geneid | 7058 |
---|---|
ensemblid | ENSG00000186340.17 |
hgncid | 11786 |
symbol | THBS2 |
name | thrombospondin 2 |
refseq_nuc | NM_003247.5 |
refseq_prot | NP_003238.2 |
ensembl_nuc | ENST00000617924.6 |
ensembl_prot | ENSP00000482784.1 |
mane_status | MANE Select |
chr | chr6 |
start | 169215785 |
end | 169253846 |
strand | - |
ver | v1.2 |
region | chr6:169215785-169253846 |
region5000 | chr6:169210785-169258846 |
regionname0 | THBS2_chr6_169215785_169253846 |
regionname5000 | THBS2_chr6_169210785_169258846 |
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 | 1172 | 362 | 70 | 81 | 154 | 16 | 39 | 109 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0002 | 0/0 | 1172 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0003 | 0/0 | 1172 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004 | 0/0 | 1172 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0005 | 0/0 | 1172 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0006 | 0/0 | 1172 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0007 | 0/0 | 1172 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0008 | 0/0 | 1172 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0009 | 0/0 | 1172 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0010 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0011 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0012 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0013 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0014 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0015 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0016 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
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 | 3519 | 170 | 17 | 38 | 89 | 4 | 20 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0002 | 0/0 | 3519 | 33 | 13 | 7 | 4 | 4 | 5 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0003 | 0/0 | 3519 | 31 | 5 | 8 | 16 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0004 | 0/0 | 3519 | 20 | 3 | 1 | 14 | 1 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0005 | 0/0 | 3519 | 18 | 6 | 6 | 4 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0006 | 0/0 | 3519 | 16 | 3 | 2 | 11 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0007 | 0/0 | 3519 | 10 | 0 | 8 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0008 | 0/0 | 3519 | 8 | 1 | 0 | 7 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0009 | 0/0 | 3519 | 8 | 0 | 3 | 5 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0010 | 0/0 | 3519 | 6 | 5 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0011 | 0/0 | 3519 | 6 | 0 | 0 | 0 | 1 | 5 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0012 | 0/0 | 3519 | 5 | 5 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0013 | 0/0 | 3519 | 4 | 0 | 2 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0014 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0015 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0016 | 0/0 | 3519 | 3 | 1 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0017 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0018 | 0/0 | 3519 | 3 | 0 | 1 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0019 | 0/0 | 3519 | 3 | 2 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0020 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0021 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0022 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0023 | 0/0 | 3519 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0024 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0025 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0026 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0027 | 0/0 | 3519 | 2 | 0 | 1 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0028 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0029 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0030 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0031 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0032 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0033 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0034 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0035 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0036 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0037 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0038 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0039 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0040 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0041 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0042 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0043 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0044 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0045 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0046 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0047 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0048 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0049 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0050 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0051 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0052 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
c0053 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2183 | 119 | 19 | 19 | 69 | 0 | 11 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0002 | 0/0 | 2176 | 80 | 27 | 17 | 24 | 6 | 6 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0003 | 0/0 | 2183 | 57 | 14 | 15 | 17 | 3 | 8 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0004 | 0/0 | 2183 | 31 | 3 | 8 | 14 | 2 | 4 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0005 | 0/0 | 2183 | 20 | 4 | 6 | 7 | 2 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0006 | 0/0 | 2183 | 18 | 0 | 0 | 18 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0007 | 0/0 | 2183 | 8 | 8 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0008 | 0/0 | 2183 | 6 | 4 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0009 | 0/0 | 2183 | 6 | 5 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0010 | 0/0 | 2183 | 6 | 0 | 4 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0011 | 1/0 | 2183 | 5 | 0 | 3 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0012 | 0/0 | 2183 | 4 | 3 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0013 | 0/0 | 2172 | 4 | 0 | 1 | 0 | 0 | 3 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0014 | 0/0 | 2183 | 3 | 2 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0015 | 0/0 | 2183 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0016 | 0/0 | 2172 | 3 | 0 | 0 | 0 | 0 | 3 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0017 | 0/0 | 2176 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0018 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0019 | 0/0 | 2183 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0020 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0021 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0022 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0023 | 0/0 | 2180 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0024 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0025 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0026 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0027 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0028 | 0/0 | 2183 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0029 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0030 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0031 | 0/0 | 2183 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0032 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0033 | 0/0 | 2183 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0034 | 0/0 | 2183 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0035 | 0/0 | 2183 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0036 | 0/0 | 2183 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0037 | 0/0 | 2183 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
t0038 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0016 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
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 | 3519 | 170 | 17 | 38 | 89 | 4 | 20 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0002 | 0/0 | 3519 | 33 | 13 | 7 | 4 | 4 | 5 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0003 | 0/0 | 3519 | 31 | 5 | 8 | 16 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0004 | 0/0 | 3519 | 20 | 3 | 1 | 14 | 1 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005 | 0/0 | 3519 | 18 | 6 | 6 | 4 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0006 | 0/0 | 3519 | 16 | 3 | 2 | 11 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0007 | 0/0 | 3519 | 10 | 0 | 8 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0008 | 0/0 | 3519 | 8 | 1 | 0 | 7 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0009 | 0/0 | 3519 | 8 | 0 | 3 | 5 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0011 | 0/0 | 3519 | 6 | 0 | 0 | 0 | 1 | 5 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0013 | 0/0 | 3519 | 4 | 0 | 2 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0014 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0015 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0016 | 0/0 | 3519 | 3 | 1 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0017 | 0/0 | 3519 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0018 | 0/0 | 3519 | 3 | 0 | 1 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0019 | 0/0 | 3519 | 3 | 2 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0022 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0023 | 0/0 | 3519 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0024 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0027 | 0/0 | 3519 | 2 | 0 | 1 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0028 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0031 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0033 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0036 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0037 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0038 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0039 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0041 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0043 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0044 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0045 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0002c0010 | 0/0 | 3519 | 6 | 5 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0003c0012 | 0/0 | 3519 | 5 | 5 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0003c0046 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004c0020 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004c0029 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004c0030 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0005c0025 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0005c0049 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0006c0026 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0007c0047 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0007c0048 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0008c0034 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0008c0053 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0009c0021 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0010c0052 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0011c0051 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0012c0050 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0013c0032 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0014c0040 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0015c0042 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0016c0035 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5701 | 92 | 6 | 12 | 63 | 0 | 10 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0003 | 0/0 | 5701 | 33 | 5 | 14 | 11 | 1 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0004 | 0/0 | 5701 | 14 | 2 | 1 | 7 | 0 | 4 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0005 | 0/0 | 5701 | 7 | 0 | 1 | 5 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0010 | 0/0 | 5701 | 6 | 0 | 4 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0011 | 1/0 | 5701 | 5 | 0 | 3 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0012 | 0/0 | 5701 | 3 | 2 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0013 | 0/0 | 5690 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0014 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0019 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0028 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0031 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0032 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0034 | 0/0 | 5701 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0035 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0036 | 0/0 | 5701 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0001t0037 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0002t0002 | 0/0 | 5694 | 29 | 13 | 6 | 3 | 4 | 3 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0002t0017 | 0/0 | 5694 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0002t0020 | 0/0 | 5694 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0002t0022 | 0/0 | 5694 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0003t0002 | 0/0 | 5694 | 29 | 5 | 7 | 15 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0003t0024 | 0/0 | 5694 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0003t0025 | 0/0 | 5694 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0004t0001 | 0/0 | 5701 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0004t0003 | 0/0 | 5701 | 8 | 2 | 0 | 4 | 1 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0004t0004 | 0/0 | 5701 | 8 | 1 | 1 | 6 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0004t0030 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0004t0033 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005t0001 | 0/0 | 5701 | 3 | 1 | 1 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005t0003 | 0/0 | 5701 | 3 | 1 | 0 | 1 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005t0004 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005t0005 | 0/0 | 5701 | 9 | 3 | 4 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005t0013 | 0/0 | 5690 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0005t0018 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0006t0006 | 0/0 | 5701 | 11 | 0 | 0 | 11 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0006t0008 | 0/0 | 5701 | 4 | 2 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0006t0027 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0007t0001 | 0/0 | 5701 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0007t0004 | 0/0 | 5701 | 7 | 0 | 5 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0008t0006 | 0/0 | 5701 | 7 | 0 | 0 | 7 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0008t0008 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0009t0002 | 0/0 | 5694 | 7 | 0 | 2 | 5 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0009t0026 | 0/0 | 5694 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0011t0003 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0011t0013 | 0/0 | 5690 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0011t0016 | 0/0 | 5690 | 3 | 0 | 0 | 0 | 0 | 3 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0013t0002 | 0/0 | 5694 | 4 | 0 | 2 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0014t0002 | 0/0 | 5694 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0015t0015 | 0/0 | 5701 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0016t0003 | 0/0 | 5701 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0016t0005 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0017t0002 | 0/0 | 5694 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0018t0005 | 0/0 | 5701 | 3 | 0 | 1 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0019t0003 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0019t0014 | 0/0 | 5701 | 2 | 1 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0022t0007 | 0/0 | 5701 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0023t0001 | 0/0 | 5701 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0024t0003 | 0/0 | 5701 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0027t0002 | 0/0 | 5694 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0027t0038 | 0/0 | 5694 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0028t0001 | 0/0 | 5701 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0031t0001 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0033t0007 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0036t0001 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0037t0003 | 0/0 | 5701 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0038t0001 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0039t0012 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0041t0001 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0043t0001 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0044t0003 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0001c0045t0003 | 0/0 | 5701 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0002c0010t0009 | 0/0 | 5701 | 6 | 5 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0003c0012t0007 | 0/0 | 5701 | 5 | 5 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0003c0046t0021 | 0/0 | 5694 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004c0020t0001 | 0/0 | 5701 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004c0029t0002 | 0/0 | 5694 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0004c0030t0003 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0005c0025t0002 | 0/0 | 5694 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0005c0025t0023 | 0/0 | 5698 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0005c0049t0004 | 0/0 | 5701 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0006c0026t0001 | 0/0 | 5701 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0007c0047t0029 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0007c0048t0002 | 0/0 | 5694 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0008c0034t0001 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0008c0053t0001 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0009c0021t0003 | 0/0 | 5701 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0010c0052t0008 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0011c0051t0001 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0012c0050t0001 | 0/0 | 5701 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0013c0032t0001 | 0/0 | 5701 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0014c0040t0002 | 0/0 | 5694 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0015c0042t0001 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
a0016c0035t0003 | 0/0 | 5701 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | copy fasta | chr6 | 169210785 | 169258846 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0010g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0011g0016 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0011g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0011g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0012g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0013g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0014g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0019g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0028g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0031g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0032g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0034g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0035g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0036g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0001t0037g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0017g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0017g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0020g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0002t0022g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0024g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0003t0025g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0030g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0004t0033g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0013g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0005t0018g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0008g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0008g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0006t0027g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0007t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0007t0004g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0007t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0007t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0007t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0007t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0008t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0009t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0009t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0009t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0009t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0009t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0009t0026g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0011t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0011t0013g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0011t0013g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0011t0016g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0011t0016g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0013t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0013t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0013t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0014t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0014t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0015t0015g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0015t0015g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0016t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0016t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0016t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0017t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0017t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0017t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0018t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0018t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0018t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0019t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0019t0014g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0019t0014g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0022t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0022t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0023t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0023t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0024t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0024t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0027t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0027t0038g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0028t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0031t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0033t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0036t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0037t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0038t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0039t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0041t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0043t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0044t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0001c0045t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0002c0010t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0002c0010t0009g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0002c0010t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0002c0010t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0003c0012t0007g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0003c0012t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0003c0012t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0003c0046t0021g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0004c0020t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0004c0020t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0004c0029t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0004c0030t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0005c0025t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0005c0025t0023g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0005c0049t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0006c0026t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0006c0026t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0007c0047t0029g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0007c0048t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0008c0034t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0008c0053t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0009c0021t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0009c0021t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0010c0052t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0011c0051t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0012c0050t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0013c0032t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0014c0040t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0015c0042t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
a0016c0035t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0159 | EUR | GBR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00099 | hp2 | a0001 | c0004 | t0003 | g0280 | EUR | GBR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0096 | EUR | GBR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00140 | hp2 | a0001 | c0001 | t0037 | g0231 | EUR | GBR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0016 | EUR | FIN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00323 | hp2 | a0001 | c0011 | t0003 | g0305 | EUR | FIN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00408 | hp1 | a0001 | c0004 | t0004 | g0252 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00423 | hp1 | a0001 | c0005 | t0004 | g0317 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00423 | hp2 | a0001 | c0003 | t0002 | g0261 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00438 | hp1 | a0001 | c0006 | t0006 | g0101 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00558 | hp1 | a0001 | c0005 | t0003 | g0327 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00609 | hp2 | a0001 | c0004 | t0030 | g0251 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00639 | hp1 | a0001 | c0004 | t0004 | g0271 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00733 | hp1 | a0001 | c0005 | t0005 | g0030 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00733 | hp2 | a0001 | c0007 | t0001 | g0009 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00735 | hp2 | a0002 | c0010 | t0009 | g0024 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00738 | hp1 | a0001 | c0007 | t0004 | g0007 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0263 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01069 | hp1 | a0001 | c0006 | t0008 | g0034 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01070 | hp2 | a0001 | c0001 | t0011 | g0122 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0284 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01081 | hp1 | a0001 | c0005 | t0005 | g0324 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01081 | hp2 | a0001 | c0007 | t0004 | g0007 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01099 | hp2 | a0001 | c0006 | t0008 | g0118 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01106 | hp1 | a0001 | c0007 | t0001 | g0009 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01109 | hp1 | a0001 | c0013 | t0002 | g0028 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0044 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01167 | hp1 | a0001 | c0007 | t0004 | g0007 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01168 | hp1 | a0001 | c0023 | t0001 | g0149 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01169 | hp1 | a0001 | c0007 | t0004 | g0115 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01169 | hp2 | a0001 | c0023 | t0001 | g0127 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01175 | hp2 | a0001 | c0001 | t0011 | g0121 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01192 | hp1 | a0001 | c0018 | t0005 | g0288 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01192 | hp2 | a0001 | c0003 | t0002 | g0297 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01243 | hp1 | a0001 | c0019 | t0014 | g0310 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01243 | hp2 | a0001 | c0002 | t0020 | g0037 | AMR | PUR | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01255 | hp1 | a0001 | c0027 | t0038 | g0346 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01257 | hp1 | a0013 | c0032 | t0001 | g0116 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01261 | hp1 | a0001 | c0009 | t0026 | g0217 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01261 | hp2 | a0001 | c0013 | t0002 | g0028 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0337 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01346 | hp2 | a0001 | c0005 | t0005 | g0325 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01361 | hp2 | a0001 | c0001 | t0011 | g0285 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01433 | hp1 | a0001 | c0007 | t0004 | g0056 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0202 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0048 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0008 | EUR | IBS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01515 | hp2 | a0001 | c0018 | t0005 | g0290 | EUR | IBS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01516 | hp1 | a0001 | c0013 | t0002 | g0303 | EUR | IBS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01516 | hp2 | a0001 | c0007 | t0004 | g0119 | EUR | IBS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0008 | EUR | IBS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01517 | hp2 | a0001 | c0013 | t0002 | g0302 | EUR | IBS | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01884 | hp1 | a0001 | c0022 | t0007 | g0189 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01891 | hp1 | a0004 | c0020 | t0001 | g0299 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01891 | hp2 | a0001 | c0036 | t0001 | g0333 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01928 | hp2 | a0001 | c0001 | t0010 | g0005 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01934 | hp1 | a0001 | c0005 | t0005 | g0030 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01934 | hp2 | a0001 | c0001 | t0010 | g0080 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01943 | hp2 | a0001 | c0001 | t0010 | g0005 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01952 | hp1 | a0001 | c0009 | t0002 | g0216 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01975 | hp1 | a0001 | c0003 | t0002 | g0262 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01975 | hp2 | a0001 | c0001 | t0034 | g0211 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01978 | hp2 | a0001 | c0009 | t0002 | g0215 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01981 | hp2 | a0001 | c0003 | t0025 | g0265 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02004 | hp1 | a0001 | c0005 | t0001 | g0321 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02004 | hp2 | a0001 | c0001 | t0010 | g0005 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02027 | hp2 | a0001 | c0004 | t0001 | g0281 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02040 | hp2 | a0001 | c0003 | t0024 | g0260 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02055 | hp1 | a0008 | c0053 | t0001 | g0312 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0065 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02056 | hp1 | a0001 | c0002 | t0022 | g0094 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0269 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02074 | hp1 | a0001 | c0006 | t0006 | g0182 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02074 | hp2 | a0001 | c0008 | t0006 | g0274 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02080 | hp2 | a0001 | c0008 | t0006 | g0245 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02132 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02135 | hp2 | a0015 | c0042 | t0001 | g0152 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02145 | hp1 | a0001 | c0033 | t0007 | g0105 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02145 | hp2 | a0012 | c0050 | t0001 | g0072 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02148 | hp1 | a0001 | c0007 | t0001 | g0009 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02155 | hp1 | a0001 | c0005 | t0005 | g0318 | EAS | CDX | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02155 | hp2 | a0001 | c0038 | t0001 | g0160 | EAS | CDX | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02165 | hp1 | a0001 | c0004 | t0004 | g0296 | EAS | CDX | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02165 | hp2 | a0001 | c0003 | t0002 | g0259 | EAS | CDX | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02258 | hp1 | a0001 | c0017 | t0002 | g0100 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02258 | hp2 | a0007 | c0048 | t0002 | g0287 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0342 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02293 | hp1 | a0001 | c0037 | t0003 | g0141 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02300 | hp1 | a0001 | c0005 | t0013 | g0306 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02300 | hp2 | a0001 | c0001 | t0036 | g0140 | AMR | PEL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02451 | hp1 | a0001 | c0024 | t0003 | g0086 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02451 | hp2 | a0001 | c0017 | t0002 | g0040 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02523 | hp1 | a0001 | c0027 | t0002 | g0322 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02572 | hp1 | a0001 | c0019 | t0003 | g0309 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02572 | hp2 | a0001 | c0019 | t0014 | g0311 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02602 | hp1 | a0001 | c0003 | t0002 | g0124 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0178 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02615 | hp1 | a0003 | c0012 | t0007 | g0042 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02615 | hp2 | a0006 | c0026 | t0001 | g0203 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0106 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02622 | hp2 | a0001 | c0004 | t0003 | g0066 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02630 | hp1 | a0001 | c0014 | t0002 | g0027 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0088 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02683 | hp1 | a0001 | c0016 | t0003 | g0144 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02683 | hp2 | a0001 | c0002 | t0017 | g0223 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02717 | hp1 | a0010 | c0052 | t0008 | g0206 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02717 | hp2 | a0001 | c0006 | t0027 | g0179 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02723 | hp2 | a0001 | c0028 | t0001 | g0029 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02735 | hp1 | a0001 | c0004 | t0003 | g0291 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02738 | hp1 | a0001 | c0016 | t0003 | g0199 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02809 | hp1 | a0003 | c0012 | t0007 | g0006 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02809 | hp2 | a0001 | c0028 | t0001 | g0029 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02818 | hp1 | a0004 | c0029 | t0002 | g0300 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02818 | hp2 | a0002 | c0010 | t0009 | g0205 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0193 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02886 | hp2 | a0004 | c0030 | t0003 | g0298 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02895 | hp1 | a0002 | c0010 | t0009 | g0023 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02895 | hp2 | a0001 | c0041 | t0001 | g0036 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0046 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02897 | hp2 | a0002 | c0010 | t0009 | g0023 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02922 | hp2 | a0003 | c0012 | t0007 | g0006 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02965 | hp1 | a0001 | c0015 | t0015 | g0017 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02965 | hp2 | a0001 | c0014 | t0002 | g0027 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0067 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02970 | hp2 | a0006 | c0026 | t0001 | g0207 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02976 | hp2 | a0009 | c0021 | t0003 | g0079 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03041 | hp2 | a0001 | c0005 | t0005 | g0323 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03098 | hp1 | a0007 | c0047 | t0029 | g0055 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0330 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03130 | hp2 | a0001 | c0015 | t0015 | g0017 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03139 | hp2 | a0003 | c0012 | t0007 | g0006 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03195 | hp1 | a0001 | c0039 | t0012 | g0045 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03225 | hp1 | a0008 | c0034 | t0001 | g0249 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03239 | hp1 | a0001 | c0045 | t0003 | g0145 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03239 | hp2 | a0001 | c0011 | t0013 | g0304 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03453 | hp1 | a0005 | c0025 | t0002 | g0110 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03486 | hp1 | a0001 | c0005 | t0018 | g0032 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03486 | hp2 | a0001 | c0008 | t0008 | g0279 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03490 | hp1 | a0001 | c0011 | t0016 | g0031 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03491 | hp2 | a0014 | c0040 | t0002 | g0229 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03492 | hp1 | a0001 | c0011 | t0016 | g0031 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03516 | hp1 | a0009 | c0021 | t0003 | g0050 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03516 | hp2 | a0001 | c0003 | t0002 | g0244 | AFR | ESN | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03540 | hp1 | a0001 | c0004 | t0004 | g0117 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | GWD | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03579 | hp2 | a0001 | c0001 | t0035 | g0329 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0104 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03688 | hp1 | a0001 | c0002 | t0017 | g0240 | SAS | STU | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03688 | hp2 | a0001 | c0011 | t0013 | g0307 | SAS | STU | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0198 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03831 | hp1 | a0001 | c0003 | t0002 | g0283 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03831 | hp2 | a0001 | c0005 | t0001 | g0328 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03834 | hp1 | a0001 | c0001 | t0013 | g0294 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03834 | hp2 | a0001 | c0001 | t0019 | g0154 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0135 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03942 | hp1 | a0001 | c0011 | t0016 | g0345 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03942 | hp2 | a0001 | c0005 | t0003 | g0326 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG04184 | hp2 | a0001 | c0001 | t0031 | g0295 | SAS | BEB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG04228 | hp2 | a0001 | c0044 | t0003 | g0058 | SAS | STU | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18522 | hp1 | a0001 | c0016 | t0005 | g0334 | AFR | YRI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18522 | hp2 | a0003 | c0012 | t0007 | g0041 | AFR | YRI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CHB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | YRI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | YRI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18942 | hp2 | a0001 | c0009 | t0002 | g0214 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18944 | hp1 | a0001 | c0004 | t0003 | g0255 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18945 | hp1 | a0016 | c0035 | t0003 | g0200 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18945 | hp2 | a0001 | c0009 | t0002 | g0013 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18954 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18956 | hp2 | a0001 | c0004 | t0004 | g0246 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18960 | hp2 | a0001 | c0006 | t0006 | g0169 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18964 | hp1 | a0001 | c0006 | t0006 | g0341 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18964 | hp2 | a0001 | c0004 | t0004 | g0257 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18968 | hp2 | a0001 | c0009 | t0002 | g0013 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18969 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18970 | hp2 | a0001 | c0006 | t0006 | g0237 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18971 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18974 | hp1 | a0001 | c0008 | t0006 | g0254 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18975 | hp1 | a0001 | c0008 | t0006 | g0253 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18977 | hp2 | a0001 | c0004 | t0003 | g0075 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18978 | hp1 | a0001 | c0004 | t0004 | g0076 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18981 | hp1 | a0001 | c0006 | t0006 | g0113 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18981 | hp2 | a0001 | c0003 | t0002 | g0248 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18985 | hp1 | a0001 | c0003 | t0002 | g0270 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18985 | hp2 | a0001 | c0008 | t0006 | g0258 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18987 | hp1 | a0001 | c0001 | t0010 | g0222 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18987 | hp2 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18990 | hp1 | a0001 | c0009 | t0002 | g0013 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18990 | hp2 | a0001 | c0043 | t0001 | g0165 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18992 | hp1 | a0001 | c0006 | t0006 | g0172 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18992 | hp2 | a0001 | c0001 | t0032 | g0184 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18994 | hp2 | a0001 | c0004 | t0001 | g0264 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18995 | hp1 | a0001 | c0005 | t0005 | g0316 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18998 | hp1 | a0001 | c0006 | t0006 | g0238 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19000 | hp2 | a0001 | c0008 | t0006 | g0276 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19002 | hp1 | a0001 | c0004 | t0033 | g0247 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19003 | hp2 | a0001 | c0031 | t0001 | g0064 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19004 | hp2 | a0001 | c0004 | t0004 | g0256 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19007 | hp1 | a0001 | c0003 | t0002 | g0278 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19007 | hp2 | a0001 | c0001 | t0010 | g0227 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19011 | hp2 | a0001 | c0004 | t0003 | g0277 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19030 | hp1 | a0001 | c0003 | t0002 | g0273 | AFR | LWK | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19030 | hp2 | a0001 | c0015 | t0015 | g0343 | AFR | LWK | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19043 | hp1 | a0003 | c0046 | t0021 | g0315 | AFR | LWK | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19043 | hp2 | a0001 | c0005 | t0003 | g0308 | AFR | LWK | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19056 | hp1 | a0001 | c0003 | t0002 | g0268 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19066 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19067 | hp2 | a0001 | c0006 | t0006 | g0068 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19068 | hp1 | a0001 | c0008 | t0006 | g0266 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19070 | hp2 | a0001 | c0006 | t0006 | g0236 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19074 | hp2 | a0001 | c0004 | t0003 | g0275 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19079 | hp1 | a0001 | c0009 | t0002 | g0218 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19083 | hp1 | a0001 | c0006 | t0006 | g0074 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19083 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19240 | hp1 | a0001 | c0006 | t0008 | g0014 | AFR | YRI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA19240 | hp2 | a0001 | c0024 | t0003 | g0099 | AFR | YRI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20129 | hp1 | a0001 | c0005 | t0001 | g0319 | AFR | ASW | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20129 | hp2 | a0011 | c0051 | t0001 | g0208 | AFR | ASW | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20752 | hp1 | a0001 | c0018 | t0005 | g0289 | EUR | TSI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20752 | hp2 | a0001 | c0001 | t0028 | g0192 | EUR | TSI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0233 | EUR | TSI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20805 | hp2 | a0001 | c0007 | t0004 | g0120 | EUR | TSI | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01123 | hp1 | a0005 | c0049 | t0004 | g0109 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0286 | AMR | CLM | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02109 | hp2 | a0001 | c0006 | t0008 | g0014 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02486 | hp1 | a0001 | c0022 | t0007 | g0038 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02559 | hp1 | a0001 | c0017 | t0002 | g0039 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG02559 | hp2 | a0004 | c0020 | t0001 | g0301 | AFR | ACB | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03471 | hp1 | a0001 | c0014 | t0002 | g0114 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG03471 | hp2 | a0002 | c0010 | t0009 | g0204 | AFR | MSL | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG06807 | hp1 | a0002 | c0010 | t0009 | g0024 | AFR | USA | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
HG06807 | hp2 | a0001 | c0005 | t0005 | g0335 | AFR | USA | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20300 | hp1 | a0005 | c0025 | t0023 | g0078 | AFR | USA | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0340 | AFR | USA | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA21309 | hp1 | a0001 | c0005 | t0005 | g0320 | AFR | LWK | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0250 | AFR | LWK | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0148 | REF | REF | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0011 | g0016 | REF | REF | THBS2_chr6_169210785_169258846 | THBS2 | chr6 | 169210785 | 169258846 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169221478
|
G | A | 1 | a0014 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.3323C>T | p.Thr1108Met | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/22 | 3468/5701 | 3323/3519 | 1108/1172 | chr6 | 169221478 | ||
chr6:169221505
|
G | A | 1 | a0013 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.3296C>T | p.Pro1099Leu | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/22 | 3441/5701 | 3296/3519 | 1099/1172 | chr6 | 169221505 | ||
chr6:169222413
|
G | C | 1 | a0011 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.3057C>G | p.Asp1019Glu | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/22 | 3202/5701 | 3057/3519 | 1019/1172 | chr6 | 169222413 | ||
chr6:169223467
|
G | A | 1 | a0015 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.2782C>T | p.Arg928Trp | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/22 | 2927/5701 | 2782/3519 | 928/1172 | chr6 | 169223467 | ||
chr6:169229589
|
C | T | 1 | a0016 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.2242G>A | p.Gly748Ser | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/22 | 2387/5701 | 2242/3519 | 748/1172 | chr6 | 169229589 | ||
chr6:169229628
|
C | T | 1 | a0008 | 2 | HG02055.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.2203G>A | p.Gly735Arg | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/22 | 2348/5701 | 2203/3519 | 735/1172 | chr6 | 169229628 | ||
chr6:169237628
|
G | A | 1 | a0010 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1297C>T | p.Arg433Cys | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/22 | 1442/5701 | 1297/3519 | 433/1172 | chr6 | 169237628 | ||
chr6:169239605
|
G | A | 2 | a0002a0003 | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
missense_variant | MODERATE | c.1123C>T | p.Leu375Phe | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/22 | 1268/5701 | 1123/3519 | 375/1172 | chr6 | 169239605 | ||
chr6:169240591
|
G | A | 1 | a0007 | 2 | HG02258.hp2 HG03098.hp1 |
missense_variant&splice_region_variant | MODERATE | c.893C>T | p.Ser298Leu | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/22 | 1038/5701 | 893/3519 | 298/1172 | chr6 | 169240591 | ||
chr6:169241770
|
T | C | 1 | a0005 | 3 | HG01123.hp1 HG03453.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.883A>G | p.Lys295Glu | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/22 | 1028/5701 | 883/3519 | 295/1172 | chr6 | 169241770 | ||
chr6:169248551
|
C | T | 2 | a0009a0012 | 3 | HG02145.hp2 HG02976.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.475G>A | p.Glu159Lys | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/22 | 620/5701 | 475/3519 | 159/1172 | chr6 | 169248551 | ||
chr6:169248628
|
G | C | 5 | a0002a0006a0010others(2): Show | 11 | HG00735.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
missense_variant | MODERATE | c.398C>G | p.Thr133Ser | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/22 | 543/5701 | 398/3519 | 133/1172 | chr6 | 169248628 | ||
chr6:169248665
|
C | T | 1 | a0004 | 4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.361G>A | p.Ala121Thr | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/22 | 506/5701 | 361/3519 | 121/1172 | chr6 | 169248665 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169220268
|
G | A | 4 | a0001c0022a0001c0033a0001c0037others(1): Show | 9 | HG01884.hp1 HG02145.hp1 HG02293.hp1 others(6): Show |
synonymous_variant | LOW | c.3441C>T | p.Gly1147Gly | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/22 | 3586/5701 | 3441/3519 | 1147/1172 | chr6 | 169220268 | ||
chr6:169220310
|
G | A | 1 | a0001c0038 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.3399C>T | p.Val1133Val | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/22 | 3544/5701 | 3399/3519 | 1133/1172 | chr6 | 169220310 | ||
chr6:169221441
|
A | G | 17 | a0001c0002a0001c0003a0001c0006others(14): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
synonymous_variant | LOW | c.3360T>C | p.Thr1120Thr | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/22 | 3505/5701 | 3360/3519 | 1120/1172 | chr6 | 169221441 | ||
chr6:169221447
|
G | C | 3 | a0001c0022a0001c0033a0003c0012 | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
synonymous_variant | LOW | c.3354C>G | p.Pro1118Pro | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/22 | 3499/5701 | 3354/3519 | 1118/1172 | chr6 | 169221447 | ||
chr6:169221504
|
G | T | 3 | a0001c0036a0008c0034a0008c0053 | 3 | HG01891.hp2 HG02055.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.3297C>A | p.Pro1099Pro | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/22 | 3442/5701 | 3297/3519 | 1099/1172 | chr6 | 169221504 | ||
chr6:169221510
|
G | A | 1 | a0001c0039 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.3291C>T | p.His1097His | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/22 | 3436/5701 | 3291/3519 | 1097/1172 | chr6 | 169221510 | ||
chr6:169222230
|
G | A | 3 | a0001c0022a0001c0033a0003c0012 | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
synonymous_variant | LOW | c.3240C>T | p.Asn1080Asn | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/22 | 3385/5701 | 3240/3519 | 1080/1172 | chr6 | 169222230 | ||
chr6:169222395
|
G | A | 12 | a0001c0002a0001c0003a0001c0009others(9): Show | 90 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
synonymous_variant | LOW | c.3075C>T | p.Ala1025Ala | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/22 | 3220/5701 | 3075/3519 | 1025/1172 | chr6 | 169222395 | ||
chr6:169223255
|
G | A | 2 | a0001c0041a0004c0020 | 3 | HG01891.hp1 HG02559.hp2 HG02895.hp2 |
synonymous_variant | LOW | c.2994C>T | p.Ile998Ile | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/22 | 3139/5701 | 2994/3519 | 998/1172 | chr6 | 169223255 | ||
chr6:169225200
|
G | A | 1 | a0001c0033 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.2718C>T | p.Pro906Pro | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/22 | 2863/5701 | 2718/3519 | 906/1172 | chr6 | 169225200 | ||
chr6:169229581
|
G | C | 2 | a0008c0034a0008c0053 | 2 | HG02055.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.2250C>G | p.Thr750Thr | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/22 | 2395/5701 | 2250/3519 | 750/1172 | chr6 | 169229581 | ||
chr6:169229629
|
G | A | 4 | a0001c0023a0002c0010a0003c0012others(1): Show | 14 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
synonymous_variant | LOW | c.2202C>T | p.Asp734Asp | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/22 | 2347/5701 | 2202/3519 | 734/1172 | chr6 | 169229629 | ||
chr6:169232010
|
G | A | 1 | a0001c0043 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.2121C>T | p.Cys707Cys | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/22 | 2266/5701 | 2121/3519 | 707/1172 | chr6 | 169232010 | ||
chr6:169232124
|
G | A | 10 | a0001c0003a0001c0004a0001c0008others(7): Show | 80 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
synonymous_variant | LOW | c.2007C>T | p.Gly669Gly | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/22 | 2152/5701 | 2007/3519 | 669/1172 | chr6 | 169232124 | ||
chr6:169234801
|
G | A | 1 | a0001c0018 | 3 | HG01192.hp1 HG01515.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.1584C>T | p.Tyr528Tyr | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/22 | 1729/5701 | 1584/3519 | 528/1172 | chr6 | 169234801 | ||
chr6:169237668
|
G | C | 18 | a0001c0003a0001c0004a0001c0008others(15): Show | 95 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
synonymous_variant | LOW | c.1257C>G | p.Ser419Ser | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/22 | 1402/5701 | 1257/3519 | 419/1172 | chr6 | 169237668 | ||
chr6:169237752
|
G | A | 2 | a0001c0044a0001c0045 | 2 | HG03239.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.1173C>T | p.Thr391Thr | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/22 | 1318/5701 | 1173/3519 | 391/1172 | chr6 | 169237752 | ||
chr6:169239651
|
G | T | 2 | a0001c0019a0001c0033 | 4 | HG01243.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
synonymous_variant | LOW | c.1077C>A | p.Thr359Thr | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/22 | 1222/5701 | 1077/3519 | 359/1172 | chr6 | 169239651 | ||
chr6:169241876
|
C | T | 4 | a0001c0007a0001c0011a0001c0014others(1): Show | 20 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(17): Show |
synonymous_variant | LOW | c.777G>A | p.Ser259Ser | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/22 | 922/5701 | 777/3519 | 259/1172 | chr6 | 169241876 | ||
chr6:169241936
|
C | T | 1 | a0001c0031 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.717G>A | p.Glu239Glu | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/22 | 862/5701 | 717/3519 | 239/1172 | chr6 | 169241936 | ||
chr6:169246264
|
G | A | 1 | a0001c0028 | 2 | HG02723.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.627C>T | p.Val209Val | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/22 | 772/5701 | 627/3519 | 209/1172 | chr6 | 169246264 | ||
chr6:169248507
|
G | A | 1 | a0001c0009 | 8 | HG01261.hp1 HG01952.hp1 HG01978.hp2 others(5): Show |
synonymous_variant | LOW | c.519C>T | p.Phe173Phe | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/22 | 664/5701 | 519/3519 | 173/1172 | chr6 | 169248507 | ||
chr6:169248672
|
G | A | 7 | a0001c0005a0001c0011a0001c0013others(4): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
synonymous_variant | LOW | c.354C>T | p.Asn118Asn | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/22 | 499/5701 | 354/3519 | 118/1172 | chr6 | 169248672 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169215851
|
G | T | 1 | a0001c0006t0027 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1971C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1971 | chr6 | 169215851 | |||||
chr6:169216002
|
C | T | 93 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(90): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
3_prime_UTR_variant | MODIFIER | c.*1820G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1820 | chr6 | 169216002 | |||||
chr6:169216017
|
C | T | 43 | a0001c0001t0003a0001c0001t0034a0001c0001t0035others(40): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1805G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1805 | chr6 | 169216017 | |||||
chr6:169216075
|
T | C | 1 | a0001c0003t0024 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1747A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1747 | chr6 | 169216075 | |||||
chr6:169216083
|
G | A | 1 | a0001c0001t0028 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1739 | chr6 | 169216083 | |||||
chr6:169216163
|
AAAC | A | 20 | a0001c0002t0002a0001c0002t0017a0001c0002t0020others(17): Show | 90 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1656_*1658delGTT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1656 | chr6 | 169216163 | |||||
chr6:169216178
|
G | A | 1 | a0001c0001t0036 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1644C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1644 | chr6 | 169216178 | |||||
chr6:169216236
|
G | A | 17 | a0001c0001t0003a0001c0001t0034a0001c0001t0035others(14): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1586C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1586 | chr6 | 169216236 | |||||
chr6:169216252
|
T | C | 63 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(60): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1570A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1570 | chr6 | 169216252 | |||||
chr6:169216256
|
C | G | 1 | a0007c0047t0029 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1566G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1566 | chr6 | 169216256 | |||||
chr6:169216300
|
A | G | 1 | a0007c0047t0029 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1522T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1522 | chr6 | 169216300 | |||||
chr6:169216308
|
G | T | 1 | a0001c0004t0033 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1514C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1514 | chr6 | 169216308 | |||||
chr6:169216328
|
C | T | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(14): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1494G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1494 | chr6 | 169216328 | |||||
chr6:169216338
|
T | G | 2 | a0001c0001t0012a0001c0039t0012 | 4 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1484 | chr6 | 169216338 | |||||
chr6:169216413
|
AAAAC | A | 19 | a0001c0002t0002a0001c0002t0017a0001c0002t0020others(16): Show | 89 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1405_*1408delGTTT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1405 | chr6 | 169216413 | |||||
chr6:169216485
|
G | A | 1 | a0001c0003t0025 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1337C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1337 | chr6 | 169216485 | |||||
chr6:169216513
|
C | CG | 63 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(60): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1308_*1309insC | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1308 | chr6 | 169216513 | |||||
chr6:169216585
|
C | T | 5 | a0001c0001t0005a0001c0001t0028a0001c0005t0005others(2): Show | 21 | HG00733.hp1 HG01081.hp1 HG01192.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1237 | chr6 | 169216585 | |||||
chr6:169216602
|
AT | A | 63 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(60): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1219delA | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1219 | chr6 | 169216602 | |||||
chr6:169216660
|
G | C | 16 | a0001c0001t0003a0001c0001t0034a0001c0001t0036others(13): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1162C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1162 | chr6 | 169216660 | |||||
chr6:169216678
|
A | C | 1 | a0001c0001t0010 | 6 | HG01928.hp2 HG01934.hp2 HG01943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1144T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1144 | chr6 | 169216678 | |||||
chr6:169216680
|
CTAA | C | 4 | a0001c0001t0013a0001c0005t0013a0001c0011t0013others(1): Show | 7 | HG02300.hp1 HG03239.hp2 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1139_*1141delTTA | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1139 | chr6 | 169216680 | |||||
chr6:169216700
|
A | G | 1 | a0001c0002t0022 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1122 | chr6 | 169216700 | |||||
chr6:169216715
|
T | G | 4 | a0001c0006t0008a0001c0006t0027a0001c0008t0008others(1): Show | 7 | HG01069.hp1 HG01099.hp2 HG02109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1107A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1107 | chr6 | 169216715 | |||||
chr6:169216787
|
T | C | 1 | a0001c0009t0026 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1035A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 1035 | chr6 | 169216787 | |||||
chr6:169216923
|
A | T | 1 | a0001c0001t0035 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 899 | chr6 | 169216923 | |||||
chr6:169216936
|
G | A | 6 | a0001c0001t0004a0001c0004t0004a0001c0005t0004others(3): Show | 34 | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*886C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 886 | chr6 | 169216936 | |||||
chr6:169217005
|
C | T | 1 | a0003c0046t0021 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*817G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 817 | chr6 | 169217005 | |||||
chr6:169217010
|
G | A | 17 | a0001c0001t0003a0001c0001t0034a0001c0001t0035others(14): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*812C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 812 | chr6 | 169217010 | |||||
chr6:169217016
|
G | A | 27 | a0001c0002t0002a0001c0002t0017a0001c0002t0020others(24): Show | 116 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*806C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 806 | chr6 | 169217016 | |||||
chr6:169217017
|
C | T | 6 | a0001c0006t0006a0001c0006t0008a0001c0006t0027others(3): Show | 25 | HG00438.hp1 HG01069.hp1 HG01099.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*805G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 805 | chr6 | 169217017 | |||||
chr6:169217074
|
A | C | 1 | a0002c0010t0009 | 6 | HG00735.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*748T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 748 | chr6 | 169217074 | |||||
chr6:169217104
|
G | A | 17 | a0001c0001t0003a0001c0001t0034a0001c0001t0035others(14): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 718 | chr6 | 169217104 | |||||
chr6:169217153
|
A | G | 1 | a0001c0015t0015 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*669T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 669 | chr6 | 169217153 | |||||
chr6:169217194
|
C | T | 1 | a0001c0002t0017 | 2 | HG02683.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 628 | chr6 | 169217194 | |||||
chr6:169217306
|
G | T | 1 | a0001c0001t0034 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 516 | chr6 | 169217306 | |||||
chr6:169217317
|
T | G | 1 | a0001c0015t0015 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*505A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 505 | chr6 | 169217317 | |||||
chr6:169217334
|
A | G | 20 | a0001c0002t0002a0001c0002t0017a0001c0002t0020others(17): Show | 90 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*488T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 488 | chr6 | 169217334 | |||||
chr6:169217334
|
A | T | 1 | a0001c0001t0032 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*488T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 488 | chr6 | 169217334 | |||||
chr6:169217335
|
T | C | 62 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(59): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*487A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 487 | chr6 | 169217335 | |||||
chr6:169217567
|
C | T | 1 | a0001c0001t0031 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 255 | chr6 | 169217567 | |||||
chr6:169217631
|
A | C | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(14): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 191 | chr6 | 169217631 | |||||
chr6:169217644
|
T | G | 1 | a0001c0001t0037 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*178A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 178 | chr6 | 169217644 | |||||
chr6:169217681
|
CAGGAGGT others(1): Show |
C | 4 | a0001c0001t0013a0001c0005t0013a0001c0011t0013others(1): Show | 7 | HG02300.hp1 HG03239.hp2 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*140delCACCTC others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 133 | chr6 | 169217681 | |||||
chr6:169217745
|
A | G | 26 | a0001c0002t0002a0001c0002t0017a0001c0002t0020others(23): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*77T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 77 | chr6 | 169217745 | |||||
chr6:169217794
|
G | A | 4 | a0001c0001t0013a0001c0005t0013a0001c0011t0013others(1): Show | 7 | HG02300.hp1 HG03239.hp2 HG03490.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*28C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 28 | chr6 | 169217794 | |||||
chr6:169217817
|
C | T | 1 | a0001c0001t0019 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 22/22 | 5 | chr6 | 169217817 | |||||
chr6:169253786
|
G | A | 2 | a0001c0011t0016a0001c0027t0038 | 4 | HG01255.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-85C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/22 | 3002 | chr6 | 169253786 | |||||
chr6:169253845
|
C | T | 1 | a0001c0005t0018 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/22 | 3061 | chr6 | 169253845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169217839
