geneid | 8027 |
---|---|
ensemblid | ENSG00000136738.15 |
hgncid | 11357 |
symbol | STAM |
name | signal transducing adaptor molecule |
refseq_nuc | NM_003473.4 |
refseq_prot | NP_003464.1 |
ensembl_nuc | ENST00000377524.8 |
ensembl_prot | ENSP00000366746.3 |
mane_status | MANE Select |
chr | chr10 |
start | 17644151 |
end | 17716824 |
strand | + |
ver | v1.2 |
region | chr10:17644151-17716824 |
region5000 | chr10:17639151-17721824 |
regionname0 | STAM_chr10_17644151_17716824 |
regionname5000 | STAM_chr10_17639151_17721824 |
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 | 540 | 422 | 92 | 80 | 197 | 16 | 35 | 161 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0002 | 0/0 | 540 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0003 | 0/0 | 540 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0004 | 0/0 | 540 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1623 | 330 | 81 | 69 | 140 | 13 | 25 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0002 | 0/0 | 1623 | 82 | 9 | 11 | 51 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0003 | 0/0 | 1623 | 4 | 0 | 0 | 4 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0004 | 0/0 | 1623 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0005 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0006 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0007 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0008 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0009 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0010 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0011 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
c0012 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
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 | 0/0 | 2234 | 127 | 23 | 13 | 77 | 3 | 11 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0002 | 1/0 | 2234 | 121 | 11 | 31 | 62 | 5 | 11 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0003 | 0/0 | 2236 | 75 | 9 | 10 | 45 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0004 | 0/0 | 2236 | 34 | 24 | 5 | 1 | 2 | 2 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0005 | 0/1 | 2237 | 20 | 1 | 12 | 4 | 2 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0006 | 0/0 | 2236 | 5 | 5 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0007 | 0/0 | 2234 | 5 | 0 | 1 | 0 | 1 | 3 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0008 | 0/0 | 2235 | 3 | 0 | 1 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0009 | 0/0 | 2237 | 3 | 1 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0010 | 0/0 | 2234 | 3 | 2 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0011 | 0/0 | 2236 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0012 | 0/0 | 2236 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0013 | 0/0 | 2236 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0014 | 0/0 | 2234 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0015 | 0/0 | 2234 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0016 | 0/0 | 2234 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0017 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0018 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0019 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0020 | 0/0 | 2236 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0021 | 0/0 | 2236 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0022 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0023 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0024 | 0/0 | 2234 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0025 | 0/0 | 2234 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0026 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0027 | 0/0 | 2234 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0028 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0029 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0030 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0031 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
t0032 | 0/0 | 2234 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
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 | 5 | 0 | 2 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0002 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1623 | 330 | 81 | 69 | 140 | 13 | 25 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002 | 0/0 | 1623 | 82 | 9 | 11 | 51 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0003 | 0/0 | 1623 | 4 | 0 | 0 | 4 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0005 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0006 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0008 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0009 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0010 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0012 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0002c0004 | 0/0 | 1623 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0003c0007 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0004c0011 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3856 | 116 | 23 | 13 | 69 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0002 | 1/0 | 3856 | 120 | 11 | 31 | 61 | 5 | 11 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0003 | 0/0 | 3858 | 7 | 7 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0004 | 0/0 | 3858 | 28 | 18 | 5 | 1 | 2 | 2 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0005 | 0/1 | 3859 | 20 | 1 | 12 | 4 | 2 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0006 | 0/0 | 3858 | 5 | 5 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0007 | 0/0 | 3856 | 5 | 0 | 1 | 0 | 1 | 3 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0008 | 0/0 | 3857 | 3 | 0 | 1 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0009 | 0/0 | 3859 | 3 | 1 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0010 | 0/0 | 3856 | 3 | 2 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0012 | 0/0 | 3858 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0014 | 0/0 | 3856 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0015 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0016 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0017 | 0/0 | 3857 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0018 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0019 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0023 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0024 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0025 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0026 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0027 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0029 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0030 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0031 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0001t0032 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0003 | 0/0 | 3858 | 68 | 2 | 10 | 45 | 3 | 8 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0004 | 0/0 | 3858 | 6 | 6 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0011 | 0/0 | 3858 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0013 | 0/0 | 3858 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0020 | 0/0 | 3858 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0021 | 0/0 | 3858 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0002t0022 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0003t0001 | 0/0 | 3856 | 4 | 0 | 0 | 4 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0005t0001 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0006t0028 | 0/0 | 3858 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0008t0001 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0009t0015 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0010t0001 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0001c0012t0002 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0002c0004t0001 | 0/0 | 3856 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0003c0007t0001 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
a0004c0011t0001 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | copy fasta | chr10 | 17639151 | 17721824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0002g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0004g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0008g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0009g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0009g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0009g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0010g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0012g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0014g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0015g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0016g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0017g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0017g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0019g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0023g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0024g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0025g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0026g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0027g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0029g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0030g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0031g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0001t0032g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0003g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0011g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0011g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0013g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0020g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0021g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0002t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0006t0028g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0008t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0009t0015g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0010t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0001c0012t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0002c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0002c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0003c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
a0004c0011t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0168 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0239 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0044 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0353 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0054 | EUR | FIN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0049 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0348 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00735 | hp1 | a0001 | c0001 | t0032 | g0225 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0352 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01074 | hp1 | a0001 | c0002 | t0021 | g0172 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0169 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01168 | hp1 | a0001 | c0001 | t0024 | g0295 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0159 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01192 | hp1 | a0001 | c0001 | t0010 | g0109 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0035 | AMR | PUR | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01346 | hp1 | a0001 | c0001 | t0014 | g0140 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01358 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0165 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01361 | hp2 | a0001 | c0001 | t0025 | g0223 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0160 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01433 | hp2 | a0001 | c0001 | t0014 | g0131 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0163 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0177 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0175 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0309 | EUR | IBS | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0389 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0162 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0357 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02055 | hp1 | a0001 | c0009 | t0015 | g0388 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0173 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02132 | hp2 | a0001 | c0010 | t0001 | g0004 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0337 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02155 | hp1 | a0001 | c0002 | t0003 | g0323 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0322 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CDX | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02258 | hp1 | a0001 | c0001 | t0017 | g0380 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0381 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0373 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0257 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02615 | hp1 | a0001 | c0002 | t0004 | g0335 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02717 | hp2 | a0001 | c0001 | t0031 | g0384 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0171 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0013 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0350 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0326 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0383 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02970 | hp1 | a0001 | c0001 | t0023 | g0187 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0164 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0390 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03209 | hp1 | a0001 | c0001 | t0029 | g0379 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0333 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03239 | hp2 | a0001 | c0008 | t0001 | g0374 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03486 | hp1 | a0001 | c0002 | t0022 | g0183 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03540 | hp2 | a0001 | c0001 | t0019 | g0110 | AFR | GWD | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03579 | hp1 | a0001 | c0006 | t0028 | g0382 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0031 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03669 | hp2 | a0001 | c0002 | t0003 | g0349 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0343 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0361 | SAS | PJL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0367 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0256 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0344 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03942 | hp2 | a0003 | c0007 | t0001 | g0099 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0216 | SAS | BEB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0170 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0080 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0212 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | CHB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | CHB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0386 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18940 | hp1 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18941 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0319 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18949 | hp2 | a0001 | c0002 | t0003 | g0329 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0318 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18954 | hp2 | a0001 | c0002 | t0003 | g0391 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18956 | hp2 | a0001 | c0002 | t0003 | g0330 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18957 | hp1 | a0001 | c0002 | t0020 | g0376 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18959 | hp1 | a0001 | c0001 | t0009 | g0311 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0331 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18963 | hp2 | a0001 | c0002 | t0011 | g0247 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18965 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18967 | hp1 | a0001 | c0002 | t0003 | g0377 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0378 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0328 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18977 | hp2 | a0001 | c0012 | t0002 | g0281 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18978 | hp2 | a0002 | c0004 | t0001 | g0112 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18979 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18981 | hp1 | a0001 | c0002 | t0003 | g0334 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0325 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18985 | hp2 | a0001 | c0001 | t0009 | g0312 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18988 | hp1 | a0001 | c0002 | t0003 | g0346 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0324 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19000 | hp1 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19001 | hp1 | a0001 | c0002 | t0003 | g0314 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19002 | hp1 | a0002 | c0004 | t0001 | g0114 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19003 | hp2 | a0004 | c0011 | t0001 | g0057 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19009 | hp1 | a0001 | c0002 | t0013 | g0332 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0205 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19058 | hp1 | a0001 | c0002 | t0011 | g0354 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19058 | hp2 | a0001 | c0001 | t0026 | g0018 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19062 | hp2 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19063 | hp1 | a0001 | c0002 | t0013 | g0022 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0320 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19068 | hp2 | a0001 | c0002 | t0003 | g0342 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19070 | hp1 | a0001 | c0002 | t0011 | g0355 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19072 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0347 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19076 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19078 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0351 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19087 | hp1 | a0001 | c0002 | t0003 | g0375 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19091 | hp1 | a0001 | c0002 | t0003 | g0327 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | YRI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0166 | AFR | ASW | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0028 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0241 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20905 | hp1 | a0001 | c0001 | t0027 | g0113 | SAS | GIH | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0147 | SAS | GIH | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0050 | AMR | CLM | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02109 | hp2 | a0001 | c0001 | t0016 | g0013 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02559 | hp1 | a0001 | c0002 | t0004 | g0336 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0387 | AFR | ACB | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0182 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0372 | AFR | USA | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
NA21309 | hp2 | a0001 | c0001 | t0030 | g0385 | AFR | LWK | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0047 | REF | REF | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0233 | REF | REF | STAM_chr10_17639151_17721824 | STAM | chr10 | 17639151 | 17721824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:17688135
|
A | C | 1 | a0004 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.406A>C | p.Lys136Gln | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/14 | 595/3856 | 406/1623 | 136/540 | chr10 | 17688135 | ||
chr10:17696848
|
C | A | 1 | a0003 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.802C>A | p.Leu268Ile | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/14 | 991/3856 | 802/1623 | 268/540 | chr10 | 17696848 | ||
chr10:17700271
|
A | T | 1 | a0002 | 2 | NA18978.hp2 NA19002.hp1 |
missense_variant | MODERATE | c.904A>T | p.Ile302Phe | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/14 | 1093/3856 | 904/1623 | 302/540 | chr10 | 17700271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:17660546
|
T | C | 1 | a0001c0005 | 1 | HG04228.hp1 | splice_region_variant&synonymous_variant | LOW | c.123T>C | p.Thr41Thr | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/14 | 312/3856 | 123/1623 | 41/540 | chr10 | 17660546 | ||
chr10:17684855
|
C | T | 1 | a0001c0012 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.225C>T | p.Asn75Asn | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/14 | 414/3856 | 225/1623 | 75/540 | chr10 | 17684855 | ||
chr10:17688140
|
A | G | 1 | a0001c0003 | 4 | NA18966.hp1 NA18983.hp2 NA19070.hp2 others(1): Show |
synonymous_variant | LOW | c.411A>G | p.Glu137Glu | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/14 | 600/3856 | 411/1623 | 137/540 | chr10 | 17688140 | ||
chr10:17688164
|
T | C | 1 | a0001c0006 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.435T>C | p.Ile145Ile | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/14 | 624/3856 | 435/1623 | 145/540 | chr10 | 17688164 | ||
chr10:17695134
|
C | T | 1 | a0001c0010 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.621C>T | p.Asn207Asn | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/14 | 810/3856 | 621/1623 | 207/540 | chr10 | 17695134 | ||
chr10:17695209
|
A | G | 1 | a0001c0009 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.696A>G | p.Lys232Lys | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/14 | 885/3856 | 696/1623 | 232/540 | chr10 | 17695209 | ||
chr10:17714597
|
T | C | 1 | a0001c0002 | 82 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(79): Show |
synonymous_variant | LOW | c.1440T>C | p.Tyr480Tyr | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1629/3856 | 1440/1623 | 480/540 | chr10 | 17714597 | ||
chr10:17714775
|
C | T | 1 | a0001c0008 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1618C>T | p.Leu540Leu | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1807/3856 | 1618/1623 | 540/540 | chr10 | 17714775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:17644183
|
C | T | 1 | a0001c0001t0032 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/14 | 157 | chr10 | 17644183 | |||||
chr10:17644235
|
G | A | 2 | a0001c0001t0005a0001c0001t0008 | 23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-105G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/14 | 105 | chr10 | 17644235 | |||||
chr10:17644335
|
C | T | 7 | a0001c0001t0005a0001c0001t0008a0001c0001t0017others(4): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/14 | 5 | chr10 | 17644335 | |||||
chr10:17714830
|
T | C | 1 | a0001c0001t0018 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 50 | chr10 | 17714830 | |||||
chr10:17714959
|
T | TCC | 2 | a0001c0001t0005a0001c0001t0009 | 23 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*186_*187dupCC | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 188 | INFO_REALIGN_3_PRIME | chr10 | 17714959 | ||||
chr10:17714967
|
C | T | 1 | a0001c0001t0027 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 187 | chr10 | 17714967 | |||||
chr10:17714976
|
A | T | 1 | a0001c0001t0007 | 5 | HG00280.hp1 HG00642.hp1 HG02602.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 196 | chr10 | 17714976 | |||||
chr10:17715079
|
C | A | 1 | a0001c0006t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 299 | chr10 | 17715079 | |||||
chr10:17715197
|
G | A | 2 | a0001c0001t0010a0001c0001t0019 | 4 | HG01192.hp1 HG02572.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*417G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 417 | chr10 | 17715197 | |||||
chr10:17715297
|
G | A | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(1): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*517G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 517 | chr10 | 17715297 | |||||
chr10:17715384
|
A | AAG | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | 127 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*608_*609dupGA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 610 | INFO_REALIGN_3_PRIME | chr10 | 17715384 | ||||
chr10:17715411
|
A | G | 1 | a0001c0002t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 631 | chr10 | 17715411 | |||||
chr10:17715474
|
G | A | 1 | a0001c0002t0020 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*694G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 694 | chr10 | 17715474 | |||||
chr10:17715491
|
T | G | 1 | a0001c0001t0014 | 2 | HG01346.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*711T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 711 | chr10 | 17715491 | |||||
chr10:17715502
|
A | AT | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(1): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*723dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 724 | INFO_REALIGN_3_PRIME | chr10 | 17715502 | ||||
chr10:17715734
|
A | C | 1 | a0001c0001t0026 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*954A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 954 | chr10 | 17715734 | |||||
chr10:17715770
|
G | A | 1 | a0001c0001t0019 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 990 | chr10 | 17715770 | |||||
chr10:17715813
|
G | A | 1 | a0001c0001t0019 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1033G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1033 | chr10 | 17715813 | |||||
chr10:17715863
|
T | C | 5 | a0001c0001t0004a0001c0001t0006a0001c0001t0018others(2): Show | 41 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1083T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1083 | chr10 | 17715863 | |||||
chr10:17715961
|
C | A | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(31): Show | 292 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*1181C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1181 | chr10 | 17715961 | |||||
chr10:17715968
|
T | G | 1 | a0001c0001t0006 | 5 | HG02615.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1188 | chr10 | 17715968 | |||||
chr10:17716014
|
T | C | 1 | a0001c0001t0024 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1234 | chr10 | 17716014 | |||||
chr10:17716109
|
C | T | 1 | a0001c0002t0021 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1329 | chr10 | 17716109 | |||||
chr10:17716220
|
A | C | 1 | a0001c0001t0016 | 2 | HG02109.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1440A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1440 | chr10 | 17716220 | |||||
chr10:17716255
|
C | G | 1 | a0001c0001t0031 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1475C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1475 | chr10 | 17716255 | |||||
chr10:17716282
|
G | T | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1502 | chr10 | 17716282 | |||||
chr10:17716417
|
C | T | 1 | a0001c0002t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1637 | chr10 | 17716417 | |||||
chr10:17716489
|
T | G | 2 | a0001c0001t0012a0001c0001t0023 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1709T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1709 | chr10 | 17716489 | |||||
chr10:17716497
|
