 110 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(107): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.64-491T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775720 | ||||||
chr7:16775735
|
C | T | 1 | a0001c0004t0002g0332 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64-476C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775735 | ||||||
chr7:16775741
|
C | T | 1 | a0001c0003t0002g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-470C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775741 | ||||||
chr7:16775752
|
C | G | 1 | a0001c0003t0002g0086 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.64-459C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775752 | ||||||
chr7:16775769
|
C | G | 13 | a0001c0001t0001g0058a0001c0001t0002g0317a0001c0001t0002g0320others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-442C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775769 | ||||||
chr7:16775917
|
G | A | 59 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0060others(56): Show | 76 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.64-294G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775917 | ||||||
chr7:16775919
|
A | G | 1 | a0001c0003t0024g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64-292A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16775919 | ||||||
chr7:16776156
|
C | G | 1 | a0001c0002t0001g0235 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.64-55C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16776156 | ||||||
chr7:16776161
|
C | G | 89 | a0001c0003t0001g0173a0001c0003t0002g0028a0001c0003t0002g0053others(86): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.64-50C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16776161 | ||||||
chr7:16776175
|
T | G | 3 | a0001c0003t0005g0176a0001c0003t0017g0177a0001c0004t0005g0175 | 3 | HG02004.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-36T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 1/5 | chr7 | 16776175 | ||||||
chr7:16776441
|
A | G | 3 | a0001c0001t0004g0234a0001c0002t0001g0233a0001c0002t0001g0266 | 3 | HG01069.hp1 HG01261.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.231+63A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776441 | ||||||
chr7:16776465
|
G | A | 10 | a0001c0001t0002g0317a0001c0001t0002g0320a0001c0001t0006g0318others(7): Show | 10 | HG01081.hp1 HG01109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+87G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776465 | ||||||
chr7:16776610
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.231+232G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776610 | ||||||
chr7:16776716
|
A | G | 1 | a0001c0002t0001g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.232-326A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776716 | ||||||
chr7:16776952
|
T | C | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.232-90T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776952 | ||||||
chr7:16776967
|
T | G | 1 | a0001c0003t0015g0301 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.232-75T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 2/5 | chr7 | 16776967 | ||||||
chr7:16777156
|
A | G | 1 | a0001c0001t0026g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.312+34A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777156 | ||||||
chr7:16777292
|
C | T | 1 | a0001c0001t0003g0010 | 3 | HG02257.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312+170C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777292 | ||||||
chr7:16777318
|
C | A | 18 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(15): Show | 20 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.312+196C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777318 | ||||||
chr7:16777324
|
C | CT | 13 | a0001c0001t0001g0038a0001c0001t0001g0299a0001c0001t0003g0012others(10): Show | 23 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.312+206dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 16777324 | |||||
chr7:16777376
|
A | C | 1 | a0001c0003t0015g0301 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.312+254A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777376 | ||||||
chr7:16777383
|
C | A | 1 | a0002c0005t0001g0189 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.312+261C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777383 | ||||||
chr7:16777387
|
A | G | 1 | a0001c0001t0004g0049 | 2 | NA18966.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.312+265A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777387 | ||||||
chr7:16777658
|
A | C | 13 | a0001c0001t0001g0058a0001c0001t0002g0317a0001c0001t0002g0320others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.313-140A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 3/5 | chr7 | 16777658 | ||||||
chr7:16778020
|
T | C | 1 | a0001c0001t0004g0049 | 2 | NA18966.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.426+109T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778020 | ||||||
chr7:16778148
|
C | G | 3 | a0001c0001t0001g0290a0001c0001t0007g0020a0001c0001t0007g0291 | 5 | HG01256.hp1 HG01361.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+237C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778148 | ||||||
chr7:16778185
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.426+274G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778185 | ||||||
chr7:16778186
|
T | C | 18 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(15): Show | 20 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.426+275T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778186 | ||||||
chr7:16778420
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0002g0326a0001c0001t0004g0057 | 3 | HG02109.hp1 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.426+509C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778420 | ||||||