|
GA | G | 228 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(225): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3512-11delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169217839 | ||||||
chr6:169217940
|
GATCT | G | 4 | a0001c0006t0008g0014a0001c0006t0008g0034a0001c0006t0008g0118others(1): Show | 5 | HG01069.hp1 HG01099.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.3512-115_3512-112d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169217940 | ||||||
chr6:169217949
|
TATGGATG others(85): Show |
T | 32 | a0001c0001t0004g0043a0001c0001t0004g0108a0001c0001t0005g0102others(29): Show | 34 | HG00733.hp1 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3512-212_3512-121d others(94): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169217949 | ||||||
chr6:169217971
|
T | A | 3 | a0001c0001t0004g0054a0001c0001t0004g0104a0001c0001t0004g0147 | 3 | HG03654.hp1 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3512-142A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169217971 | ||||||
chr6:169217978
|
GATGGGTG others(102): Show |
G | 28 | a0001c0001t0004g0054a0001c0001t0004g0061a0001c0001t0004g0089others(25): Show | 30 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.3512-258_3512-150d others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169217978 | ||||||
chr6:169217993
|
GAGATGGG others(5): Show |
G | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512-176_3512-165d others(14): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169217993 | ||||||
chr6:169218040
|
AGATG | A | 137 | a0001c0001t0001g0332a0001c0001t0003g0012a0001c0001t0003g0018others(134): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.3512-215_3512-212d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218040 | ||||||
chr6:169218040
|
AGATGGAT others(5): Show |
A | 6 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0221others(3): Show | 6 | HG00673.hp1 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.3512-223_3512-212d others(14): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218040 | ||||||
chr6:169218077
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-248C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218077 | ||||||
chr6:169218092
|
GTGGGTGG others(5): Show |
G | 1 | a0007c0047t0029g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3512-275_3512-264d others(14): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218092 | ||||||
chr6:169218174
|
G | GATGGATG others(22): Show |
1 | a0001c0033t0007g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3512-374_3512-346d others(31): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218174 | ||||||
chr6:169218195
|
A | T | 1 | a0001c0001t0003g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3512-366T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218195 | ||||||
chr6:169218224
|
ATGGT | A | 154 | a0001c0001t0004g0054a0001c0001t0004g0061a0001c0001t0004g0089others(151): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.3512-399_3512-396d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218224 | ||||||
chr6:169218228
|
T | G | 56 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(53): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.3512-399A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218228 | ||||||
chr6:169218231
|
G | A | 1 | a0015c0042t0001g0152 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3512-402C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218231 | ||||||
chr6:169218236
|
C | G | 222 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(219): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.3512-407G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218236 | ||||||
chr6:169218265
|
A | ATGGGTGG others(18): Show |
1 | a0001c0004t0030g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3512-437_3512-436i others(27): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218265 | ||||||
chr6:169218267
|
G | A | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3512-438C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218267 | ||||||
chr6:169218273
|
A | G | 1 | a0001c0004t0030g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3512-444T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218273 | ||||||
chr6:169218280
|
T | G | 1 | a0001c0004t0030g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3512-451A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218280 | ||||||
chr6:169218282
|
G | A | 1 | a0001c0004t0030g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3512-453C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218282 | ||||||
chr6:169218298
|
G | A | 1 | a0001c0004t0030g0251 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3512-469C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218298 | ||||||
chr6:169218322
|
G | T | 1 | a0001c0001t0028g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3512-493C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218322 | ||||||
chr6:169218359
|
T | TGATG | 160 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(157): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.3512-534_3512-531d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218359 | ||||||
chr6:169218382
|
A | G | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3512-553T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218382 | ||||||
chr6:169218388
|
G | C | 3 | a0001c0001t0004g0054a0001c0001t0004g0104a0001c0001t0004g0147 | 3 | HG03654.hp1 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3512-559C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218388 | ||||||
chr6:169218414
|
GGATGGAT others(2): Show |
G | 4 | a0001c0024t0003g0086a0001c0024t0003g0099a0009c0021t0003g0050others(1): Show | 4 | HG02451.hp1 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3512-594_3512-586d others(11): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218414 | ||||||
chr6:169218471
|
A | ATGAG | 99 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(96): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3512-646_3512-643d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218471 | ||||||
chr6:169218490
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-661T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218490 | ||||||
chr6:169218491
|
T | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-662A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218491 | ||||||
chr6:169218493
|
G | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-664C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218493 | ||||||
chr6:169218517
|
AGATG | A | 5 | a0001c0001t0001g0332a0002c0010t0009g0023a0002c0010t0009g0024others(2): Show | 7 | HG00735.hp2 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3512-692_3512-689d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218517 | ||||||
chr6:169218523
|
A | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-694T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218523 | ||||||
chr6:169218546
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-717T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218546 | ||||||
chr6:169218566
|
C | A | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512-737G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218566 | ||||||
chr6:169218570
|
G | A | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512-741C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218570 | ||||||
chr6:169218578
|
A | G | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512-749T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218578 | ||||||
chr6:169218579
|
T | C | 4 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(1): Show | 6 | HG00735.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3512-750A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218579 | ||||||
chr6:169218582
|
A | G | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512-753T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218582 | ||||||
chr6:169218585
|
A | T | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3512-756T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218585 | ||||||
chr6:169218598
|
T | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-769A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218598 | ||||||
chr6:169218618
|
A | G | 1 | a0001c0002t0002g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3512-789T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218618 | ||||||
chr6:169218619
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-790T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218619 | ||||||
chr6:169218626
|
GATGGATG others(18): Show |
G | 60 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(57): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.3512-822_3512-798d others(27): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218626 | ||||||
chr6:169218639
|
G | A | 1 | a0001c0036t0001g0333 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3512-810C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218639 | ||||||
chr6:169218670
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3512-841G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218670 | ||||||
chr6:169218679
|
A | AGATG | 205 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(202): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.3512-854_3512-851d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218679 | ||||||
chr6:169218682
|
TGGATGGA others(2): Show |
T | 18 | a0001c0006t0006g0068a0001c0006t0006g0074a0001c0006t0006g0101others(15): Show | 18 | HG00438.hp1 HG02074.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3512-862_3512-854d others(11): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218682 | ||||||
chr6:169218683
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-854C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218683 | ||||||
chr6:169218689
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-860T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218689 | ||||||
chr6:169218690
|
T | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-861A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218690 | ||||||
chr6:169218693
|
G | A | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3512-864C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218693 | ||||||
chr6:169218694
|
A | T | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3512-865T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218694 | ||||||
chr6:169218695
|
T | C | 60 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(57): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.3512-866A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218695 | ||||||
chr6:169218695
|
T | G | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3512-866A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218695 | ||||||
chr6:169218705
|
GATGAGAC others(1): Show |
G | 18 | a0001c0006t0006g0068a0001c0006t0006g0074a0001c0006t0006g0101others(15): Show | 18 | HG00438.hp1 HG02074.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3512-884_3512-877d others(10): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218705 | ||||||
chr6:169218715
|
G | A | 18 | a0001c0006t0006g0068a0001c0006t0006g0074a0001c0006t0006g0101others(15): Show | 18 | HG00438.hp1 HG02074.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3512-886C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218715 | ||||||
chr6:169218715
|
GTGGA | G | 6 | a0001c0022t0007g0038a0001c0022t0007g0189a0001c0033t0007g0105others(3): Show | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3512-890_3512-887d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218715 | ||||||
chr6:169218747
|
AGATG | A | 26 | a0001c0001t0001g0332a0001c0006t0006g0068a0001c0006t0006g0074others(23): Show | 27 | HG00438.hp1 HG01069.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.3512-922_3512-919d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218747 | ||||||
chr6:169218793
|
G | GTGGACGA others(2): Show |
74 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(71): Show | 89 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.3512-965_3512-964i others(11): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218793 | ||||||
chr6:169218793
|
G | GTGGATGA others(2): Show |
147 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(144): Show | 158 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.3512-973_3512-965d others(11): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218793 | ||||||
chr6:169218814
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3512-985T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218814 | ||||||
chr6:169218829
|
AGATG | A | 99 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(96): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3512-1004_3512-100 others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218829 | ||||||
chr6:169218869
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3512-1040C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169218869 | ||||||
chr6:169219020
|
AGTGG | A | 28 | a0001c0001t0004g0054a0001c0001t0004g0061a0001c0001t0004g0089others(25): Show | 30 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.3511+1174_3511+117 others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219020 | ||||||
chr6:169219021
|
G | A | 32 | a0001c0001t0004g0043a0001c0001t0004g0108a0001c0001t0005g0102others(29): Show | 34 | HG00733.hp1 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3511+1177C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219021 | ||||||
chr6:169219039
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+1159T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219039 | ||||||
chr6:169219052
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+1146T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219052 | ||||||
chr6:169219052
|
AGATG | A | 3 | a0001c0041t0001g0036a0004c0020t0001g0299a0004c0020t0001g0301 | 3 | HG01891.hp1 HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3511+1142_3511+114 others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219052 | ||||||
chr6:169219062
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1136T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219062 | ||||||
chr6:169219079
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1119T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219079 | ||||||
chr6:169219083
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1115T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219083 | ||||||
chr6:169219089
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1109T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219089 | ||||||
chr6:169219110
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1088T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219110 | ||||||
chr6:169219113
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1085T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219113 | ||||||
chr6:169219117
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1081T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219117 | ||||||
chr6:169219122
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1076T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219122 | ||||||
chr6:169219127
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1071T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219127 | ||||||
chr6:169219130
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1068T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219130 | ||||||
chr6:169219144
|
A | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+1054T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219144 | ||||||
chr6:169219151
|
A | T | 2 | a0001c0001t0001g0063a0001c0001t0032g0184 | 2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3511+1047T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219151 | ||||||
chr6:169219153
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1045T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219153 | ||||||
chr6:169219156
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1042T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219156 | ||||||
chr6:169219160
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1038T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219160 | ||||||
chr6:169219162
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1036A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219162 | ||||||
chr6:169219162
|
T | TG | 13 | a0001c0002t0002g0002a0001c0002t0002g0107a0001c0002t0002g0170others(10): Show | 17 | HG01167.hp2 HG01884.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.3511+1035dupC | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219162 | ||||||
chr6:169219168
|
T | C | 57 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(54): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.3511+1030A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219168 | ||||||
chr6:169219170
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1028T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219170 | ||||||
chr6:169219171
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1027T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219171 | ||||||
chr6:169219180
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1018A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219180 | ||||||
chr6:169219184
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1014C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219184 | ||||||
chr6:169219194
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1004C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219194 | ||||||
chr6:169219196
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+1002C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219196 | ||||||
chr6:169219200
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+998T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219200 | ||||||
chr6:169219201
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+997A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219201 | ||||||
chr6:169219208
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0032g0184 | 2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3511+990T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219208 | ||||||
chr6:169219209
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+989A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219209 | ||||||
chr6:169219211
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+987T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219211 | ||||||
chr6:169219212
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+986T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219212 | ||||||
chr6:169219213
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+985T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219213 | ||||||
chr6:169219213
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+985T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219213 | ||||||
chr6:169219217
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+981T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219217 | ||||||
chr6:169219220
|
AGTGG | A | 106 | a0001c0001t0013g0294a0001c0002t0002g0002a0001c0002t0002g0008others(103): Show | 123 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.3511+974_3511+977d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219220 | ||||||
chr6:169219221
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+977C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219221 | ||||||
chr6:169219223
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+975C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219223 | ||||||
chr6:169219228
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+970C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219228 | ||||||
chr6:169219229
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+969C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219229 | ||||||
chr6:169219235
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+963C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219235 | ||||||
chr6:169219237
|
A | G | 1 | a0001c0001t0004g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3511+961T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219237 | ||||||
chr6:169219241
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+957T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219241 | ||||||
chr6:169219244
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+954T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219244 | ||||||
chr6:169219246
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+952T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219246 | ||||||
chr6:169219252
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+946T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219252 | ||||||
chr6:169219252
|
AGGTGGAT others(5): Show |
A | 99 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(96): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3511+934_3511+945d others(14): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219252 | ||||||
chr6:169219262
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+936C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219262 | ||||||
chr6:169219263
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+935A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219263 | ||||||
chr6:169219264
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+934C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219264 | ||||||
chr6:169219274
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+924T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219274 | ||||||
chr6:169219279
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+919A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219279 | ||||||
chr6:169219282
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+916T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219282 | ||||||
chr6:169219285
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+913T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219285 | ||||||
chr6:169219289
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+909T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219289 | ||||||
chr6:169219299
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+899T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219299 | ||||||
chr6:169219300
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+898A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219300 | ||||||
chr6:169219302
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+896C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219302 | ||||||
chr6:169219303
|
G | GTGGT | 6 | a0001c0001t0001g0060a0001c0001t0001g0230a0001c0001t0001g0232others(3): Show | 6 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.3511+891_3511+894d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219303 | ||||||
chr6:169219311
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+887T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219311 | ||||||
chr6:169219315
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+883T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219315 | ||||||
chr6:169219318
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+880T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219318 | ||||||
chr6:169219320
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+878T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219320 | ||||||
chr6:169219328
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+870C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219328 | ||||||
chr6:169219329
|
T | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+869A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219329 | ||||||
chr6:169219330
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+868C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219330 | ||||||
chr6:169219331
|
T | G | 57 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(54): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.3511+867A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219331 | ||||||
chr6:169219336
|
G | A | 2 | a0001c0004t0003g0277a0001c0037t0003g0141 | 2 | HG02293.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3511+862C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219336 | ||||||
chr6:169219340
|
G | A | 57 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(54): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.3511+858C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219340 | ||||||
chr6:169219340
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+858C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219340 | ||||||
chr6:169219344
|
A | G | 164 | a0001c0001t0004g0054a0001c0001t0004g0061a0001c0001t0004g0089others(161): Show | 186 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.3511+854T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219344 | ||||||
chr6:169219345
|
T | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+853A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219345 | ||||||
chr6:169219346
|
G | GGATGA | 3 | a0001c0001t0003g0201a0001c0004t0003g0277a0001c0037t0003g0141 | 3 | HG02293.hp1 NA19000.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3511+851_3511+852i others(7): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219346 | ||||||
chr6:169219346
|
G | GGATGGAT others(2): Show |
54 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(51): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.3511+851_3511+852i others(11): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219346 | ||||||
chr6:169219346
|
G | GGATGGAT others(6): Show |
1 | a0001c0001t0004g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3511+851_3511+852i others(15): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219346 | ||||||
chr6:169219346
|
G | GGATGGAT others(10): Show |
93 | a0001c0001t0004g0054a0001c0001t0004g0061a0001c0001t0004g0089others(90): Show | 100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.3511+851_3511+852i others(19): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219346 | ||||||
chr6:169219346
|
G | GGGTGGAT others(14): Show |
71 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(68): Show | 86 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.3511+851_3511+852i others(23): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219346 | ||||||
chr6:169219348
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+850T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219348 | ||||||
chr6:169219348
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+850T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219348 | ||||||
chr6:169219352
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+846T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219352 | ||||||
chr6:169219353
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+845A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219353 | ||||||
chr6:169219354
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+844C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219354 | ||||||
chr6:169219363
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+835T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219363 | ||||||
chr6:169219364
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+834T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219364 | ||||||
chr6:169219371
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+827T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219371 | ||||||
chr6:169219376
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+822C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219376 | ||||||
chr6:169219381
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+817T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219381 | ||||||
chr6:169219386
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+812A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219386 | ||||||
chr6:169219389
|
A | T | 2 | a0001c0001t0001g0063a0001c0001t0032g0184 | 2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3511+809T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219389 | ||||||
chr6:169219393
|
A | C | 1 | a0001c0008t0008g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3511+805T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219393 | ||||||
chr6:169219395
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+803C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219395 | ||||||
chr6:169219396
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+802C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219396 | ||||||
chr6:169219401
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+797C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219401 | ||||||
chr6:169219405
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0032g0184 | 2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3511+793T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219405 | ||||||
chr6:169219407
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+791C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219407 | ||||||
chr6:169219409
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+789T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219409 | ||||||
chr6:169219411
|
G | A | 7 | a0001c0001t0001g0063a0001c0006t0008g0014a0001c0006t0008g0034others(4): Show | 8 | HG01069.hp1 HG01099.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3511+787C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219411 | ||||||
chr6:169219414
|
A | C | 6 | a0001c0022t0007g0038a0001c0022t0007g0189a0001c0033t0007g0105others(3): Show | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3511+784T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219414 | ||||||
chr6:169219414
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+784T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219414 | ||||||
chr6:169219415
|
T | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+783A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219415 | ||||||
chr6:169219416
|
A | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+782T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219416 | ||||||
chr6:169219420
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+778C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219420 | ||||||
chr6:169219422
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+776C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219422 | ||||||
chr6:169219425
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+773C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219425 | ||||||
chr6:169219426
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+772C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219426 | ||||||
chr6:169219428
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+770C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219428 | ||||||
chr6:169219432
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+766C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219432 | ||||||
chr6:169219434
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+764T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219434 | ||||||
chr6:169219435
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+763A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219435 | ||||||
chr6:169219436
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+762C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219436 | ||||||
chr6:169219437
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+761T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219437 | ||||||
chr6:169219443
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+755T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219443 | ||||||
chr6:169219446
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+752C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219446 | ||||||
chr6:169219448
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+750A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219448 | ||||||
chr6:169219457
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+741T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219457 | ||||||
chr6:169219458
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+740A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219458 | ||||||
chr6:169219460
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+738T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219460 | ||||||
chr6:169219465
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+733G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219465 | ||||||
chr6:169219466
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+732G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219466 | ||||||
chr6:169219481
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+717T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219481 | ||||||
chr6:169219485
|
T | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+713A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219485 | ||||||
chr6:169219486
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+712T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219486 | ||||||
chr6:169219494
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0032g0184 | 2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3511+704C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219494 | ||||||
chr6:169219511
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+687G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219511 | ||||||
chr6:169219512
|
AAGCAGAT others(59): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+620_3511+685d others(68): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219512 | ||||||
chr6:169219516
|
A | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+682T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219516 | ||||||
chr6:169219531
|
A | C | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+667T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219531 | ||||||
chr6:169219545
|
C | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+653G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219545 | ||||||
chr6:169219553
|
C | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+645G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219553 | ||||||
chr6:169219557
|
C | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+641G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219557 | ||||||
chr6:169219558
|
T | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+640A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219558 | ||||||
chr6:169219568
|
C | T | 11 | a0001c0001t0003g0018a0001c0001t0003g0022a0001c0001t0003g0138others(8): Show | 13 | HG00558.hp2 HG00735.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.3511+630G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219568 | ||||||
chr6:169219570
|
C | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+628G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219570 | ||||||
chr6:169219580
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3511+618C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219580 | ||||||
chr6:169219587
|
C | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+611G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219587 | ||||||
chr6:169219588
|
A | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+610T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219588 | ||||||
chr6:169219590
|
C | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+608G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219590 | ||||||
chr6:169219592
|
G | A | 76 | a0001c0001t0032g0184a0001c0002t0002g0002a0001c0002t0002g0008others(73): Show | 91 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.3511+606C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219592 | ||||||
chr6:169219593
|
C | G | 2 | a0001c0001t0001g0063a0001c0001t0032g0184 | 2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.3511+605G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219593 | ||||||
chr6:169219608
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+590C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219608 | ||||||
chr6:169219612
|
T | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+586A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219612 | ||||||
chr6:169219630
|
C | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+568G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219630 | ||||||
chr6:169219636
|
C | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+562G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219636 | ||||||
chr6:169219637
|
C | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+561G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219637 | ||||||
chr6:169219652
|
T | G | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+546A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219652 | ||||||
chr6:169219653
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+545C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219653 | ||||||
chr6:169219720
|
C | T | 60 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(57): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.3511+478G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219720 | ||||||
chr6:169219721
|
G | T | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+477C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219721 | ||||||
chr6:169219739
|
T | A | 1 | a0001c0001t0003g0171 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3511+459A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219739 | ||||||
chr6:169219770
|
G | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+428C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219770 | ||||||
chr6:169219787
|
T | A | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+411A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219787 | ||||||
chr6:169219838
|
T | C | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3511+360A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219838 | ||||||
chr6:169219838
|
T | TTTCCTTC others(1): Show |
235 | a0001c0001t0001g0332a0001c0001t0003g0012a0001c0001t0003g0018others(232): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.3511+352_3511+359d others(10): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219838 | ||||||
chr6:169219885
|
A | C | 1 | a0001c0001t0032g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3511+313T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219885 | ||||||
chr6:169219925
|
ACT | A | 3 | a0001c0041t0001g0036a0004c0020t0001g0299a0004c0020t0001g0301 | 3 | HG01891.hp1 HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3511+271_3511+272d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169219925 | ||||||
chr6:169220056
|
G | A | 60 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(57): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.3511+142C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220056 | ||||||
chr6:169220066
|
CAT | C | 3 | a0001c0041t0001g0036a0004c0020t0001g0299a0004c0020t0001g0301 | 3 | HG01891.hp1 HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3511+130_3511+131d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220066 | ||||||
chr6:169220124
|
G | C | 12 | a0001c0006t0008g0014a0001c0006t0008g0034a0001c0006t0008g0118others(9): Show | 15 | HG01069.hp1 HG01099.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3511+74C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220124 | ||||||
chr6:169220127
|
C | T | 6 | a0001c0001t0003g0336a0001c0001t0003g0337a0001c0001t0003g0339others(3): Show | 6 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.3511+71G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220127 | ||||||
chr6:169220149
|
T | C | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3511+49A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220149 | ||||||
chr6:169220152
|
T | C | 240 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0003g0012others(237): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.3511+46A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220152 | ||||||
chr6:169220179
|
C | T | 8 | a0001c0001t0003g0033a0001c0001t0003g0035a0001c0001t0003g0176others(5): Show | 8 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3511+19G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 21/21 | chr6 | 169220179 | ||||||
chr6:169220355
|
AAAG | A | 74 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(71): Show | 89 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.3372-21_3372-19del others(3): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220355 | ||||||
chr6:169220445
|
C | T | 3 | a0001c0036t0001g0333a0008c0034t0001g0249a0008c0053t0001g0312 | 3 | HG01891.hp2 HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3372-108G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220445 | ||||||
chr6:169220446
|
G | A | 75 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(72): Show | 90 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.3372-109C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220446 | ||||||
chr6:169220665
|
C | T | 99 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(96): Show | 115 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.3372-328G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220665 | ||||||
chr6:169220736
|
G | A | 60 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(57): Show | 64 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.3372-399C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220736 | ||||||
chr6:169220787
|
A | G | 1 | a0001c0003t0002g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3372-450T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220787 | ||||||
chr6:169220827
|
G | A | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3372-490C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220827 | ||||||
chr6:169220834
|
C | T | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | NA18953.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.3372-497G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220834 | ||||||
chr6:169220896
|
A | G | 5 | a0001c0001t0001g0332a0002c0010t0009g0023a0002c0010t0009g0024others(2): Show | 7 | HG00735.hp2 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3371+534T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169220896 | ||||||
chr6:169221041
|
T | C | 222 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(219): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.3371+389A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169221041 | ||||||
chr6:169221075
|
C | T | 1 | a0001c0001t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3371+355G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169221075 | ||||||
chr6:169221143
|
A | G | 1 | a0001c0006t0008g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3371+287T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169221143 | ||||||
chr6:169221261
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3371+169T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169221261 | ||||||
chr6:169221336
|
A | C | 1 | a0001c0002t0002g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3371+94T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169221336 | ||||||
chr6:169221409
|
G | T | 2 | a0001c0041t0001g0036a0004c0020t0001g0299 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3371+21C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 20/21 | chr6 | 169221409 | ||||||
chr6:169221536
|
G | A | 1 | a0001c0016t0003g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3274-9C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221536 | ||||||
chr6:169221666
|
T | G | 10 | a0001c0006t0008g0014a0001c0006t0008g0034a0001c0006t0008g0118others(7): Show | 11 | HG01069.hp1 HG01099.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3274-139A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221666 | ||||||
chr6:169221692
|
G | A | 27 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0135others(24): Show | 28 | HG00733.hp1 HG01081.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3274-165C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221692 | ||||||
chr6:169221706
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3274-179C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221706 | ||||||
chr6:169221734
|
A | T | 239 | a0001c0001t0001g0332a0001c0001t0003g0012a0001c0001t0003g0018others(236): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.3274-207T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221734 | ||||||
chr6:169221744
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3274-217T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221744 | ||||||
chr6:169221769
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3274-242G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221769 | ||||||
chr6:169221920
|
T | C | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3273+277A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169221920 | ||||||
chr6:169222030
|
C | T | 1 | a0001c0005t0018g0032 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3273+167G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169222030 | ||||||
chr6:169222106
|
G | T | 3 | a0001c0001t0014g0330a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3273+91C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169222106 | ||||||
chr6:169222168
|
G | A | 66 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(63): Show | 72 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3273+29C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 19/21 | chr6 | 169222168 | ||||||
chr6:169222543
|
C | A | 103 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(100): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.3002-75G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222543 | ||||||
chr6:169222563
|
G | A | 40 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(37): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.3002-95C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222563 | ||||||
chr6:169222639
|
G | A | 222 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(219): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.3002-171C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222639 | ||||||
chr6:169222794
|
CAA | C | 160 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(157): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.3002-328_3002-327d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222794 | ||||||
chr6:169222794
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0015t0015g0017a0001c0015t0015g0343 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3002-337_3002-327d others(13): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222794 | ||||||
chr6:169222805
|
AAAGAAAA others(5): Show |
A | 57 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(54): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.3002-349_3002-338d others(14): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222805 | ||||||
chr6:169222806
|
AAGAAAAA others(4): Show |
A | 1 | a0001c0004t0003g0255 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3002-349_3002-339d others(13): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222806 | ||||||
chr6:169222813
|
A | G | 3 | a0001c0002t0002g0146a0001c0002t0002g0198a0001c0002t0002g0233 | 3 | HG03710.hp1 HG04184.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3002-345T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222813 | ||||||
chr6:169222817
|
G | A | 2 | a0001c0001t0005g0313a0001c0001t0035g0329 | 2 | HG03579.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.3002-349C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222817 | ||||||
chr6:169222817
|
GA | G | 162 | a0001c0001t0004g0043a0001c0001t0004g0054a0001c0001t0004g0061others(159): Show | 182 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.3002-350delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222817 | ||||||
chr6:169222818
|
A | G | 60 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(57): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.3002-350T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222818 | ||||||
chr6:169222833
|
AG | A | 103 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(100): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.3002-366delC | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222833 | ||||||
chr6:169222872
|
G | A | 1 | a0001c0002t0002g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3001+376C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222872 | ||||||
chr6:169222977
|
C | A | 28 | a0001c0006t0006g0068a0001c0006t0006g0074a0001c0006t0006g0101others(25): Show | 29 | HG00438.hp1 HG01069.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3001+271G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169222977 | ||||||
chr6:169223065
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0095 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3001+183G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169223065 | ||||||
chr6:169223207
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3001+41G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 18/21 | chr6 | 169223207 | ||||||
chr6:169223527
|
G | A | 3 | a0001c0003t0002g0244a0001c0003t0002g0250a0001c0003t0002g0273 | 3 | HG03516.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2774-52C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223527 | ||||||
chr6:169223733
|
A | T | 3 | a0001c0041t0001g0036a0004c0020t0001g0299a0004c0020t0001g0301 | 3 | HG01891.hp1 HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2774-258T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223733 | ||||||
chr6:169223763
|
A | G | 1 | a0001c0033t0007g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2774-288T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223763 | ||||||
chr6:169223883
|
A | G | 1 | a0001c0001t0004g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2774-408T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223883 | ||||||
chr6:169223903
|
G | A | 55 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(52): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.2774-428C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223903 | ||||||
chr6:169223950
|
T | G | 52 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(49): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2774-475A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223950 | ||||||
chr6:169223999
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2774-524C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169223999 | ||||||
chr6:169224007
|
A | G | 3 | a0001c0036t0001g0333a0008c0034t0001g0249a0008c0053t0001g0312 | 3 | HG01891.hp2 HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2774-532T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224007 | ||||||
chr6:169224050
|
CAT | C | 5 | a0001c0022t0007g0038a0001c0022t0007g0189a0003c0012t0007g0006others(2): Show | 7 | HG01884.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2774-577_2774-576d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224050 | ||||||
chr6:169224064
|
A | G | 1 | a0003c0012t0007g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2774-589T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224064 | ||||||
chr6:169224077
|
G | A | 236 | a0001c0001t0001g0332a0001c0001t0003g0012a0001c0001t0003g0018others(233): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2774-602C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224077 | ||||||
chr6:169224079
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2774-604A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224079 | ||||||
chr6:169224133
|
T | G | 52 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(49): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2774-658A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224133 | ||||||
chr6:169224136
|
C | T | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2774-661G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224136 | ||||||
chr6:169224141
|
T | TAGAA | 239 | a0001c0001t0001g0332a0001c0001t0003g0012a0001c0001t0003g0018others(236): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2774-667_2774-666i others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224141 | ||||||
chr6:169224265
|
C | T | 6 | a0001c0022t0007g0038a0001c0022t0007g0189a0001c0033t0007g0105others(3): Show | 8 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2774-790G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224265 | ||||||
chr6:169224406
|
C | T | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2773+739G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224406 | ||||||
chr6:169224409
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2773+736C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224409 | ||||||
chr6:169224427
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2773+718G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224427 | ||||||
chr6:169224522
|
AAG | A | 17 | a0001c0001t0001g0332a0001c0001t0013g0294a0001c0005t0013g0306others(14): Show | 20 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2773+621_2773+622d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224522 | ||||||
chr6:169224594
|
A | G | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2773+551T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224594 | ||||||
chr6:169224606
|
C | A | 17 | a0001c0001t0001g0332a0001c0001t0013g0294a0001c0005t0013g0306others(14): Show | 20 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2773+539G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224606 | ||||||
chr6:169224627
|
C | T | 67 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0022others(64): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2773+518G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224627 | ||||||
chr6:169224656
|
G | T | 2 | a0001c0015t0015g0017a0001c0015t0015g0343 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2773+489C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224656 | ||||||
chr6:169224674
|
C | T | 104 | a0001c0002t0002g0002a0001c0002t0002g0008a0001c0002t0002g0057others(101): Show | 120 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2773+471G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224674 | ||||||
chr6:169224675
|
G | A | 17 | a0001c0001t0001g0332a0001c0001t0013g0294a0001c0005t0013g0306others(14): Show | 20 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2773+470C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224675 | ||||||
chr6:169224805
|
A | G | 17 | a0001c0001t0001g0332a0001c0001t0013g0294a0001c0005t0013g0306others(14): Show | 20 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2773+340T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224805 | ||||||
chr6:169224828
|
G | A | 3 | a0001c0001t0004g0043a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG02486.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2773+317C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224828 | ||||||
chr6:169224857
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0004g0104 | 2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2773+288G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224857 | ||||||
chr6:169224969
|
G | A | 9 | a0001c0002t0002g0062a0001c0002t0002g0084a0001c0002t0002g0112others(6): Show | 9 | HG00544.hp2 HG01123.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.2773+176C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224969 | ||||||
chr6:169224973
|
G | A | 8 | a0001c0001t0001g0332a0001c0036t0001g0333a0002c0010t0009g0023others(5): Show | 10 | HG00735.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2773+172C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169224973 | ||||||
chr6:169225124
|
A | G | 7 | a0001c0003t0002g0124a0001c0003t0002g0283a0001c0003t0002g0284others(4): Show | 8 | HG01074.hp1 HG01109.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2773+21T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 17/21 | chr6 | 169225124 | ||||||
chr6:169225450
|
C | T | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2539-71G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225450 | ||||||
chr6:169225465
|
C | T | 1 | a0001c0005t0005g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2539-86G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225465 | ||||||
chr6:169225509
|
C | T | 8 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0036t0001g0333others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2539-130G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225509 | ||||||
chr6:169225512
|
C | T | 2 | a0001c0008t0008g0279a0001c0017t0002g0100 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2539-133G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225512 | ||||||
chr6:169225610
|
A | G | 2 | a0001c0014t0002g0027a0001c0014t0002g0114 | 3 | HG02630.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2539-231T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225610 | ||||||
chr6:169225641
|
C | T | 2 | a0001c0001t0001g0331a0001c0001t0004g0108 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2539-262G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225641 | ||||||
chr6:169225695
|
G | A | 65 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0004g0054others(62): Show | 72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.2539-316C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225695 | ||||||
chr6:169225748
|
A | G | 6 | a0001c0001t0001g0331a0001c0001t0004g0108a0001c0001t0012g0044others(3): Show | 6 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2539-369T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225748 | ||||||
chr6:169225776
|
C | T | 1 | a0001c0004t0001g0264 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2539-397G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225776 | ||||||
chr6:169225779
|
A | G | 170 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0087others(167): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2539-400T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225779 | ||||||
chr6:169225807
|
T | C | 1 | a0001c0014t0002g0027 | 2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2538+373A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225807 | ||||||
chr6:169225954
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2538+226T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225954 | ||||||
chr6:169225970
|
T | C | 108 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0221others(105): Show | 123 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2538+210A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169225970 | ||||||
chr6:169226027
|
G | C | 1 | a0001c0004t0004g0296 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2538+153C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226027 | ||||||
chr6:169226086
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0003g0022a0001c0001t0003g0201others(10): Show | 15 | HG02027.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.2538+94T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226086 | ||||||
chr6:169226100
|
C | T | 109 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0221others(106): Show | 125 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.2538+80G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226100 | ||||||
chr6:169226116
|
C | T | 1 | a0001c0008t0006g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2538+64G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226116 | ||||||
chr6:169226123
|
G | A | 2 | a0001c0003t0002g0067a0001c0017t0002g0100 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2538+57C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226123 | ||||||
chr6:169226130
|
C | T | 2 | a0001c0003t0002g0067a0001c0017t0002g0100 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2538+50G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226130 | ||||||
chr6:169226149
|
T | C | 68 | a0001c0001t0001g0077a0001c0001t0001g0241a0001c0001t0001g0331others(65): Show | 75 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.2538+31A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226149 | ||||||
chr6:169226150
|
C | T | 26 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0014g0330others(23): Show | 31 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.2538+30G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 16/21 | chr6 | 169226150 | ||||||
chr6:169226386
|
G | A | 1 | a0001c0006t0006g0101 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2420-88C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226386 | ||||||
chr6:169226486
|
T | C | 47 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0002t0002g0084others(44): Show | 56 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.2420-188A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226486 | ||||||
chr6:169226502
|
A | C | 1 | a0001c0002t0002g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2420-204T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226502 | ||||||
chr6:169226606
|
A | G | 8 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329others(5): Show | 9 | HG01891.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2420-308T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226606 | ||||||
chr6:169226611
|
T | G | 1 | a0001c0013t0002g0303 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2420-313A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226611 | ||||||
chr6:169226642
|
T | C | 1 | a0001c0033t0007g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2420-344A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226642 | ||||||
chr6:169226728
|
A | G | 1 | a0001c0001t0003g0243 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2420-430T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226728 | ||||||
chr6:169226735
|
C | T | 84 | a0001c0001t0001g0123a0001c0001t0001g0221a0001c0001t0001g0230others(81): Show | 95 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2420-437G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226735 | ||||||
chr6:169226855
|
G | A | 10 | a0001c0001t0003g0033a0001c0001t0003g0190a0001c0002t0002g0106others(7): Show | 11 | HG01069.hp1 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.2420-557C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226855 | ||||||
chr6:169226872
|
A | T | 54 | a0001c0001t0003g0176a0001c0001t0005g0202a0001c0002t0002g0084others(51): Show | 64 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2420-574T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226872 | ||||||
chr6:169226885
|
G | T | 1 | a0001c0006t0008g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2420-587C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226885 | ||||||
chr6:169226909
|
G | A | 2 | a0001c0002t0002g0057a0001c0002t0002g0159 | 2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2420-611C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226909 | ||||||
chr6:169226942
|
A | G | 126 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0221others(123): Show | 143 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.2420-644T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226942 | ||||||
chr6:169226950
|
A | T | 61 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0221others(58): Show | 68 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.2420-652T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169226950 | ||||||
chr6:169227046
|
G | A | 1 | a0001c0002t0002g0286 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2420-748C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227046 | ||||||
chr6:169227088
|
G | C | 120 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0123others(117): Show | 133 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2420-790C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227088 | ||||||
chr6:169227162
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(241): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.2420-864A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227162 | ||||||
chr6:169227163
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(122): Show | 144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2420-865C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227163 | ||||||
chr6:169227172
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(241): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.2420-874T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227172 | ||||||
chr6:169227174
|
G | C | 2 | a0008c0034t0001g0249a0008c0053t0001g0312 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2420-876C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227174 | ||||||
chr6:169227186
|
G | A | 23 | a0001c0002t0022g0094a0001c0003t0002g0067a0001c0003t0002g0193others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.2420-888C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227186 | ||||||
chr6:169227188
|
C | T | 1 | a0001c0001t0001g0344 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2420-890G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227188 | ||||||
chr6:169227205
|
C | T | 120 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0123others(117): Show | 133 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2420-907G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227205 | ||||||
chr6:169227214
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2419+908G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227214 | ||||||
chr6:169227246
|
C | T | 2 | a0001c0001t0003g0171a0001c0006t0006g0172 | 2 | NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2419+876G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227246 | ||||||
chr6:169227252
|
G | C | 112 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0123others(109): Show | 121 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2419+870C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227252 | ||||||
chr6:169227326
|
T | C | 120 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0123others(117): Show | 133 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2419+796A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227326 | ||||||
chr6:169227328
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(241): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.2419+794T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227328 | ||||||
chr6:169227335
|
G | A | 3 | a0001c0001t0003g0012a0001c0001t0003g0175a0001c0001t0003g0187 | 5 | HG01069.hp2 HG01071.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2419+787C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227335 | ||||||
chr6:169227439
|
C | T | 83 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(80): Show | 95 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2419+683G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227439 | ||||||
chr6:169227636
|
T | C | 122 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0123others(119): Show | 135 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.2419+486A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227636 | ||||||
chr6:169227699
|
A | G | 2 | a0008c0034t0001g0249a0008c0053t0001g0312 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2419+423T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227699 | ||||||
chr6:169227711
|
T | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(120): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2419+411A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227711 | ||||||
chr6:169227804
|
