geneid | 23554 |
---|---|
ensemblid | ENSG00000106025.9 |
hgncid | 21641 |
symbol | TSPAN12 |
name | tetraspanin 12 |
refseq_nuc | NM_012338.4 |
refseq_prot | NP_036470.1 |
ensembl_nuc | ENST00000222747.8 |
ensembl_prot | ENSP00000222747.3 |
mane_status | MANE Select |
chr | chr7 |
start | 120787320 |
end | 120858144 |
strand | - |
ver | v1.2 |
region | chr7:120787320-120858144 |
region5000 | chr7:120782320-120863144 |
regionname0 | TSPAN12_chr7_120787320_120858144 |
regionname5000 | TSPAN12_chr7_120782320_120863144 |
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 | 305 | 292 | 90 | 52 | 124 | 2 | 22 | 98 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0002 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0003 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 918 | 254 | 72 | 41 | 121 | 1 | 18 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
c0002 | 1/0 | 918 | 36 | 16 | 11 | 3 | 1 | 4 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
c0003 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
c0004 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
c0005 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
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 | 1668 | 168 | 63 | 28 | 65 | 1 | 10 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0002 | 0/0 | 1669 | 73 | 4 | 14 | 48 | 0 | 7 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0003 | 1/0 | 1668 | 29 | 15 | 7 | 2 | 0 | 4 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0004 | 0/0 | 1669 | 8 | 2 | 5 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0005 | 0/0 | 1668 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0006 | 0/0 | 1668 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0007 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0008 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0009 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0010 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0011 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0012 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
t0013 | 0/0 | 1669 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
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 | 6 | 0 | 2 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0002 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 918 | 254 | 72 | 41 | 121 | 1 | 18 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0002 | 1/0 | 918 | 36 | 16 | 11 | 3 | 1 | 4 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0003 | 0/0 | 918 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0002c0004 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0003c0005 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2585 | 166 | 63 | 26 | 65 | 1 | 10 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0002 | 0/0 | 2586 | 71 | 2 | 14 | 48 | 0 | 7 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0003 | 0/0 | 2585 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0005 | 0/0 | 2585 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0006 | 0/0 | 2585 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0007 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0009 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0010 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0011 | 0/0 | 2585 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0012 | 0/0 | 2585 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0001t0013 | 0/0 | 2586 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0002t0003 | 1/0 | 2585 | 27 | 14 | 6 | 2 | 0 | 4 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0002t0004 | 0/0 | 2586 | 8 | 2 | 5 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0002t0008 | 0/0 | 2585 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0001c0003t0002 | 0/0 | 2586 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0002c0004t0001 | 0/0 | 2585 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
a0003c0005t0001 | 0/0 | 2585 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | copy fasta | chr7 | 120782320 | 120863144 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0002 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0003g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0005g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0011g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0001t0013g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0002t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0001c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0002c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
a0003c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00423 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0067 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0223 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0074 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01168 | hp2 | a0003 | c0005 | t0001 | g0116 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0054 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01258 | hp2 | a0001 | c0002 | t0004 | g0220 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0202 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01934 | hp2 | a0001 | c0002 | t0004 | g0180 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0181 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02004 | hp2 | a0002 | c0004 | t0001 | g0126 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02015 | hp1 | a0001 | c0001 | t0013 | g0179 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0069 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02071 | hp1 | a0001 | c0002 | t0008 | g0060 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02257 | hp1 | a0001 | c0001 | t0012 | g0176 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0063 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0066 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0065 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0053 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0052 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02970 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0188 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0169 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0068 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0073 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | ESN | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03710 | hp2 | a0001 | c0001 | t0011 | g0101 | SAS | PJL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0189 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0168 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18943 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18959 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19075 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0059 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0089 | AFR | YRI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0197 | EUR | TSI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0064 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0056 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ACB | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0219 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | USA | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
NA21309 | hp2 | a0001 | c0002 | t0004 | g0182 | AFR | LWK | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0050 | REF | REF | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0156 | REF | REF | TSPAN12_chr7_120782320_120863144 | TSPAN12 | chr7 | 120782320 | 120863144 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:120787321
|
T | A | 1 | a0001 | 1 | HG02071.hp1 | splice_region_variant | LOW | c.*1271A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | chr7 | 120787321 | ||||||
chr7:120787322
|
A | C | 1 | a0001 | 1 | HG03579.hp2 | splice_region_variant | LOW | c.*1270T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | chr7 | 120787322 | ||||||
chr7:120788677
|
A | G | 1 | a0003 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.833T>C | p.Leu278Pro | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1228/2585 | 833/918 | 278/305 | chr7 | 120788677 | ||
chr7:120840030
|
G | T | 1 | a0002 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.146C>A | p.Thr49Lys | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/8 | 541/2585 | 146/918 | 49/305 | chr7 | 120840030 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:120788745
|
C | A | 4 | a0001c0001a0001c0003a0002c0004others(1): Show | 258 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(255): Show |
synonymous_variant | LOW | c.765G>T | p.Pro255Pro | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1160/2585 | 765/918 | 255/305 | chr7 | 120788745 | ||
chr7:120815738
|
C | T | 1 | a0001c0003 | 2 | HG03209.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.351G>A | p.Gln117Gln | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/8 | 746/2585 | 351/918 | 117/305 | chr7 | 120815738 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:120787349
|
T | A | 1 | a0001c0001t0011 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1243A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1243 | chr7 | 120787349 | |||||
chr7:120787453
|
T | A | 1 | a0001c0001t0005 | 7 | HG00558.hp1 NA18954.hp1 NA18970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1139A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 1139 | chr7 | 120787453 | |||||
chr7:120788150
|
C | T | 1 | a0001c0001t0009 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 442 | chr7 | 120788150 | |||||
chr7:120788553
|
G | A | 13 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(10): Show | 256 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 8/8 | 39 | chr7 | 120788553 | |||||
chr7:120857825
|
G | A | 1 | a0001c0001t0012 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1062 | chr7 | 120857825 | |||||
chr7:120857880
|
G | A | 1 | a0001c0001t0006 | 2 | HG03209.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-131C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1117 | chr7 | 120857880 | |||||
chr7:120857905
|
C | T | 1 | a0001c0001t0007 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1142 | chr7 | 120857905 | |||||
chr7:120857961
|
C | G | 1 | a0001c0001t0013 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1198 | chr7 | 120857961 | |||||
chr7:120857999
|
G | GA | 4 | a0001c0001t0002a0001c0001t0013a0001c0002t0004others(1): Show | 82 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
5_prime_UTR_variant | MODIFIER | c.-251dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/8 | 1237 | chr7 | 120857999 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:120788978
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.613-81A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120788978 | ||||||
chr7:120788983
|
G | A | 3 | a0001c0002t0003g0064a0001c0002t0003g0168a0001c0002t0003g0169 | 3 | HG02486.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-86C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120788983 | ||||||
chr7:120789519
|
T | C | 3 | a0001c0001t0001g0083a0001c0003t0002g0188a0001c0003t0002g0189 | 3 | HG01433.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.613-622A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789519 | ||||||
chr7:120789753
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.613-856A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789753 | ||||||
chr7:120789850
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613-953C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789850 | ||||||
chr7:120789989
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-1092A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120789989 | ||||||
chr7:120790008
|
C | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0040others(11): Show | 17 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.613-1111G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790008 | ||||||
chr7:120790022
|
G | A | 1 | a0001c0002t0003g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.613-1125C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790022 | ||||||
chr7:120790074
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.613-1177A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790074 | ||||||
chr7:120790092
|
G | A | 1 | a0001c0002t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.613-1195C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790092 | ||||||
chr7:120790240
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0006g0177a0001c0001t0006g0178others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-1343C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790240 | ||||||
chr7:120790341
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.613-1444G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790341 | ||||||
chr7:120790342
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.613-1445A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790342 | ||||||
chr7:120790360
|
T | G | 1 | a0001c0001t0002g0198 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.613-1463A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790360 | ||||||
chr7:120790362
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.613-1465C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790362 | ||||||
chr7:120790376
|
G | T | 1 | a0001c0002t0003g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.613-1479C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790376 | ||||||
chr7:120790473
|
G | C | 3 | a0001c0002t0003g0064a0001c0002t0003g0168a0001c0002t0003g0169 | 3 | HG02486.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-1576C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790473 | ||||||
chr7:120790685
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613-1788T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790685 | ||||||
chr7:120790754
|
C | T | 9 | a0001c0002t0003g0014a0001c0002t0003g0053a0001c0002t0003g0054others(6): Show | 10 | HG01243.hp1 HG01934.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-1857G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790754 | ||||||
chr7:120790981
|
T | A | 2 | a0001c0002t0003g0014a0001c0002t0003g0056 | 3 | HG02559.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.613-2084A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120790981 | ||||||
chr7:120791060
|
G | A | 2 | a0001c0002t0003g0053a0001c0002t0003g0054 | 2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.613-2163C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791060 | ||||||
chr7:120791327
|