chr7:16778474
|
A | T | 1 | a0002c0005t0001g0189 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.427-529A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778474 | ||||||
chr7:16778549
|
T | C | 94 | a0001c0001t0001g0069a0001c0001t0001g0117a0001c0001t0001g0118others(91): Show | 118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.427-454T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778549 | ||||||
chr7:16778637
|
C | T | 16 | a0001c0003t0001g0267a0001c0003t0002g0053a0001c0003t0002g0055others(13): Show | 21 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.427-366C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778637 | ||||||
chr7:16778779
|
C | G | 2 | a0001c0001t0001g0221a0001c0002t0005g0256 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.427-224C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778779 | ||||||
chr7:16778851
|
T | G | 63 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0003g0162others(60): Show | 81 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.427-152T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778851 | ||||||
chr7:16778933
|
G | A | 27 | a0001c0001t0001g0221a0001c0001t0002g0317a0001c0001t0002g0320others(24): Show | 28 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.427-70G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 4/5 | chr7 | 16778933 | ||||||
chr7:16779174
|
A | G | 94 | a0001c0001t0001g0069a0001c0001t0001g0117a0001c0001t0001g0118others(91): Show | 118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.540+58A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779174 | ||||||
chr7:16779182
|
C | A | 3 | a0001c0001t0001g0058a0001c0001t0002g0326a0001c0001t0004g0057 | 3 | HG02109.hp1 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.540+66C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779182 | ||||||
chr7:16779298
|
G | C | 1 | a0001c0004t0010g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.540+182G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779298 | ||||||
chr7:16779327
|
T | C | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0304 | 3 | HG02809.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.540+211T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779327 | ||||||
chr7:16779632
|
A | G | 19 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(16): Show | 21 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.540+516A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779632 | ||||||
chr7:16779670
|
C | G | 72 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0300others(69): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.540+554C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779670 | ||||||
chr7:16779771
|
A | G | 1 | a0001c0002t0008g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.540+655A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779771 | ||||||
chr7:16779772
|
T | C | 1 | a0001c0001t0001g0047 | 2 | HG02080.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.540+656T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779772 | ||||||
chr7:16779776
|
C | CT | 75 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0157others(72): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.540+673dupT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16779776 | |||||
chr7:16779776
|
C | CTT | 19 | a0001c0001t0001g0069a0001c0001t0003g0064a0001c0001t0003g0065others(16): Show | 21 | HG00423.hp2 HG01074.hp1 HG02165.hp2 others(18): Show |
intron_variant | MODIFIER | c.540+672_540+673dup others(2): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16779776 | |||||
chr7:16779803
|
G | A | 18 | a0001c0001t0001g0060a0001c0003t0001g0267a0001c0003t0002g0053others(15): Show | 23 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.540+687G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779803 | ||||||
chr7:16779811
|
A | G | 111 | a0001c0001t0001g0060a0001c0001t0001g0069a0001c0001t0001g0117others(108): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.540+695A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779811 | ||||||
chr7:16779860
|
C | A | 1 | a0002c0005t0001g0189 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.540+744C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779860 | ||||||
chr7:16779870
|
C | G | 2 | a0001c0004t0001g0115a0001c0004t0001g0116 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.540+754C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779870 | ||||||
chr7:16779881
|
C | T | 24 | a0001c0001t0001g0221a0001c0001t0002g0317a0001c0001t0002g0320others(21): Show | 25 | HG00280.hp2 HG01081.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.540+765C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779881 | ||||||
chr7:16779920
|
C | A | 3 | a0001c0002t0001g0147a0001c0002t0001g0167a0001c0002t0001g0169 | 3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+804C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779920 | ||||||
chr7:16779927
|
A | G | 3 | a0001c0002t0001g0147a0001c0002t0001g0167a0001c0002t0001g0169 | 3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+811A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779927 | ||||||
chr7:16779932
|
C | T | 3 | a0001c0002t0001g0147a0001c0002t0001g0167a0001c0002t0001g0169 | 3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+816C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779932 | ||||||
chr7:16779933
|
A | G | 3 | a0001c0002t0001g0147a0001c0002t0001g0167a0001c0002t0001g0169 | 3 | NA18940.hp1 NA18957.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.540+817A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16779933 | ||||||
chr7:16780032
|