A | G | 1 | a0001c0002t0013 | 2 | NA19009.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1717A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1717 | chr10 | 17716497 | |||||
chr10:17716521
|
T | C | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(1): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1741T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1741 | chr10 | 17716521 | |||||
chr10:17716525
|
G | A | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(1): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1745G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1745 | chr10 | 17716525 | |||||
chr10:17716548
|
A | G | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(1): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1768A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1768 | chr10 | 17716548 | |||||
chr10:17716612
|
C | G | 2 | a0001c0001t0012a0001c0001t0023 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1832 | chr10 | 17716612 | |||||
chr10:17716623
|
T | C | 1 | a0001c0002t0022 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1843T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1843 | chr10 | 17716623 | |||||
chr10:17716740
|
C | A | 2 | a0001c0001t0015a0001c0009t0015 | 2 | HG01884.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1960C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 14/14 | 1960 | chr10 | 17716740 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:17644392
|
G | C | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+13G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644392 | ||||||
chr10:17644430
|
C | G | 1 | a0001c0002t0003g0391 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.40+51C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644430 | ||||||
chr10:17644450
|
A | C | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.40+71A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644450 | ||||||
chr10:17644665
|
G | A | 1 | a0001c0002t0003g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.40+286G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644665 | ||||||
chr10:17644946
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+567C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17644946 | ||||||
chr10:17645072
|
C | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+693C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645072 | ||||||
chr10:17645101
|
A | G | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.40+722A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645101 | ||||||
chr10:17645128
|
T | A | 30 | a0001c0001t0001g0030a0001c0001t0002g0033a0001c0001t0002g0036others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.40+749T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645128 | ||||||
chr10:17645149
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+770G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645149 | ||||||
chr10:17645219
|
A | G | 1 | a0001c0001t0004g0387 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40+840A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645219 | ||||||
chr10:17645554
|
T | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(103): Show | 114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.40+1175T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645554 | ||||||
chr10:17645776
|
G | A | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(58): Show | 68 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.40+1397G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645776 | ||||||
chr10:17645862
|
GCTT | G | 3 | a0001c0001t0010g0109a0001c0001t0010g0111a0001c0001t0019g0110 | 3 | HG01192.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.40+1487_40+1489del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17645862 | |||||
chr10:17645960
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.40+1581A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17645960 | ||||||
chr10:17646071
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.40+1692T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646071 | ||||||
chr10:17646110
|
C | T | 1 | a0001c0001t0012g0386 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.40+1731C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646110 | ||||||
chr10:17646279
|
T | C | 1 | a0001c0002t0003g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.40+1900T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646279 | ||||||
chr10:17646376
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+1997A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646376 | ||||||
chr10:17646490
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.40+2111A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646490 | ||||||
chr10:17646511
|
A | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+2132A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646511 | ||||||
chr10:17646607
|
G | A | 8 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(5): Show | 8 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+2228G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646607 | ||||||
chr10:17646759
|
A | T | 1 | a0001c0001t0010g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.40+2380A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17646759 | ||||||
chr10:17647117
|
C | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+2738C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647117 | ||||||
chr10:17647118
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.40+2739G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647118 | ||||||
chr10:17647167
|
A | G | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.40+2788A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647167 | ||||||
chr10:17647302
|
T | G | 16 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+2923T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647302 | ||||||
chr10:17647389
|
A | G | 20 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0362others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.40+3010A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647389 | ||||||
chr10:17647423
|
A | C | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.40+3044A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647423 | ||||||
chr10:17647462
|
A | G | 16 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+3083A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647462 | ||||||
chr10:17647578
|
T | G | 20 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0362others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.40+3199T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647578 | ||||||
chr10:17647612
|
T | C | 11 | a0001c0001t0002g0390a0001c0001t0004g0016a0001c0001t0004g0174others(8): Show | 12 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.40+3233T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647612 | ||||||
chr10:17647652
|
G | A | 2 | a0001c0001t0012g0182a0001c0001t0012g0386 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.40+3273G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647652 | ||||||
chr10:17647821
|
C | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 16 | HG02132.hp2 NA18940.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+3442C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647821 | ||||||
chr10:17647822
|
G | A | 9 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+3443G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647822 | ||||||
chr10:17647829
|
G | C | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.40+3450G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647829 | ||||||
chr10:17647854
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108 | 5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+3475C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17647854 | ||||||
chr10:17648012
|
AGAC | A | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+3637_40+3639del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17648012 | |||||
chr10:17648052
|
A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0357 | 3 | HG01256.hp2 HG01258.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.40+3673A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648052 | ||||||
chr10:17648239
|
C | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+3860C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648239 | ||||||
chr10:17648350
|
A | G | 1 | a0001c0001t0002g0356 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.40+3971A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648350 | ||||||
chr10:17648405
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40+4026G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648405 | ||||||
chr10:17648462
|
C | T | 51 | a0001c0001t0002g0316a0001c0002t0003g0007a0001c0002t0003g0008others(48): Show | 56 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.40+4083C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648462 | ||||||
chr10:17648558
|
A | G | 3 | a0001c0001t0002g0310a0001c0001t0009g0311a0001c0001t0009g0312 | 3 | NA18954.hp1 NA18959.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.40+4179A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648558 | ||||||
chr10:17648582
|
G | A | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.40+4203G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648582 | ||||||
chr10:17648587
|
C | CTAGACGC others(50): Show |
1 | a0001c0001t0002g0309 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.40+4208_40+4209ins others(57): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648587 | ||||||
chr10:17648588
|
G | A | 2 | a0001c0001t0002g0309a0001c0009t0015g0388 | 2 | HG01517.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+4209G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648588 | ||||||
chr10:17648670
|
C | G | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+4291C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648670 | ||||||
chr10:17648683
|
T | C | 285 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(282): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.40+4304T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648683 | ||||||
chr10:17648842
|
A | G | 8 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(5): Show | 8 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+4463A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648842 | ||||||
chr10:17648963
|
A | G | 1 | a0001c0003t0001g0151 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.40+4584A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648963 | ||||||
chr10:17648980
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.40+4601T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17648980 | ||||||
chr10:17649141
|
C | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+4762C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649141 | ||||||
chr10:17649393
|
TA | T | 240 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(237): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.40+5030delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17649393 | |||||
chr10:17649427
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.40+5048T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649427 | ||||||
chr10:17649502
|
T | G | 11 | a0001c0001t0002g0390a0001c0001t0004g0016a0001c0001t0004g0174others(8): Show | 12 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.40+5123T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649502 | ||||||
chr10:17649523
|
A | G | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+5144A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649523 | ||||||
chr10:17649636
|
G | A | 261 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(258): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.40+5257G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649636 | ||||||
chr10:17649673
|
G | C | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.40+5294G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649673 | ||||||
chr10:17649715
|
G | A | 1 | a0001c0001t0001g0011 | 2 | NA18947.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.40+5336G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649715 | ||||||
chr10:17649904
|
G | A | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.40+5525G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649904 | ||||||
chr10:17649944
|
C | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+5565C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17649944 | ||||||
chr10:17650168
|
G | A | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.40+5789G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650168 | ||||||
chr10:17650189
|
A | G | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+5810A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650189 | ||||||
chr10:17650311
|
C | A | 261 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(258): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.40+5932C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650311 | ||||||
chr10:17650451
|
A | G | 102 | a0001c0001t0001g0158a0001c0001t0002g0390a0001c0001t0003g0024others(99): Show | 106 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.40+6072A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650451 | ||||||
chr10:17650453
|
T | G | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+6074T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650453 | ||||||
chr10:17650472
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.40+6093G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650472 | ||||||
chr10:17650505
|
A | G | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.40+6126A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650505 | ||||||
chr10:17650527
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.40+6148C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650527 | ||||||
chr10:17650544
|
T | C | 1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.40+6165T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650544 | ||||||
chr10:17650606
|
C | T | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+6227C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650606 | ||||||
chr10:17650607
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+6228G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650607 | ||||||
chr10:17650699
|
C | G | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+6320C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650699 | ||||||
chr10:17650759
|
C | T | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+6380C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650759 | ||||||
chr10:17650866
|
C | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+6487C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650866 | ||||||
chr10:17650867
|
C | G | 1 | a0001c0001t0002g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.40+6488C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650867 | ||||||
chr10:17650917
|
T | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(102): Show | 113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.40+6538T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650917 | ||||||
chr10:17650924
|
G | A | 2 | a0001c0001t0004g0032a0001c0001t0004g0055 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.40+6545G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650924 | ||||||
chr10:17650925
|
C | T | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+6546C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650925 | ||||||
chr10:17650926
|
G | A | 1 | a0001c0002t0003g0375 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.40+6547G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650926 | ||||||
chr10:17650958
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+6579A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650958 | ||||||
chr10:17650982
|
G | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.40+6603G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17650982 | ||||||
chr10:17651035
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+6656A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651035 | ||||||
chr10:17651060
|
G | A | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+6681G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651060 | ||||||
chr10:17651060
|
G | C | 1 | a0001c0001t0004g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40+6681G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651060 | ||||||
chr10:17651064
|
C | CA | 24 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0119others(21): Show | 24 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+6712dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | |||||
chr10:17651064
|
CA | C | 87 | a0001c0001t0001g0030a0001c0001t0001g0058a0001c0001t0001g0070others(84): Show | 89 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.40+6712delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | |||||
chr10:17651064
|
CAA | C | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(126): Show | 140 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.40+6711_40+6712del others(2): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | |||||
chr10:17651064
|
CAAA | C | 11 | a0001c0001t0001g0029a0001c0001t0004g0215a0001c0001t0005g0054others(8): Show | 11 | HG00323.hp2 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+6710_40+6712del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17651064 | |||||
chr10:17651536
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+7157A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651536 | ||||||
chr10:17651563
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+7184T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651563 | ||||||
chr10:17651581
|
A | G | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+7202A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651581 | ||||||
chr10:17651625
|
G | A | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40+7246G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651625 | ||||||
chr10:17651649
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.40+7270C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651649 | ||||||
chr10:17651804
|
T | C | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.40+7425T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651804 | ||||||
chr10:17651873
|
C | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+7494C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651873 | ||||||
chr10:17651913
|
G | C | 255 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(252): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.40+7534G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651913 | ||||||
chr10:17651974
|
A | G | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40+7595A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17651974 | ||||||
chr10:17652041
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.40+7662A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652041 | ||||||
chr10:17652042
|
A | G | 2 | a0002c0004t0001g0112a0002c0004t0001g0114 | 2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.40+7663A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652042 | ||||||
chr10:17652098
|
A | G | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+7719A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652098 | ||||||
chr10:17652247
|
TA | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0359a0001c0001t0001g0362others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+7878delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17652247 | |||||
chr10:17652286
|
T | C | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+7907T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652286 | ||||||
chr10:17652313
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.40+7934A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652313 | ||||||
chr10:17652336
|
C | T | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG02027.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.40+7957C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652336 | ||||||
chr10:17652450
|
A | G | 31 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0174others(28): Show | 33 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-8014A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652450 | ||||||
chr10:17652508
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-7956T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652508 | ||||||
chr10:17652551
|
C | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-7913C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652551 | ||||||
chr10:17652596
|
T | C | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.41-7868T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652596 | ||||||
chr10:17652606
|
G | A | 255 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(252): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.41-7858G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652606 | ||||||
chr10:17652654
|
C | T | 1 | a0001c0002t0003g0349 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41-7810C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652654 | ||||||
chr10:17652757
|
T | C | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41-7707T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652757 | ||||||
chr10:17652865
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.41-7599T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652865 | ||||||
chr10:17652957
|
C | G | 7 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0358others(4): Show | 7 | HG01192.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-7507C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652957 | ||||||
chr10:17652997
|
T | C | 1 | a0001c0002t0003g0315 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.41-7467T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17652997 | ||||||
chr10:17653185
|
A | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-7279A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653185 | ||||||
chr10:17653284
|
C | T | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.41-7180C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653284 | ||||||
chr10:17653324
|
T | A | 1 | a0001c0001t0002g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.41-7140T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653324 | ||||||
chr10:17653337
|
T | G | 1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41-7127T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653337 | ||||||
chr10:17653355
|
A | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-7109A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653355 | ||||||
chr10:17653395
|
A | T | 18 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.41-7069A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653395 | ||||||
chr10:17653471
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-6993T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653471 | ||||||
chr10:17653524
|
C | T | 7 | a0001c0001t0004g0175a0001c0001t0004g0176a0001c0001t0004g0177others(4): Show | 7 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-6940C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653524 | ||||||
chr10:17653587
|
C | A | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0033others(7): Show | 10 | HG00099.hp1 HG02109.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.41-6877C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653587 | ||||||
chr10:17653618
|
T | G | 1 | a0001c0001t0004g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.41-6846T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653618 | ||||||
chr10:17653718
|
G | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-6746G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653718 | ||||||
chr10:17653773
|
A | G | 35 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0001t0001g0116others(32): Show | 36 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.41-6691A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653773 | ||||||
chr10:17653789
|
G | A | 1 | a0001c0001t0004g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.41-6675G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653789 | ||||||
chr10:17653938
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-6526A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17653938 | ||||||
chr10:17654025
|
C | T | 1 | a0001c0002t0003g0375 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.41-6439C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654025 | ||||||
chr10:17654074
|
G | T | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-6390G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654074 | ||||||
chr10:17654105
|
G | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-6359G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654105 | ||||||
chr10:17654214
|
G | GTTA | 74 | a0001c0001t0002g0231a0001c0001t0002g0316a0001c0002t0003g0007others(71): Show | 79 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.41-6229_41-6227dup others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17654214 | |||||
chr10:17654226
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-6238A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654226 | ||||||
chr10:17654228
|
T | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-6236T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654228 | ||||||
chr10:17654229
|
A | G | 1 | a0001c0001t0004g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.41-6235A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654229 | ||||||
chr10:17654246
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0124 | 2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.41-6218G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654246 | ||||||
chr10:17654284
|
A | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-6180A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654284 | ||||||
chr10:17654285
|
T | C | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-6179T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654285 | ||||||
chr10:17654324
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0002g0232 | 2 | HG01071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.41-6140G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654324 | ||||||
chr10:17654359
|
A | T | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.41-6105A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654359 | ||||||
chr10:17654367
|
C | T | 2 | a0001c0003t0001g0122a0001c0003t0001g0123 | 2 | NA18966.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.41-6097C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654367 | ||||||
chr10:17654373
|
C | T | 2 | a0001c0001t0005g0053a0001c0001t0005g0054 | 2 | HG00323.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.41-6091C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654373 | ||||||
chr10:17654513
|
C | T | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-5951C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654513 | ||||||
chr10:17654517
|
C | T | 6 | a0001c0001t0004g0204a0001c0001t0004g0211a0001c0001t0004g0213others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-5947C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654517 | ||||||
chr10:17654587
|
T | A | 4 | a0001c0002t0003g0320a0001c0002t0003g0321a0001c0002t0003g0322others(1): Show | 4 | HG02155.hp1 HG02165.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-5877T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654587 | ||||||
chr10:17654702
|
G | A | 4 | a0001c0001t0009g0383a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-5762G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654702 | ||||||
chr10:17654709
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.41-5755T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654709 | ||||||
chr10:17654725
|