T | G | 1 | a0001c0001t0002g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.613-2430A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791327 | ||||||
chr7:120791328
|
C | CA | 16 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(13): Show | 20 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.613-2432dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791328 | ||||||
chr7:120791416
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-2519A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791416 | ||||||
chr7:120791425
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.613-2528A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791425 | ||||||
chr7:120791453
|
A | G | 4 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-2556T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791453 | ||||||
chr7:120791500
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.613-2603A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791500 | ||||||
chr7:120791561
|
G | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 19 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.613-2664C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791561 | ||||||
chr7:120791916
|
T | C | 53 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 67 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.613-3019A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791916 | ||||||
chr7:120791936
|
G | C | 1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.613-3039C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120791936 | ||||||
chr7:120792023
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.613-3126A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792023 | ||||||
chr7:120792033
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613-3136G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792033 | ||||||
chr7:120792075
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.613-3178T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792075 | ||||||
chr7:120792164
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0199a0001c0001t0002g0201 | 6 | NA18956.hp2 NA18969.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-3267C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792164 | ||||||
chr7:120792344
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-3447G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792344 | ||||||
chr7:120792489
|
ATGAATAG others(24): Show |
A | 2 | a0001c0001t0001g0055a0001c0001t0001g0171 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.613-3623_613-3593d others(33): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792489 | ||||||
chr7:120792673
|
T | A | 1 | a0001c0003t0002g0189 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.613-3776A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792673 | ||||||
chr7:120792913
|
T | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG02630.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-4016A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792913 | ||||||
chr7:120792967
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0084 | 3 | HG00558.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.613-4070C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120792967 | ||||||
chr7:120793150
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.613-4253G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793150 | ||||||
chr7:120793363
|
T | C | 2 | a0001c0002t0003g0069a0001c0002t0003g0070 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.613-4466A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793363 | ||||||
chr7:120793416
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-4519G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793416 | ||||||
chr7:120793699
|
A | T | 1 | a0001c0002t0003g0015 | 2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.613-4802T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793699 | ||||||
chr7:120793716
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-4819G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793716 | ||||||
chr7:120793874
|
C | A | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0028others(16): Show | 22 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.613-4977G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793874 | ||||||
chr7:120793893
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0012g0176 | 2 | HG00738.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.613-4996A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120793893 | ||||||
chr7:120794129
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.613-5232A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794129 | ||||||
chr7:120794142
|
G | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-5245C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794142 | ||||||
chr7:120794468
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.613-5571A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794468 | ||||||
chr7:120794678
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.613-5781G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794678 | ||||||
chr7:120794699
|
A | G | 53 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 67 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.613-5802T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794699 | ||||||
chr7:120794774
|
A | ACAGT | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 149 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.613-5881_613-5878d others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794774 | ||||||
chr7:120794972
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.613-6075A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120794972 | ||||||
chr7:120795072
|
T | C | 1 | a0001c0002t0004g0220 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.613-6175A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120795072 | ||||||
chr7:120795246
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.613-6349A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120795246 | ||||||
chr7:120795584
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 153 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.613-6687A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120795584 | ||||||
chr7:120796003
|
C | G | 2 | a0001c0001t0006g0177a0001c0001t0006g0178 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.613-7106G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796003 | ||||||
chr7:120796068
|
CA | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 153 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.613-7172delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796068 | ||||||
chr7:120796107
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.613-7210G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796107 | ||||||
chr7:120796516
|
G | A | 1 | a0003c0005t0001g0116 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.613-7619C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796516 | ||||||
chr7:120796529
|
T | C | 1 | a0001c0001t0005g0022 | 2 | NA18970.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.613-7632A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796529 | ||||||
chr7:120796549
|
G | A | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.613-7652C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796549 | ||||||
chr7:120796739
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0010g0078 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.613-7842A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796739 | ||||||
chr7:120796826
|
CTCCACTT others(2): Show |
C | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-7938_613-7930d others(11): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796826 | ||||||
chr7:120796894
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.613-7997C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796894 | ||||||
chr7:120796930
|
C | T | 1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.613-8033G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796930 | ||||||
chr7:120796948
|
G | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-8051C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120796948 | ||||||
chr7:120797016
|
G | T | 1 | a0001c0001t0005g0118 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.613-8119C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797016 | ||||||
chr7:120797088
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.613-8191G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797088 | ||||||
chr7:120797104
|
C | A | 2 | a0001c0002t0003g0052a0001c0002t0003g0089 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.613-8207G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797104 | ||||||
chr7:120797138
|
CAG | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0079others(2): Show | 8 | HG00558.hp2 NA18952.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.613-8243_613-8242d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797138 | ||||||
chr7:120797144
|
C | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 278 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.613-8247G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797144 | ||||||
chr7:120797223
|
A | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0028others(15): Show | 21 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.613-8326T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797223 | ||||||
chr7:120797553
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 251 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.613-8656G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797553 | ||||||
chr7:120797611
|
T | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.613-8714A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797611 | ||||||
chr7:120797740
|
C | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+8809G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120797740 | ||||||
chr7:120798158
|
A | G | 56 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.612+8391T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798158 | ||||||
chr7:120798180
|
C | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.612+8369G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798180 | ||||||
chr7:120798194
|
G | A | 7 | a0001c0001t0002g0196a0001c0001t0002g0207a0001c0001t0002g0208others(4): Show | 7 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+8355C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798194 | ||||||
chr7:120798349
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02145.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.612+8200C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798349 | ||||||
chr7:120798416
|
T | C | 1 | a0001c0001t0001g0016 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.612+8133A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798416 | ||||||
chr7:120798507
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 149 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.612+8042C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798507 | ||||||
chr7:120798527
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(90): Show | 119 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.612+8022C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798527 | ||||||
chr7:120798643
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+7906G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798643 | ||||||
chr7:120798835
|
A | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(99): Show | 128 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.612+7714T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798835 | ||||||
chr7:120798851
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.612+7698G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798851 | ||||||
chr7:120798871
|
ATTCTTT | A | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+7672_612+7677d others(8): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798871 | ||||||
chr7:120798980
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.612+7569G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798980 | ||||||
chr7:120798997
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.612+7552G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120798997 | ||||||
chr7:120799082
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 18 | HG00597.hp1 HG01975.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.612+7467C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799082 | ||||||
chr7:120799109
|
G | A | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.612+7440C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799109 | ||||||
chr7:120799278
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.612+7271C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799278 | ||||||
chr7:120799354
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.612+7195G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799354 | ||||||
chr7:120799460
|
A | C | 1 | a0001c0001t0001g0002 | 5 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+7089T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799460 | ||||||
chr7:120799462
|
TTACATAA others(15): Show |
T | 2 | a0001c0001t0001g0017a0001c0001t0001g0084 | 3 | HG00558.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.612+7065_612+7086d others(24): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799462 | ||||||
chr7:120799465
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 252 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.612+7084G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799465 | ||||||
chr7:120799506
|
T | TTAATTAT others(17): Show |
4 | a0001c0001t0001g0043a0001c0001t0001g0146a0001c0001t0002g0190others(1): Show | 4 | HG02004.hp2 HG03927.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+7019_612+7042d others(26): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799506 | ||||||
chr7:120799506
|
T | TTAATTAT others(55): Show |
1 | a0001c0001t0002g0198 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.612+7042_612+7043i others(64): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799506 | ||||||
chr7:120799520
|
TTAATTAT others(19): Show |
T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.612+7003_612+7028d others(28): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799520 | ||||||
chr7:120799524
|
TTATATAT others(15): Show |
T | 1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.612+7003_612+7024d others(24): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799524 | ||||||
chr7:120799527
|