A | G | 19 | a0001c0001t0001g0060a0001c0001t0004g0074a0001c0003t0001g0267others(16): Show | 24 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+916A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780032 | ||||||
chr7:16780074
|
T | C | 19 | a0001c0001t0001g0060a0001c0001t0004g0074a0001c0003t0001g0267others(16): Show | 24 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+958T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780074 | ||||||
chr7:16780203
|
G | A | 1 | a0001c0003t0012g0025 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.540+1087G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780203 | ||||||
chr7:16780425
|
T | A | 1 | a0001c0001t0001g0298 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1309T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780425 | ||||||
chr7:16780434
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1318C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780434 | ||||||
chr7:16780434
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0033others(22): Show | 39 | HG00544.hp2 HG00621.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.540+1318C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780434 | ||||||
chr7:16780437
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1321C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780437 | ||||||
chr7:16780439
|
T | G | 1 | a0001c0001t0001g0298 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1323T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780439 | ||||||
chr7:16780441
|
A | T | 1 | a0001c0001t0001g0298 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540+1325A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780441 | ||||||
chr7:16780463
|
A | G | 1 | a0001c0002t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.540+1347A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780463 | ||||||
chr7:16780534
|
G | A | 1 | a0001c0003t0007g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.540+1418G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780534 | ||||||
chr7:16780761
|
A | C | 1 | a0001c0002t0001g0279 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.540+1645A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16780761 | ||||||
chr7:16781170
|
C | T | 1 | a0001c0001t0004g0230 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.540+2054C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781170 | ||||||
chr7:16781274
|
G | A | 8 | a0001c0001t0001g0221a0001c0001t0004g0123a0001c0001t0014g0122others(5): Show | 9 | HG00280.hp2 HG01433.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.541-2143G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781274 | ||||||
chr7:16781279
|
A | G | 22 | a0001c0001t0001g0060a0001c0001t0004g0074a0001c0001t0006g0310others(19): Show | 27 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.541-2138A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781279 | ||||||
chr7:16781372
|
G | C | 78 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0003g0065others(75): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.541-2045G>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781372 | ||||||
chr7:16781379
|
T | A | 1 | a0001c0002t0005g0068 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.541-2038T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781379 | ||||||
chr7:16781458
|
T | C | 59 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(56): Show | 78 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.541-1959T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781458 | ||||||
chr7:16781539
|
A | G | 4 | a0001c0001t0001g0221a0001c0001t0020g0276a0001c0002t0005g0256others(1): Show | 4 | HG00280.hp2 HG01433.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1878A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781539 | ||||||
chr7:16781591
|
G | A | 74 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0237others(71): Show | 91 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.541-1826G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781591 | ||||||
chr7:16781730
|
G | A | 207 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0035others(204): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.541-1687G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781730 | ||||||
chr7:16781746
|
A | G | 1 | a0001c0003t0002g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.541-1671A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781746 | ||||||
chr7:16781811
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0242 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.541-1606G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781811 | ||||||
chr7:16781931
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.541-1486G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781931 | ||||||
chr7:16781963
|
G | A | 1 | a0001c0001t0007g0034 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.541-1454G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781963 | ||||||
chr7:16781987
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.541-1430A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16781987 | ||||||
chr7:16782012
|
T | C | 313 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(310): Show | 407 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.541-1405T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782012 | ||||||
chr7:16782021
|
C | T | 1 | a0001c0004t0002g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.541-1396C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782021 | ||||||
chr7:16782100
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.541-1317T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782100 | ||||||
chr7:16782245
|
A | G | 2 | a0001c0004t0008g0031a0001c0004t0009g0120 | 3 | HG02723.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.541-1172A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782245 | ||||||