A | G | 2 | a0001c0001t0002g0298a0001c0001t0002g0299 | 2 | NA18968.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.41-5739A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654725 | ||||||
chr10:17654758
|
T | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-5706T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654758 | ||||||
chr10:17654793
|
G | A | 14 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-5671G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654793 | ||||||
chr10:17654795
|
C | G | 14 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-5669C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654795 | ||||||
chr10:17654834
|
G | A | 100 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(97): Show | 104 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.41-5630G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17654834 | ||||||
chr10:17655023
|
T | A | 2 | a0001c0001t0004g0032a0001c0001t0004g0055 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.41-5441T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655023 | ||||||
chr10:17655052
|
A | G | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-5412A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655052 | ||||||
chr10:17655201
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.41-5263T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655201 | ||||||
chr10:17655324
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-5140T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655324 | ||||||
chr10:17655342
|
T | C | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.41-5122T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655342 | ||||||
chr10:17655346
|
A | T | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-5118A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655346 | ||||||
chr10:17655348
|
G | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-5116G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655348 | ||||||
chr10:17655358
|
G | C | 1 | a0001c0001t0002g0361 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.41-5106G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655358 | ||||||
chr10:17655440
|
T | C | 1 | a0001c0001t0001g0367 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-5024T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655440 | ||||||
chr10:17655487
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.41-4977C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655487 | ||||||
chr10:17655488
|
G | A | 102 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(99): Show | 106 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.41-4976G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655488 | ||||||
chr10:17655516
|
C | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-4948C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655516 | ||||||
chr10:17655526
|
T | C | 2 | a0001c0003t0001g0118a0001c0003t0001g0151 | 2 | NA19070.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.41-4938T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655526 | ||||||
chr10:17655534
|
A | G | 6 | a0001c0001t0004g0017a0001c0001t0004g0197a0001c0001t0004g0198others(3): Show | 7 | HG00642.hp2 HG02976.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-4930A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655534 | ||||||
chr10:17655603
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.41-4861G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655603 | ||||||
chr10:17655644
|
T | G | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41-4820T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655644 | ||||||
chr10:17655707
|
A | C | 9 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG02145.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-4757A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655707 | ||||||
chr10:17655880
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.41-4584C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655880 | ||||||
chr10:17655938
|
C | T | 1 | a0001c0008t0001g0374 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41-4526C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17655938 | ||||||
chr10:17655942
|
CGT | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-4517_41-4516del others(2): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17655942 | |||||
chr10:17656074
|
C | T | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-4390C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656074 | ||||||
chr10:17656111
|
A | G | 394 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(391): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.41-4353A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656111 | ||||||
chr10:17656245
|
G | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-4219G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656245 | ||||||
chr10:17656280
|
C | T | 53 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0028others(50): Show | 55 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.41-4184C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656280 | ||||||
chr10:17656288
|
C | T | 4 | a0001c0001t0009g0383a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4176C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656288 | ||||||
chr10:17656292
|
T | TC | 4 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-4172_41-4171ins others(1): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656292 | ||||||
chr10:17656293
|
T | A | 4 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-4171T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656293 | ||||||
chr10:17656293
|
T | C | 26 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(23): Show | 29 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.41-4171T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656293 | ||||||
chr10:17656293
|
T | TA | 15 | a0001c0001t0001g0106a0001c0001t0002g0298a0001c0001t0004g0016others(12): Show | 16 | HG01243.hp2 HG01255.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.41-4150dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17656293 | |||||
chr10:17656293
|
TA | T | 92 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0115others(89): Show | 95 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.41-4150delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17656293 | |||||
chr10:17656294
|
A | C | 2 | a0001c0001t0005g0052a0001c0001t0005g0054 | 2 | HG00323.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.41-4170A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656294 | ||||||
chr10:17656495
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.41-3969T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656495 | ||||||
chr10:17656515
|
C | G | 4 | a0001c0002t0003g0320a0001c0002t0003g0321a0001c0002t0003g0322others(1): Show | 4 | HG02155.hp1 HG02165.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3949C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656515 | ||||||
chr10:17656529
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.41-3935C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656529 | ||||||
chr10:17656563
|
C | T | 3 | a0001c0001t0001g0029a0001c0006t0028g0382a0001c0009t0015g0388 | 3 | HG02055.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.41-3901C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656563 | ||||||
chr10:17656564
|
G | A | 1 | a0001c0001t0012g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.41-3900G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656564 | ||||||
chr10:17656567
|
A | T | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-3897A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656567 | ||||||
chr10:17656614
|
C | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(102): Show | 113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.41-3850C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656614 | ||||||
chr10:17656738
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0104 | 3 | NA18944.hp1 NA18963.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.41-3726C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656738 | ||||||
chr10:17656857
|
C | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-3607C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656857 | ||||||
chr10:17656879
|
T | C | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.41-3585T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656879 | ||||||
chr10:17656966
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0003g0155a0001c0001t0003g0156others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3498C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17656966 | ||||||
chr10:17657044
|
A | G | 4 | a0001c0001t0001g0358a0001c0001t0012g0182a0001c0001t0012g0386others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3420A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657044 | ||||||
chr10:17657049
|
A | G | 4 | a0001c0001t0001g0358a0001c0001t0012g0182a0001c0001t0012g0386others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3415A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657049 | ||||||
chr10:17657056
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-3408T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657056 | ||||||
chr10:17657144
|
C | G | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-3320C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657144 | ||||||
chr10:17657196
|
T | A | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(266): Show | 287 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.41-3268T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657196 | ||||||
chr10:17657223
|
G | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-3241G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657223 | ||||||
chr10:17657239
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.41-3225C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657239 | ||||||
chr10:17657343
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41-3121C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657343 | ||||||
chr10:17657399
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-3065T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657399 | ||||||
chr10:17657471
|
G | T | 2 | a0001c0002t0003g0322a0001c0002t0003g0323 | 2 | HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.41-2993G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657471 | ||||||
chr10:17657593
|
T | G | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-2871T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657593 | ||||||
chr10:17657608
|
A | G | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.41-2856A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657608 | ||||||
chr10:17657660
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.41-2804A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657660 | ||||||
chr10:17657685
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0070 | 2 | HG01975.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.41-2779A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657685 | ||||||
chr10:17657704
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0104 | 3 | NA18944.hp1 NA18963.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.41-2760G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657704 | ||||||
chr10:17657841
|
T | TTCTC | 3 | a0001c0001t0015g0389a0001c0006t0028g0382a0001c0009t0015g0388 | 3 | HG01884.hp2 HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.41-2617_41-2614dup others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17657841 | |||||
chr10:17657849
|
C | CTCTCT | 29 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(26): Show | 32 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.41-2614_41-2613ins others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17657849 | |||||
chr10:17657890
|
C | T | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2574C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657890 | ||||||
chr10:17657903
|
C | A | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.41-2561C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17657903 | ||||||
chr10:17658197
|
GT | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-2257delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17658197 | |||||
chr10:17658231
|
T | G | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-2233T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658231 | ||||||
chr10:17658246
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.41-2218G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658246 | ||||||
chr10:17658302
|
A | G | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.41-2162A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658302 | ||||||
chr10:17658308
|
T | G | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41-2156T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658308 | ||||||
chr10:17658432
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-2032A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658432 | ||||||
chr10:17658446
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0002g0150 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.41-2018A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658446 | ||||||
chr10:17658527
|
TC | T | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-1936delC | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658527 | ||||||
chr10:17658536
|
G | A | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.41-1928G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658536 | ||||||
chr10:17658539
|
C | G | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-1925C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658539 | ||||||
chr10:17658573
|
C | T | 1 | a0001c0002t0021g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.41-1891C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658573 | ||||||
chr10:17658738
|
C | G | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.41-1726C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658738 | ||||||
chr10:17658738
|
C | T | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.41-1726C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658738 | ||||||
chr10:17658809
|
T | G | 1 | a0001c0001t0005g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.41-1655T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658809 | ||||||
chr10:17658853
|
A | T | 2 | a0001c0001t0001g0152a0001c0001t0002g0150 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.41-1611A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658853 | ||||||
chr10:17658859
|
G | A | 31 | a0001c0001t0001g0029a0001c0001t0002g0236a0001c0001t0005g0003others(28): Show | 34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-1605G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658859 | ||||||
chr10:17658925
|
A | C | 1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41-1539A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658925 | ||||||
chr10:17658926
|
T | A | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.41-1538T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658926 | ||||||
chr10:17658965
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-1499A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17658965 | ||||||
chr10:17659115
|
C | CT | 112 | a0001c0001t0001g0158a0001c0001t0002g0316a0001c0001t0003g0024others(109): Show | 119 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.41-1339dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659115 | |||||
chr10:17659117
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.41-1347T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659117 | ||||||
chr10:17659265
|
G | A | 31 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(28): Show | 34 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.41-1199G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659265 | ||||||
chr10:17659374
|
C | T | 1 | a0001c0001t0030g0385 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41-1090C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659374 | ||||||
chr10:17659463
|
C | CT | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(182): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.41-979dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659463 | |||||
chr10:17659463
|
C | CTTTTT | 20 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(17): Show | 23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.41-983_41-979dupTT others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659463 | |||||
chr10:17659463
|
CT | C | 14 | a0001c0001t0002g0230a0001c0001t0002g0237a0001c0001t0002g0238others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-979delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17659463 | |||||
chr10:17659560
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.41-904T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659560 | ||||||
chr10:17659595
|
G | A | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-869G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659595 | ||||||
chr10:17659614
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-850G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659614 | ||||||
chr10:17659631
|
G | A | 2 | a0001c0001t0004g0032a0001c0001t0004g0055 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.41-833G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659631 | ||||||
chr10:17659768
|
T | G | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41-696T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659768 | ||||||
chr10:17659948
|
C | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-516C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17659948 | ||||||
chr10:17660032
|
T | G | 1 | a0001c0001t0004g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.41-432T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660032 | ||||||
chr10:17660049
|
C | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.41-415C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660049 | ||||||
chr10:17660049
|
C | CA | 24 | a0001c0001t0001g0119a0001c0001t0001g0367a0001c0001t0001g0369others(21): Show | 27 | HG02071.hp2 HG02074.hp1 HG02698.hp2 others(24): Show |
intron_variant | MODIFIER | c.41-405dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17660049 | |||||
chr10:17660049
|
C | CAA | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-406_41-405dupAA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 17660049 | |||||
chr10:17660095
|
T | C | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.41-369T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660095 | ||||||
chr10:17660119
|
T | C | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.41-345T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660119 | ||||||
chr10:17660123
|
A | G | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41-341A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660123 | ||||||
chr10:17660154
|
A | G | 16 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.41-310A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660154 | ||||||
chr10:17660264
|
T | C | 30 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.41-200T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660264 | ||||||
chr10:17660337
|
A | C | 1 | a0001c0001t0006g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.41-127A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 1/13 | chr10 | 17660337 | ||||||
chr10:17660599
|
C | T | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125+51C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660599 | ||||||
chr10:17660617
|
G | A | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+69G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660617 | ||||||
chr10:17660641
|
C | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(103): Show | 114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.125+93C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660641 | ||||||
chr10:17660658
|
G | A | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125+110G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17660658 | ||||||
chr10:17661293
|
G | T | 1 | a0001c0001t0002g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.125+745G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661293 | ||||||
chr10:17661480
|
A | C | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+932A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661480 | ||||||
chr10:17661488
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0041a0001c0001t0005g0042others(8): Show | 13 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.125+940G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661488 | ||||||
chr10:17661501
|
G | T | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(254): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.125+953G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661501 | ||||||
chr10:17661556
|
C | T | 1 | a0001c0002t0013g0332 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.125+1008C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661556 | ||||||
chr10:17661586
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.125+1038A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661586 | ||||||
chr10:17661613
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+1065T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661613 | ||||||
chr10:17661629
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+1081T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661629 | ||||||
chr10:17661695
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+1147T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661695 | ||||||
chr10:17661711
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.125+1163A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661711 | ||||||
chr10:17661742
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+1194A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661742 | ||||||
chr10:17661784
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+1236T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661784 | ||||||
chr10:17661872
|
C | T | 2 | a0001c0002t0003g0322a0001c0002t0003g0323 | 2 | HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.125+1324C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661872 | ||||||
chr10:17661908
|
T | TC | 271 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(268): Show | 289 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.125+1363dupC | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17661908 | |||||
chr10:17661972
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.125+1424T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661972 | ||||||
chr10:17661995
|
C | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(103): Show | 114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.125+1447C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17661995 | ||||||
chr10:17662063
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.125+1515G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662063 | ||||||
chr10:17662256
|
G | A | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+1708G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662256 | ||||||
chr10:17662373
|
A | G | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+1825A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662373 | ||||||
chr10:17662446
|
C | T | 1 | a0001c0002t0003g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.125+1898C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662446 | ||||||
chr10:17662543
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.125+1995G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662543 | ||||||
chr10:17662544
|
A | G | 1 | a0001c0001t0001g0366 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125+1996A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662544 | ||||||
chr10:17662634
|
A | T | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(256): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.125+2086A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662634 | ||||||
chr10:17662889
|
C | T | 4 | a0001c0001t0009g0383a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+2341C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662889 | ||||||
chr10:17662902
|
C | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+2354C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662902 | ||||||
chr10:17662966
|
C | G | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.125+2418C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17662966 | ||||||
chr10:17663025
|
C | T | 1 | a0001c0001t0001g0360 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.125+2477C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663025 | ||||||
chr10:17663195
|
T | C | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+2647T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663195 | ||||||
chr10:17663214
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125+2666G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663214 | ||||||
chr10:17663288
|
A | T | 1 | a0001c0005t0001g0080 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125+2740A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663288 | ||||||
chr10:17663288
|
AT | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+2746delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17663288 | |||||
chr10:17663334
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.125+2786A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663334 | ||||||
chr10:17663340
|
A | T | 1 | a0001c0002t0003g0348 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.125+2792A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663340 | ||||||
chr10:17663453
|
G | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+2905G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663453 | ||||||
chr10:17663508
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | NA18970.hp1 NA18991.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.125+2960T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663508 | ||||||
chr10:17663653
|
A | G | 4 | a0001c0001t0002g0033a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG02109.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+3105A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663653 | ||||||
chr10:17663898
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+3350A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663898 | ||||||
chr10:17663909
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+3361A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663909 | ||||||
chr10:17663921
|
C | A | 32 | a0001c0001t0001g0029a0001c0001t0005g0003a0001c0001t0005g0009others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.125+3373C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663921 | ||||||
chr10:17663949
|
G | T | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+3401G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17663949 | ||||||
chr10:17664009
|
A | G | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+3461A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664009 | ||||||
chr10:17664081
|
AAT | A | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+3535_125+3536d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17664081 | |||||
chr10:17664114
|
G | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(212): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.125+3566G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664114 | ||||||
chr10:17664137
|
C | T | 41 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0154others(38): Show | 43 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.125+3589C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664137 | ||||||
chr10:17664147
|
C | T | 73 | a0001c0001t0001g0158a0001c0001t0003g0024a0001c0001t0003g0025others(70): Show | 76 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.125+3599C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664147 | ||||||