G | A | 80 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(77): Show | 92 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2419+318C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227804 | ||||||
chr6:169227827
|
A | T | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2419+295T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227827 | ||||||
chr6:169227854
|
G | A | 62 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0221others(59): Show | 69 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.2419+268C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227854 | ||||||
chr6:169227856
|
C | T | 9 | a0001c0001t0003g0339a0002c0010t0009g0023a0002c0010t0009g0024others(6): Show | 13 | HG00735.hp2 HG01168.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2419+266G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227856 | ||||||
chr6:169227863
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(242): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2419+259A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227863 | ||||||
chr6:169227989
|
G | C | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2419+133C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169227989 | ||||||
chr6:169228074
|
CA | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(116): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2419+47delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169228074 | ||||||
chr6:169228074
|
CAA | C | 129 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0123others(126): Show | 143 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.2419+46_2419+47del others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 15/21 | chr6 | 169228074 | ||||||
chr6:169228358
|
T | C | 5 | a0001c0005t0003g0326a0001c0016t0003g0144a0001c0016t0003g0199others(2): Show | 5 | HG02683.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2260-77A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228358 | ||||||
chr6:169228385
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2260-104A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228385 | ||||||
chr6:169228424
|
G | A | 1 | a0001c0001t0001g0148 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2260-143C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228424 | ||||||
chr6:169228503
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(242): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2260-222T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228503 | ||||||
chr6:169228645
|
C | T | 2 | a0001c0014t0002g0027a0001c0014t0002g0114 | 3 | HG02630.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2260-364G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228645 | ||||||
chr6:169228646
|
G | A | 1 | a0004c0020t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2260-365C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228646 | ||||||
chr6:169228649
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0195a0001c0001t0001g0272 | 3 | HG00673.hp2 NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2260-368G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228649 | ||||||
chr6:169228721
|
C | T | 2 | a0007c0047t0029g0055a0007c0048t0002g0287 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2260-440G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228721 | ||||||
chr6:169228831
|
A | G | 2 | a0008c0034t0001g0249a0008c0053t0001g0312 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2260-550T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228831 | ||||||
chr6:169228906
|
C | CA | 126 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0186others(123): Show | 145 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2260-626dupT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228906 | ||||||
chr6:169228906
|
C | CAA | 6 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(3): Show | 6 | HG02055.hp2 HG02622.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2260-627_2260-626d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228906 | ||||||
chr6:169228906
|
CA | C | 10 | a0001c0001t0001g0052a0001c0001t0001g0081a0001c0001t0012g0046others(7): Show | 12 | HG00323.hp2 HG00738.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2260-626delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228906 | ||||||
chr6:169228923
|
AG | A | 28 | a0001c0001t0001g0026a0001c0001t0003g0176a0001c0001t0005g0102others(25): Show | 30 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2260-643delC | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228923 | ||||||
chr6:169228926
|
GTT | G | 28 | a0001c0001t0001g0026a0001c0001t0003g0176a0001c0001t0005g0102others(25): Show | 30 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2259+644_2259+645d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228926 | ||||||
chr6:169228951
|
C | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(242): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2259+621G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228951 | ||||||
chr6:169228996
|
A | C | 2 | a0008c0034t0001g0249a0008c0053t0001g0312 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2259+576T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169228996 | ||||||
chr6:169229041
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2259+531T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169229041 | ||||||
chr6:169229113
|
A | G | 4 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259+459T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169229113 | ||||||
chr6:169229265
|
G | A | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2259+307C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169229265 | ||||||
chr6:169229469
|
A | G | 2 | a0001c0015t0015g0017a0001c0015t0015g0343 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2259+103T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169229469 | ||||||
chr6:169229531
|
C | T | 4 | a0001c0016t0005g0334a0004c0020t0001g0299a0004c0020t0001g0301others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+41G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169229531 | ||||||
chr6:169229539
|
C | T | 2 | a0001c0001t0003g0176a0001c0001t0005g0202 | 2 | HG01433.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2259+33G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 14/21 | chr6 | 169229539 | ||||||
chr6:169229688
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(254): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.2152-9C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169229688 | ||||||
chr6:169229766
|
G | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(120): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2152-87C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169229766 | ||||||
chr6:169229815
|
G | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(243): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.2152-136C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169229815 | ||||||
chr6:169230118
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0157others(2): Show | 7 | HG02132.hp1 HG02135.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.2152-439G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230118 | ||||||
chr6:169230220
|
C | CA | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(230): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.2152-542dupT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230220 | ||||||
chr6:169230245
|
G | A | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(230): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.2152-566C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230245 | ||||||
chr6:169230370
|
TC | T | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2152-692delG | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230370 | ||||||
chr6:169230497
|
G | A | 3 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329 | 3 | HG03098.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2152-818C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230497 | ||||||
chr6:169230506
|
C | T | 3 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329 | 3 | HG03098.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2152-827G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230506 | ||||||
chr6:169230558
|
G | A | 1 | a0001c0004t0003g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2152-879C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230558 | ||||||
chr6:169230705
|
G | A | 13 | a0001c0002t0022g0094a0001c0004t0003g0075a0001c0004t0004g0076others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.2152-1026C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230705 | ||||||
chr6:169230878
|
C | A | 58 | a0001c0001t0001g0026a0001c0001t0003g0176a0001c0001t0005g0102others(55): Show | 62 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.2151+1102G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230878 | ||||||
chr6:169230988
|
A | G | 1 | a0001c0011t0016g0345 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2151+992T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169230988 | ||||||
chr6:169231085
|
C | G | 2 | a0001c0001t0001g0166a0001c0043t0001g0165 | 2 | NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2151+895G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231085 | ||||||
chr6:169231328
|
G | A | 1 | a0001c0044t0003g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2151+652C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231328 | ||||||
chr6:169231483
|
C | T | 2 | a0001c0001t0001g0092a0001c0002t0002g0159 | 2 | HG00099.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.2151+497G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231483 | ||||||
chr6:169231787
|
C | T | 1 | a0001c0005t0001g0328 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2151+193G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231787 | ||||||
chr6:169231812
|
G | A | 81 | a0001c0001t0001g0331a0001c0001t0012g0046a0001c0001t0012g0047others(78): Show | 93 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.2151+168C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231812 | ||||||
chr6:169231870
|
C | CCTTCCAA others(11): Show |
27 | a0001c0001t0001g0026a0001c0001t0001g0331a0001c0001t0001g0332others(24): Show | 29 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.2151+109_2151+110i others(20): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231870 | ||||||
chr6:169231876
|
A | AAAT | 12 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2151+101_2151+103d others(5): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231876 | ||||||
chr6:169231899
|
C | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(111): Show | 126 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2151+81G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231899 | ||||||
chr6:169231906
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2151+74G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 13/21 | chr6 | 169231906 | ||||||
chr6:169232206
|
G | C | 1 | a0001c0003t0002g0067 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.1933-8C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232206 | ||||||
chr6:169232210
|
AG | A | 19 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0150others(16): Show | 20 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.1933-13delC | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232210 | ||||||
chr6:169232213
|
G | A | 3 | a0001c0003t0002g0244a0001c0003t0002g0250a0001c0003t0002g0273 | 3 | HG03516.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1933-15C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232213 | ||||||
chr6:169232275
|
C | T | 2 | a0001c0001t0001g0239a0001c0005t0001g0319 | 2 | HG00642.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1933-77G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232275 | ||||||
chr6:169232283
|
C | T | 62 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0221others(59): Show | 69 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1933-85G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232283 | ||||||
chr6:169232359
|
T | G | 1 | a0001c0006t0006g0074 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1933-161A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232359 | ||||||
chr6:169232368
|
A | C | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1933-170T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232368 | ||||||
chr6:169232398
|
T | G | 4 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1933-200A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232398 | ||||||
chr6:169232469
|
G | A | 1 | a0001c0004t0004g0296 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1932+195C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232469 | ||||||
chr6:169232469
|
G | C | 73 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0123others(70): Show | 84 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.1932+195C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232469 | ||||||
chr6:169232477
|
A | ACG | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(171): Show | 199 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1932+185_1932+186d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232477 | ||||||
chr6:169232482
|
C | T | 1 | a0010c0052t0008g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1932+182G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232482 | ||||||
chr6:169232513
|
C | G | 55 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(52): Show | 62 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1932+151G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232513 | ||||||
chr6:169232556
|
C | A | 57 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(54): Show | 65 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1932+108G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232556 | ||||||
chr6:169232633
|
G | T | 1 | a0001c0005t0005g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1932+31C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232633 | ||||||
chr6:169232651
|
C | T | 8 | a0001c0001t0035g0329a0001c0003t0002g0067a0001c0003t0002g0193others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1932+13G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232651 | ||||||
chr6:169232653
|
G | T | 1 | a0001c0001t0001g0015 | 2 | NA18998.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1932+11C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 12/21 | chr6 | 169232653 | ||||||
chr6:169232820
|
C | T | 1 | a0001c0002t0002g0008 | 3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
splice_region_variant&intron_variant | LOW | c.1780-4G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 11/21 | chr6 | 169232820 | ||||||
chr6:169233090
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(137): Show | 159 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1652-73G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233090 | ||||||
chr6:169233115
|
T | C | 6 | a0001c0016t0005g0334a0001c0017t0002g0039a0001c0017t0002g0040others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1652-98A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233115 | ||||||
chr6:169233211
|
C | G | 22 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(19): Show | 24 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.1652-194G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233211 | ||||||
chr6:169233215
|
G | A | 25 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(22): Show | 28 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1652-198C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233215 | ||||||
chr6:169233227
|
C | T | 1 | a0011c0051t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1652-210G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233227 | ||||||
chr6:169233240
|
T | C | 193 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(190): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1652-223A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233240 | ||||||
chr6:169233279
|
C | T | 4 | a0001c0016t0005g0334a0004c0020t0001g0299a0004c0020t0001g0301others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1652-262G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233279 | ||||||
chr6:169233283
|
A | T | 33 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(30): Show | 40 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1652-266T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233283 | ||||||
chr6:169233366
|
C | T | 25 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(22): Show | 28 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1652-349G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233366 | ||||||
chr6:169233429
|
A | C | 1 | a0001c0003t0002g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1652-412T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233429 | ||||||
chr6:169233439
|
C | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1652-422G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233439 | ||||||
chr6:169233555
|
A | G | 25 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(22): Show | 28 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1652-538T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233555 | ||||||
chr6:169233562
|
ACCACACA others(935): Show |
A | 8 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1651+230_1652-546d others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233562 | ||||||
chr6:169233622
|
A | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1652-605T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233622 | ||||||
chr6:169233706
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1652-689C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233706 | ||||||
chr6:169233822
|
A | G | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(308): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1652-805T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169233822 | ||||||
chr6:169234010
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1651+724G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169234010 | ||||||
chr6:169234082
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0052others(5): Show | 11 | HG00544.hp2 NA18939.hp1 NA18959.hp2 others(8): Show |
intron_variant | MODIFIER | c.1651+652C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169234082 | ||||||
chr6:169234335
|
ACAC | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(131): Show | 152 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1651+396_1651+398d others(5): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169234335 | ||||||
chr6:169234714
|
C | T | 133 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(130): Show | 151 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1651+20G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 10/21 | chr6 | 169234714 | ||||||
chr6:169234912
|
G | A | 1 | a0001c0001t0035g0329 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.1478-5C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169234912 | ||||||
chr6:169234915
|
G | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(131): Show | 152 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(149): Show |
splice_region_variant&intron_variant | LOW | c.1478-8C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169234915 | ||||||
chr6:169234925
|
CA | C | 134 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(131): Show | 152 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1478-19delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169234925 | ||||||
chr6:169234961
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0010g0222 | 2 | HG02129.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1478-54C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169234961 | ||||||
chr6:169235041
|
T | C | 1 | a0001c0005t0003g0326 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1478-134A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235041 | ||||||
chr6:169235068
|
C | T | 2 | a0001c0001t0004g0225a0001c0005t0005g0323 | 2 | HG03041.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1478-161G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235068 | ||||||
chr6:169235110
|
T | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(322): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1478-203A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235110 | ||||||
chr6:169235189
|
T | C | 1 | a0001c0001t0003g0096 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1478-282A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235189 | ||||||
chr6:169235457
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1478-550C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235457 | ||||||
chr6:169235511
|
G | A | 15 | a0001c0003t0002g0262a0001c0004t0003g0075a0001c0004t0003g0255others(12): Show | 16 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1478-604C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235511 | ||||||
chr6:169235586
|
C | T | 1 | a0001c0033t0007g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1478-679G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235586 | ||||||
chr6:169235676
|
G | A | 15 | a0001c0001t0004g0155a0001c0003t0002g0067a0001c0003t0002g0193others(12): Show | 15 | HG01891.hp1 HG02055.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1478-769C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235676 | ||||||
chr6:169235743
|
C | T | 1 | a0001c0001t0003g0096 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1478-836G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235743 | ||||||
chr6:169235796
|
A | C | 1 | a0001c0006t0006g0172 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1478-889T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235796 | ||||||
chr6:169235815
|
A | ACACT | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(322): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1478-912_1478-909d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235815 | ||||||
chr6:169235947
|
T | TCCCCATC others(11): Show |
1 | a0001c0001t0031g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1478-1058_1478-104 others(22): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235947 | ||||||
chr6:169235947
|
TCCCCATC others(11): Show |
T | 1 | a0001c0005t0004g0317 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1478-1058_1478-104 others(22): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235947 | ||||||
chr6:169235965
|
CCCCCATC others(68): Show |
C | 1 | a0013c0032t0001g0116 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1477+1130_1478-105 others(79): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169235965 | ||||||
chr6:169236088
|
CCCATCCA others(37): Show |
C | 2 | a0001c0014t0002g0027a0001c0014t0002g0114 | 3 | HG02630.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1477+1038_1477+108 others(48): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236088 | ||||||
chr6:169236132
|
ACCATCCA others(10): Show |
A | 95 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0063others(92): Show | 103 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1477+1021_1477+103 others(21): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236132 | ||||||
chr6:169236149
|
C | CCCATCCA others(302): Show |
39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(36): Show | 47 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1477+1020_1477+102 others(313): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236149 | ||||||
chr6:169236149
|
C | CCCATCCA others(301): Show |
1 | a0001c0001t0010g0222 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1477+1020_1477+102 others(312): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236149 | ||||||
chr6:169236154
|
CCACACTC others(9): Show |
C | 1 | a0001c0006t0006g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1477+1000_1477+101 others(20): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236154 | ||||||
chr6:169236211
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1477+959G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236211 | ||||||
chr6:169236217
|
ACACT | A | 87 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(84): Show | 95 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1477+949_1477+952d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236217 | ||||||
chr6:169236265
|
C | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1477+905G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236265 | ||||||
chr6:169236287
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+883G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236287 | ||||||
chr6:169236291
|
T | C | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+879A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236291 | ||||||
chr6:169236299
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+871G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236299 | ||||||
chr6:169236301
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+869G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236301 | ||||||
chr6:169236303
|
G | C | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+867C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236303 | ||||||
chr6:169236324
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+846G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236324 | ||||||
chr6:169236325
|
TCC | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(37): Show | 48 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1477+843_1477+844d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236325 | ||||||
chr6:169236326
|
C | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1477+844G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236326 | ||||||
chr6:169236327
|
C | CCCCATCC others(317): Show |
33 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0063others(30): Show | 34 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1477+842_1477+843i others(326): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236327 | ||||||
chr6:169236327
|
C | CCCCATCC others(317): Show |
1 | a0001c0006t0006g0068 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1477+842_1477+843i others(326): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236327 | ||||||
chr6:169236327
|
C | CCCCATCC others(315): Show |
1 | a0001c0006t0006g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1477+842_1477+843i others(324): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236327 | ||||||
chr6:169236405
|
C | A | 87 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(84): Show | 95 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1477+765G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236405 | ||||||
chr6:169236408
|
ATAAACAC others(37): Show |
A | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1477+718_1477+761d others(46): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236408 | ||||||
chr6:169236491
|
C | CTCCA | 245 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(242): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1477+675_1477+678d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236491 | ||||||
chr6:169236498
|
T | A | 1 | a0001c0006t0006g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1477+672A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236498 | ||||||
chr6:169236529
|
C | T | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1477+641G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236529 | ||||||
chr6:169236581
|
TCACTCCC others(22): Show |
T | 3 | a0001c0018t0005g0288a0001c0018t0005g0289a0001c0018t0005g0290 | 3 | HG01192.hp1 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1477+560_1477+588d others(31): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236581 | ||||||
chr6:169236586
|
C | T | 1 | a0008c0034t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1477+584G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236586 | ||||||
chr6:169236616
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1477+554C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236616 | ||||||
chr6:169236645
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0085others(5): Show | 10 | NA18966.hp1 NA18969.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+525C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236645 | ||||||
chr6:169236774
|
G | A | 2 | a0001c0001t0035g0329a0001c0038t0001g0160 | 2 | HG02155.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1477+396C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236774 | ||||||
chr6:169236823
|
G | A | 25 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(22): Show | 28 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1477+347C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236823 | ||||||
chr6:169236919
|
T | C | 1 | a0001c0001t0031g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1477+251A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169236919 | ||||||
chr6:169237137
|
G | A | 2 | a0001c0019t0014g0310a0001c0019t0014g0311 | 2 | HG01243.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1477+33C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 9/21 | chr6 | 169237137 | ||||||
chr6:169237361
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(253): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1301-15C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/21 | chr6 | 169237361 | ||||||
chr6:169237374
|
G | T | 24 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 27 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1301-28C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/21 | chr6 | 169237374 | ||||||
chr6:169237424
|
C | T | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(254): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1301-78G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/21 | chr6 | 169237424 | ||||||
chr6:169237518
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1300+107G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/21 | chr6 | 169237518 | ||||||
chr6:169237579
|
G | A | 3 | a0001c0003t0002g0193a0001c0004t0003g0065a0001c0004t0003g0066 | 3 | HG02055.hp2 HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1300+46C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/21 | chr6 | 169237579 | ||||||
chr6:169237606
|
T | A | 60 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0221others(57): Show | 67 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1300+19A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 8/21 | chr6 | 169237606 | ||||||
chr6:169237816
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(254): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1130-21C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169237816 | ||||||
chr6:169237843
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1130-48C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169237843 | ||||||
chr6:169237877
|
C | T | 60 | a0001c0001t0001g0070a0001c0001t0001g0123a0001c0001t0001g0221others(57): Show | 67 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1130-82G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169237877 | ||||||
chr6:169237958
|
G | A | 6 | a0001c0002t0002g0002a0001c0002t0002g0170a0001c0002t0002g0177others(3): Show | 10 | HG01167.hp2 HG01884.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1130-163C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169237958 | ||||||
chr6:169238117
|
C | T | 136 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0221others(133): Show | 148 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1130-322G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238117 | ||||||
chr6:169238194
|
C | A | 2 | a0001c0007t0004g0007a0001c0007t0004g0115 | 4 | HG00738.hp1 HG01081.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-399G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238194 | ||||||
chr6:169238282
|
A | C | 4 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-487T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238282 | ||||||
chr6:169238330
|
A | G | 3 | a0001c0013t0002g0028a0001c0013t0002g0302a0001c0013t0002g0303 | 4 | HG01109.hp1 HG01261.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-535T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238330 | ||||||
chr6:169238359
|
C | G | 1 | a0001c0004t0033g0247 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1130-564G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238359 | ||||||
chr6:169238372
|
T | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1130-577A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238372 | ||||||
chr6:169238438
|
G | T | 4 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-643C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238438 | ||||||
chr6:169238657
|
T | TTCTGCAT others(8): Show |
1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1130-877_1130-863d others(17): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238657 | ||||||
chr6:169238696
|
A | C | 36 | a0001c0001t0001g0070a0001c0001t0001g0224a0001c0001t0001g0338others(33): Show | 42 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1130-901T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238696 | ||||||
chr6:169238758
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(67): Show | 79 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1129+841A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238758 | ||||||
chr6:169238793
|
A | G | 24 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 27 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1129+806T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238793 | ||||||
chr6:169238873
|
T | G | 1 | a0001c0005t0004g0317 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1129+726A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169238873 | ||||||
chr6:169239005
|