T | A | 1 | a0001c0001t0001g0025 | 2 | HG02071.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.612+7022A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799527 | ||||||
chr7:120799534
|
TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+7003_612+7014d others(14): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799534 | ||||||
chr7:120799546
|
A | AATTATAT others(15): Show |
3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0083 | 3 | HG01433.hp1 HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.612+7002_612+7003i others(24): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799546 | ||||||
chr7:120799570
|
T | A | 39 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 48 | HG00558.hp2 HG00741.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.612+6979A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799570 | ||||||
chr7:120799599
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(85): Show | 112 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.612+6950A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799599 | ||||||
chr7:120799605
|
A | ATT | 4 | a0001c0001t0001g0021a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 5 | HG00621.hp1 NA18947.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.612+6942_612+6943d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799605 | ||||||
chr7:120799640
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.612+6909G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799640 | ||||||
chr7:120799700
|
TTATTA | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+6844_612+6848d others(7): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799700 | ||||||
chr7:120799720
|
TTTA | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+6826_612+6828d others(5): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799720 | ||||||
chr7:120799739
|
TTA | T | 3 | a0001c0001t0006g0177a0001c0001t0006g0178a0001c0001t0009g0035 | 3 | HG03209.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.612+6808_612+6809d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799739 | ||||||
chr7:120799783
|
A | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+6766T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799783 | ||||||
chr7:120799913
|
A | T | 1 | a0001c0002t0004g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.612+6636T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799913 | ||||||
chr7:120799914
|
T | A | 1 | a0001c0002t0004g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.612+6635A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120799914 | ||||||
chr7:120800190
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+6359C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800190 | ||||||
chr7:120800250
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+6299C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800250 | ||||||
chr7:120800292
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.612+6257C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800292 | ||||||
chr7:120800653
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.612+5896C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800653 | ||||||
chr7:120800744
|
G | GTT | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(58): Show | 82 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.612+5803_612+5804d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800744 | ||||||
chr7:120800744
|
G | GTTT | 42 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(39): Show | 48 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.612+5802_612+5804d others(5): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800744 | ||||||
chr7:120800744
|
G | GTTTT | 7 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0090others(4): Show | 8 | HG02145.hp2 HG02647.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+5801_612+5804d others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800744 | ||||||
chr7:120800754
|
G | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 153 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.612+5795C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800754 | ||||||
chr7:120800844
|
GTTCACCT others(21): Show |
G | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+5677_612+5704d others(30): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120800844 | ||||||
chr7:120801033
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.612+5516C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801033 | ||||||
chr7:120801123
|
T | A | 1 | a0001c0001t0009g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.612+5426A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801123 | ||||||
chr7:120801327
|
T | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+5222A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801327 | ||||||
chr7:120801586
|
C | G | 1 | a0001c0001t0002g0007 | 4 | NA18969.hp2 NA18994.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.612+4963G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801586 | ||||||
chr7:120801727
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.612+4822G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801727 | ||||||
chr7:120801935
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+4614T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120801935 | ||||||
chr7:120802317
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0106 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.612+4232C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120802317 | ||||||
chr7:120803018
|
A | G | 1 | a0001c0002t0004g0220 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.612+3531T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803018 | ||||||
chr7:120803131
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 126 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.612+3418C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803131 | ||||||
chr7:120803256
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.612+3293G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803256 | ||||||
chr7:120803416
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.612+3133A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803416 | ||||||
chr7:120803773
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.612+2776A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120803773 | ||||||
chr7:120804048
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+2501A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120804048 | ||||||
chr7:120804074
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.612+2475C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120804074 | ||||||
chr7:120804337
|
T | G | 56 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.612+2212A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120804337 | ||||||
chr7:120805014
|
C | T | 2 | a0001c0001t0001g0057a0003c0005t0001g0116 | 2 | HG01168.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.612+1535G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805014 | ||||||
chr7:120805080
|
G | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(82): Show | 105 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.612+1469C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805080 | ||||||
chr7:120805269
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0147 | 3 | HG03490.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.612+1280A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805269 | ||||||
chr7:120805299
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.612+1250T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805299 | ||||||
chr7:120805498
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.612+1051G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805498 | ||||||
chr7:120805815
|
C | A | 1 | a0001c0001t0001g0016 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.612+734G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120805815 | ||||||
chr7:120806074
|
A | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(89): Show | 118 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.612+475T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120806074 | ||||||
chr7:120806335
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.612+214C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120806335 | ||||||
chr7:120806538
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.612+11A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 7/7 | chr7 | 120806538 | ||||||
chr7:120806832
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.469-140A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806832 | ||||||
chr7:120806855
|
G | T | 1 | a0001c0002t0003g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.469-163C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806855 | ||||||
chr7:120806871
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-179C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806871 | ||||||
chr7:120806874
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.469-182A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806874 | ||||||
chr7:120806992
|
T | C | 1 | a0001c0001t0002g0236 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.469-300A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120806992 | ||||||
chr7:120807152
|
A | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.469-460T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807152 | ||||||
chr7:120807406
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 253 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.469-714C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807406 | ||||||
chr7:120807580
|
C | T | 1 | a0001c0002t0003g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.469-888G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807580 | ||||||
chr7:120807707
|
T | A | 1 | a0001c0001t0002g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.469-1015A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807707 | ||||||
chr7:120807799
|
A | G | 1 | a0001c0002t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.469-1107T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807799 | ||||||
chr7:120807816
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.469-1124G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807816 | ||||||
chr7:120807884
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.469-1192A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120807884 | ||||||
chr7:120808245
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-1553A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808245 | ||||||
chr7:120808325
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 126 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.469-1633A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808325 | ||||||
chr7:120808543
|
T | C | 2 | a0001c0001t0002g0193a0001c0001t0002g0195 | 2 | NA18944.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.469-1851A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808543 | ||||||
chr7:120808670
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+1793G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808670 | ||||||
chr7:120808683
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.468+1780G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808683 | ||||||
chr7:120808748
|
G | A | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468+1715C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808748 | ||||||
chr7:120808749
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0010g0078 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.468+1714T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808749 | ||||||
chr7:120808830
|
T | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0028others(15): Show | 21 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.468+1633A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120808830 | ||||||
chr7:120809003
|
G | A | 1 | a0001c0001t0005g0118 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.468+1460C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809003 | ||||||
chr7:120809037
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0136a0001c0001t0011g0101 | 3 | HG01123.hp1 HG01168.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.468+1426G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809037 | ||||||
chr7:120809071
|
T | C | 2 | a0001c0002t0003g0069a0001c0002t0003g0070 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.468+1392A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809071 | ||||||
chr7:120809141
|
T | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02145.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.468+1322A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809141 | ||||||
chr7:120809149
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+1314C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809149 | ||||||
chr7:120809191
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.468+1272A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809191 | ||||||
chr7:120809396
|
C | G | 1 | a0001c0001t0010g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.468+1067G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809396 | ||||||
chr7:120809729
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.468+734C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809729 | ||||||
chr7:120809756
|
A | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 126 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.468+707T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809756 | ||||||
chr7:120809759
|
C | T | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468+704G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809759 | ||||||
chr7:120809877
|
T | A | 2 | a0001c0002t0003g0069a0001c0002t0003g0070 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.468+586A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120809877 | ||||||
chr7:120810216
|
G | A | 1 | a0001c0002t0008g0060 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.468+247C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120810216 | ||||||
chr7:120810430
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.468+33G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 6/7 | chr7 | 120810430 | ||||||
chr7:120810604
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 253 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(250): Show |
intron_variant | MODIFIER | c.361-34C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810604 | ||||||
chr7:120810624
|
T | TCA | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(94): Show | 127 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-56_361-55dupTG | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | ||||||