chr10:17664167
|
A | G | 34 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(31): Show | 34 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.125+3619A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664167 | ||||||
chr10:17664341
|
T | C | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+3793T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664341 | ||||||
chr10:17664354
|
G | A | 1 | a0001c0002t0004g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.125+3806G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664354 | ||||||
chr10:17664377
|
C | T | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+3829C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664377 | ||||||
chr10:17664387
|
A | C | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.125+3839A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664387 | ||||||
chr10:17664461
|
C | T | 40 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(37): Show | 44 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+3913C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664461 | ||||||
chr10:17664594
|
G | C | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+4046G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664594 | ||||||
chr10:17664684
|
T | C | 6 | a0001c0001t0004g0204a0001c0001t0004g0211a0001c0001t0004g0213others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+4136T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664684 | ||||||
chr10:17664772
|
C | A | 1 | a0001c0001t0005g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.125+4224C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664772 | ||||||
chr10:17664799
|
A | G | 7 | a0001c0001t0001g0286a0001c0001t0002g0038a0001c0001t0002g0227others(4): Show | 7 | NA18943.hp2 NA18947.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+4251A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664799 | ||||||
chr10:17664840
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0027 | 2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.125+4292G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664840 | ||||||
chr10:17664843
|
C | T | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125+4295C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664843 | ||||||
chr10:17664992
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0088 | 2 | HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.125+4444T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17664992 | ||||||
chr10:17665005
|
T | G | 1 | a0001c0001t0005g0053 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.125+4457T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665005 | ||||||
chr10:17665100
|
C | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(100): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.125+4552C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665100 | ||||||
chr10:17665102
|
A | G | 2 | a0001c0001t0004g0017a0001c0001t0004g0201 | 3 | HG02976.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125+4554A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665102 | ||||||
chr10:17665150
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.125+4602T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665150 | ||||||
chr10:17665153
|
CAGT | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(101): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.125+4606_125+4608d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665153 | ||||||
chr10:17665226
|
T | C | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+4678T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665226 | ||||||
chr10:17665424
|
A | G | 2 | a0001c0002t0003g0170a0001c0002t0003g0171 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.125+4876A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665424 | ||||||
chr10:17665465
|
T | A | 1 | a0001c0002t0003g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.125+4917T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665465 | ||||||
chr10:17665554
|
T | A | 1 | a0001c0002t0003g0334 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.125+5006T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665554 | ||||||
chr10:17665669
|
C | T | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.125+5121C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665669 | ||||||
chr10:17665766
|
G | A | 2 | a0001c0001t0004g0032a0001c0001t0004g0055 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.125+5218G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665766 | ||||||
chr10:17665872
|
C | T | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+5324C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665872 | ||||||
chr10:17665950
|
T | C | 1 | a0001c0002t0004g0335 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125+5402T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665950 | ||||||
chr10:17665983
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.125+5435A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665983 | ||||||
chr10:17665994
|
C | A | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.125+5446C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17665994 | ||||||
chr10:17666385
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0017g0381 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+5838_125+5839i others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666385 | |||||
chr10:17666387
|
A | AT | 141 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(138): Show | 151 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.125+5864dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666387
|
A | ATT | 59 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0001t0001g0060others(56): Show | 60 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.125+5863_125+5864d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666387
|
A | ATTT | 10 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG00438.hp1 HG01346.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+5862_125+5864d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666387
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0017g0380a0001c0001t0029g0379 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.125+5853_125+5864d others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666387
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+5851_125+5864d others(16): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666387
|
A | T | 1 | a0001c0001t0017g0381 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+5839A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666387 | ||||||
chr10:17666387
|
AT | A | 10 | a0001c0001t0002g0018a0001c0001t0002g0237a0001c0001t0002g0245others(7): Show | 10 | NA18948.hp2 NA18963.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+5864delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666387
|
ATTTTTTT others(4): Show |
A | 24 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0005g0003others(21): Show | 27 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.125+5854_125+5864d others(13): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17666387 | |||||
chr10:17666443
|
G | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(91): Show | 100 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.125+5895G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666443 | ||||||
chr10:17666479
|
C | G | 34 | a0001c0001t0001g0158a0001c0001t0003g0155a0001c0001t0003g0156others(31): Show | 37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.125+5931C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666479 | ||||||
chr10:17666507
|
G | A | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+5959G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666507 | ||||||
chr10:17666519
|
T | C | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+5971T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666519 | ||||||
chr10:17666551
|
T | C | 1 | a0001c0001t0008g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.125+6003T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666551 | ||||||
chr10:17666587
|
C | T | 4 | a0001c0001t0004g0055a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+6039C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666587 | ||||||
chr10:17666598
|
C | T | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0002t0003g0170 | 3 | HG02258.hp1 HG02280.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.125+6050C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666598 | ||||||
chr10:17666662
|
G | A | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+6114G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666662 | ||||||
chr10:17666677
|
A | G | 2 | a0001c0002t0003g0170a0001c0002t0003g0171 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.125+6129A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666677 | ||||||
chr10:17666729
|
C | G | 1 | a0001c0002t0003g0334 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.125+6181C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666729 | ||||||
chr10:17666837
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.125+6289A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17666837 | ||||||
chr10:17667103
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0304 | 2 | NA18961.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.125+6555G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667103 | ||||||
chr10:17667112
|
C | T | 14 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+6564C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667112 | ||||||
chr10:17667128
|
A | AT | 145 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0185others(142): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.125+6595dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17667128 | |||||
chr10:17667128
|
ATT | A | 248 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(245): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.125+6594_125+6595d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17667128 | |||||
chr10:17667158
|
C | G | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.125+6610C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667158 | ||||||
chr10:17667163
|
G | A | 14 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+6615G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667163 | ||||||
chr10:17667229
|
C | T | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.125+6681C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667229 | ||||||
chr10:17667312
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.125+6764A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667312 | ||||||
chr10:17667383
|
A | T | 1 | a0001c0002t0003g0334 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.125+6835A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667383 | ||||||
chr10:17667402
|
G | A | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.125+6854G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667402 | ||||||
chr10:17667560
|
A | G | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+7012A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667560 | ||||||
chr10:17667580
|
A | C | 1 | a0001c0001t0010g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.125+7032A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667580 | ||||||
chr10:17667624
|
A | G | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+7076A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667624 | ||||||
chr10:17667677
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+7129A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667677 | ||||||
chr10:17667757
|
T | G | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+7209T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667757 | ||||||
chr10:17667915
|
GA | G | 8 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(5): Show | 8 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+7369delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17667915 | |||||
chr10:17667928
|
G | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+7380G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667928 | ||||||
chr10:17667965
|
T | C | 18 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.125+7417T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17667965 | ||||||
chr10:17668061
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+7513T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668061 | ||||||
chr10:17668089
|
A | G | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+7541A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668089 | ||||||
chr10:17668115
|
T | A | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.125+7567T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668115 | ||||||
chr10:17668178
|
T | A | 1 | a0001c0001t0002g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.125+7630T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668178 | ||||||
chr10:17668275
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(96): Show | 107 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.125+7727G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668275 | ||||||
chr10:17668488
|
C | T | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+7940C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668488 | ||||||
chr10:17668640
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+8092C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668640 | ||||||
chr10:17668906
|
A | C | 18 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.125+8358A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17668906 | ||||||
chr10:17669051
|
A | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0058others(48): Show | 53 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.125+8503A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669051 | ||||||
chr10:17669216
|
C | T | 2 | a0001c0001t0006g0203a0001c0001t0006g0209 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.125+8668C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669216 | ||||||
chr10:17669340
|
G | T | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+8792G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669340 | ||||||
chr10:17669354
|
G | GT | 11 | a0001c0001t0002g0228a0001c0001t0002g0230a0001c0001t0002g0248others(8): Show | 11 | HG01175.hp1 HG01243.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.125+8821dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669354 | |||||
chr10:17669412
|
A | C | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+8864A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669412 | ||||||
chr10:17669438
|
G | A | 261 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(258): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.125+8890G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669438 | ||||||
chr10:17669622
|
G | A | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+9074G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669622 | ||||||
chr10:17669732
|
C | T | 3 | a0001c0002t0003g0345a0001c0002t0003g0346a0001c0002t0003g0347 | 3 | NA18988.hp1 NA19010.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.125+9184C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669732 | ||||||
chr10:17669774
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.125+9226C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669774 | ||||||
chr10:17669783
|
C | T | 10 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+9235C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669783 | ||||||
chr10:17669801
|
C | T | 1 | a0001c0001t0005g0042 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.125+9253C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669801 | ||||||
chr10:17669811
|
C | T | 2 | a0001c0001t0009g0311a0001c0001t0009g0312 | 2 | NA18959.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.125+9263C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669811 | ||||||
chr10:17669825
|
G | A | 3 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0252 | 3 | HG01981.hp1 HG02300.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.125+9277G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669825 | ||||||
chr10:17669848
|
C | T | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.125+9300C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669848 | ||||||
chr10:17669884
|
C | CT | 66 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 73 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(70): Show |
intron_variant | MODIFIER | c.125+9355dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | |||||
chr10:17669884
|
C | CTT | 57 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0058others(54): Show | 59 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.125+9354_125+9355d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | |||||
chr10:17669884
|
C | CTTTT | 21 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(18): Show | 24 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+9352_125+9355d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | |||||
chr10:17669884
|
CT | C | 48 | a0001c0001t0001g0368a0001c0001t0001g0372a0001c0001t0001g0373others(45): Show | 50 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.125+9355delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17669884 | |||||
chr10:17669921
|
G | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+9373G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669921 | ||||||
chr10:17669951
|
C | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.125+9403C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669951 | ||||||
chr10:17669985
|
C | T | 8 | a0001c0001t0002g0023a0001c0001t0002g0273a0001c0001t0002g0274others(5): Show | 9 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.125+9437C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17669985 | ||||||
chr10:17670171
|
A | G | 10 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+9623A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670171 | ||||||
chr10:17670191
|
C | T | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.125+9643C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670191 | ||||||
chr10:17670232
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+9684T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670232 | ||||||
chr10:17670250
|
A | T | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+9702A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670250 | ||||||
chr10:17670298
|
G | A | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+9750G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670298 | ||||||
chr10:17670298
|
G | T | 2 | a0001c0002t0003g0325a0001c0002t0003g0331 | 2 | NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.125+9750G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670298 | ||||||
chr10:17670453
|
A | C | 43 | a0001c0001t0001g0029a0001c0002t0003g0008a0001c0002t0003g0022others(40): Show | 45 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+9905A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670453 | ||||||
chr10:17670735
|
T | C | 1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+10187T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670735 | ||||||
chr10:17670744
|
A | G | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+10196A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670744 | ||||||
chr10:17670758
|
T | TTATC | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+10213_125+1021 others(8): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670758 | |||||
chr10:17670782
|
T | TAAGAAAC others(798): Show |
1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.125+10240_125+1024 others(809): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAC others(801): Show |
1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+10240_125+1024 others(812): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(800): Show |
1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+10245_125+1024 others(811): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(799): Show |
1 | a0001c0001t0030g0385 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(800): Show |
1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+10245_125+1024 others(811): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(799): Show |
7 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0044others(4): Show | 7 | HG00280.hp2 HG01081.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(801): Show |
1 | a0001c0001t0008g0039 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.125+10245_125+1024 others(812): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(800): Show |
15 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0040others(12): Show | 16 | HG00323.hp2 HG00609.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.125+10245_125+1024 others(811): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(799): Show |
1 | a0001c0001t0005g0003 | 3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670782
|
T | TAAGAAAT others(799): Show |
1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125+10245_125+1024 others(810): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17670782 | |||||
chr10:17670809
|
C | A | 16 | a0001c0001t0001g0362a0001c0001t0001g0363a0001c0001t0001g0364others(13): Show | 16 | HG01106.hp2 HG02071.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.125+10261C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670809 | ||||||
chr10:17670853
|
T | G | 8 | a0001c0001t0002g0018a0001c0001t0002g0219a0001c0001t0002g0237others(5): Show | 8 | NA18948.hp2 NA18965.hp1 NA19001.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+10305T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17670853 | ||||||
chr10:17671014
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.125+10466T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671014 | ||||||
chr10:17671102
|
A | G | 6 | a0001c0001t0004g0017a0001c0001t0004g0197a0001c0001t0004g0198others(3): Show | 7 | HG00642.hp2 HG02976.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+10554A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671102 | ||||||
chr10:17671246
|
C | T | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125+10698C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671246 | ||||||
chr10:17671458
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.125+10910A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671458 | ||||||
chr10:17671578
|
C | T | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.125+11030C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671578 | ||||||
chr10:17671724
|
C | G | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125+11176C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671724 | ||||||
chr10:17671968
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.125+11420A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671968 | ||||||
chr10:17671986
|
G | A | 6 | a0001c0001t0009g0383a0001c0001t0017g0380a0001c0001t0017g0381others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+11438G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17671986 | ||||||
chr10:17672069
|
A | G | 1 | a0001c0002t0003g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.125+11521A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672069 | ||||||
chr10:17672183
|
G | A | 1 | a0001c0001t0030g0385 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125+11635G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672183 | ||||||
chr10:17672288
|
A | G | 4 | a0001c0002t0003g0008a0001c0002t0003g0216a0001c0002t0003g0327others(1): Show | 6 | HG04184.hp2 NA18971.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+11740A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672288 | ||||||
chr10:17672391
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(111): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.125+11843A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672391 | ||||||
chr10:17672423
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.125+11875T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672423 | ||||||
chr10:17672575
|
C | T | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.125+12027C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672575 | ||||||
chr10:17672674
|
A | G | 1 | a0001c0001t0004g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-12001A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672674 | ||||||
chr10:17672818
|
G | T | 32 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(29): Show | 33 | HG00642.hp2 HG01243.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.126-11857G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672818 | ||||||
chr10:17672833
|
AGTGTGAT others(2): Show |
A | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-11837_126-1182 others(13): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17672833 | |||||
chr10:17672867
|
T | TAAGAG | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.126-11805_126-1180 others(9): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17672867 | |||||
chr10:17672990
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0002g0150others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-11685G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17672990 | ||||||
chr10:17673023
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.126-11652A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673023 | ||||||
chr10:17673156
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108 | 5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-11519T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673156 | ||||||
chr10:17673279
|
T | C | 2 | a0001c0002t0003g0314a0001c0002t0003g0317 | 2 | NA19001.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.126-11396T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673279 | ||||||
chr10:17673289
|
T | TTAG | 2 | a0001c0001t0001g0014a0001c0001t0001g0104 | 3 | NA18944.hp1 NA18963.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.126-11385_126-1138 others(7): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17673289 | |||||
chr10:17673293
|
C | T | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-11382C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673293 | ||||||
chr10:17673294
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126-11381G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673294 | ||||||
chr10:17673329
|
A | G | 1 | a0001c0002t0003g0344 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.126-11346A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673329 | ||||||
chr10:17673398
|
G | A | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.126-11277G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673398 | ||||||
chr10:17673410
|
G | T | 1 | a0001c0001t0002g0282 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126-11265G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673410 | ||||||
chr10:17673463
|
C | T | 9 | a0001c0001t0002g0275a0001c0001t0004g0017a0001c0001t0004g0032others(6): Show | 10 | HG00642.hp2 HG00738.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-11212C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673463 | ||||||
chr10:17673603
|
G | C | 1 | a0001c0001t0004g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.126-11072G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673603 | ||||||
chr10:17673649
|
G | A | 2 | a0001c0002t0003g0034a0001c0002t0003g0035 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-11026G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673649 | ||||||
chr10:17673673
|
C | A | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-11002C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17673673 | ||||||
chr10:17674014
|
G | C | 2 | a0001c0002t0003g0034a0001c0002t0003g0035 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-10661G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674014 | ||||||