T | G | 2 | a0001c0001t0001g0239a0001c0005t0001g0319 | 2 | HG00642.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1129+594A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239005 | ||||||
chr6:169239087
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1129+512C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239087 | ||||||
chr6:169239263
|
T | C | 111 | a0001c0001t0001g0123a0001c0001t0001g0221a0001c0001t0001g0230others(108): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1129+336A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239263 | ||||||
chr6:169239275
|
G | A | 20 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(17): Show | 22 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.1129+324C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239275 | ||||||
chr6:169239324
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1129+275A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239324 | ||||||
chr6:169239331
|
C | T | 22 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(19): Show | 25 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129+268G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239331 | ||||||
chr6:169239332
|
G | A | 4 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129+267C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239332 | ||||||
chr6:169239565
|
A | T | 1 | a0001c0002t0002g0008 | 3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1129+34T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239565 | ||||||
chr6:169239589
|
C | T | 1 | a0001c0002t0017g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1129+10G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 7/21 | chr6 | 169239589 | ||||||
chr6:169239745
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1033-50G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169239745 | ||||||
chr6:169239806
|
C | T | 114 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(111): Show | 131 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1033-111G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169239806 | ||||||
chr6:169239816
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1033-121T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169239816 | ||||||
chr6:169239904
|
T | A | 35 | a0001c0001t0001g0070a0001c0001t0001g0224a0001c0001t0001g0338others(32): Show | 41 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1033-209A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169239904 | ||||||
chr6:169240065
|
T | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(76): Show | 94 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1033-370A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169240065 | ||||||
chr6:169240111
|
C | T | 2 | a0001c0017t0002g0039a0001c0017t0002g0040 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1032+341G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169240111 | ||||||
chr6:169240162
|
A | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(68): Show | 82 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1032+290T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169240162 | ||||||
chr6:169240416
|
G | A | 2 | a0001c0002t0002g0057a0001c0002t0002g0159 | 2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1032+36C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169240416 | ||||||
chr6:169240429
|
A | G | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1032+23T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169240429 | ||||||
chr6:169240434
|
C | T | 72 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(69): Show | 80 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1032+18G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 6/21 | chr6 | 169240434 | ||||||
chr6:169240637
|
A | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(69): Show | 83 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.892-45T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169240637 | ||||||
chr6:169240832
|
C | T | 8 | a0001c0001t0001g0071a0001c0001t0001g0148a0001c0001t0001g0197others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-240G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169240832 | ||||||
chr6:169240877
|
C | T | 3 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.892-285G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169240877 | ||||||
chr6:169240971
|
AGCTCCTG others(55): Show |
A | 2 | a0001c0015t0015g0017a0001c0015t0015g0343 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.892-441_892-380del others(62): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169240971 | ||||||
chr6:169240997
|
C | T | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.892-405G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169240997 | ||||||
chr6:169241001
|
G | A | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.892-409C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241001 | ||||||
chr6:169241046
|
G | A | 1 | a0001c0005t0005g0324 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.892-454C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241046 | ||||||
chr6:169241066
|
C | T | 4 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(1): Show | 4 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-474G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241066 | ||||||
chr6:169241072
|
CCCCTGCC others(5): Show |
C | 1 | a0001c0003t0002g0273 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892-492_892-481del others(12): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241072 | ||||||
chr6:169241091
|
C | T | 1 | a0001c0004t0003g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.892-499G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241091 | ||||||
chr6:169241142
|
G | A | 1 | a0001c0001t0011g0122 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.892-550C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241142 | ||||||
chr6:169241143
|
ACAGT | A | 16 | a0001c0003t0002g0278a0001c0003t0002g0292a0001c0004t0003g0275others(13): Show | 16 | HG01192.hp1 HG01515.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.892-555_892-552del others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241143 | ||||||
chr6:169241174
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.892-582A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241174 | ||||||
chr6:169241180
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(134): Show | 156 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.891+582A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241180 | ||||||
chr6:169241239
|
C | G | 1 | a0001c0004t0001g0281 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.891+523G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241239 | ||||||
chr6:169241270
|
G | C | 15 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(12): Show | 16 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+492C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241270 | ||||||
chr6:169241285
|
C | T | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+477G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241285 | ||||||
chr6:169241287
|
G | A | 80 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(77): Show | 93 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.891+475C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241287 | ||||||
chr6:169241288
|
C | T | 19 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(16): Show | 21 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.891+474G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241288 | ||||||
chr6:169241296
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.891+466G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241296 | ||||||
chr6:169241340
|
G | A | 3 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.891+422C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241340 | ||||||
chr6:169241347
|
C | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(31): Show | 40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+415G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241347 | ||||||
chr6:169241358
|
T | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+404A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241358 | ||||||
chr6:169241400
|
GGTGTGTG others(1): Show |
G | 38 | a0001c0001t0001g0059a0001c0001t0001g0081a0001c0001t0001g0123others(35): Show | 39 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.891+354_891+361del others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241400 | ||||||
chr6:169241415
|
GTATGTGT others(5): Show |
G | 2 | a0001c0001t0004g0093a0001c0002t0022g0094 | 2 | HG02056.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.891+335_891+346del others(12): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241415 | ||||||
chr6:169241417
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0014g0330 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.891+333_891+344dup others(12): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241417 | ||||||
chr6:169241417
|
ATGTGTGT others(5): Show |
A | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(133): Show | 157 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.891+333_891+344del others(12): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241417 | ||||||
chr6:169241429
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0003g0033a0001c0006t0006g0113 | 2 | HG02922.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.891+323_891+332del others(10): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241429 | ||||||
chr6:169241439
|
A | ATG | 28 | a0001c0001t0001g0026a0001c0001t0001g0332a0001c0001t0005g0102others(25): Show | 30 | HG00438.hp1 HG00558.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.891+321_891+322dup others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241439 | ||||||
chr6:169241439
|
A | ATGTG | 9 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(6): Show | 10 | HG00423.hp1 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+319_891+322dup others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241439 | ||||||
chr6:169241440
|
T | A | 3 | a0001c0003t0002g0244a0001c0003t0002g0250a0001c0003t0002g0273 | 3 | HG03516.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.891+322A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241440 | ||||||
chr6:169241498
|
A | G | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.891+264T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241498 | ||||||
chr6:169241680
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.891+82C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241680 | ||||||
chr6:169241725
|
GCCCTATG others(12): Show |
G | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.891+18_891+36delGG others(17): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241725 | ||||||
chr6:169241738
|
C | T | 3 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329 | 3 | HG03098.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.891+24G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 5/21 | chr6 | 169241738 | ||||||
chr6:169242002
|
G | A | 2 | a0001c0033t0007g0105a0008c0034t0001g0249 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.695-44C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242002 | ||||||
chr6:169242032
|
G | A | 21 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(18): Show | 26 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.695-74C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242032 | ||||||
chr6:169242040
|
C | T | 1 | a0001c0003t0002g0262 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.695-82G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242040 | ||||||
chr6:169242043
|
C | T | 6 | a0001c0017t0002g0039a0001c0017t0002g0040a0004c0020t0001g0299others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-85G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242043 | ||||||
chr6:169242058
|
G | T | 2 | a0001c0007t0001g0009a0001c0007t0004g0119 | 4 | HG00733.hp2 HG01106.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-100C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242058 | ||||||
chr6:169242085
|
A | G | 5 | a0001c0017t0002g0100a0001c0024t0003g0086a0001c0024t0003g0099others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-127T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242085 | ||||||
chr6:169242147
|
T | C | 70 | a0001c0001t0031g0295a0001c0003t0002g0001a0001c0003t0002g0048others(67): Show | 78 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.695-189A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242147 | ||||||
chr6:169242148
|
G | A | 69 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(66): Show | 77 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.695-190C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242148 | ||||||
chr6:169242188
|
G | C | 4 | a0004c0020t0001g0299a0004c0020t0001g0301a0004c0029t0002g0300others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-230C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242188 | ||||||
chr6:169242206
|
C | T | 55 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(52): Show | 62 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.695-248G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242206 | ||||||
chr6:169242241
|
T | G | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-283A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242241 | ||||||
chr6:169242254
|
G | T | 42 | a0001c0001t0001g0123a0001c0001t0001g0221a0001c0001t0001g0230others(39): Show | 44 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.695-296C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242254 | ||||||
chr6:169242257
|
G | A | 5 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-299C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242257 | ||||||
chr6:169242295
|
C | T | 16 | a0001c0001t0001g0026a0001c0004t0003g0075a0001c0004t0003g0255others(13): Show | 18 | HG00408.hp1 HG00609.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-337G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242295 | ||||||
chr6:169242388
|
C | T | 4 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(1): Show | 4 | HG02486.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-430G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242388 | ||||||
chr6:169242425
|
T | C | 1 | a0001c0002t0002g0177 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.695-467A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242425 | ||||||
chr6:169242563
|
T | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-605A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242563 | ||||||
chr6:169242565
|
A | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-607T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242565 | ||||||
chr6:169242567
|
T | TTCCCACC others(94): Show |
1 | a0001c0004t0004g0256 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.695-610_695-609ins others(101): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242567 | ||||||
chr6:169242578
|
C | CCACCTT | 13 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-621_695-620ins others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242578 | ||||||
chr6:169242578
|
C | CCACCTTC others(116): Show |
1 | a0001c0004t0003g0255 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.695-621_695-620ins others(123): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242578 | ||||||
chr6:169242582
|
A | AC | 12 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(9): Show | 13 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-625_695-624ins others(1): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242582 | ||||||
chr6:169242583
|
A | C | 12 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(9): Show | 13 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-625T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242583 | ||||||
chr6:169242583
|
A | T | 2 | a0001c0004t0003g0255a0001c0004t0004g0256 | 2 | NA18944.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.695-625T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242583 | ||||||
chr6:169242584
|
A | C | 2 | a0001c0004t0003g0255a0001c0004t0004g0256 | 2 | NA18944.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.695-626T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242584 | ||||||
chr6:169242584
|
A | G | 12 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(9): Show | 13 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-626T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242584 | ||||||
chr6:169242585
|
T | C | 12 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(9): Show | 13 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-627A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242585 | ||||||
chr6:169242598
|
A | AC | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-641dupG | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242598 | ||||||
chr6:169242600
|
A | ATTCCCAC others(692): Show |
1 | a0008c0053t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.695-643_695-642ins others(699): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242600
|
A | ATTCCCAC others(100): Show |
160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(157): Show | 188 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.695-643_695-642ins others(107): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242600
|
A | ATTCCCAC others(201): Show |
1 | a0001c0002t0002g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.695-643_695-642ins others(208): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242600
|
A | ATTCCCAC others(42): Show |
1 | a0001c0003t0002g0261 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.695-643_695-642ins others(49): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242600
|
A | ATTCCCAC others(26): Show |
1 | a0001c0033t0007g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.695-675_695-643dup others(33): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242600
|
A | ATTCCCAC others(26): Show |
2 | a0001c0014t0002g0027a0001c0014t0002g0114 | 3 | HG02630.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.695-643_695-642ins others(33): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242600
|
A | C | 18 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0313others(15): Show | 20 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.695-642T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242600 | ||||||
chr6:169242601
|
T | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-643A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242601 | ||||||
chr6:169242601
|
T | TTCCCACC others(117): Show |
19 | a0001c0001t0001g0134a0001c0001t0001g0164a0001c0001t0001g0338others(16): Show | 19 | HG00544.hp1 HG00597.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.695-644_695-643ins others(124): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242601 | ||||||
chr6:169242601
|
T | TTCCCACC others(161): Show |
6 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(3): Show | 10 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-644_695-643ins others(168): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242601 | ||||||
chr6:169242601
|
T | TTCCCACC others(144): Show |
1 | a0003c0012t0007g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.695-644_695-643ins others(151): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242601 | ||||||
chr6:169242616
|
C | T | 35 | a0001c0001t0001g0123a0001c0001t0001g0221a0001c0001t0001g0230others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.695-658G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242616 | ||||||
chr6:169242617
|
G | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(260): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.695-659C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242617 | ||||||
chr6:169242618
|
C | CTCCACCT others(715): Show |
1 | a0001c0003t0002g0248 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.695-661_695-660ins others(722): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242618 | ||||||
chr6:169242618
|
C | CTCCCACC others(9): Show |
6 | a0001c0017t0002g0039a0001c0017t0002g0040a0004c0020t0001g0299others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-661_695-660ins others(16): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242618 | ||||||
chr6:169242618
|
C | CTCCCACC others(108): Show |
2 | a0001c0002t0002g0008a0001c0004t0004g0117 | 4 | HG00639.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-661_695-660ins others(115): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242618 | ||||||
chr6:169242618
|
C | CTCCCACC others(83): Show |
3 | a0001c0005t0003g0308a0001c0005t0018g0032a0001c0036t0001g0333 | 3 | HG01891.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.695-661_695-660ins others(90): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242618 | ||||||
chr6:169242618
|
C | T | 2 | a0001c0004t0003g0255a0001c0004t0004g0256 | 2 | NA18944.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.695-660G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242618 | ||||||
chr6:169242624
|
C | CCTTCCCA others(782): Show |
1 | a0001c0001t0031g0295 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.695-667_695-666ins others(789): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242624 | ||||||
chr6:169242624
|
C | CCTTCCCA others(658): Show |
1 | a0001c0003t0002g0267 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.695-667_695-666ins others(665): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242624 | ||||||
chr6:169242624
|
C | CCTTCCCA others(724): Show |
22 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0051others(19): Show | 27 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.695-667_695-666ins others(731): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242624 | ||||||
chr6:169242624
|
C | CCTTCCCA others(707): Show |
4 | a0001c0003t0002g0259a0001c0003t0024g0260a0001c0009t0002g0013others(1): Show | 6 | HG02040.hp2 HG02165.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-667_695-666ins others(714): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242624 | ||||||
chr6:169242624
|
C | T | 1 | a0001c0003t0002g0248 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.695-666G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242624 | ||||||
chr6:169242631
|
A | ACCTTCCC others(64): Show |
4 | a0001c0016t0003g0144a0001c0016t0003g0199a0001c0044t0003g0058others(1): Show | 4 | HG02683.hp1 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-674_695-673ins others(71): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242631 | ||||||
chr6:169242631
|
A | ACCTTCCC others(31): Show |
1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-674_695-673ins others(38): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242631 | ||||||
chr6:169242633
|
C | CTTCCCAT | 12 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(9): Show | 13 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-676_695-675ins others(7): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242633 | ||||||
chr6:169242633
|
C | CTTCCTAT others(8): Show |
17 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(14): Show | 19 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.695-676_695-675ins others(15): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242633 | ||||||
chr6:169242633
|
C | CTTCCTAT others(65): Show |
1 | a0001c0005t0005g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695-676_695-675ins others(72): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242633 | ||||||
chr6:169242633
|
CA | C | 32 | a0001c0001t0001g0123a0001c0001t0001g0221a0001c0001t0001g0230others(29): Show | 33 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.695-676delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242633 | ||||||
chr6:169242634
|
A | ACTCCCAC others(818): Show |
1 | a0001c0018t0005g0290 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.695-677_695-676ins others(825): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242634
|
A | ACTCCCAC others(692): Show |
10 | a0001c0003t0002g0244a0001c0003t0002g0250a0001c0003t0002g0273others(7): Show | 10 | HG01192.hp1 HG01255.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-677_695-676ins others(699): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242634
|
A | ACTCCCAC others(675): Show |
10 | a0001c0003t0002g0278a0001c0004t0003g0275a0001c0004t0003g0277others(7): Show | 10 | HG02074.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-677_695-676ins others(682): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242634
|
A | ACTCCCAC others(675): Show |
1 | a0007c0047t0029g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695-677_695-676ins others(682): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242634
|
A | ACTCCCAC others(857): Show |
1 | a0008c0034t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.695-677_695-676ins others(864): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242634
|
A | C | 30 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(27): Show | 33 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.695-676T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242634
|
A | G | 31 | a0001c0001t0031g0295a0001c0003t0002g0001a0001c0003t0002g0048others(28): Show | 38 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.695-676T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242634 | ||||||
chr6:169242635
|
C | CCT | 5 | a0001c0016t0003g0144a0001c0016t0003g0199a0001c0044t0003g0058others(2): Show | 5 | HG02683.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-678_695-677ins others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242635 | ||||||
chr6:169242635
|
C | CTCCCACC others(51): Show |
4 | a0004c0020t0001g0299a0004c0020t0001g0301a0004c0029t0002g0300others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-735_695-678dup others(58): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242635 | ||||||
chr6:169242635
|
C | T | 62 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0221others(59): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.695-677G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242635 | ||||||
chr6:169242639
|
C | T | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-681G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242639 | ||||||
chr6:169242641
|
C | T | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-683G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242641 | ||||||
chr6:169242649
|
C | T | 8 | a0001c0005t0003g0327a0002c0010t0009g0023a0002c0010t0009g0024others(5): Show | 12 | HG00558.hp1 HG00735.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-691G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242649 | ||||||
chr6:169242650
|
C | T | 1 | a0001c0005t0005g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.695-692G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242650 | ||||||
chr6:169242650
|
CA | C | 8 | a0001c0005t0003g0327a0002c0010t0009g0023a0002c0010t0009g0024others(5): Show | 12 | HG00558.hp1 HG00735.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-693delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242650 | ||||||
chr6:169242651
|
A | G | 4 | a0001c0005t0005g0316a0001c0019t0003g0309a0001c0019t0014g0310others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-693T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242651 | ||||||
chr6:169242652
|
C | CTCCCACC others(1): Show |
16 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 18 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-702_695-695dup others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242652 | ||||||
chr6:169242652
|
C | T | 8 | a0001c0005t0003g0327a0002c0010t0009g0023a0002c0010t0009g0024others(5): Show | 12 | HG00558.hp1 HG00735.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-694G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242652 | ||||||
chr6:169242667
|
C | CTTCCCAT others(8): Show |
1 | a0001c0005t0005g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.695-710_695-709ins others(15): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242667 | ||||||
chr6:169242668
|
A | C | 1 | a0001c0005t0005g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.695-710T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242668 | ||||||
chr6:169242669
|
C | CTCCCACC others(18): Show |
1 | a0001c0001t0001g0331 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.695-712_695-711ins others(25): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242669 | ||||||
chr6:169242669
|
C | CTCCCACC others(51): Show |
1 | a0001c0001t0014g0330 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.695-712_695-711ins others(58): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242669 | ||||||
chr6:169242669
|
C | CTCCCACC others(67): Show |
2 | a0001c0001t0004g0043a0001c0001t0035g0329 | 2 | HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.695-712_695-711ins others(74): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242669 | ||||||
chr6:169242669
|
C | T | 2 | a0001c0005t0005g0316a0003c0046t0021g0315 | 2 | NA18995.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.695-711G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242669 | ||||||
chr6:169242674
|
A | G | 2 | a0001c0002t0002g0008a0001c0004t0004g0117 | 4 | HG00639.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-716T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242674 | ||||||
chr6:169242675
|
C | T | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-717G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242675 | ||||||
chr6:169242675
|
CCTTCCCA others(9): Show |
C | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-733_695-718del others(16): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242675 | ||||||
chr6:169242677
|
T | TTCCCACC others(160): Show |
2 | a0001c0019t0003g0309a0001c0019t0014g0310 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.695-720_695-719ins others(167): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242677 | ||||||
chr6:169242677
|
T | TTCCCACC others(985): Show |
1 | a0001c0019t0014g0311 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.695-720_695-719ins others(992): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242677 | ||||||
chr6:169242683
|
C | CCTTCCCA others(1): Show |
5 | a0001c0001t0011g0285a0001c0003t0002g0124a0001c0003t0002g0283others(2): Show | 5 | HG01074.hp1 HG01192.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-733_695-726dup others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242683 | ||||||
chr6:169242685
|
T | C | 2 | a0001c0005t0005g0316a0001c0005t0005g0320 | 2 | NA18995.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.695-727A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242685 | ||||||
chr6:169242685
|
T | TTCCCACC others(59): Show |
3 | a0001c0001t0001g0134a0001c0002t0002g0008a0001c0004t0004g0117 | 5 | HG00544.hp1 HG00639.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-728_695-727ins others(66): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242685 | ||||||
chr6:169242691
|
T | C | 26 | a0001c0001t0001g0026a0001c0001t0001g0134a0001c0001t0005g0102others(23): Show | 30 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.695-733A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242691 | ||||||
chr6:169242691
|
T | TCTTCCCA others(92): Show |
1 | a0001c0001t0001g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.695-734_695-733ins others(99): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242691 | ||||||
chr6:169242691
|
T | TCTTCCCA others(404): Show |
1 | a0001c0001t0001g0091 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.695-734_695-733ins others(411): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242691 | ||||||
chr6:169242691
|
T | TCTTCCCA others(100): Show |
9 | a0001c0001t0001g0059a0001c0001t0001g0081a0001c0001t0001g0161others(6): Show | 10 | HG01167.hp2 HG02027.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-734_695-733ins others(107): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242691 | ||||||
chr6:169242692
|
C | CTTCCCAC others(116): Show |
16 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 18 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-735_695-734ins others(123): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242692 | ||||||
chr6:169242715
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(169): Show | 197 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.695-757T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242715 | ||||||
chr6:169242718
|
T | TTCCCACC others(1327): Show |
1 | a0001c0003t0002g0261 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.695-761_695-760ins others(1334): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242718
|
T | TTCCCACC others(1244): Show |
3 | a0001c0003t0002g0124a0001c0003t0002g0283a0001c0003t0002g0297 | 3 | HG01192.hp2 HG02602.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.695-761_695-760ins others(1251): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242718
|
T | TTCCCACC others(1335): Show |
2 | a0001c0001t0011g0285a0001c0003t0002g0284 | 2 | HG01074.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.695-761_695-760ins others(1342): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242718
|
T | TTCCCACC others(678): Show |
1 | a0001c0004t0003g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.695-761_695-760ins others(685): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242718
|
T | TTCCCACC others(570): Show |
18 | a0001c0003t0002g0001a0001c0003t0002g0048a0001c0003t0002g0259others(15): Show | 23 | HG00639.hp1 HG00738.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.695-761_695-760ins others(577): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242718
|
T | TTCCCACC others(578): Show |
1 | a0001c0004t0004g0076 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.695-761_695-760ins others(585): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242718