chr7:120810624
|
T | TCACA | 16 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0048others(13): Show | 17 | HG01123.hp1 HG01168.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.361-58_361-55dupTG others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | ||||||
chr7:120810624
|
T | TCACACA | 4 | a0001c0001t0001g0021a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 5 | HG00621.hp1 NA18947.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-60_361-55dupTG others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | ||||||
chr7:120810624
|
TCA | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0086others(68): Show | 89 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.361-56_361-55delTG | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | ||||||
chr7:120810624
|
TCACA | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 15 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.361-58_361-55delTG others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | ||||||
chr7:120810624
|
TCACACA | T | 3 | a0001c0002t0003g0062a0001c0003t0002g0188a0001c0003t0002g0189 | 3 | HG03209.hp1 NA18906.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.361-60_361-55delTG others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810624 | ||||||
chr7:120810672
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-102C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810672 | ||||||
chr7:120810682
|
C | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(115): Show | 147 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.361-112G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810682 | ||||||
chr7:120810715
|
G | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0003g0014others(4): Show | 8 | HG01243.hp1 HG01975.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-145C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120810715 | ||||||
chr7:120811049
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-479G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811049 | ||||||
chr7:120811150
|
T | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-580A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811150 | ||||||
chr7:120811578
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(97): Show | 126 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.361-1008C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811578 | ||||||
chr7:120811594
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-1024G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811594 | ||||||
chr7:120811869
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.361-1299C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811869 | ||||||
chr7:120811896
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-1326C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120811896 | ||||||
chr7:120812330
|
G | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-1760C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812330 | ||||||
chr7:120812360
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-1790G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812360 | ||||||
chr7:120812416
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG02071.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.361-1846G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812416 | ||||||
chr7:120812573
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.361-2003A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812573 | ||||||
chr7:120812760
|
C | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0028others(15): Show | 21 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.361-2190G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812760 | ||||||
chr7:120812885
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-2315G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812885 | ||||||
chr7:120812887
|
A | G | 1 | a0001c0001t0002g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.361-2317T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812887 | ||||||
chr7:120812894
|
C | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-2324G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812894 | ||||||
chr7:120812936
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.361-2366A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120812936 | ||||||
chr7:120813016
|
A | C | 1 | a0001c0001t0002g0237 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.361-2446T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813016 | ||||||
chr7:120813019
|
C | G | 1 | a0001c0001t0010g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.361-2449G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813019 | ||||||
chr7:120813197
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.360+2532A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813197 | ||||||
chr7:120813588
|
A | C | 1 | a0001c0001t0010g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.360+2141T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813588 | ||||||
chr7:120813897
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.360+1832A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120813897 | ||||||
chr7:120814057
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.360+1672C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120814057 | ||||||
chr7:120814433
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.360+1296G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120814433 | ||||||
chr7:120814801
|
T | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 18 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.360+928A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120814801 | ||||||
chr7:120815587
|
A | T | 4 | a0001c0001t0001g0075a0001c0001t0006g0177a0001c0001t0006g0178others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+142T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120815587 | ||||||
chr7:120815695
|
T | C | 1 | a0001c0001t0002g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.360+34A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 5/7 | chr7 | 120815695 | ||||||
chr7:120815824
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.286-21T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120815824 | ||||||
chr7:120816137
|
A | G | 1 | a0001c0001t0005g0103 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.286-334T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816137 | ||||||
chr7:120816209
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286-406T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816209 | ||||||
chr7:120816252
|
A | G | 1 | a0001c0001t0001g0025 | 2 | HG02071.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.286-449T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816252 | ||||||
chr7:120816365
|
C | CA | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(91): Show | 120 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.286-563dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816365 | ||||||
chr7:120816551
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.286-748C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816551 | ||||||
chr7:120816917
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.286-1114G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120816917 | ||||||
chr7:120817127
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-1324C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817127 | ||||||
chr7:120817171
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-1368G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817171 | ||||||
chr7:120817172
|
G | A | 56 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-1369C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817172 | ||||||
chr7:120817236
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0084 | 3 | HG00558.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.286-1433T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817236 | ||||||
chr7:120817403
|
GATT | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(142): Show | 173 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.286-1603_286-1601d others(5): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817403 | ||||||
chr7:120817416
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-1613G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817416 | ||||||
chr7:120817920
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.286-2117G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120817920 | ||||||
chr7:120818016
|
G | A | 1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.286-2213C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818016 | ||||||
chr7:120818218
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG00597.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.286-2415C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818218 | ||||||
chr7:120818269
|
AT | A | 4 | a0001c0001t0001g0075a0001c0001t0006g0177a0001c0001t0006g0178others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2467delA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818269 | ||||||
chr7:120818440
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.286-2637C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818440 | ||||||
chr7:120818671
|
C | T | 1 | a0001c0001t0010g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.286-2868G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818671 | ||||||
chr7:120818924
|
T | C | 37 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(34): Show | 40 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-3121A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120818924 | ||||||
chr7:120819230
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-3427G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819230 | ||||||
chr7:120819376
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286-3573C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819376 | ||||||
chr7:120819439
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286-3636T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819439 | ||||||
chr7:120819477
|
A | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-3674T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819477 | ||||||
chr7:120819650
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-3847G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819650 | ||||||
chr7:120819703
|
T | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-3900A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819703 | ||||||
chr7:120819776
|
C | T | 1 | a0001c0002t0003g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.286-3973G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120819776 | ||||||
chr7:120820018
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0164 | 2 | NA18969.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.286-4215A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820018 | ||||||
chr7:120820062
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.286-4259A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820062 | ||||||
chr7:120820177
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286-4374A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820177 | ||||||
chr7:120820346
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-4543G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820346 | ||||||
chr7:120820407
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-4604G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820407 | ||||||
chr7:120820657
|
C | T | 1 | a0001c0001t0002g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.286-4854G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820657 | ||||||
chr7:120820731
|
G | C | 8 | a0001c0001t0002g0005a0001c0001t0002g0185a0001c0001t0002g0206others(5): Show | 12 | HG01123.hp2 HG01192.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.286-4928C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820731 | ||||||
chr7:120820876
|
C | T | 58 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(55): Show | 72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.286-5073G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820876 | ||||||
chr7:120820939
|
A | G | 37 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(34): Show | 40 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-5136T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820939 | ||||||
chr7:120820976
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.286-5173A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120820976 | ||||||
chr7:120821000
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.286-5197G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821000 | ||||||
chr7:120821382
|
A | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.286-5579T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821382 | ||||||
chr7:120821429
|
T | TA | 38 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(35): Show | 41 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.286-5627dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821429 | ||||||
chr7:120821429
|
TA | T | 10 | a0001c0001t0001g0047a0001c0001t0001g0138a0001c0001t0002g0031others(7): Show | 11 | HG02015.hp1 HG02015.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-5627delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821429 | ||||||
chr7:120821490
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.286-5687C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821490 | ||||||
chr7:120821607
|
G | T | 56 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-5804C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821607 | ||||||
chr7:120821682
|
C | A | 1 | a0001c0001t0010g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.286-5879G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821682 | ||||||
chr7:120821892
|
G | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.286-6089C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120821892 | ||||||
chr7:120822159
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.286-6356G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822159 | ||||||
chr7:120822170
|
T | G | 1 | a0001c0001t0002g0195 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.286-6367A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822170 | ||||||
chr7:120822247
|
T | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-6444A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822247 | ||||||
chr7:120822345
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286-6542T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822345 | ||||||