chr10:17674014
|
G | GC | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.126-10661_126-1066 others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674014 | ||||||
chr10:17674097
|
T | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-10578T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674097 | ||||||
chr10:17674294
|
T | G | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126-10381T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674294 | ||||||
chr10:17674405
|
C | T | 6 | a0001c0002t0004g0326a0001c0002t0004g0333a0001c0002t0004g0335others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-10270C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674405 | ||||||
chr10:17674737
|
G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(97): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.126-9938G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674737 | ||||||
chr10:17674870
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-9805A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674870 | ||||||
chr10:17674872
|
G | A | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(241): Show | 259 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.126-9803G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674872 | ||||||
chr10:17674879
|
T | C | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.126-9796T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674879 | ||||||
chr10:17674909
|
C | A | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-9766C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674909 | ||||||
chr10:17674931
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126-9744A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17674931 | ||||||
chr10:17675099
|
T | G | 1 | a0001c0001t0001g0362 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.126-9576T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675099 | ||||||
chr10:17675109
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-9566T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675109 | ||||||
chr10:17675503
|
C | CA | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(101): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.126-9158dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675503 | |||||
chr10:17675503
|
C | CAA | 7 | a0001c0001t0015g0389a0001c0001t0017g0380a0001c0001t0017g0381others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-9159_126-9158d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675503 | |||||
chr10:17675503
|
C | CAAA | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.126-9160_126-9158d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675503 | |||||
chr10:17675579
|
G | A | 1 | a0001c0001t0007g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.126-9096G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675579 | ||||||
chr10:17675700
|
T | G | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.126-8975T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675700 | ||||||
chr10:17675799
|
A | AT | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-8867dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17675799 | |||||
chr10:17675862
|
C | T | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126-8813C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675862 | ||||||
chr10:17675894
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.126-8781T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675894 | ||||||
chr10:17675960
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.126-8715C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17675960 | ||||||
chr10:17676008
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.126-8667G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676008 | ||||||
chr10:17676068
|
A | G | 10 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.126-8607A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676068 | ||||||
chr10:17676144
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126-8531C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676144 | ||||||
chr10:17676283
|
A | G | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.126-8392A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676283 | ||||||
chr10:17676304
|
G | A | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-8371G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676304 | ||||||
chr10:17676334
|
T | C | 1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126-8341T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676334 | ||||||
chr10:17676495
|
G | A | 13 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-8180G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676495 | ||||||
chr10:17676557
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.126-8118C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676557 | ||||||
chr10:17676578
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG00609.hp2 NA18970.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-8097A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676578 | ||||||
chr10:17676582
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.126-8093A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676582 | ||||||
chr10:17676699
|
A | G | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.126-7976A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676699 | ||||||
chr10:17676700
|
T | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(177): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.126-7975T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676700 | ||||||
chr10:17676798
|
A | G | 3 | a0001c0001t0002g0224a0001c0001t0002g0298a0001c0001t0002g0299 | 3 | HG00423.hp2 NA18968.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.126-7877A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676798 | ||||||
chr10:17676808
|
C | A | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-7867C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17676808 | ||||||
chr10:17676896
|
C | CAT | 19 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.126-7765_126-7764d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17676896 | |||||
chr10:17677001
|
G | C | 3 | a0001c0001t0001g0367a0001c0001t0002g0300a0001c0001t0002g0301 | 3 | HG02027.hp2 HG02165.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.126-7674G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677001 | ||||||
chr10:17677078
|
G | A | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.126-7597G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677078 | ||||||
chr10:17677089
|
C | T | 1 | a0001c0001t0002g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.126-7586C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677089 | ||||||
chr10:17677135
|
G | T | 7 | a0001c0001t0002g0033a0001c0001t0002g0184a0001c0001t0002g0188others(4): Show | 7 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-7540G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677135 | ||||||
chr10:17677243
|
A | G | 16 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-7432A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677243 | ||||||
chr10:17677247
|
C | A | 30 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(27): Show | 33 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.126-7428C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677247 | ||||||
chr10:17677263
|
C | A | 7 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-7412C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677263 | ||||||
chr10:17677283
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.126-7392T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677283 | ||||||
chr10:17677391
|
G | A | 2 | a0001c0001t0004g0032a0001c0001t0004g0055 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.126-7284G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677391 | ||||||
chr10:17677495
|
G | A | 1 | a0001c0001t0012g0182 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.126-7180G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677495 | ||||||
chr10:17677797
|
A | G | 8 | a0001c0001t0002g0226a0001c0001t0002g0270a0001c0001t0002g0271others(5): Show | 8 | HG01123.hp1 HG01993.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-6878A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677797 | ||||||
chr10:17677808
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126-6867C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677808 | ||||||
chr10:17677849
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-6826A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677849 | ||||||
chr10:17677873
|
G | A | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(99): Show | 110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.126-6802G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677873 | ||||||
chr10:17677947
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.126-6728G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677947 | ||||||
chr10:17677951
|
G | A | 13 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-6724G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17677951 | ||||||
chr10:17677965
|
C | CT | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(99): Show | 110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.126-6706dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17677965 | |||||
chr10:17678049
|
A | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-6626A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678049 | ||||||
chr10:17678049
|
A | G | 1 | a0001c0002t0003g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.126-6626A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678049 | ||||||
chr10:17678073
|
C | A | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-6602C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678073 | ||||||
chr10:17678219
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-6456A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678219 | ||||||
chr10:17678260
|
A | ATTTTTTT others(1): Show |
21 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(18): Show | 24 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.126-6412_126-6405d others(10): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17678260 | |||||
chr10:17678260
|
A | ATTTTTTT others(3): Show |
9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-6414_126-6405d others(12): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17678260 | |||||
chr10:17678260
|
AT | A | 110 | a0001c0001t0001g0029a0001c0001t0001g0358a0001c0001t0001g0359others(107): Show | 113 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.126-6405delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17678260 | |||||
chr10:17678337
|
C | G | 19 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.126-6338C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678337 | ||||||
chr10:17678366
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.126-6309T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678366 | ||||||
chr10:17678496
|
C | T | 16 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-6179C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678496 | ||||||
chr10:17678534
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0056others(9): Show | 13 | HG00609.hp2 HG02129.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-6141G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678534 | ||||||
chr10:17678581
|
G | A | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126-6094G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678581 | ||||||
chr10:17678750
|
C | T | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-5925C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678750 | ||||||
chr10:17678938
|
T | A | 1 | a0001c0001t0004g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.126-5737T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678938 | ||||||
chr10:17678985
|
C | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.126-5690C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17678985 | ||||||
chr10:17679028
|
A | G | 1 | a0001c0001t0002g0299 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.126-5647A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679028 | ||||||
chr10:17679037
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126-5638T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679037 | ||||||
chr10:17679043
|
G | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-5632G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679043 | ||||||
chr10:17679089
|
A | G | 1 | a0001c0002t0003g0348 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.126-5586A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679089 | ||||||
chr10:17679317
|
C | T | 35 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(32): Show | 39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-5358C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679317 | ||||||
chr10:17679379
|
A | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108 | 5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-5296A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679379 | ||||||
chr10:17679491
|
T | G | 1 | a0001c0001t0002g0254 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.126-5184T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679491 | ||||||
chr10:17679502
|
C | G | 35 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(32): Show | 39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-5173C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679502 | ||||||
chr10:17679574
|
C | T | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126-5101C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679574 | ||||||
chr10:17679575
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.126-5100G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679575 | ||||||
chr10:17679579
|
G | GT | 6 | a0001c0001t0001g0108a0001c0001t0004g0032a0001c0001t0004g0055others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-5084dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679579 | |||||
chr10:17679579
|
GT | G | 28 | a0001c0001t0001g0124a0001c0001t0005g0003a0001c0001t0005g0009others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-5084delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679579 | |||||
chr10:17679579
|
GTT | G | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-5085_126-5084d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679579 | |||||
chr10:17679669
|
G | A | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-5006G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17679669 | ||||||
chr10:17679751
|
GTTTCTTT others(5): Show |
G | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-4915_126-4904d others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17679751 | |||||
chr10:17680027
|
A | T | 1 | a0001c0001t0005g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.126-4648A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680027 | ||||||
chr10:17680038
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126-4637A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680038 | ||||||
chr10:17680053
|
T | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-4622T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680053 | ||||||
chr10:17680146
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126-4529G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680146 | ||||||
chr10:17680163
|
C | A | 6 | a0001c0001t0004g0215a0001c0001t0006g0203a0001c0001t0006g0207others(3): Show | 6 | HG02615.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-4512C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680163 | ||||||
chr10:17680210
|
G | A | 8 | a0001c0001t0002g0006a0001c0001t0002g0220a0001c0001t0002g0258others(5): Show | 9 | HG00280.hp1 HG00642.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-4465G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680210 | ||||||
chr10:17680265
|
AT | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(100): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.126-4409delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680265 | ||||||
chr10:17680379
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(100): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.126-4296A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680379 | ||||||
chr10:17680416
|
C | CT | 8 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(5): Show | 8 | HG00280.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-4244dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | |||||
chr10:17680416
|
CT | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0152others(5): Show | 8 | HG00099.hp1 HG02630.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-4244delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | |||||
chr10:17680416
|
CTT | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.126-4245_126-4244d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | |||||
chr10:17680416
|
CTTT | C | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-4246_126-4244d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17680416 | |||||
chr10:17680541
|
G | T | 8 | a0001c0001t0002g0033a0001c0001t0002g0184a0001c0001t0002g0188others(5): Show | 8 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-4134G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680541 | ||||||
chr10:17680768
|
G | C | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.126-3907G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680768 | ||||||
chr10:17680817
|
T | C | 4 | a0001c0001t0009g0383a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-3858T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680817 | ||||||
chr10:17680835
|
T | C | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-3840T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680835 | ||||||
chr10:17680865
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-3810C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17680865 | ||||||
chr10:17681060
|
G | A | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126-3615G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681060 | ||||||
chr10:17681071
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0145 | 2 | NA19082.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.126-3604G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681071 | ||||||
chr10:17681090
|
A | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.126-3585A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681090 | ||||||
chr10:17681134
|
C | G | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-3541C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681134 | ||||||
chr10:17681134
|
C | T | 35 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(32): Show | 39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-3541C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681134 | ||||||
chr10:17681146
|
T | A | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-3529T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681146 | ||||||
chr10:17681169
|
G | A | 1 | a0001c0001t0004g0387 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.126-3506G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681169 | ||||||
chr10:17681197
|
C | CT | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(143): Show | 157 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.126-3460dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17681197 | |||||
chr10:17681197
|
C | CTT | 15 | a0001c0001t0001g0029a0001c0001t0001g0102a0001c0001t0001g0108others(12): Show | 16 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-3461_126-3460d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17681197 | |||||
chr10:17681217
|
A | C | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-3458A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681217 | ||||||
chr10:17681218
|
T | C | 50 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(47): Show | 56 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.126-3457T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681218 | ||||||
chr10:17681225
|
G | T | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.126-3450G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681225 | ||||||
chr10:17681253
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.126-3422G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681253 | ||||||
chr10:17681276
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.126-3399C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681276 | ||||||
chr10:17681379
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.126-3296C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681379 | ||||||
chr10:17681395
|
A | G | 1 | a0001c0001t0012g0386 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.126-3280A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681395 | ||||||
chr10:17681441
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.126-3234C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681441 | ||||||
chr10:17681641
|
G | A | 2 | a0001c0002t0003g0338a0001c0002t0003g0339 | 2 | NA18968.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.126-3034G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681641 | ||||||
chr10:17681715
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.126-2960A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681715 | ||||||
chr10:17681737
|
C | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-2938C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681737 | ||||||
chr10:17681842
|
A | G | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-2833A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681842 | ||||||
chr10:17681867
|
A | G | 2 | a0001c0001t0005g0046a0001c0001t0005g0052 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.126-2808A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681867 | ||||||
chr10:17681892
|
A | G | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126-2783A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17681892 | ||||||
chr10:17682004
|
T | C | 90 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(87): Show | 95 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.126-2671T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682004 | ||||||
chr10:17682123
|
C | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 91 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.126-2552C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682123 | ||||||
chr10:17682178
|
T | G | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.126-2497T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682178 | ||||||
chr10:17682184
|
T | G | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.126-2491T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682184 | ||||||
chr10:17682234
|
G | C | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-2441G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682234 | ||||||
chr10:17682241
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.126-2434C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682241 | ||||||
chr10:17682435
|
A | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(46): Show | 55 | HG00597.hp1 HG00609.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.126-2240A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682435 | ||||||
chr10:17682452
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.126-2223A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682452 | ||||||
chr10:17682504
|
G | A | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-2171G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682504 | ||||||
chr10:17682529
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-2146T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682529 | ||||||
chr10:17682909
|
T | C | 1 | a0001c0002t0003g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.126-1766T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682909 | ||||||
chr10:17682925
|
T | G | 37 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(34): Show | 41 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.126-1750T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17682925 | ||||||
chr10:17683110
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126-1565T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683110 | ||||||
chr10:17683236
|
T | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.126-1439T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683236 | ||||||
chr10:17683239
|
C | T | 16 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-1436C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683239 | ||||||
chr10:17683250
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.126-1425A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683250 | ||||||
chr10:17683307
|
T | C | 36 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(33): Show | 40 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.126-1368T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683307 | ||||||
chr10:17683367
|
G | T | 35 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(32): Show | 39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-1308G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683367 | ||||||
chr10:17683389
|
C | G | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126-1286C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683389 | ||||||
chr10:17683410
|
C | T | 60 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0028others(57): Show | 62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.126-1265C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683410 | ||||||
chr10:17683432
|
A | G | 38 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(35): Show | 42 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.126-1243A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683432 | ||||||
chr10:17683504
|
G | A | 7 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-1171G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683504 | ||||||
chr10:17683689
|
T | C | 36 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(33): Show | 40 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.126-986T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683689 | ||||||
chr10:17683712
|
A | C | 18 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-963A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683712 | ||||||
chr10:17683787
|
C | T | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126-888C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683787 | ||||||
chr10:17683856
|
C | T | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(247): Show | 265 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.126-819C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683856 | ||||||
chr10:17683913
|
C | G | 1 | a0001c0002t0003g0339 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.126-762C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683913 | ||||||
chr10:17683940
|
C | T | 35 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(32): Show | 39 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-735C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17683940 | ||||||
chr10:17684048
|
T | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-627T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684048 | ||||||
chr10:17684071
|
G | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(242): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.126-604G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684071 | ||||||
chr10:17684155
|
G | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.126-520G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684155 | ||||||
chr10:17684306
|
G | A | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.126-369G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684306 | ||||||