|
T | TTCCCACC others(537): Show |
1 | a0001c0004t0003g0255 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.695-761_695-760ins others(544): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242718 | ||||||
chr6:169242741
|
C | T | 20 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(17): Show | 22 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-783G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242741 | ||||||
chr6:169242751
|
T | TTCCCACC others(612): Show |
8 | a0001c0004t0004g0246a0001c0004t0004g0252a0001c0004t0004g0257others(5): Show | 9 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.695-794_695-793ins others(619): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242751 | ||||||
chr6:169242751
|
T | TTCCCACC others(712): Show |
1 | a0001c0008t0006g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.695-794_695-793ins others(719): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242751 | ||||||
chr6:169242751
|
T | TTCCCACC others(604): Show |
1 | a0001c0004t0003g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.695-794_695-793ins others(611): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242751 | ||||||
chr6:169242751
|
T | TTCCCACC others(913): Show |
2 | a0001c0013t0002g0302a0001c0013t0002g0303 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.695-794_695-793ins others(920): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242751 | ||||||
chr6:169242764
|
A | ACATTCCC others(505): Show |
1 | a0001c0004t0004g0256 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.695-807_695-806ins others(512): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242764 | ||||||
chr6:169242764
|
A | AG | 12 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(9): Show | 13 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-807_695-806ins others(1): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242764 | ||||||
chr6:169242765
|
T | C | 17 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(14): Show | 19 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.695-807A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242765 | ||||||
chr6:169242766
|
C | A | 16 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 18 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-808G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242766 | ||||||
chr6:169242766
|
C | G | 13 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-808G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242766 | ||||||
chr6:169242767
|
T | C | 13 | a0001c0004t0003g0075a0001c0004t0004g0246a0001c0004t0004g0252others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-809A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242767 | ||||||
chr6:169242767
|
T | TTCCCACC others(61): Show |
1 | a0001c0004t0003g0255 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.695-810_695-809ins others(68): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242767 | ||||||
chr6:169242767
|
T | TTCCCATC others(126): Show |
1 | a0004c0020t0001g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.695-942_695-810dup others(133): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242767 | ||||||
chr6:169242773
|
T | C | 16 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 18 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-815A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242773 | ||||||
chr6:169242773
|
T | TCTTCCCA others(323): Show |
1 | a0001c0001t0001g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.695-816_695-815ins others(330): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242773 | ||||||
chr6:169242790
|
CA | C | 16 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 18 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-833delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242790 | ||||||
chr6:169242792
|
C | T | 16 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 18 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-834G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242792 | ||||||
chr6:169242799
|
C | CTTCCCAC others(50): Show |
1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-842_695-841ins others(57): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242799 | ||||||
chr6:169242800
|
T | TTCCCACC others(397): Show |
1 | a0001c0005t0005g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.695-843_695-842ins others(404): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242800 | ||||||
chr6:169242800
|
T | TTCCCACC others(493): Show |
1 | a0001c0005t0005g0316 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.695-843_695-842ins others(500): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242800 | ||||||
chr6:169242800
|
T | TTCCCACC others(493): Show |
1 | a0001c0005t0005g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695-843_695-842ins others(500): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242800 | ||||||
chr6:169242814
|
C | CCGCTCCC others(313): Show |
13 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0313others(10): Show | 14 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-857_695-856ins others(320): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242814 | ||||||
chr6:169242814
|
C | CCGCTCCC others(248): Show |
2 | a0001c0001t0001g0026a0001c0005t0001g0321 | 3 | HG01070.hp1 HG01071.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.695-857_695-856ins others(255): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242814 | ||||||
chr6:169242815
|
C | T | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-857G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242815 | ||||||
chr6:169242815
|
CA | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-858delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242815 | ||||||
chr6:169242816
|
A | ACTCCCAC others(10): Show |
15 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(12): Show | 17 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-859_695-858ins others(17): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242816 | ||||||
chr6:169242816
|
A | G | 8 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(5): Show | 8 | HG01346.hp2 HG02486.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.695-858T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242816 | ||||||
chr6:169242817
|
C | T | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-859G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242817 | ||||||
chr6:169242824
|
C | CA | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-867_695-866ins others(1): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242824 | ||||||
chr6:169242825
|
T | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-867A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(854): Show |
1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-868_695-867ins others(861): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(725): Show |
1 | a0001c0002t0002g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.695-868_695-867ins others(732): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(855): Show |
1 | a0001c0001t0001g0166 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.695-868_695-867ins others(862): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(733): Show |
1 | a0001c0001t0003g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.695-868_695-867ins others(740): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(937): Show |
2 | a0001c0001t0001g0063a0001c0043t0001g0165 | 2 | NA18966.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.695-868_695-867ins others(944): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(1005): Show |
1 | a0011c0051t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.695-868_695-867ins others(1012): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(520): Show |
1 | a0001c0001t0001g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.695-868_695-867ins others(527): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(626): Show |
6 | a0001c0001t0001g0091a0001c0001t0001g0134a0001c0001t0001g0143others(3): Show | 8 | HG00544.hp1 HG00639.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-868_695-867ins others(633): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(740): Show |
4 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(1): Show | 4 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-868_695-867ins others(747): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(733): Show |
1 | a0001c0016t0003g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.695-868_695-867ins others(740): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242825
|
T | TTCCCACC others(841): Show |
1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.695-868_695-867ins others(848): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242825 | ||||||
chr6:169242832
|
C | CTTCCCAC others(42): Show |
4 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(1): Show | 4 | HG02486.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-875_695-874ins others(49): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242832 | ||||||
chr6:169242840
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695-882G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242840 | ||||||
chr6:169242848
|
T | C | 230 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(227): Show | 265 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.695-890A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242848 | ||||||
chr6:169242849
|
G | A | 4 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(1): Show | 4 | HG02486.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-891C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242849 | ||||||
chr6:169242850
|
CTCCCACC others(1): Show |
C | 3 | a0001c0003t0002g0067a0001c0019t0003g0309a0001c0019t0014g0310 | 3 | HG01243.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.695-900_695-893del others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242850 | ||||||
chr6:169242858
|
T | TTCCCACC others(92): Show |
1 | a0001c0019t0014g0311 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.695-901_695-900ins others(99): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242858 | ||||||
chr6:169242864
|
C | CCTTCCCA others(9): Show |
10 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343others(7): Show | 15 | HG00735.hp2 HG01167.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-907_695-906ins others(16): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242864 | ||||||
chr6:169242872
|
C | T | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(161): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.695-914G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242872 | ||||||
chr6:169242873
|
C | A | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-915G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242873 | ||||||
chr6:169242879
|
A | ACCTTCCC others(14): Show |
1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-922_695-921ins others(21): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242879 | ||||||
chr6:169242880
|
C | T | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(161): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.695-922G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242880 | ||||||
chr6:169242881
|
CA | C | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(161): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.695-924delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242881 | ||||||
chr6:169242883
|
C | CTCCCACC others(1): Show |
3 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-933_695-926dup others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242883 | ||||||
chr6:169242883
|
C | CTCCCACC others(411): Show |
1 | a0002c0010t0009g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.695-926_695-925ins others(418): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242883 | ||||||
chr6:169242883
|
C | CTCCCACC others(304): Show |
6 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(3): Show | 10 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-926_695-925ins others(311): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242883 | ||||||
chr6:169242883
|
C | T | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(161): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.695-925G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242883 | ||||||
chr6:169242897
|
G | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(172): Show | 205 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.695-939C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242897 | ||||||
chr6:169242898
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(162): Show | 190 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.695-940A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242898 | ||||||
chr6:169242899
|
G | A | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(161): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.695-941C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242899 | ||||||
chr6:169242906
|
T | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(172): Show | 205 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.695-948A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242906 | ||||||
chr6:169242912
|
C | CACCTTCC others(279): Show |
3 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-955_695-954ins others(286): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242912 | ||||||
chr6:169242921
|
AC | A | 8 | a0001c0005t0003g0327a0002c0010t0009g0023a0002c0010t0009g0024others(5): Show | 12 | HG00558.hp1 HG00735.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-964delG | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242921 | ||||||
chr6:169242924
|
A | G | 3 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-966T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242924 | ||||||
chr6:169242925
|
C | T | 8 | a0001c0005t0003g0327a0002c0010t0009g0023a0002c0010t0009g0024others(5): Show | 12 | HG00558.hp1 HG00735.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-967G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242925 | ||||||
chr6:169242932
|
C | A | 3 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-974G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242932 | ||||||
chr6:169242932
|
C | CTTCCCAC others(9): Show |
22 | a0001c0001t0001g0026a0001c0001t0001g0331a0001c0001t0004g0043others(19): Show | 24 | HG00423.hp1 HG00438.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.695-975_695-974ins others(16): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242932 | ||||||
chr6:169242933
|
T | TTCCCACC others(562): Show |
7 | a0001c0003t0002g0051a0001c0009t0002g0013a0001c0009t0002g0214others(4): Show | 9 | HG01261.hp1 HG01952.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.695-976_695-975ins others(569): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242933 | ||||||
chr6:169242936
|
C | T | 3 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-978G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242936 | ||||||
chr6:169242940
|
C | A | 8 | a0001c0001t0001g0242a0002c0010t0009g0023a0002c0010t0009g0024others(5): Show | 12 | HG00735.hp2 HG02135.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-982G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242940 | ||||||
chr6:169242941
|
T | TTCCCACC others(51): Show |
3 | a0001c0004t0003g0255a0001c0004t0004g0246a0001c0008t0006g0245 | 3 | HG02080.hp2 NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.695-984_695-983ins others(58): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242941 | ||||||
chr6:169242947
|
C | CTGCTCCC others(373): Show |
1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-990_695-989ins others(380): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242947 | ||||||
chr6:169242947
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695-989G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242947 | ||||||
chr6:169242948
|
C | A | 20 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(17): Show | 22 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.695-990G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242948 | ||||||
chr6:169242949
|
T | TTCCCACC others(2): Show |
11 | a0001c0004t0003g0075a0001c0004t0004g0252a0001c0004t0004g0256others(8): Show | 12 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-992_695-991ins others(9): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242949 | ||||||
chr6:169242951
|
C | CCCACCGC others(510): Show |
1 | a0001c0001t0001g0163 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.695-994_695-993ins others(517): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(518): Show |
2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18942.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.695-994_695-993ins others(525): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(411): Show |
1 | a0001c0001t0001g0164 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(418): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(462): Show |
1 | a0001c0001t0003g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.695-994_695-993ins others(469): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(305): Show |
34 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(31): Show | 40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.695-994_695-993ins others(312): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(411): Show |
1 | a0001c0016t0005g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(418): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(395): Show |
1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(402): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(411): Show |
2 | a0001c0001t0001g0049a0001c0028t0001g0029 | 3 | HG02109.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.695-994_695-993ins others(418): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(411): Show |
100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(97): Show | 116 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.695-994_695-993ins others(418): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(395): Show |
1 | a0001c0002t0002g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(402): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(460): Show |
1 | a0001c0001t0001g0142 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.695-994_695-993ins others(467): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(738): Show |
3 | a0001c0001t0001g0128a0006c0026t0001g0207a0012c0050t0001g0072 | 3 | HG02145.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.695-994_695-993ins others(745): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(608): Show |
1 | a0001c0001t0001g0059 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(615): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(419): Show |
1 | a0006c0026t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.695-994_695-993ins others(426): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(452): Show |
1 | a0001c0002t0002g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(459): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(321): Show |
10 | a0001c0001t0003g0033a0001c0001t0003g0035a0001c0001t0003g0190others(7): Show | 11 | HG01069.hp1 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.695-994_695-993ins others(328): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCGC others(452): Show |
1 | a0001c0001t0001g0344 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.695-994_695-993ins others(459): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | CCCACCTT others(749): Show |
1 | a0001c0001t0001g0020 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.695-994_695-993ins others(756): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242951
|
C | T | 3 | a0001c0002t0002g0170a0001c0015t0015g0017a0001c0015t0015g0343 | 4 | HG01167.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-993G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242951 | ||||||
chr6:169242957
|
TTCCCACT others(2): Show |
T | 20 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(17): Show | 22 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.695-1008_695-1000d others(11): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242957 | ||||||
chr6:169242964
|
T | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(177): Show | 207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.695-1006A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242964 | ||||||
chr6:169242965
|
G | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(165): Show | 194 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.695-1007C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242965 | ||||||
chr6:169242970
|
C | CACCTTCC others(84): Show |
7 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(4): Show | 11 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.695-1013_695-1012i others(93): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242970 | ||||||
chr6:169242970
|
C | CGCCTTCC others(559): Show |
1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695-1013_695-1012i others(568): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242970 | ||||||
chr6:169242970
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(163): Show | 192 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.695-1012G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242970 | ||||||
chr6:169242977
|
C | G | 1 | a0001c0001t0037g0231 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.695-1019G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242977 | ||||||
chr6:169242988
|
C | CCACTCCC others(19): Show |
1 | a0001c0001t0001g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.695-1031_695-1030i others(28): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242988 | ||||||
chr6:169242988
|
C | CT | 20 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(17): Show | 22 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.695-1031_695-1030i others(3): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242988 | ||||||
chr6:169242989
|
A | G | 21 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(18): Show | 23 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.695-1031T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242989 | ||||||
chr6:169242990
|
T | C | 21 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(18): Show | 23 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.695-1032A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242990 | ||||||
chr6:169242993
|
G | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(207): Show | 243 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.695-1035C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242993 | ||||||
chr6:169242993
|
G | GCACCTTC others(92): Show |
26 | a0001c0001t0001g0123a0001c0001t0001g0221a0001c0001t0001g0232others(23): Show | 27 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.695-1134_695-1036d others(101): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169242993 | ||||||
chr6:169243004
|
C | CT | 3 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.695-1047_695-1046i others(3): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243004 | ||||||
chr6:169243005
|
C | G | 3 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.695-1047G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243005 | ||||||
chr6:169243006
|
T | C | 3 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.695-1048A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243006 | ||||||
chr6:169243011
|
A | ACCTTCCC others(27): Show |
2 | a0001c0004t0003g0255a0001c0008t0006g0245 | 2 | HG02080.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.695-1054_695-1053i others(36): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243011 | ||||||
chr6:169243011
|
A | ACTGCTCC others(68): Show |
3 | a0001c0013t0002g0028a0001c0013t0002g0302a0001c0013t0002g0303 | 4 | HG01109.hp1 HG01261.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-1054_695-1053i others(77): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243011 | ||||||
chr6:169243011
|
A | ACTGCTCC others(76): Show |
8 | a0001c0004t0003g0075a0001c0004t0004g0252a0001c0004t0004g0256others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-1054_695-1053i others(85): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243011 | ||||||
chr6:169243013
|
A | C | 5 | a0001c0004t0004g0246a0001c0005t0003g0327a0001c0019t0003g0309others(2): Show | 5 | HG00558.hp1 HG01243.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-1055T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243013 | ||||||
chr6:169243014
|
T | C | 13 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0252others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-1056A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243014 | ||||||
chr6:169243017
|
C | G | 20 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(17): Show | 22 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.695-1059G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243017 | ||||||
chr6:169243035
|
AC | A | 19 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(16): Show | 21 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.695-1078delG | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243035 | ||||||
chr6:169243036
|
C | G | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-1078G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243036 | ||||||
chr6:169243037
|
C | T | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-1079G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243037 | ||||||
chr6:169243038
|
G | A | 20 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(17): Show | 22 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.695-1080C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243038 | ||||||
chr6:169243039
|
C | A | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.695-1081G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(291): Show |
1 | a0001c0006t0006g0182 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.695-1082_695-1081i others(300): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(1): Show |
13 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0252others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-1089_695-1082d others(10): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(307): Show |
2 | a0001c0001t0001g0332a0001c0016t0005g0334 | 2 | HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.695-1082_695-1081i others(316): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(306): Show |
1 | a0001c0006t0006g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.695-1082_695-1081i others(315): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(299): Show |
1 | a0001c0001t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.695-1082_695-1081i others(308): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(307): Show |
2 | a0001c0015t0015g0017a0001c0015t0015g0343 | 3 | HG02965.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.695-1082_695-1081i others(316): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(291): Show |
1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.695-1082_695-1081i others(300): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(307): Show |
152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(149): Show | 176 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.695-1082_695-1081i others(316): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(365): Show |
1 | a0001c0001t0003g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.695-1082_695-1081i others(374): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(307): Show |
1 | a0001c0001t0028g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.695-1082_695-1081i others(316): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | CTCCCACC others(306): Show |
1 | a0001c0001t0001g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.695-1082_695-1081i others(315): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243039
|
C | T | 19 | a0001c0001t0001g0063a0001c0001t0001g0091a0001c0001t0001g0134others(16): Show | 21 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.695-1081G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243039 | ||||||
chr6:169243041
|
C | T | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.695-1083G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243041 | ||||||
chr6:169243045
|
C | T | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.695-1087G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243045 | ||||||
chr6:169243046
|
C | CTTCCCAC others(299): Show |
3 | a0001c0006t0008g0014a0001c0006t0008g0034a0001c0022t0007g0038 | 4 | HG01069.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-1089_695-1088i others(308): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243046 | ||||||
chr6:169243046
|
C | CTTCCCAC others(282): Show |
1 | a0001c0002t0020g0037 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.695-1089_695-1088i others(291): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243046 | ||||||
chr6:169243061
|
C | CCGCTCCC others(282): Show |
7 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(4): Show | 11 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.695-1104_695-1103i others(291): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243061 | ||||||
chr6:169243063
|
A | ACTCCCAC others(18): Show |
1 | a0001c0001t0004g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.695-1106_695-1105i others(27): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243063 | ||||||
chr6:169243063
|
A | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(198): Show | 230 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.695-1105T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243063 | ||||||
chr6:169243064
|
C | T | 7 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(4): Show | 11 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.695-1106G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243064 | ||||||
chr6:169243072
|
T | TTCCCACC others(561): Show |
1 | a0001c0003t0002g0248 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.695-1115_695-1114i others(570): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243072 | ||||||
chr6:169243087
|
T | C | 22 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(19): Show | 27 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.695-1129A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243087 | ||||||
chr6:169243087
|
T | TGCTCCCA others(42): Show |
1 | a0001c0001t0001g0230 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.695-1130_695-1129i others(51): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243087 | ||||||
chr6:169243113
|
A | G | 1 | a0001c0004t0004g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.695-1155T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243113 | ||||||
chr6:169243114
|
C | CTCCCACC others(18): Show |
6 | a0001c0017t0002g0039a0001c0017t0002g0040a0004c0020t0001g0299others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-1157_695-1156i others(27): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243114 | ||||||
chr6:169243118
|
T | C | 28 | a0001c0001t0001g0230a0001c0004t0003g0075a0001c0004t0003g0255others(25): Show | 33 | HG00408.hp1 HG00609.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.695-1160A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243118 | ||||||
chr6:169243126
|
C | T | 1 | a0002c0010t0009g0205 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.695-1168G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243126 | ||||||
chr6:169243138
|
G | A | 1 | a0001c0004t0004g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.695-1180C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243138 | ||||||
chr6:169243162
|
A | C | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-1204T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243162 | ||||||
chr6:169243172
|
C | CTCCCACC others(85): Show |
13 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0252others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-1215_695-1214i others(94): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243172 | ||||||
chr6:169243183
|
C | T | 1 | a0001c0005t0003g0326 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.695-1225G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243183 | ||||||
chr6:169243184
|
C | G | 2 | a0006c0026t0001g0207a0012c0050t0001g0072 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.695-1226G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243184 | ||||||
chr6:169243188
|
T | TCTCCCAC others(10): Show |
1 | a0001c0001t0001g0019 | 2 | NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.695-1247_695-1231d others(19): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243188 | ||||||
chr6:169243202
|
A | G | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-1244T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243202 | ||||||
chr6:169243211
|
A | T | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.695-1253T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243211 | ||||||
chr6:169243252
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(179): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.695-1294C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243252 | ||||||
chr6:169243310
|
C | T | 1 | a0001c0017t0002g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.695-1352G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243310 | ||||||
chr6:169243390
|
C | T | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(78): Show | 92 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.695-1432G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243390 | ||||||
chr6:169243402
|
G | C | 4 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-1444C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243402 | ||||||