chr7:120822364
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286-6561T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822364 | ||||||
chr7:120822423
|
T | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-6620A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822423 | ||||||
chr7:120822527
|
CAAAGCAG | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-6731_286-6725d others(9): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822527 | ||||||
chr7:120822587
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.286-6784T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822587 | ||||||
chr7:120822730
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0095others(6): Show | 13 | HG00423.hp2 HG02074.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.286-6927G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822730 | ||||||
chr7:120822901
|
G | A | 56 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-7098C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822901 | ||||||
chr7:120822955
|
G | A | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286-7152C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120822955 | ||||||
chr7:120823235
|
C | T | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-7432G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823235 | ||||||
chr7:120823236
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0010g0078 | 2 | HG03579.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.286-7433A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823236 | ||||||
chr7:120823296
|
GAT | G | 56 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 70 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.286-7495_286-7494d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823296 | ||||||
chr7:120823314
|
T | C | 1 | a0001c0001t0002g0211 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.286-7511A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120823314 | ||||||
chr7:120824000
|
G | A | 2 | a0001c0001t0006g0177a0001c0001t0006g0178 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.286-8197C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824000 | ||||||
chr7:120824012
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286-8209C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824012 | ||||||
chr7:120824112
|
A | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-8309T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824112 | ||||||
chr7:120824133
|
G | C | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.286-8330C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824133 | ||||||
chr7:120824276
|
C | CA | 19 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 24 | HG00597.hp1 HG01975.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.286-8474dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824276 | ||||||
chr7:120824276
|
C | CAA | 37 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0057others(34): Show | 44 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.286-8475_286-8474d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824276 | ||||||
chr7:120824495
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-8692G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824495 | ||||||
chr7:120824515
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.286-8712C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824515 | ||||||
chr7:120824552
|
T | C | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286-8749A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824552 | ||||||
chr7:120824839
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.286-9036G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120824839 | ||||||
chr7:120825043
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286-9240G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825043 | ||||||
chr7:120825090
|
C | T | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.286-9287G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825090 | ||||||
chr7:120825100
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-9297T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825100 | ||||||
chr7:120825262
|
G | C | 2 | a0001c0002t0004g0181a0001c0002t0004g0182 | 2 | HG01978.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286-9459C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825262 | ||||||
chr7:120825276
|
C | T | 2 | a0001c0002t0003g0067a0001c0002t0003g0071 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.286-9473G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825276 | ||||||
chr7:120825505
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-9702A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825505 | ||||||
chr7:120825824
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.286-10021C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825824 | ||||||
chr7:120825903
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.286-10100G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825903 | ||||||
chr7:120825913
|
A | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(143): Show | 174 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.286-10110T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825913 | ||||||
chr7:120825986
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.286-10183A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120825986 | ||||||
chr7:120826005
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(7): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-10202C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826005 | ||||||
chr7:120826171
|
A | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-10368T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826171 | ||||||
chr7:120826426
|
T | C | 58 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(55): Show | 72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.286-10623A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826426 | ||||||
chr7:120826496
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.286-10693A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826496 | ||||||
chr7:120826548
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.286-10745A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826548 | ||||||
chr7:120826924
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.286-11121G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826924 | ||||||
chr7:120826955
|
A | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.286-11152T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826955 | ||||||
chr7:120826992
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.286-11189T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120826992 | ||||||
chr7:120827005
|
G | A | 1 | a0001c0001t0012g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286-11202C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827005 | ||||||
chr7:120827122
|
T | TAATAGCT others(311): Show |
1 | a0001c0001t0001g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.286-11320_286-1131 others(322): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827122 | ||||||
chr7:120827122
|
T | TAATAGCT others(312): Show |
4 | a0001c0001t0001g0043a0001c0001t0001g0091a0001c0001t0001g0092others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-11320_286-1131 others(323): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827122 | ||||||
chr7:120827122
|
T | TAATAGCT others(316): Show |
1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.286-11320_286-1131 others(327): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827122 | ||||||
chr7:120827515
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 19 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+11262G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827515 | ||||||
chr7:120827871
|
C | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+10906G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827871 | ||||||
chr7:120827993
|
G | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 18 | HG00597.hp1 HG01975.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.285+10784C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827993 | ||||||
chr7:120827995
|
A | T | 1 | a0001c0002t0004g0219 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285+10782T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120827995 | ||||||
chr7:120828015
|
A | G | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.285+10762T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828015 | ||||||
chr7:120828158
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+10619T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828158 | ||||||
chr7:120828189
|
T | C | 3 | a0001c0001t0002g0007a0001c0001t0002g0199a0001c0001t0002g0201 | 6 | NA18956.hp2 NA18969.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+10588A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828189 | ||||||
chr7:120828443
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.285+10334G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828443 | ||||||
chr7:120828554
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285+10223G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828554 | ||||||
chr7:120828655
|
C | CT | 65 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0040others(62): Show | 80 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.285+10121dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | ||||||
chr7:120828655
|
C | CTT | 8 | a0001c0001t0001g0090a0001c0001t0002g0190a0001c0001t0002g0204others(5): Show | 8 | HG02074.hp2 HG02486.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+10120_285+1012 others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | ||||||
chr7:120828655
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.285+10122G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | ||||||
chr7:120828655
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0195 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285+10112_285+1012 others(14): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828655 | ||||||
chr7:120828888
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.285+9889T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828888 | ||||||
chr7:120828949
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285+9828A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120828949 | ||||||
chr7:120829220
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+9557C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829220 | ||||||
chr7:120829266
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+9511G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829266 | ||||||
chr7:120829388
|
A | AT | 4 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0129others(1): Show | 8 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+9388dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829388 | ||||||
chr7:120829636
|
T | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.285+9141A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120829636 | ||||||
chr7:120830006
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+8771G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120830006 | ||||||
chr7:120830556
|
A | T | 1 | a0001c0002t0003g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.285+8221T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120830556 | ||||||
chr7:120830698
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.285+8079C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120830698 | ||||||
chr7:120831099
|
T | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+7678A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831099 | ||||||
chr7:120831308
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0077 | 6 | HG02109.hp2 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+7469C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831308 | ||||||
chr7:120831327
|
CAG | C | 6 | a0001c0001t0002g0031a0001c0001t0002g0229a0001c0001t0002g0230others(3): Show | 7 | HG02015.hp2 NA18962.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+7448_285+7449d others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831327 | ||||||
chr7:120831499
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.285+7278T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831499 | ||||||
chr7:120831923
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+6854G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120831923 | ||||||
chr7:120832004
|
CAAAT | C | 36 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(33): Show | 39 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.285+6769_285+6772d others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832004 | ||||||
chr7:120832006
|
A | C | 1 | a0002c0004t0001g0126 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.285+6771T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832006 | ||||||
chr7:120832402
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.285+6375G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832402 | ||||||
chr7:120832504
|
C | T | 1 | a0001c0001t0002g0236 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.285+6273G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832504 | ||||||
chr7:120832590
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+6187C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832590 | ||||||
chr7:120832729
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0013g0179 | 2 | HG02015.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.285+6048C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832729 | ||||||
chr7:120832916
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+5861C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832916 | ||||||
chr7:120832990
|
G | A | 1 | a0001c0002t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+5787C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120832990 | ||||||
chr7:120833296
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.285+5481G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833296 | ||||||
chr7:120833418
|
A | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0075a0001c0001t0001g0086others(5): Show | 12 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+5359T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833418 | ||||||
chr7:120833484
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5293A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833484 | ||||||
chr7:120833537
|
C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0171 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.285+5240G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833537 | ||||||