chr10:17684422
|
CT | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(17): Show | 24 | HG00597.hp1 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.126-242delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr10 | 17684422 | |||||
chr10:17684538
|
G | A | 22 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0154others(19): Show | 24 | HG00673.hp1 NA18941.hp1 NA18949.hp2 others(21): Show |
intron_variant | MODIFIER | c.126-137G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684538 | ||||||
chr10:17684574
|
A | G | 60 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0028others(57): Show | 62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.126-101A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684574 | ||||||
chr10:17684649
|
A | G | 6 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0002g0275others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-26A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 2/13 | chr10 | 17684649 | ||||||
chr10:17685091
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.297+164C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685091 | ||||||
chr10:17685209
|
A | G | 4 | a0001c0001t0002g0242a0001c0001t0002g0309a0001c0001t0024g0295others(1): Show | 4 | HG00639.hp1 HG01168.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+282A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685209 | ||||||
chr10:17685242
|
C | T | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.297+315C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685242 | ||||||
chr10:17685494
|
G | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.297+567G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685494 | ||||||
chr10:17685507
|
G | T | 1 | a0001c0001t0005g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.297+580G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685507 | ||||||
chr10:17685515
|
G | C | 34 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(31): Show | 38 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.297+588G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685515 | ||||||
chr10:17685609
|
A | G | 1 | a0001c0002t0003g0344 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.297+682A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685609 | ||||||
chr10:17685614
|
A | C | 5 | a0001c0001t0001g0152a0001c0001t0001g0358a0001c0001t0002g0390others(2): Show | 5 | HG02630.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+687A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685614 | ||||||
chr10:17685648
|
A | G | 2 | a0001c0002t0003g0338a0001c0002t0003g0339 | 2 | NA18968.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.297+721A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685648 | ||||||
chr10:17685815
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.297+888A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685815 | ||||||
chr10:17685965
|
T | C | 1 | a0001c0001t0002g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.297+1038T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685965 | ||||||
chr10:17685993
|
T | A | 1 | a0001c0002t0003g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.297+1066T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17685993 | ||||||
chr10:17686099
|
C | T | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.297+1172C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686099 | ||||||
chr10:17686118
|
T | C | 36 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(33): Show | 40 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+1191T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686118 | ||||||
chr10:17686181
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(97): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.297+1254C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686181 | ||||||
chr10:17686200
|
G | A | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.297+1273G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686200 | ||||||
chr10:17686217
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.297+1290A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686217 | ||||||
chr10:17686279
|
C | G | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.297+1352C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686279 | ||||||
chr10:17686295
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0358 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.297+1368C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686295 | ||||||
chr10:17686315
|
TTC | T | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+1392_297+1393d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17686315 | |||||
chr10:17686355
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+1428T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686355 | ||||||
chr10:17686374
|
C | T | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+1447C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686374 | ||||||
chr10:17686378
|
C | CT | 40 | a0001c0001t0001g0096a0001c0001t0001g0138a0001c0001t0001g0186others(37): Show | 43 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.297+1467dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17686378 | |||||
chr10:17686378
|
C | CTTT | 10 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 11 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+1465_297+1467d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17686378 | |||||
chr10:17686413
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0098 | 2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.297+1486G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686413 | ||||||
chr10:17686496
|
C | T | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.298-1531C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686496 | ||||||
chr10:17686514
|
A | T | 395 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(392): Show | 425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.298-1513A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686514 | ||||||
chr10:17686518
|
A | C | 18 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.298-1509A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686518 | ||||||
chr10:17686746
|
G | A | 2 | a0001c0002t0003g0170a0001c0002t0003g0171 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.298-1281G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686746 | ||||||
chr10:17686929
|
T | C | 6 | a0001c0001t0001g0149a0001c0001t0002g0150a0001c0001t0010g0109others(3): Show | 6 | HG01192.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1098T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686929 | ||||||
chr10:17686968
|
C | G | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-1059C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17686968 | ||||||
chr10:17687202
|
C | T | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-825C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687202 | ||||||
chr10:17687292
|
T | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(102): Show | 113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.298-735T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687292 | ||||||
chr10:17687327
|
T | C | 2 | a0001c0001t0001g0102a0001c0005t0001g0080 | 2 | HG02027.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.298-700T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687327 | ||||||
chr10:17687350
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.298-677C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687350 | ||||||
chr10:17687373
|
A | T | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.298-654A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687373 | ||||||
chr10:17687394
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.298-633C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687394 | ||||||
chr10:17687421
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(95): Show | 106 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.298-606G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687421 | ||||||
chr10:17687495
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.298-532C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687495 | ||||||
chr10:17687500
|
CA | C | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(241): Show | 259 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.298-518delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17687500 | |||||
chr10:17687519
|
A | G | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-508A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687519 | ||||||
chr10:17687533
|
G | A | 1 | a0004c0011t0001g0057 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.298-494G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687533 | ||||||
chr10:17687534
|
T | G | 1 | a0004c0011t0001g0057 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.298-493T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687534 | ||||||
chr10:17687731
|
T | A | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298-296T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687731 | ||||||
chr10:17687733
|
CT | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108 | 5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-292delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr10 | 17687733 | |||||
chr10:17687738
|
C | G | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.298-289C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687738 | ||||||
chr10:17687833
|
A | C | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-194A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687833 | ||||||
chr10:17687965
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.298-62T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 4/13 | chr10 | 17687965 | ||||||
chr10:17688246
|
T | G | 3 | a0001c0001t0001g0358a0001c0001t0030g0385a0001c0001t0031g0384 | 3 | HG02630.hp1 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.444+73T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688246 | ||||||
chr10:17688259
|
G | A | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.444+86G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688259 | ||||||
chr10:17688313
|
G | A | 2 | a0001c0001t0002g0265a0001c0001t0002g0266 | 2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.444+140G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688313 | ||||||
chr10:17688417
|
C | T | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.444+244C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688417 | ||||||
chr10:17688485
|
C | T | 1 | a0001c0001t0005g0003 | 3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.444+312C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688485 | ||||||
chr10:17688510
|
T | A | 1 | a0001c0002t0004g0350 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+337T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688510 | ||||||
chr10:17688514
|
G | C | 1 | a0001c0002t0004g0350 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+341G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688514 | ||||||
chr10:17688520
|
T | G | 1 | a0001c0002t0004g0350 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+347T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688520 | ||||||
chr10:17688530
|
T | C | 1 | a0001c0002t0004g0350 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+357T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688530 | ||||||
chr10:17688562
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+389A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688562 | ||||||
chr10:17688573
|
C | A | 5 | a0001c0001t0004g0204a0001c0001t0004g0211a0001c0001t0004g0213others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+400C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688573 | ||||||
chr10:17688582
|
C | T | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.444+409C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688582 | ||||||
chr10:17688628
|
AT | A | 40 | a0001c0001t0005g0046a0001c0002t0003g0008a0001c0002t0003g0022others(37): Show | 42 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.444+469delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 17688628 | |||||
chr10:17688682
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.444+509C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688682 | ||||||
chr10:17688730
|
T | C | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.444+557T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688730 | ||||||
chr10:17688888
|
T | A | 7 | a0001c0001t0004g0175a0001c0001t0004g0176a0001c0001t0004g0177others(4): Show | 7 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+715T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688888 | ||||||
chr10:17688939
|
A | G | 1 | a0001c0001t0027g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.444+766A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17688939 | ||||||
chr10:17689026
|
A | T | 15 | a0001c0002t0003g0028a0001c0002t0003g0031a0001c0002t0003g0159others(12): Show | 15 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+853A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689026 | ||||||
chr10:17689178
|
C | T | 6 | a0001c0002t0004g0326a0001c0002t0004g0333a0001c0002t0004g0335others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+1005C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689178 | ||||||
chr10:17689220
|
G | C | 1 | a0001c0001t0018g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.444+1047G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689220 | ||||||
chr10:17689273
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+1100T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689273 | ||||||
chr10:17689295
|
A | G | 1 | a0001c0001t0004g0387 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444+1122A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689295 | ||||||
chr10:17689387
|
A | G | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.444+1214A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689387 | ||||||
chr10:17689389
|
G | A | 6 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0002g0275others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+1216G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689389 | ||||||
chr10:17689391
|
C | T | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+1218C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689391 | ||||||
chr10:17689470
|
C | T | 395 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(392): Show | 425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.444+1297C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689470 | ||||||
chr10:17689566
|
A | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0056others(11): Show | 15 | HG00609.hp2 HG02129.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1393A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689566 | ||||||
chr10:17689643
|
A | G | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.444+1470A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689643 | ||||||
chr10:17689748
|
T | A | 1 | a0001c0002t0003g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.444+1575T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689748 | ||||||
chr10:17689758
|
A | G | 42 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0154others(39): Show | 44 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+1585A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689758 | ||||||
chr10:17689971
|
C | A | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+1798C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17689971 | ||||||
chr10:17690077
|
C | T | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.444+1904C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690077 | ||||||
chr10:17690423
|
T | C | 1 | a0001c0001t0005g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.444+2250T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690423 | ||||||
chr10:17690463
|
C | T | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+2290C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690463 | ||||||
chr10:17690476
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.444+2303A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690476 | ||||||
chr10:17690795
|
G | A | 2 | a0001c0001t0014g0131a0001c0001t0014g0140 | 2 | HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.445-2427G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690795 | ||||||
chr10:17690822
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-2400A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690822 | ||||||
chr10:17690827
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.445-2395T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17690827 | ||||||
chr10:17691010
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.445-2212A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691010 | ||||||
chr10:17691015
|
G | A | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.445-2207G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691015 | ||||||
chr10:17691086
|
A | G | 2 | a0001c0002t0003g0034a0001c0002t0003g0035 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.445-2136A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691086 | ||||||
chr10:17691104
|
A | C | 1 | a0001c0001t0002g0269 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.445-2118A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691104 | ||||||
chr10:17691170
|
T | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-2052T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691170 | ||||||
chr10:17691185
|
T | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(160): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.445-2037T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691185 | ||||||
chr10:17691202
|
T | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-2020T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691202 | ||||||
chr10:17691247
|
G | A | 1 | a0001c0001t0004g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.445-1975G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691247 | ||||||
chr10:17691337
|
T | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(21): Show | 28 | HG00597.hp1 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.445-1885T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691337 | ||||||
chr10:17691385
|
G | A | 2 | a0001c0001t0001g0102a0001c0005t0001g0080 | 2 | HG02027.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.445-1837G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691385 | ||||||
chr10:17691504
|
C | T | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445-1718C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691504 | ||||||
chr10:17691511
|
C | CTGTCTCA others(1): Show |
26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.445-1711_445-1710i others(10): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691511 | ||||||
chr10:17691513
|
A | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-1709A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691513 | ||||||
chr10:17691828
|
G | A | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.445-1394G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691828 | ||||||
chr10:17691850
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.445-1372T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691850 | ||||||
chr10:17691928
|
G | A | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.445-1294G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691928 | ||||||
chr10:17691963
|
A | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0136a0001c0001t0001g0142 | 3 | HG00438.hp1 HG00621.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.445-1259A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17691963 | ||||||
chr10:17692085
|
C | T | 3 | a0001c0001t0004g0211a0001c0001t0004g0213a0001c0001t0004g0214 | 3 | HG02451.hp1 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.445-1137C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692085 | ||||||
chr10:17692154
|
T | A | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.445-1068T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692154 | ||||||
chr10:17692247
|
G | A | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(238): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.445-975G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692247 | ||||||
chr10:17692277
|
T | G | 37 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(34): Show | 41 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.445-945T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692277 | ||||||
chr10:17692304
|
AGGTTGAG | A | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.445-915_445-909del others(7): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | 17692304 | |||||
chr10:17692361
|
C | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.445-861C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692361 | ||||||
chr10:17692363
|
A | G | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-859A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692363 | ||||||
chr10:17692374
|
G | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.445-848G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692374 | ||||||
chr10:17692403
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.445-819G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692403 | ||||||
chr10:17692547
|
G | A | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.445-675G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692547 | ||||||
chr10:17692767
|
T | C | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-455T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 5/13 | chr10 | 17692767 | ||||||
chr10:17693328
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.535+16C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693328 | ||||||
chr10:17693392
|
G | T | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.535+80G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693392 | ||||||
chr10:17693478
|
G | A | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535+166G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693478 | ||||||
chr10:17693479
|
T | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.535+167T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693479 | ||||||
chr10:17693508
|
T | C | 35 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(32): Show | 38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.535+196T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693508 | ||||||
chr10:17693516
|
T | C | 33 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(30): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.535+204T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693516 | ||||||
chr10:17693588
|
C | G | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535+276C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693588 | ||||||
chr10:17693588
|
C | T | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.535+276C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693588 | ||||||
chr10:17693621
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.535+309G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693621 | ||||||
chr10:17693677
|
T | C | 10 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 11 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.535+365T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693677 | ||||||
chr10:17693720
|
T | C | 3 | a0001c0001t0005g0009a0001c0001t0005g0040a0001c0001t0008g0039 | 4 | NA18983.hp1 NA18993.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.535+408T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693720 | ||||||
chr10:17693889
|
GT | G | 33 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(30): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.535+579delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 17693889 | |||||
chr10:17693976
|
A | G | 33 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(30): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.535+664A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693976 | ||||||
chr10:17693985
|
G | A | 33 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(30): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.535+673G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17693985 | ||||||
chr10:17694183
|
A | T | 1 | a0001c0001t0002g0254 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.536-866A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694183 | ||||||
chr10:17694248
|
T | A | 33 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(30): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.536-801T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694248 | ||||||
chr10:17694535
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.536-514T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694535 | ||||||
chr10:17694555
|
A | G | 10 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(7): Show | 10 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.536-494A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694555 | ||||||
chr10:17694586
|
G | C | 38 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0021others(35): Show | 43 | HG00323.hp1 HG00673.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.536-463G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694586 | ||||||
chr10:17694841
|
C | G | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.536-208C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694841 | ||||||
chr10:17694875
|
G | A | 33 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(30): Show | 36 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.536-174G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694875 | ||||||
chr10:17694884
|
T | G | 23 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0174others(20): Show | 25 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.536-165T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694884 | ||||||
chr10:17694889
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0124 | 2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.536-160A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 6/13 | chr10 | 17694889 | ||||||
chr10:17695245
|
A | G | 2 | a0001c0001t0002g0023a0001c0001t0002g0357 | 3 | HG01256.hp2 HG01258.hp1 HG01978.hp1 |
splice_region_variant&intron_variant | LOW | c.728+4A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695245 | ||||||
chr10:17695295
|
T | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.728+54T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695295 | ||||||
chr10:17695362
|
G | A | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.728+121G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695362 | ||||||
chr10:17695570
|
T | A | 1 | a0001c0001t0002g0244 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.728+329T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695570 | ||||||
chr10:17695661
|
C | G | 35 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(32): Show | 38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.728+420C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695661 | ||||||
chr10:17695718
|
T | C | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.728+477T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695718 | ||||||
chr10:17695869
|
G | A | 13 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(10): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.728+628G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17695869 | ||||||
chr10:17696023
|
G | T | 1 | a0001c0001t0005g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.729-752G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696023 | ||||||
chr10:17696066
|
G | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.729-709G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696066 | ||||||