chr7:16782255
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0259a0001c0001t0019g0136 | 3 | HG01074.hp2 HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.541-1162C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782255 | ||||||
chr7:16782350
|
ACT | A | 22 | a0001c0001t0001g0194a0001c0001t0003g0010a0001c0001t0003g0125others(19): Show | 25 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.541-1062_541-1061d others(4): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16782350 | |||||
chr7:16782429
|
G | A | 27 | a0001c0001t0007g0034a0001c0001t0014g0122a0001c0002t0005g0023others(24): Show | 31 | HG00280.hp2 HG00733.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.541-988G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782429 | ||||||
chr7:16782440
|
G | T | 2 | a0001c0001t0004g0040a0001c0001t0004g0230 | 3 | HG00280.hp1 HG01934.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.541-977G>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782440 | ||||||
chr7:16782452
|
A | T | 1 | a0002c0005t0001g0189 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.541-965A>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782452 | ||||||
chr7:16782597
|
G | A | 113 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0047others(110): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.541-820G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782597 | ||||||
chr7:16782691
|
T | G | 2 | a0001c0001t0003g0269a0001c0001t0003g0271 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.541-726T>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782691 | ||||||
chr7:16782799
|
T | A | 1 | a0001c0003t0024g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.541-618T>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782799 | ||||||
chr7:16782813
|
A | G | 4 | a0001c0002t0001g0008a0001c0002t0001g0132a0001c0002t0001g0134others(1): Show | 7 | HG00558.hp1 NA18942.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-604A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782813 | ||||||
chr7:16782818
|
T | C | 2 | a0001c0004t0008g0031a0001c0004t0009g0120 | 3 | HG02723.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.541-599T>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782818 | ||||||
chr7:16782841
|
A | G | 3 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0271 | 3 | HG03130.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.541-576A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782841 | ||||||
chr7:16782883
|
G | A | 5 | a0001c0001t0001g0227a0001c0001t0001g0259a0001c0001t0002g0317others(2): Show | 5 | HG01074.hp2 HG01081.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-534G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782883 | ||||||
chr7:16782946
|
A | G | 1 | a0001c0001t0004g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541-471A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782946 | ||||||
chr7:16782980
|
C | A | 3 | a0001c0002t0010g0319a0001c0004t0005g0174a0001c0004t0010g0321 | 3 | HG01243.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.541-437C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16782980 | ||||||
chr7:16783048
|
C | T | 3 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0271 | 3 | HG03130.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.541-369C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783048 | ||||||
chr7:16783062
|
CCCTGTGA others(6): Show |
C | 1 | a0002c0005t0001g0189 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.541-353_541-341del others(13): Show |
TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16783062 | |||||
chr7:16783124
|
A | C | 1 | a0001c0001t0001g0254 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-293A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783124 | ||||||
chr7:16783128
|
C | T | 116 | a0001c0001t0001g0150a0001c0001t0001g0229a0001c0001t0001g0237others(113): Show | 161 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.541-289C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783128 | ||||||
chr7:16783133
|
A | C | 1 | a0001c0001t0001g0254 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-284A>C | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783133 | ||||||
chr7:16783191
|
C | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(98): Show | 129 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.541-226C>T | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783191 | ||||||
chr7:16783213
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-204A>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783213 | ||||||
chr7:16783214
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.541-203G>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783214 | ||||||
chr7:16783250
|
C | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(107): Show | 142 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.541-167C>G | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783250 | ||||||
chr7:16783252
|
C | A | 1 | a0001c0003t0001g0173 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.541-165C>A | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783252 | ||||||
chr7:16783311
|
TG | T | 20 | a0001c0001t0014g0122a0001c0002t0005g0023a0001c0002t0005g0024others(17): Show | 23 | HG00280.hp2 HG00733.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.541-105delG | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | chr7 | 16783311 | ||||||
chr7:16783396
|
AT | A | 29 | a0001c0001t0003g0007a0001c0001t0003g0010a0001c0001t0003g0012others(26): Show | 42 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.541-12delT | TSPAN13 | ENSG00000106537.8 | transcript | ENST00000262067.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 16783396 |