chr7:120833699
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285+5078A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120833699 | ||||||
chr7:120834000
|
G | C | 125 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(122): Show | 146 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.285+4777C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834000 | ||||||
chr7:120834010
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+4767A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834010 | ||||||
chr7:120834114
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(144): Show | 175 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.285+4663C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834114 | ||||||
chr7:120834128
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.285+4649A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834128 | ||||||
chr7:120834132
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.285+4645C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834132 | ||||||
chr7:120834261
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0127 | 4 | NA18962.hp1 NA18975.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+4516T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834261 | ||||||
chr7:120834388
|
G | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+4389C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834388 | ||||||
chr7:120834481
|
G | T | 2 | a0001c0001t0006g0177a0001c0001t0006g0178 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.285+4296C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834481 | ||||||
chr7:120834520
|
A | G | 36 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(33): Show | 39 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.285+4257T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834520 | ||||||
chr7:120834587
|
T | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+4190A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834587 | ||||||
chr7:120834633
|
C | A | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+4144G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834633 | ||||||
chr7:120834691
|
T | C | 2 | a0001c0001t0002g0215a0001c0001t0002g0218 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.285+4086A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834691 | ||||||
chr7:120834748
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+4029A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834748 | ||||||
chr7:120834955
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.285+3822A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120834955 | ||||||
chr7:120835275
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3502C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835275 | ||||||
chr7:120835432
|
A | T | 1 | a0001c0001t0002g0232 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.285+3345T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835432 | ||||||
chr7:120835468
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+3309T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835468 | ||||||
chr7:120835471
|
T | A | 7 | a0001c0001t0002g0196a0001c0001t0002g0207a0001c0001t0002g0208others(4): Show | 7 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3306A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835471 | ||||||
chr7:120835537
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+3240C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835537 | ||||||
chr7:120835955
|
C | CA | 2 | a0001c0001t0003g0013a0001c0002t0003g0071 | 3 | HG00735.hp1 HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.285+2821dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120835955 | ||||||
chr7:120836091
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0104 | 3 | NA18949.hp1 NA19065.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.285+2686G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836091 | ||||||
chr7:120836102
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0057others(38): Show | 48 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.285+2675G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836102 | ||||||
chr7:120836316
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0091 | 2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.285+2461C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836316 | ||||||
chr7:120836491
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.285+2286T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836491 | ||||||
chr7:120836550
|
T | C | 1 | a0001c0002t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+2227A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836550 | ||||||
chr7:120836553
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.285+2224C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836553 | ||||||
chr7:120836591
|
C | T | 2 | a0001c0001t0006g0177a0001c0001t0006g0178 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.285+2186G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836591 | ||||||
chr7:120836771
|
T | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(95): Show | 118 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.285+2006A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836771 | ||||||
chr7:120836789
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285+1988A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120836789 | ||||||
chr7:120837008
|
G | A | 1 | a0001c0002t0004g0220 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.285+1769C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837008 | ||||||
chr7:120837152
|
G | A | 2 | a0001c0002t0003g0168a0001c0002t0003g0169 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.285+1625C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837152 | ||||||
chr7:120837311
|
A | AT | 4 | a0001c0001t0002g0207a0001c0001t0002g0222a0001c0002t0004g0181others(1): Show | 4 | HG01071.hp2 HG01081.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1465dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837311 | ||||||
chr7:120837315
|
A | AT | 110 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(107): Show | 132 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.285+1461dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837315 | ||||||
chr7:120837315
|
A | T | 5 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0222others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1462T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837315 | ||||||
chr7:120837318
|
T | TA | 18 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 22 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.285+1458_285+1459i others(3): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837318 | ||||||
chr7:120837372
|
C | T | 1 | a0001c0002t0004g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.285+1405G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837372 | ||||||
chr7:120837404
|
C | T | 59 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(56): Show | 73 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.285+1373G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837404 | ||||||
chr7:120837436
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0228 | 2 | HG01255.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.285+1341G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837436 | ||||||
chr7:120837792
|
T | G | 1 | a0001c0003t0002g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285+985A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837792 | ||||||
chr7:120837804
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+973C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837804 | ||||||
chr7:120837876
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.285+901A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837876 | ||||||
chr7:120837982
|
TAA | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+793_285+794del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837982 | ||||||
chr7:120837988
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+789G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120837988 | ||||||
chr7:120838296
|
C | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0158 | 3 | NA18612.hp1 NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.285+481G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120838296 | ||||||
chr7:120838497
|
T | G | 1 | a0001c0002t0008g0060 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.285+280A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120838497 | ||||||
chr7:120838601
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.285+176G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 4/7 | chr7 | 120838601 | ||||||
chr7:120839149
|
T | C | 1 | a0001c0002t0004g0223 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-237A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839149 | ||||||
chr7:120839319
|
T | A | 1 | a0001c0001t0002g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.150-407A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839319 | ||||||
chr7:120839812
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.149+215A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839812 | ||||||
chr7:120839926
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.149+101A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 3/7 | chr7 | 120839926 | ||||||
chr7:120840132
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(15): Show | 22 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-23G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840132 | ||||||
chr7:120840156
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67-47A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840156 | ||||||
chr7:120840202
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.67-93T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840202 | ||||||
chr7:120840221
|
T | C | 2 | a0001c0001t0002g0191a0001c0001t0002g0203 | 2 | HG00642.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.67-112A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840221 | ||||||
chr7:120840420
|
G | A | 19 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(16): Show | 23 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-311C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840420 | ||||||
chr7:120840491
|
C | CA | 19 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(16): Show | 23 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-383dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840491 | ||||||
chr7:120840504
|
A | AG | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 293 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(290): Show |
intron_variant | MODIFIER | c.67-396_67-395insC | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840504 | ||||||
chr7:120840575
|
T | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-466A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840575 | ||||||
chr7:120840633
|
T | C | 32 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0057others(29): Show | 35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-524A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840633 | ||||||
chr7:120840697
|
TACTCA | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG02145.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67-593_67-589delTG others(3): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120840697 | ||||||
chr7:120841077
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.67-968G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841077 | ||||||
chr7:120841103
|
G | A | 3 | a0001c0001t0001g0055a0001c0002t0003g0053a0001c0002t0003g0054 | 3 | HG01243.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.67-994C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841103 | ||||||
chr7:120841194
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.67-1085G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841194 | ||||||
chr7:120841232
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-1123C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841232 | ||||||
chr7:120841281
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.67-1172T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841281 | ||||||
chr7:120841515
|
C | T | 32 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0057others(29): Show | 35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-1406G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841515 | ||||||
chr7:120841633
|
A | ATTAAGC | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0002t0003g0014others(1): Show | 5 | HG01975.hp1 HG02559.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1525_67-1524ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841633 | ||||||
chr7:120841633
|
A | ATTAAGT | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(232): Show | 288 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(285): Show |
intron_variant | MODIFIER | c.67-1525_67-1524ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841633 | ||||||
chr7:120841649
|
T | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0076others(7): Show | 13 | HG00558.hp2 HG02559.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-1540A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841649 | ||||||
chr7:120841723
|
A | C | 1 | a0001c0001t0001g0018 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.67-1614T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841723 | ||||||
chr7:120841764
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-1655G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120841764 | ||||||
chr7:120842033
|
G | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-1924C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842033 | ||||||
chr7:120842053
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.67-1944T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842053 | ||||||
chr7:120842448
|
TA | T | 9 | a0001c0001t0001g0049a0001c0001t0001g0121a0001c0001t0001g0122others(6): Show | 9 | HG00738.hp2 HG01081.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-2340delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842448 | ||||||
chr7:120842448
|
TAA | T | 133 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(130): Show | 156 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.67-2341_67-2340del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842448 | ||||||
chr7:120842448
|
TAAA | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0002g0186others(3): Show | 7 | HG01074.hp2 HG01192.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-2342_67-2340del others(3): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842448 | ||||||