chr10:17696106
|
G | T | 127 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0185others(124): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.729-669G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696106 | ||||||
chr10:17696164
|
A | AT | 18 | a0001c0001t0001g0152a0001c0001t0001g0359a0001c0001t0001g0362others(15): Show | 18 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.729-598dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 17696164 | |||||
chr10:17696199
|
G | A | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.729-576G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696199 | ||||||
chr10:17696274
|
T | C | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.729-501T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696274 | ||||||
chr10:17696303
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.729-472G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696303 | ||||||
chr10:17696314
|
G | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0357 | 3 | HG01256.hp2 HG01258.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.729-461G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696314 | ||||||
chr10:17696379
|
T | G | 1 | a0001c0001t0004g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.729-396T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696379 | ||||||
chr10:17696414
|
A | G | 1 | a0001c0001t0001g0373 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.729-361A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696414 | ||||||
chr10:17696485
|
A | G | 34 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(31): Show | 37 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.729-290A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696485 | ||||||
chr10:17696627
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.729-148T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696627 | ||||||
chr10:17696754
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.729-21A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 7/13 | chr10 | 17696754 | ||||||
chr10:17696892
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0098 | 2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.823+23A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17696892 | ||||||
chr10:17696982
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.823+113C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17696982 | ||||||
chr10:17697076
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.823+207T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697076 | ||||||
chr10:17697097
|
G | C | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.823+228G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697097 | ||||||
chr10:17697175
|
C | T | 1 | a0001c0002t0003g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.823+306C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697175 | ||||||
chr10:17697220
|
C | T | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823+351C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697220 | ||||||
chr10:17697244
|
A | G | 1 | a0001c0001t0004g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+375A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697244 | ||||||
chr10:17697284
|
A | AT | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108 | 5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+417dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17697284 | |||||
chr10:17697407
|
T | A | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.823+538T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697407 | ||||||
chr10:17697645
|
A | C | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823+776A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697645 | ||||||
chr10:17697660
|
T | G | 10 | a0001c0001t0002g0221a0001c0001t0002g0235a0001c0001t0002g0254others(7): Show | 10 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+791T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697660 | ||||||
chr10:17697722
|
C | CTATT | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.823+855_823+856ins others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17697722 | |||||
chr10:17697798
|
T | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0002g0150others(4): Show | 7 | HG01192.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+929T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697798 | ||||||
chr10:17697804
|
G | A | 351 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(348): Show | 378 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(375): Show |
intron_variant | MODIFIER | c.823+935G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697804 | ||||||
chr10:17697844
|
A | G | 2 | a0001c0001t0010g0111a0001c0001t0010g0212 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.823+975A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697844 | ||||||
chr10:17697850
|
G | A | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.823+981G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17697850 | ||||||
chr10:17698093
|
C | G | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.823+1224C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698093 | ||||||
chr10:17698125
|
G | C | 1 | a0001c0001t0002g0234 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.823+1256G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698125 | ||||||
chr10:17698148
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(96): Show | 107 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.823+1279G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698148 | ||||||
chr10:17698260
|
C | T | 1 | a0001c0001t0029g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.823+1391C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698260 | ||||||
chr10:17698302
|
T | C | 2 | a0001c0001t0002g0265a0001c0001t0002g0266 | 2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.823+1433T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698302 | ||||||
chr10:17698412
|
C | T | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.823+1543C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698412 | ||||||
chr10:17698421
|
C | CT | 20 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0359others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+1565dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17698421 | |||||
chr10:17698459
|
A | G | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1590A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698459 | ||||||
chr10:17698463
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1594G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698463 | ||||||
chr10:17698494
|
C | G | 4 | a0001c0001t0009g0383a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1625C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698494 | ||||||
chr10:17698500
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(95): Show | 106 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.823+1631G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698500 | ||||||
chr10:17698507
|
AAG | A | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.823+1642_823+1643d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 17698507 | |||||
chr10:17698655
|
G | A | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1536G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698655 | ||||||
chr10:17698795
|
G | A | 1 | a0001c0002t0022g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.824-1396G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698795 | ||||||
chr10:17698865
|
A | G | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.824-1326A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698865 | ||||||
chr10:17698923
|
C | G | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.824-1268C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698923 | ||||||
chr10:17698974
|
T | C | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0195 | 3 | HG02109.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.824-1217T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698974 | ||||||
chr10:17698989
|
A | G | 11 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(8): Show | 12 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1202A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17698989 | ||||||
chr10:17699047
|
A | C | 8 | a0001c0001t0004g0204a0001c0001t0004g0205a0001c0001t0004g0206others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-1144A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699047 | ||||||
chr10:17699060
|
T | G | 1 | a0001c0001t0032g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.824-1131T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699060 | ||||||
chr10:17699108
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.824-1083A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699108 | ||||||
chr10:17699186
|
A | G | 11 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(8): Show | 12 | HG01255.hp2 HG01256.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.824-1005A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699186 | ||||||
chr10:17699213
|
A | G | 1 | a0001c0001t0002g0390 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.824-978A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699213 | ||||||
chr10:17699270
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.824-921T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699270 | ||||||
chr10:17699361
|
T | A | 1 | a0001c0001t0005g0040 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.824-830T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699361 | ||||||
chr10:17699412
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(95): Show | 106 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.824-779G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699412 | ||||||
chr10:17699488
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.824-703T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699488 | ||||||
chr10:17699492
|
T | C | 1 | a0001c0001t0006g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.824-699T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699492 | ||||||
chr10:17699672
|
C | T | 72 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 75 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.824-519C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699672 | ||||||
chr10:17699691
|
A | G | 13 | a0001c0001t0004g0016a0001c0001t0004g0032a0001c0001t0004g0055others(10): Show | 14 | HG01243.hp2 HG01255.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.824-500A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699691 | ||||||
chr10:17699697
|
C | T | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.824-494C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699697 | ||||||
chr10:17699768
|
A | AC | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.824-423_824-422ins others(1): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 8/13 | chr10 | 17699768 | ||||||
chr10:17700348
|
A | G | 1 | a0001c0001t0031g0384 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.912+69A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700348 | ||||||
chr10:17700351
|
A | C | 3 | a0001c0001t0017g0380a0001c0001t0017g0381a0001c0001t0029g0379 | 3 | HG02258.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.912+72A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700351 | ||||||
chr10:17700466
|
G | A | 2 | a0001c0001t0001g0067a0004c0011t0001g0057 | 2 | NA18940.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.912+187G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700466 | ||||||
chr10:17700563
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.912+284C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700563 | ||||||
chr10:17700570
|
T | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0056others(11): Show | 16 | HG00609.hp2 HG02109.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.912+291T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700570 | ||||||
chr10:17700587
|
A | AT | 35 | a0001c0001t0001g0358a0001c0001t0002g0150a0001c0001t0004g0032others(32): Show | 38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.912+322dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17700587 | |||||
chr10:17700587
|
AT | A | 120 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0286others(117): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.912+322delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17700587 | |||||
chr10:17700606
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.912+327A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700606 | ||||||
chr10:17700611
|
T | C | 2 | a0001c0001t0001g0359a0001c0001t0001g0365 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.912+332T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700611 | ||||||
chr10:17700672
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.912+393A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700672 | ||||||
chr10:17700725
|
C | G | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.912+446C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700725 | ||||||
chr10:17700770
|
A | C | 128 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0185others(125): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.912+491A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700770 | ||||||
chr10:17700792
|
CA | C | 14 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.912+514delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700792 | ||||||
chr10:17700813
|
C | T | 2 | a0001c0001t0007g0256a0001c0001t0007g0257 | 2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.912+534C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700813 | ||||||
chr10:17700823
|
A | G | 1 | a0001c0001t0009g0312 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.912+544A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700823 | ||||||
chr10:17700881
|
A | T | 4 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0002t0003g0034others(1): Show | 4 | HG01243.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+602A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700881 | ||||||
chr10:17700925
|
T | C | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+646T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700925 | ||||||
chr10:17700987
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.912+708C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700987 | ||||||
chr10:17700987
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.912+708C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17700987 | ||||||
chr10:17701228
|
G | T | 83 | a0001c0001t0002g0390a0001c0001t0003g0024a0001c0001t0003g0025others(80): Show | 89 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.912+949G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701228 | ||||||
chr10:17701273
|
AAAT | A | 116 | a0001c0001t0001g0286a0001c0001t0002g0001a0001c0001t0002g0002others(113): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.912+997_912+999del others(3): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17701273 | |||||
chr10:17701319
|
A | G | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.912+1040A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701319 | ||||||
chr10:17701385
|
A | G | 1 | a0001c0001t0002g0237 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.912+1106A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701385 | ||||||
chr10:17701727
|
C | A | 4 | a0001c0001t0002g0228a0001c0001t0002g0249a0001c0001t0002g0290others(1): Show | 4 | NA18952.hp2 NA18961.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.912+1448C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701727 | ||||||
chr10:17701727
|
C | T | 1 | a0001c0001t0002g0292 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.912+1448C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701727 | ||||||
chr10:17701765
|
G | A | 3 | a0001c0002t0003g0377a0001c0002t0003g0378a0001c0002t0020g0376 | 3 | NA18957.hp1 NA18967.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.912+1486G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701765 | ||||||
chr10:17701861
|
G | C | 58 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0021others(55): Show | 63 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.912+1582G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701861 | ||||||
chr10:17701890
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.912+1611A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17701890 | ||||||
chr10:17701894
|
AAC | A | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.912+1619_912+1620d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17701894 | |||||
chr10:17702220
|
A | C | 18 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.912+1941A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702220 | ||||||
chr10:17702303
|
C | A | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.912+2024C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702303 | ||||||
chr10:17702373
|
A | C | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.913-2058A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702373 | ||||||
chr10:17702454
|
C | T | 2 | a0001c0002t0003g0034a0001c0002t0003g0035 | 2 | HG01243.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.913-1977C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702454 | ||||||
chr10:17702585
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0130others(4): Show | 7 | NA18944.hp2 NA19010.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-1846A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702585 | ||||||
chr10:17702748
|
G | A | 9 | a0001c0001t0002g0390a0001c0001t0003g0024a0001c0001t0003g0025others(6): Show | 9 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1683G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702748 | ||||||
chr10:17702776
|
G | A | 1 | a0001c0001t0005g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.913-1655G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702776 | ||||||
chr10:17702785
|
A | G | 28 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(25): Show | 31 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.913-1646A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702785 | ||||||
chr10:17702802
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.913-1629C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702802 | ||||||
chr10:17702806
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.913-1625G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702806 | ||||||
chr10:17702823
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108 | 5 | NA18952.hp1 NA18961.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.913-1608C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702823 | ||||||
chr10:17702829
|
G | A | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.913-1602G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702829 | ||||||
chr10:17702861
|
C | T | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG02630.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.913-1570C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702861 | ||||||
chr10:17702980
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.913-1451G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17702980 | ||||||
chr10:17703008
|
C | CA | 40 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(37): Show | 41 | HG00140.hp1 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.913-1404dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703008 | |||||
chr10:17703008
|
C | CAAA | 9 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0185others(6): Show | 9 | HG01192.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1406_913-1404d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703008 | |||||
chr10:17703008
|
CA | C | 14 | a0001c0001t0001g0063a0001c0001t0001g0104a0001c0001t0001g0126others(11): Show | 14 | HG00323.hp1 HG00558.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.913-1404delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703008 | |||||
chr10:17703015
|
AAAAAAAA others(6): Show |
A | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.913-1411_913-1399d others(15): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703015 | |||||
chr10:17703018
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-1408_913-1399d others(12): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703018 | |||||
chr10:17703023
|
AAAAAG | A | 9 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0001g0084others(6): Show | 9 | HG02622.hp2 HG02970.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.913-1383_913-1379d others(7): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703023 | |||||
chr10:17703023
|
AAAAAGAA others(3): Show |
A | 3 | a0001c0001t0001g0029a0001c0001t0030g0385a0001c0001t0031g0384 | 3 | HG02717.hp2 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.913-1388_913-1379d others(12): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703023 | |||||
chr10:17703026
|
AAG | A | 104 | a0001c0001t0001g0286a0001c0001t0002g0001a0001c0001t0002g0002others(101): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.913-1403_913-1402d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703026 | |||||
chr10:17703027
|
AG | A | 8 | a0001c0001t0002g0228a0001c0001t0002g0238a0001c0001t0002g0249others(5): Show | 8 | NA18943.hp2 NA18952.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-1403delG | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703027 | ||||||
chr10:17703125
|
A | G | 127 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0185others(124): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.913-1306A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703125 | ||||||
chr10:17703198
|
T | C | 3 | a0001c0002t0003g0338a0001c0002t0003g0339a0001c0002t0003g0351 | 3 | NA18968.hp2 NA19004.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.913-1233T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703198 | ||||||
chr10:17703231
|
C | G | 2 | a0001c0002t0003g0162a0001c0002t0003g0167 | 2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.913-1200C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703231 | ||||||
chr10:17703331
|
G | GT | 7 | a0001c0001t0001g0358a0001c0001t0002g0219a0001c0001t0002g0316others(4): Show | 7 | HG00323.hp1 HG01175.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-1086dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703331 | |||||
chr10:17703331
|
GT | G | 6 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0124others(3): Show | 6 | HG02965.hp2 NA18987.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.913-1086delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 17703331 | |||||
chr10:17703377
|
A | G | 1 | a0001c0001t0004g0308 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.913-1054A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703377 | ||||||
chr10:17703481
|
C | G | 3 | a0001c0001t0002g0275a0001c0001t0002g0283a0001c0001t0032g0225 | 3 | HG00735.hp1 HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.913-950C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703481 | ||||||
chr10:17703501
|
A | T | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.913-930A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703501 | ||||||
chr10:17703551
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.913-880A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703551 | ||||||
chr10:17703589
|
A | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.913-842A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703589 | ||||||
chr10:17703594
|
C | A | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.913-837C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703594 | ||||||
chr10:17703595
|
A | G | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-836A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703595 | ||||||
chr10:17703630
|
A | C | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.913-801A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703630 | ||||||
chr10:17703663
|
A | C | 1 | a0001c0001t0004g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.913-768A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703663 | ||||||
chr10:17703997
|
G | A | 321 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(318): Show | 346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.913-434G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17703997 | ||||||
chr10:17704001
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0002g0150 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.913-430T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704001 | ||||||
chr10:17704074
|
T | C | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.913-357T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704074 | ||||||
chr10:17704088
|
G | A | 2 | a0001c0001t0014g0131a0001c0001t0014g0140 | 2 | HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.913-343G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704088 | ||||||
chr10:17704178
|
G | T | 1 | a0001c0001t0023g0187 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.913-253G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704178 | ||||||
chr10:17704302
|
C | A | 27 | a0001c0001t0004g0032a0001c0001t0004g0055a0001c0001t0005g0003others(24): Show | 30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.913-129C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704302 | ||||||
chr10:17704306
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.913-125A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 9/13 | chr10 | 17704306 | ||||||
chr10:17704612
|
A | C | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1000+94A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704612 | ||||||
chr10:17704697
|
T | A | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1000+179T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704697 | ||||||
chr10:17704719
|
G | A | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1000+201G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704719 | ||||||
chr10:17704752
|
T | C | 17 | a0001c0001t0004g0017a0001c0001t0004g0032a0001c0001t0004g0055others(14): Show | 18 | HG00642.hp2 HG01884.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1001-218T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704752 | ||||||
chr10:17704754
|
G | A | 2 | a0001c0001t0001g0029a0001c0006t0028g0382 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1001-216G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704754 | ||||||
chr10:17704769
|
C | T | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(98): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1001-201C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704769 | ||||||
chr10:17704935
|
A | G | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1001-35A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 10/13 | chr10 | 17704935 | ||||||
chr10:17705054
|
G | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1055+30G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705054 | ||||||
chr10:17705109
|
T | TA | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1055+95dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 17705109 | |||||
chr10:17705122
|
T | C | 8 | a0001c0001t0002g0033a0001c0001t0002g0184a0001c0001t0002g0188others(5): Show | 8 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1055+98T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705122 | ||||||
chr10:17705190
|
T | C | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1055+166T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705190 | ||||||
chr10:17705276
|
A | G | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1055+252A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705276 | ||||||
chr10:17705390
|