chr7:120842610
|
T | A | 4 | a0001c0001t0001g0075a0001c0001t0006g0177a0001c0001t0006g0178others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-2501A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842610 | ||||||
chr7:120842624
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2515C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842624 | ||||||
chr7:120842831
|
A | G | 1 | a0001c0001t0011g0101 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.67-2722T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842831 | ||||||
chr7:120842881
|
A | T | 2 | a0001c0001t0006g0177a0001c0001t0006g0178 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.67-2772T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842881 | ||||||
chr7:120842904
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-2795G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842904 | ||||||
chr7:120842905
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0104others(1): Show | 6 | HG01975.hp2 NA18949.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-2796C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120842905 | ||||||
chr7:120843041
|
C | T | 64 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(61): Show | 78 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.67-2932G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843041 | ||||||
chr7:120843117
|
A | T | 1 | a0001c0001t0010g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.67-3008T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843117 | ||||||
chr7:120843124
|
G | A | 94 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(91): Show | 112 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.67-3015C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843124 | ||||||
chr7:120843205
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-3096T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843205 | ||||||
chr7:120843282
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-3173A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843282 | ||||||
chr7:120843445
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-3336T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843445 | ||||||
chr7:120843476
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.67-3367C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843476 | ||||||
chr7:120843486
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.67-3377G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843486 | ||||||
chr7:120843667
|
T | A | 94 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(91): Show | 112 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.67-3558A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843667 | ||||||
chr7:120843707
|
G | C | 4 | a0001c0001t0001g0075a0001c0001t0006g0177a0001c0001t0006g0178others(1): Show | 4 | HG03130.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-3598C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843707 | ||||||
chr7:120843804
|
G | A | 5 | a0001c0002t0003g0015a0001c0002t0003g0052a0001c0002t0003g0063others(2): Show | 6 | HG01496.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-3695C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843804 | ||||||
chr7:120843843
|
A | G | 58 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(55): Show | 72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.67-3734T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843843 | ||||||
chr7:120843855
|
G | A | 1 | a0001c0002t0003g0014 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.67-3746C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843855 | ||||||
chr7:120843999
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.67-3890G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120843999 | ||||||
chr7:120844028
|
C | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG00597.hp2 NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.67-3919G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844028 | ||||||
chr7:120844336
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.67-4227G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844336 | ||||||
chr7:120844343
|
C | T | 1 | a0001c0002t0003g0089 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.67-4234G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844343 | ||||||
chr7:120844418
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-4309C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844418 | ||||||
chr7:120844565
|
T | G | 1 | a0001c0002t0004g0223 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.67-4456A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844565 | ||||||
chr7:120844628
|
C | T | 6 | a0001c0001t0002g0031a0001c0001t0002g0229a0001c0001t0002g0230others(3): Show | 7 | HG02015.hp2 NA18962.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-4519G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844628 | ||||||
chr7:120844629
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.67-4520C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120844629 | ||||||
chr7:120845241
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.67-5132C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845241 | ||||||
chr7:120845373
|
C | T | 32 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0057others(29): Show | 35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-5264G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845373 | ||||||
chr7:120845497
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-5388T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845497 | ||||||
chr7:120845711
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67-5602C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845711 | ||||||
chr7:120845768
|
G | C | 1 | a0001c0001t0002g0225 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.67-5659C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845768 | ||||||
chr7:120845826
|
T | C | 1 | a0001c0001t0009g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67-5717A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845826 | ||||||
chr7:120845936
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-5827A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120845936 | ||||||
chr7:120846006
|
A | C | 1 | a0001c0001t0006g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.67-5897T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846006 | ||||||
chr7:120846112
|
G | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.67-6003C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846112 | ||||||
chr7:120846114
|
G | C | 9 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-6005C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846114 | ||||||
chr7:120846459
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.67-6350A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846459 | ||||||
chr7:120846516
|
CA | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-6408delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846516 | ||||||
chr7:120846695
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67-6586G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846695 | ||||||
chr7:120846743
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(145): Show | 176 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.67-6634A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846743 | ||||||
chr7:120846843
|
G | A | 1 | a0001c0002t0004g0180 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.67-6734C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120846843 | ||||||
chr7:120847131
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0104 | 5 | NA18949.hp1 NA18971.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-7022G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847131 | ||||||
chr7:120847233
|
C | CA | 12 | a0001c0001t0001g0084a0001c0001t0001g0165a0001c0001t0001g0166others(9): Show | 14 | HG00621.hp2 HG01981.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-7125dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847233 | ||||||
chr7:120847233
|
C | CAA | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-7126_67-7125dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847233 | ||||||
chr7:120847233
|
CA | C | 40 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0055others(37): Show | 43 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.67-7125delT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847233 | ||||||
chr7:120847244
|
A | C | 6 | a0001c0001t0005g0022a0001c0001t0005g0103a0001c0001t0005g0109others(3): Show | 7 | HG00558.hp1 NA18954.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-7135T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847244 | ||||||
chr7:120847246
|
AAC | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0171others(1): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-7139_67-7138del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847246 | ||||||
chr7:120847247
|
AC | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0036others(22): Show | 31 | HG00558.hp2 HG00642.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.67-7139delG | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847247 | ||||||
chr7:120847248
|
C | A | 75 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0028others(72): Show | 89 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.67-7139G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847248 | ||||||
chr7:120847530
|
T | C | 1 | a0001c0003t0002g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-7421A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847530 | ||||||
chr7:120847808
|
T | C | 65 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(62): Show | 79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.67-7699A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847808 | ||||||
chr7:120847875
|
C | T | 1 | a0001c0002t0008g0060 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67-7766G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847875 | ||||||
chr7:120847966
|
G | A | 1 | a0001c0002t0003g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.67-7857C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120847966 | ||||||
chr7:120848015
|
C | T | 1 | a0001c0001t0002g0230 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.67-7906G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848015 | ||||||
chr7:120848027
|
C | T | 2 | a0001c0003t0002g0188a0001c0003t0002g0189 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.67-7918G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848027 | ||||||
chr7:120848169
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67-8060A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848169 | ||||||
chr7:120848196
|
C | G | 1 | a0003c0005t0001g0116 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67-8087G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848196 | ||||||
chr7:120848297
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.67-8188T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848297 | ||||||
chr7:120848506
|
TG | T | 4 | a0001c0002t0003g0015a0001c0002t0003g0052a0001c0002t0003g0063others(1): Show | 5 | HG01496.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+8191delC | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848506 | ||||||
chr7:120848550
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.66+8148T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848550 | ||||||
chr7:120848580
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.66+8118T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848580 | ||||||
chr7:120848715
|
A | C | 1 | a0001c0002t0003g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+7983T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848715 | ||||||
chr7:120848723
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.66+7975C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848723 | ||||||
chr7:120848787
|
T | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | HG02559.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+7911A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848787 | ||||||
chr7:120848857
|
A | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+7841T>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120848857 | ||||||
chr7:120849082
|
G | A | 1 | a0001c0002t0003g0074 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.66+7616C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849082 | ||||||
chr7:120849385
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+7313C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849385 | ||||||
chr7:120849409
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.66+7289A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849409 | ||||||
chr7:120849601
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.66+7097T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849601 | ||||||
chr7:120849657
|
C | T | 32 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0057others(29): Show | 35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.66+7041G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849657 | ||||||
chr7:120849950
|
C | T | 1 | a0001c0002t0003g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+6748G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120849950 | ||||||
chr7:120850009
|
TGA | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0099a0001c0001t0001g0110others(3): Show | 7 | HG00621.hp1 HG02083.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+6687_66+6688del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850009 | ||||||
chr7:120850464
|
C | T | 1 | a0001c0001t0005g0109 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.66+6234G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850464 | ||||||
chr7:120850549
|
T | C | 2 | a0001c0001t0002g0227a0001c0001t0002g0233 | 2 | HG02074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.66+6149A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850549 | ||||||
chr7:120850753
|
G | A | 65 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(62): Show | 79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.66+5945C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850753 | ||||||
chr7:120850874
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.66+5824C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850874 | ||||||
chr7:120850979
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.66+5719G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850979 | ||||||
chr7:120850985
|