C | T | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-198C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705390 | ||||||
chr10:17705449
|
A | G | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1056-139A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705449 | ||||||
chr10:17705501
|
C | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1056-87C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 11/13 | chr10 | 17705501 | ||||||
chr10:17705813
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(100): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1209+72A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17705813 | ||||||
chr10:17705880
|
T | C | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1209+139T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17705880 | ||||||
chr10:17705905
|
C | CA | 27 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0359others(24): Show | 27 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1209+181dupA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17705905 | |||||
chr10:17705905
|
CA | C | 22 | a0001c0001t0001g0063a0001c0001t0005g0003a0001c0001t0005g0009others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1209+181delA | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17705905 | |||||
chr10:17705909
|
A | G | 1 | a0001c0001t0015g0389 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1209+168A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17705909 | ||||||
chr10:17706052
|
C | T | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1209+311C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706052 | ||||||
chr10:17706053
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1209+312G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706053 | ||||||
chr10:17706064
|
T | G | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1209+323T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706064 | ||||||
chr10:17706127
|
T | G | 18 | a0001c0001t0001g0015a0001c0001t0001g0115a0001c0001t0001g0120others(15): Show | 19 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.1209+386T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706127 | ||||||
chr10:17706154
|
A | T | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+413A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706154 | ||||||
chr10:17706173
|
G | A | 289 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(286): Show | 315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1209+432G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706173 | ||||||
chr10:17706199
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1209+458C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706199 | ||||||
chr10:17706215
|
T | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+474T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706215 | ||||||
chr10:17706223
|
T | A | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1209+482T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706223 | ||||||
chr10:17706229
|
TTTG | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(46): Show | 56 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1209+503_1209+505d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706229 | |||||
chr10:17706232
|
G | T | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+491G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706232 | ||||||
chr10:17706247
|
T | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+506T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706247 | ||||||
chr10:17706256
|
T | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+515T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706256 | ||||||
chr10:17706259
|
C | G | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1209+518C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706259 | ||||||
chr10:17706261
|
T | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+520T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706261 | ||||||
chr10:17706264
|
A | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+523A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706264 | ||||||
chr10:17706270
|
G | T | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+529G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706270 | ||||||
chr10:17706272
|
T | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+531T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706272 | ||||||
chr10:17706274
|
A | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+533A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706274 | ||||||
chr10:17706285
|
T | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(100): Show | 111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1209+544T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706285 | ||||||
chr10:17706308
|
A | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+567A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706308 | ||||||
chr10:17706317
|
T | G | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+576T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706317 | ||||||
chr10:17706369
|
C | CT | 68 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0059others(65): Show | 70 | HG00140.hp1 HG00621.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1209+655dupT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
C | CTT | 97 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0061others(94): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1209+654_1209+655d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
C | CTTT | 33 | a0001c0001t0001g0125a0001c0001t0002g0002a0001c0001t0002g0006others(30): Show | 38 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1209+653_1209+655d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
C | CTTTT | 14 | a0001c0001t0002g0023a0001c0001t0002g0184a0001c0001t0002g0226others(11): Show | 16 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1209+652_1209+655d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
CT | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(64): Show | 73 | HG00609.hp2 HG01069.hp1 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.1209+655delT | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
CTT | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0056others(11): Show | 15 | HG01884.hp2 HG02055.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.1209+654_1209+655d others(4): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
CTTTT | C | 20 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(17): Show | 23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1209+652_1209+655d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706369
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0224a0001c0001t0002g0298a0001c0001t0002g0299 | 3 | HG00423.hp2 NA18968.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1209+644_1209+655d others(14): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17706369 | |||||
chr10:17706373
|
T | A | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+632T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706373 | ||||||
chr10:17706373
|
T | C | 5 | a0001c0001t0005g0047a0001c0001t0005g0050a0001c0001t0009g0312others(2): Show | 5 | HG01123.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209+632T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706373 | ||||||
chr10:17706374
|
T | C | 20 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(17): Show | 23 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1209+633T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706374 | ||||||
chr10:17706401
|
C | T | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209+660C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706401 | ||||||
chr10:17706402
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1209+661G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706402 | ||||||
chr10:17706413
|
C | T | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+672C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706413 | ||||||
chr10:17706417
|
G | T | 1 | a0001c0002t0003g0329 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1209+676G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706417 | ||||||
chr10:17706668
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1209+927C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706668 | ||||||
chr10:17706701
|
C | T | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1209+960C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706701 | ||||||
chr10:17706722
|
G | T | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209+981G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17706722 | ||||||
chr10:17707029
|
G | C | 3 | a0001c0001t0012g0182a0001c0001t0012g0386a0001c0001t0023g0187 | 3 | HG02970.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1209+1288G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707029 | ||||||
chr10:17707079
|
A | G | 31 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0174others(28): Show | 33 | HG00642.hp2 HG01255.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.1209+1338A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707079 | ||||||
chr10:17707175
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(97): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1209+1434C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707175 | ||||||
chr10:17707308
|
G | C | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(230): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1210-1468G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707308 | ||||||
chr10:17707334
|
C | T | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1210-1442C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707334 | ||||||
chr10:17707358
|
C | G | 58 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0021others(55): Show | 63 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1210-1418C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707358 | ||||||
chr10:17707480
|
G | A | 2 | a0001c0001t0005g0046a0001c0001t0005g0052 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1210-1296G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707480 | ||||||
chr10:17707488
|
G | A | 1 | a0001c0009t0015g0388 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1210-1288G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707488 | ||||||
chr10:17707585
|
T | C | 1 | a0001c0002t0003g0342 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1210-1191T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707585 | ||||||
chr10:17707587
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1210-1189G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707587 | ||||||
chr10:17707879
|
G | T | 1 | a0001c0001t0005g0047 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1210-897G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707879 | ||||||
chr10:17707915
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1210-861G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17707915 | ||||||
chr10:17708035
|
C | T | 2 | a0001c0002t0003g0313a0001c0002t0003g0342 | 2 | HG00558.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1210-741C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708035 | ||||||
chr10:17708073
|
G | T | 1 | a0001c0001t0009g0312 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1210-703G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708073 | ||||||
chr10:17708081
|
G | A | 3 | a0001c0001t0009g0383a0001c0001t0015g0389a0001c0009t0015g0388 | 3 | HG01884.hp2 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1210-695G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708081 | ||||||
chr10:17708096
|
T | C | 1 | a0001c0001t0002g0298 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1210-680T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708096 | ||||||
chr10:17708162
|
T | G | 13 | a0001c0001t0002g0221a0001c0001t0002g0259a0001c0001t0002g0261others(10): Show | 16 | NA18939.hp2 NA18940.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1210-614T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708162 | ||||||
chr10:17708171
|
T | G | 1 | a0001c0001t0010g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1210-605T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708171 | ||||||
chr10:17708261
|
C | G | 5 | a0001c0001t0006g0203a0001c0001t0006g0207a0001c0001t0006g0208others(2): Show | 5 | HG02615.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1210-515C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708261 | ||||||
chr10:17708264
|
C | T | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1210-512C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708264 | ||||||
chr10:17708545
|
A | C | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(101): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1210-231A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708545 | ||||||
chr10:17708594
|
C | CATCA | 8 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(5): Show | 8 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210-180_1210-177d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr10 | 17708594 | |||||
chr10:17708636
|
C | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(131): Show | 142 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1210-140C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 12/13 | chr10 | 17708636 | ||||||
chr10:17708969
|
T | G | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+18T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17708969 | ||||||
chr10:17709003
|
A | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1385+52A>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709003 | ||||||
chr10:17709047
|
T | C | 21 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1385+96T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709047 | ||||||
chr10:17709055
|
C | T | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+104C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709055 | ||||||
chr10:17709113
|
A | G | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1385+162A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709113 | ||||||
chr10:17709163
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1385+212A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709163 | ||||||
chr10:17709220
|
T | A | 3 | a0001c0001t0001g0134a0001c0003t0001g0118a0001c0003t0001g0151 | 3 | NA18944.hp2 NA19070.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1385+269T>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709220 | ||||||
chr10:17709323
|
C | T | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1385+372C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709323 | ||||||
chr10:17709342
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1385+391G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709342 | ||||||
chr10:17709354
|
CTCTT | C | 2 | a0001c0001t0002g0019a0001c0001t0002g0262 | 3 | HG00738.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1385+405_1385+408d others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709354 | |||||
chr10:17709477
|
A | C | 44 | a0001c0002t0003g0008a0001c0002t0003g0022a0001c0002t0003g0154others(41): Show | 46 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.1385+526A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709477 | ||||||
chr10:17709590
|
G | A | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1385+639G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709590 | ||||||
chr10:17709682
|
C | T | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1385+731C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709682 | ||||||
chr10:17709731
|
G | C | 5 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0364others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385+780G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709731 | ||||||
chr10:17709776
|
C | T | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1385+825C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709776 | ||||||
chr10:17709798
|
G | A | 92 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(89): Show | 95 | HG00323.hp1 HG00558.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1385+847G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17709798 | ||||||
chr10:17709963
|
G | GCAGGATT others(309): Show |
7 | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0070others(4): Show | 7 | HG01257.hp2 HG01975.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(320): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(310): Show |
3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0097 | 3 | NA18970.hp1 NA18982.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(321): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(310): Show |
61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(58): Show | 68 | HG00140.hp1 HG00423.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(321): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(310): Show |
1 | a0004c0011t0001g0057 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(321): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(311): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | NA18991.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(322): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(311): Show |
26 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0064others(23): Show | 27 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1385+1026_1385+102 others(322): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(311): Show |
1 | a0001c0001t0001g0067 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(322): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(312): Show |
1 | a0001c0001t0001g0065 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(323): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709963
|
G | GCAGGATT others(313): Show |
1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(324): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709963 | |||||
chr10:17709969
|
T | TTTTTTTT others(308): Show |
1 | a0001c0001t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1385+1026_1385+102 others(319): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17709969 | |||||
chr10:17710145
|
G | A | 5 | a0001c0001t0006g0203a0001c0001t0006g0207a0001c0001t0006g0208others(2): Show | 5 | HG02615.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385+1194G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710145 | ||||||
chr10:17710247
|
G | A | 1 | a0001c0002t0003g0345 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1385+1296G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710247 | ||||||
chr10:17710443
|
CAT | C | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1385+1493_1385+149 others(6): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710443 | ||||||
chr10:17710594
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1385+1643C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710594 | ||||||
chr10:17710746
|
C | T | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1385+1795C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710746 | ||||||
chr10:17710855
|
A | G | 1 | a0001c0001t0004g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1385+1904A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710855 | ||||||
chr10:17710909
|
A | G | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1385+1958A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710909 | ||||||
chr10:17710972
|
G | T | 2 | a0001c0002t0003g0170a0001c0002t0003g0171 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1385+2021G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17710972 | ||||||
chr10:17711045
|
A | G | 34 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(31): Show | 38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1385+2094A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711045 | ||||||
chr10:17711159
|
C | G | 36 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(33): Show | 40 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1385+2208C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711159 | ||||||
chr10:17711271
|
C | T | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+2320C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711271 | ||||||
chr10:17711294
|
C | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1385+2343C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711294 | ||||||
chr10:17711328
|
A | G | 7 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1385+2377A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711328 | ||||||
chr10:17711701
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1385+2750A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711701 | ||||||
chr10:17711785
|
C | G | 3 | a0001c0001t0023g0187a0001c0001t0030g0385a0001c0001t0031g0384 | 3 | HG02717.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1386-2758C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711785 | ||||||
chr10:17711797
|
G | A | 1 | a0001c0001t0005g0043 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1386-2746G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711797 | ||||||
chr10:17711857
|
C | T | 2 | a0001c0001t0017g0380a0001c0001t0017g0381 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1386-2686C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711857 | ||||||
chr10:17711871
|
T | C | 25 | a0001c0001t0004g0017a0001c0001t0004g0032a0001c0001t0004g0055others(22): Show | 26 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1386-2672T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711871 | ||||||
chr10:17711942
|
C | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1386-2601C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17711942 | ||||||
chr10:17712150
|
C | A | 54 | a0001c0002t0003g0007a0001c0002t0003g0008a0001c0002t0003g0021others(51): Show | 59 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1386-2393C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712150 | ||||||
chr10:17712183
|
A | G | 1 | a0001c0001t0001g0363 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1386-2360A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712183 | ||||||
chr10:17712266
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1386-2277C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712266 | ||||||
chr10:17712526
|
A | C | 2 | a0001c0001t0015g0389a0001c0009t0015g0388 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1386-2017A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712526 | ||||||
chr10:17712538
|
C | T | 251 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(248): Show | 266 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1386-2005C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712538 | ||||||
chr10:17712555
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1386-1988A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712555 | ||||||
chr10:17712705
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1386-1838T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712705 | ||||||
chr10:17712763
|
G | C | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386-1780G>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712763 | ||||||
chr10:17712810
|
T | C | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1386-1733T>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712810 | ||||||
chr10:17712813
|
A | G | 114 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(111): Show | 120 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1386-1730A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712813 | ||||||
chr10:17712861
|
CGGAGCGG others(2): Show |
C | 17 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(14): Show | 21 | HG00597.hp1 NA18944.hp1 NA18945.hp1 others(18): Show |
intron_variant | MODIFIER | c.1386-1673_1386-166 others(13): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17712861 | |||||
chr10:17712908
|
T | G | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1386-1635T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712908 | ||||||
chr10:17712986
|
C | T | 1 | a0001c0002t0003g0345 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1386-1557C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17712986 | ||||||
chr10:17713004
|
C | G | 4 | a0001c0001t0002g0242a0001c0001t0002g0309a0001c0001t0024g0295others(1): Show | 4 | HG00639.hp1 HG01168.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386-1539C>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713004 | ||||||
chr10:17713026
|
A | G | 34 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(31): Show | 38 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1386-1517A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713026 | ||||||
chr10:17713155
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1386-1388T>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713155 | ||||||
chr10:17713175
|
C | T | 1 | a0001c0002t0003g0353 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1386-1368C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713175 | ||||||
chr10:17713189
|
C | T | 25 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(22): Show | 28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1386-1354C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713189 | ||||||
chr10:17713291
|
A | C | 27 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(24): Show | 30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1386-1252A>C | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713291 | ||||||
chr10:17713389
|
TTGCCTAT others(27): Show |
T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1386-1143_1386-111 others(38): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17713389 | |||||
chr10:17713668
|
A | G | 3 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0365 | 3 | HG01069.hp1 HG01071.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1386-875A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713668 | ||||||
chr10:17713932
|
C | T | 24 | a0001c0001t0004g0017a0001c0001t0004g0032a0001c0001t0004g0055others(21): Show | 25 | HG00642.hp2 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1386-611C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713932 | ||||||
chr10:17713936
|
G | T | 9 | a0001c0001t0004g0016a0001c0001t0004g0174a0001c0001t0004g0175others(6): Show | 10 | HG01255.hp2 HG01256.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386-607G>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17713936 | ||||||
chr10:17714059
|
A | G | 1 | a0001c0001t0009g0383 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1386-484A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714059 | ||||||
chr10:17714312
|
A | ACCC | 22 | a0001c0001t0005g0003a0001c0001t0005g0009a0001c0001t0005g0010others(19): Show | 25 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1386-225_1386-223d others(5): Show |
STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr10 | 17714312 | |||||
chr10:17714336
|
A | G | 1 | a0001c0002t0003g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1386-207A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714336 | ||||||
chr10:17714405
|
C | T | 1 | a0001c0006t0028g0382 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1386-138C>T | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714405 | ||||||
chr10:17714448
|
A | G | 2 | a0001c0001t0030g0385a0001c0001t0031g0384 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1386-95A>G | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714448 | ||||||
chr10:17714452
|
G | A | 2 | a0001c0002t0004g0335a0001c0002t0004g0350 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1386-91G>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714452 | ||||||
chr10:17714534
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1386-9C>A | STAM | ENSG00000136738.15 | transcript | ENST00000377524.8 | protein_coding | 13/13 | chr10 | 17714534 |