C | T | 1 | a0001c0001t0012g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+5713G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120850985 | ||||||
chr7:120851060
|
T | C | 65 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(62): Show | 79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.66+5638A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851060 | ||||||
chr7:120851232
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.66+5466C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851232 | ||||||
chr7:120851398
|
G | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0045others(4): Show | 9 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+5300C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851398 | ||||||
chr7:120851570
|
A | G | 1 | a0001c0002t0003g0063 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.66+5128T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851570 | ||||||
chr7:120851905
|
T | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0028others(14): Show | 20 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+4793A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851905 | ||||||
chr7:120851928
|
T | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(147): Show | 178 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.66+4770A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120851928 | ||||||
chr7:120852020
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.66+4678C>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852020 | ||||||
chr7:120852023
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.66+4675C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852023 | ||||||
chr7:120852069
|
T | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+4629A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852069 | ||||||
chr7:120852191
|
T | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0036others(13): Show | 19 | HG00558.hp2 HG01433.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.66+4507A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852191 | ||||||
chr7:120852452
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0108 | 3 | HG02572.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.66+4246G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852452 | ||||||
chr7:120852516
|
A | T | 1 | a0001c0002t0004g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.66+4182T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852516 | ||||||
chr7:120852517
|
T | C | 1 | a0001c0002t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.66+4181A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852517 | ||||||
chr7:120852610
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+4088C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852610 | ||||||
chr7:120852644
|
T | C | 4 | a0001c0002t0003g0061a0001c0002t0003g0062a0001c0002t0004g0180others(1): Show | 4 | HG01934.hp2 HG02071.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+4054A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852644 | ||||||
chr7:120852728
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+3970A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852728 | ||||||
chr7:120852837
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.66+3861C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852837 | ||||||
chr7:120852855
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+3843T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852855 | ||||||
chr7:120852998
|
C | T | 2 | a0001c0001t0002g0031a0001c0001t0002g0229 | 3 | NA18962.hp2 NA19081.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.66+3700G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120852998 | ||||||
chr7:120853007
|
C | A | 1 | a0001c0001t0002g0228 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.66+3691G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853007 | ||||||
chr7:120853090
|
A | AT | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(114): Show | 140 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.66+3607dupA | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853090 | ||||||
chr7:120853090
|
A | ATT | 33 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0055others(30): Show | 37 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.66+3606_66+3607dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853090 | ||||||
chr7:120853217
|
C | T | 1 | a0001c0001t0005g0103 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.66+3481G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853217 | ||||||
chr7:120853242
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0091 | 2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.66+3456G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853242 | ||||||
chr7:120853316
|
T | A | 97 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 117 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.66+3382A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853316 | ||||||
chr7:120853362
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 9 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+3336G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853362 | ||||||
chr7:120853371
|
T | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.66+3327A>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853371 | ||||||
chr7:120853449
|
C | A | 1 | a0001c0001t0005g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.66+3249G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853449 | ||||||
chr7:120853471
|
G | GAT | 15 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 21 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+3225_66+3226dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
G | GATAGAT | 2 | a0001c0002t0003g0015a0001c0002t0003g0066 | 3 | HG01496.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.66+3226_66+3227ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
G | GATAT | 4 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0174others(1): Show | 4 | HG02886.hp1 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3223_66+3226dup others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
G | GATATAT | 12 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0040others(9): Show | 13 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+3221_66+3226dup others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
G | GATATATA others(1): Show |
14 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0055others(11): Show | 15 | HG01243.hp1 HG01934.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+3219_66+3226dup others(8): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
G | GATATATA others(3): Show |
1 | a0001c0001t0003g0013 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.66+3217_66+3226dup others(10): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
G | GATATATA others(5): Show |
1 | a0001c0002t0003g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.66+3215_66+3226dup others(12): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853471
|
GAT | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0163a0001c0001t0001g0171others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3225_66+3226del others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853471 | ||||||
chr7:120853493
|
T | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 26 | HG00558.hp2 HG01074.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.66+3205A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | ||||||
chr7:120853493
|
T | TAC | 5 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG02818.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+3203_66+3204dup others(2): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | ||||||
chr7:120853493
|
T | TACAC | 7 | a0001c0001t0002g0031a0001c0001t0002g0229a0001c0001t0002g0230others(4): Show | 8 | HG02015.hp2 NA18962.hp2 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+3201_66+3204dup others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | ||||||
chr7:120853493
|
T | TATAC | 57 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(54): Show | 72 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+3204_66+3205ins others(4): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | ||||||
chr7:120853493
|
T | TATATAC | 17 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0193others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.66+3204_66+3205ins others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853493 | ||||||
chr7:120853505
|
T | C | 3 | a0001c0001t0001g0166a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | NA18977.hp2 NA18989.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.66+3193A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853505 | ||||||
chr7:120853533
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.66+3165A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853533 | ||||||
chr7:120853572
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.66+3126G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853572 | ||||||
chr7:120853769
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.66+2929C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853769 | ||||||
chr7:120853862
|
G | A | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0238 | 3 | NA18971.hp1 NA19063.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.66+2836C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853862 | ||||||
chr7:120853872
|
C | CA | 61 | a0001c0001t0001g0034a0001c0001t0001g0166a0001c0001t0002g0004others(58): Show | 75 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.66+2825dupT | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853872 | ||||||
chr7:120853884
|
A | G | 32 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0057others(29): Show | 35 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.66+2814T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120853884 | ||||||
chr7:120854189
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.66+2509A>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120854189 | ||||||
chr7:120854357
|
C | A | 89 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(86): Show | 107 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.66+2341G>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120854357 | ||||||
chr7:120854805
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.66+1893T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120854805 | ||||||
chr7:120855006
|
A | G | 1 | a0001c0001t0009g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.66+1692T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855006 | ||||||
chr7:120855363
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.66+1335C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855363 | ||||||
chr7:120855523
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(147): Show | 178 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.66+1175C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855523 | ||||||
chr7:120855771
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.66+927T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855771 | ||||||
chr7:120855891
|
A | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0044others(5): Show | 10 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+807T>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855891 | ||||||
chr7:120855967
|
T | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 8 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+731A>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120855967 | ||||||
chr7:120856330
|
A | G | 9 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+368T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120856330 | ||||||
chr7:120856612
|
AGCCATGC others(6): Show |
A | 1 | a0001c0001t0002g0240 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.66+73_66+85delCAAA others(9): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120856612 | ||||||
chr7:120856626
|
G | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0091others(4): Show | 7 | HG01070.hp1 HG02647.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+72C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 2/7 | chr7 | 120856626 | ||||||
chr7:120856917
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 10 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-84G>A | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120856917 | ||||||
chr7:120857219
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-70-386T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857219 | ||||||
chr7:120857371
|
C | CGGGGCG | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG02145.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71+443_-71+448dup others(6): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857371 | ||||||
chr7:120857396
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(147): Show | 178 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.-71+424T>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857396 | ||||||
chr7:120857397
|
G | A | 63 | a0001c0001t0001g0166a0001c0001t0002g0004a0001c0001t0002g0005others(60): Show | 77 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-71+423C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857397 | ||||||
chr7:120857397
|
G | GGGCGGGG others(5): Show |
1 | a0001c0001t0002g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-71+422_-71+423ins others(12): Show |
TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857397 | ||||||
chr7:120857513
|
G | A | 3 | a0001c0001t0001g0167a0001c0002t0003g0168a0001c0002t0003g0169 | 3 | HG02970.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-71+307C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857513 | ||||||
chr7:120857586
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02630.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71+234C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857586 | ||||||
chr7:120857588
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-71+232G>C | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857588 | ||||||
chr7:120857592
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-71+228C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857592 | ||||||
chr7:120857652
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0174 | 3 | HG02486.hp2 HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-71+168C>G | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857652 | ||||||
chr7:120857707
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-71+113C>T | TSPAN12 | ENSG00000106025.9 | transcript | ENST00000222747.8 | protein_coding | 1/7 | chr7 | 120857707 |