chr6:169243499
|
C | T | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-1541G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243499 | ||||||
chr6:169243590
|
C | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(190): Show | 225 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.695-1632G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243590 | ||||||
chr6:169243631
|
C | T | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-1673G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243631 | ||||||
chr6:169243784
|
T | C | 24 | a0001c0001t0001g0026a0001c0001t0001g0331a0001c0001t0004g0043others(21): Show | 26 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.695-1826A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243784 | ||||||
chr6:169243891
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(183): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.695-1933G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243891 | ||||||
chr6:169243937
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(183): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.695-1979G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243937 | ||||||
chr6:169243986
|
A | G | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.695-2028T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243986 | ||||||
chr6:169243991
|
TGAA | T | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-2036_695-2034d others(5): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169243991 | ||||||
chr6:169244053
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(191): Show | 226 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.695-2095G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244053 | ||||||
chr6:169244095
|
G | A | 14 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(11): Show | 15 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.694+2102C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244095 | ||||||
chr6:169244134
|
T | A | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.694+2063A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244134 | ||||||
chr6:169244142
|
T | A | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.694+2055A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244142 | ||||||
chr6:169244158
|
C | A | 1 | a0001c0014t0002g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.694+2039G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244158 | ||||||
chr6:169244164
|
G | GT | 14 | a0001c0001t0031g0295a0001c0003t0002g0048a0001c0003t0002g0270others(11): Show | 14 | HG00558.hp1 HG01496.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.694+2032dupA | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244164 | ||||||
chr6:169244164
|
G | GTT | 15 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(12): Show | 16 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.694+2031_694+2032d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244164 | ||||||
chr6:169244164
|
GT | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(151): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.694+2032delA | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244164 | ||||||
chr6:169244164
|
GTT | G | 57 | a0001c0001t0001g0049a0001c0001t0001g0085a0001c0001t0001g0098others(54): Show | 63 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.694+2031_694+2032d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244164 | ||||||
chr6:169244164
|
GTTT | G | 8 | a0001c0001t0003g0033a0001c0001t0004g0043a0001c0001t0014g0330others(5): Show | 8 | HG02055.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+2030_694+2032d others(5): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244164 | ||||||
chr6:169244164
|
GTTTTTT | G | 13 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(10): Show | 14 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.694+2027_694+2032d others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244164 | ||||||
chr6:169244168
|
T | G | 2 | a0001c0001t0001g0332a0001c0016t0005g0334 | 2 | HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.694+2029A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244168 | ||||||
chr6:169244172
|
T | G | 1 | a0001c0033t0007g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.694+2025A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244172 | ||||||
chr6:169244313
|
A | AAC | 22 | a0001c0001t0001g0003a0001c0001t0001g0063a0001c0001t0004g0043others(19): Show | 26 | HG01109.hp1 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.694+1882_694+1883d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
A | AACAC | 189 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(186): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.694+1880_694+1883d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
A | AACACAC | 66 | a0001c0001t0001g0081a0001c0001t0001g0087a0001c0001t0001g0123others(63): Show | 74 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.694+1878_694+1883d others(8): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
A | AACACACA others(1): Show |
10 | a0001c0001t0001g0220a0001c0001t0004g0054a0001c0001t0014g0330others(7): Show | 10 | HG02451.hp2 HG02559.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+1876_694+1883d others(10): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
A | AACACACA others(5): Show |
3 | a0002c0010t0009g0024a0002c0010t0009g0205a0003c0012t0007g0006 | 6 | HG00735.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+1872_694+1883d others(14): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
A | AACACACA others(7): Show |
3 | a0002c0010t0009g0204a0003c0012t0007g0041a0007c0047t0029g0055 | 3 | HG03098.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.694+1870_694+1883d others(16): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
A | AACACACA others(9): Show |
1 | a0002c0010t0009g0023 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.694+1868_694+1883d others(18): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244313
|
AAC | A | 30 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(27): Show | 32 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.694+1882_694+1883d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244313 | ||||||
chr6:169244424
|
C | G | 4 | a0001c0003t0002g0067a0001c0003t0002g0193a0001c0004t0003g0065others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+1773G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244424 | ||||||
chr6:169244434
|
T | C | 18 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(15): Show | 19 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.694+1763A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244434 | ||||||
chr6:169244503
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0132 | 2 | NA18942.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.694+1694G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244503 | ||||||
chr6:169244600
|
GCA | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(199): Show | 234 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.694+1595_694+1596d others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244600 | ||||||
chr6:169244600
|
GCACA | G | 17 | a0001c0004t0003g0075a0001c0004t0003g0255a0001c0004t0004g0246others(14): Show | 18 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.694+1593_694+1596d others(6): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244600 | ||||||
chr6:169244766
|
A | T | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.694+1431T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244766 | ||||||
chr6:169244767
|
T | A | 1 | a0001c0031t0001g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.694+1430A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244767 | ||||||
chr6:169244839
|
G | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(190): Show | 225 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.694+1358C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244839 | ||||||
chr6:169244897
|
C | A | 1 | a0008c0053t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.694+1300G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244897 | ||||||
chr6:169244969
|
C | T | 1 | a0001c0007t0004g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.694+1228G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244969 | ||||||
chr6:169244998
|
A | C | 1 | a0001c0001t0010g0222 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.694+1199T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169244998 | ||||||
chr6:169245033
|
T | C | 19 | a0001c0001t0001g0026a0001c0001t0005g0102a0001c0001t0005g0103others(16): Show | 21 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.694+1164A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245033 | ||||||
chr6:169245121
|
C | T | 8 | a0002c0010t0009g0023a0002c0010t0009g0024a0002c0010t0009g0204others(5): Show | 12 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.694+1076G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245121 | ||||||
chr6:169245141
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.694+1056G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245141 | ||||||
chr6:169245252
|
ATCTT | A | 17 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0313others(14): Show | 18 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.694+941_694+944del others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245252 | ||||||
chr6:169245320
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.694+877C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245320 | ||||||
chr6:169245455
|
T | C | 1 | a0001c0001t0013g0294 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.694+742A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245455 | ||||||
chr6:169245520
|
T | C | 3 | a0001c0001t0014g0330a0001c0005t0003g0326a0008c0053t0001g0312 | 3 | HG02055.hp1 HG03098.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.694+677A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245520 | ||||||
chr6:169245521
|
G | A | 2 | a0001c0005t0003g0326a0008c0053t0001g0312 | 2 | HG02055.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.694+676C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245521 | ||||||
chr6:169245531
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0131 | 2 | HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.694+666T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245531 | ||||||
chr6:169245562
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0003g0196 | 2 | HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.694+635C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245562 | ||||||
chr6:169245588
|
C | G | 2 | a0001c0001t0001g0197a0008c0034t0001g0249 | 2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.694+609G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245588 | ||||||
chr6:169245598
|
T | C | 8 | a0001c0001t0001g0070a0001c0001t0001g0197a0001c0001t0001g0331others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+599A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245598 | ||||||
chr6:169245609
|
G | A | 1 | a0001c0004t0004g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.694+588C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245609 | ||||||
chr6:169245610
|
C | G | 10 | a0001c0001t0001g0128a0001c0001t0012g0044a0001c0001t0012g0046others(7): Show | 11 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.694+587G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245610 | ||||||
chr6:169245618
|
C | T | 28 | a0001c0001t0001g0129a0001c0001t0004g0130a0001c0003t0002g0001others(25): Show | 33 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.694+579G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245618 | ||||||
chr6:169245620
|
A | G | 12 | a0001c0001t0001g0128a0001c0001t0012g0044a0001c0001t0012g0046others(9): Show | 13 | HG01109.hp2 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.694+577T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245620 | ||||||
chr6:169245660
|
C | T | 3 | a0001c0004t0004g0252a0001c0004t0004g0296a0001c0004t0030g0251 | 3 | HG00408.hp1 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.694+537G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245660 | ||||||
chr6:169245661
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.694+536C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245661 | ||||||
chr6:169245664
|
T | C | 5 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(2): Show | 5 | HG01109.hp2 HG02165.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+533A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245664 | ||||||
chr6:169245702
|
G | A | 25 | a0001c0001t0001g0128a0001c0001t0001g0331a0001c0001t0014g0330others(22): Show | 27 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.694+495C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245702 | ||||||
chr6:169245786
|
T | C | 1 | a0001c0005t0003g0327 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.694+411A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245786 | ||||||
chr6:169245791
|
C | CA | 75 | a0001c0001t0001g0053a0001c0001t0001g0069a0001c0001t0001g0070others(72): Show | 81 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.694+405dupT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245791 | ||||||
chr6:169245791
|
CA | C | 15 | a0001c0001t0001g0085a0001c0001t0001g0128a0001c0005t0013g0306others(12): Show | 18 | HG00323.hp2 HG01109.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.694+405delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245791 | ||||||
chr6:169245965
|
G | T | 95 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0003g0293others(92): Show | 105 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.694+232C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169245965 | ||||||
chr6:169246006
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0052others(6): Show | 12 | HG00544.hp2 NA18939.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.694+191T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169246006 | ||||||
chr6:169246104
|
A | C | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.694+93T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169246104 | ||||||
chr6:169246107
|
GCACACAC others(7): Show |
G | 2 | a0001c0007t0004g0007a0001c0007t0004g0115 | 4 | HG00738.hp1 HG01081.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+76_694+89delTG others(12): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169246107 | ||||||
chr6:169246187
|
A | T | 6 | a0001c0001t0004g0043a0001c0017t0002g0039a0001c0017t0002g0040others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+10T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 4/21 | chr6 | 169246187 | ||||||
chr6:169246307
|
T | C | 2 | a0001c0001t0001g0331a0001c0001t0014g0330 | 2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.610-26A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246307 | ||||||
chr6:169246314
|
A | G | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.610-33T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246314 | ||||||
chr6:169246455
|
T | C | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.610-174A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246455 | ||||||
chr6:169246525
|
A | C | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-244T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246525 | ||||||
chr6:169246527
|
T | C | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-246A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246527 | ||||||
chr6:169246530
|
T | A | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-249A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246530 | ||||||
chr6:169246531
|
T | C | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-250A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246531 | ||||||
chr6:169246531
|
T | G | 17 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(14): Show | 18 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.610-250A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246531 | ||||||
chr6:169246532
|
C | G | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-251G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246532 | ||||||
chr6:169246535
|
A | G | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-254T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246535 | ||||||
chr6:169246536
|
A | T | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-255T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246536 | ||||||
chr6:169246537
|
A | T | 1 | a0001c0001t0010g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-256T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246537 | ||||||
chr6:169246656
|
T | G | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.610-375A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246656 | ||||||
chr6:169246727
|
C | T | 66 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0003g0293others(63): Show | 72 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.610-446G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246727 | ||||||
chr6:169246760
|
T | C | 1 | a0001c0001t0003g0342 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.610-479A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246760 | ||||||
chr6:169246800
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.610-519A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246800 | ||||||
chr6:169246825
|
A | G | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.610-544T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246825 | ||||||
chr6:169246868
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.610-587T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246868 | ||||||
chr6:169246874
|
C | T | 10 | a0001c0005t0013g0306a0001c0011t0003g0305a0001c0011t0013g0304others(7): Show | 12 | HG00323.hp2 HG01109.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.610-593G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246874 | ||||||
chr6:169246880
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.610-599C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246880 | ||||||
chr6:169246927
|
T | C | 76 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0003g0293others(73): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.610-646A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169246927 | ||||||
chr6:169247089
|
C | A | 22 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(19): Show | 24 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.610-808G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247089 | ||||||
chr6:169247108
|
T | C | 2 | a0003c0012t0007g0041a0003c0012t0007g0042 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.610-827A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247108 | ||||||
chr6:169247118
|
T | G | 15 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(12): Show | 16 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.610-837A>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247118 | ||||||
chr6:169247235
|
C | T | 1 | a0001c0003t0002g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.610-954G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247235 | ||||||
chr6:169247240
|
G | A | 10 | a0001c0001t0004g0108a0001c0002t0002g0106a0001c0002t0002g0107others(7): Show | 12 | HG01123.hp1 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.610-959C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247240 | ||||||
chr6:169247306
|
G | A | 57 | a0001c0001t0001g0272a0001c0001t0003g0293a0001c0001t0011g0285others(54): Show | 63 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.610-1025C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247306 | ||||||
chr6:169247349
|
G | T | 1 | a0008c0053t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.609+1068C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247349 | ||||||
chr6:169247352
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.609+1065G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247352 | ||||||
chr6:169247373
|
A | C | 1 | a0001c0003t0002g0244 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.609+1044T>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247373 | ||||||
chr6:169247495
|
A | G | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.609+922T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247495 | ||||||
chr6:169247514
|
A | G | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.609+903T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247514 | ||||||
chr6:169247518
|
G | A | 2 | a0001c0014t0002g0114a0003c0046t0021g0315 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.609+899C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247518 | ||||||
chr6:169247527
|
T | TG | 75 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0001g0332others(72): Show | 81 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.609+889dupC | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247527 | ||||||
chr6:169247531
|
G | GT | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.609+885_609+886ins others(1): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247531 | ||||||
chr6:169247655
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.609+762A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247655 | ||||||
chr6:169247736
|
ATGAG | A | 4 | a0001c0001t0001g0332a0001c0001t0004g0043a0001c0016t0005g0334others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+677_609+680del others(4): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247736 | ||||||
chr6:169247772
|
C | T | 66 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0003g0293others(63): Show | 72 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.609+645G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247772 | ||||||
chr6:169247935
|
T | C | 76 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0003g0293others(73): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.609+482A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247935 | ||||||
chr6:169247982
|
C | T | 1 | a0006c0026t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.609+435G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247982 | ||||||
chr6:169247985
|
G | T | 22 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(19): Show | 24 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.609+432C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169247985 | ||||||
chr6:169248049
|
CTG | C | 105 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0001g0332others(102): Show | 115 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.609+366_609+367del others(2): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248049 | ||||||
chr6:169248066
|
G | A | 7 | a0001c0001t0001g0332a0001c0016t0005g0334a0001c0036t0001g0333others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+351C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248066 | ||||||
chr6:169248265
|
G | A | 22 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(19): Show | 24 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.609+152C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248265 | ||||||
chr6:169248281
|
A | G | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.609+136T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248281 | ||||||
chr6:169248285
|
C | G | 22 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(19): Show | 24 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.609+132G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248285 | ||||||
chr6:169248347
|
C | T | 1 | a0001c0003t0002g0051 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.609+70G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248347 | ||||||
chr6:169248391
|
G | A | 1 | a0001c0028t0001g0029 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.609+26C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 3/21 | chr6 | 169248391 | ||||||
chr6:169249420
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.53-447C>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249420 | ||||||
chr6:169249720
|
C | T | 3 | a0001c0001t0001g0332a0001c0016t0005g0334a0001c0036t0001g0333 | 3 | HG01891.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-747G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249720 | ||||||
chr6:169249728
|
A | G | 1 | a0005c0025t0023g0078 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-755T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249728 | ||||||
chr6:169249732
|
T | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(330): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.53-759A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249732 | ||||||
chr6:169249751
|
C | T | 2 | a0001c0005t0003g0308a0001c0005t0018g0032 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.53-778G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249751 | ||||||
chr6:169249801
|
T | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(141): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.53-828A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249801 | ||||||
chr6:169249836
|
A | G | 1 | a0001c0019t0003g0309 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.53-863T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249836 | ||||||
chr6:169249902
|
C | T | 1 | a0008c0053t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.52+831G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249902 | ||||||
chr6:169249903
|
G | A | 1 | a0001c0002t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.52+830C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169249903 | ||||||
chr6:169250000
|
A | T | 3 | a0001c0001t0001g0332a0001c0016t0005g0334a0001c0036t0001g0333 | 3 | HG01891.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.52+733T>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250000 | ||||||
chr6:169250031
|
GA | G | 37 | a0001c0001t0001g0077a0001c0005t0001g0319a0001c0005t0001g0321others(34): Show | 41 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.52+701delT | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250031 | ||||||
chr6:169250070
|
G | A | 40 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(37): Show | 44 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.52+663C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250070 | ||||||
chr6:169250071
|
C | A | 40 | a0001c0001t0001g0331a0001c0001t0004g0043a0001c0001t0014g0330others(37): Show | 44 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.52+662G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250071 | ||||||
chr6:169250081
|
C | G | 4 | a0004c0020t0001g0299a0004c0020t0001g0301a0004c0029t0002g0300others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+652G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250081 | ||||||
chr6:169250135
|
C | T | 106 | a0001c0001t0001g0272a0001c0001t0001g0331a0001c0001t0001g0332others(103): Show | 116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.52+598G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250135 | ||||||
chr6:169250339
|
CT | C | 6 | a0001c0009t0002g0013a0001c0009t0002g0214a0001c0009t0002g0215others(3): Show | 8 | HG01261.hp1 HG01952.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+393delA | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250339 | ||||||
chr6:169250366
|
T | C | 1 | a0001c0001t0003g0219 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.52+367A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250366 | ||||||
chr6:169250472
|
T | C | 2 | a0001c0005t0003g0308a0001c0005t0018g0032 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.52+261A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250472 | ||||||
chr6:169250512
|
T | A | 3 | a0001c0001t0001g0332a0001c0016t0005g0334a0001c0036t0001g0333 | 3 | HG01891.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.52+221A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250512 | ||||||
chr6:169250575
|
T | C | 1 | a0001c0006t0006g0113 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.52+158A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250575 | ||||||
chr6:169250637
|
T | C | 3 | a0001c0019t0003g0309a0001c0019t0014g0310a0001c0019t0014g0311 | 3 | HG01243.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.52+96A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250637 | ||||||
chr6:169250676
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.52+57C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 2/21 | chr6 | 169250676 | ||||||
chr6:169250828
|
G | C | 5 | a0001c0001t0004g0043a0001c0017t0002g0039a0001c0017t0002g0040others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-22C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169250828 | ||||||
chr6:169250980
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-174C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169250980 | ||||||
chr6:169251046
|
A | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0052others(48): Show | 58 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-22-240T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251046 | ||||||
chr6:169251249
|
C | T | 58 | a0001c0001t0001g0272a0001c0001t0003g0243a0001c0001t0003g0293others(55): Show | 64 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-22-443G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251249 | ||||||
chr6:169251315
|
A | G | 1 | a0001c0004t0003g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-22-509T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251315 | ||||||
chr6:169251319
|
TAAA | T | 15 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(12): Show | 16 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-516_-22-514del others(3): Show |
THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251319 | ||||||
chr6:169251407
|
T | A | 5 | a0001c0001t0004g0043a0001c0017t0002g0039a0001c0017t0002g0040others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-601A>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251407 | ||||||
chr6:169251554
|
C | T | 3 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329 | 3 | HG03098.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-22-748G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251554 | ||||||
chr6:169251618
|
C | T | 1 | a0001c0005t0004g0317 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-22-812G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251618 | ||||||
chr6:169251830
|
A | AC | 31 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0053others(28): Show | 34 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-22-1025dupG | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251830 | ||||||
chr6:169251830
|
AC | A | 103 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0221others(100): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-22-1025delG | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251830 | ||||||
chr6:169251833
|
C | T | 1 | a0001c0003t0002g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-22-1027G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251833 | ||||||
chr6:169251834
|
C | A | 58 | a0001c0001t0001g0272a0001c0001t0003g0243a0001c0001t0003g0293others(55): Show | 64 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-22-1028G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251834 | ||||||
chr6:169251840
|
C | A | 3 | a0001c0001t0004g0043a0003c0012t0007g0041a0003c0012t0007g0042 | 3 | HG02486.hp2 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-1034G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251840 | ||||||
chr6:169251853
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22-1047G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251853 | ||||||
chr6:169251917
|
C | T | 1 | a0008c0053t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-22-1111G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251917 | ||||||
chr6:169251974
|
C | G | 1 | a0001c0005t0005g0335 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-1168G>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169251974 | ||||||
chr6:169252034
|
G | A | 4 | a0004c0020t0001g0299a0004c0020t0001g0301a0004c0029t0002g0300others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-1228C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252034 | ||||||
chr6:169252119
|
G | A | 3 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329 | 3 | HG03098.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-22-1313C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252119 | ||||||
chr6:169252164
|
G | A | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-22-1358C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252164 | ||||||
chr6:169252244
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-22-1438T>C | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252244 | ||||||
chr6:169252297
|
G | C | 32 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(29): Show | 36 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-23+1427C>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252297 | ||||||
chr6:169252319
|
C | A | 1 | a0008c0053t0001g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-23+1405G>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252319 | ||||||
chr6:169252395
|
G | A | 2 | a0001c0001t0005g0313a0001c0001t0005g0314 | 2 | NA18977.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-23+1329C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252395 | ||||||
chr6:169252416
|
G | A | 1 | a0003c0046t0021g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-23+1308C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252416 | ||||||
chr6:169252473
|
G | A | 15 | a0001c0005t0001g0319a0001c0005t0001g0321a0001c0005t0001g0328others(12): Show | 16 | HG00423.hp1 HG00558.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23+1251C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252473 | ||||||
chr6:169252757
|
C | T | 5 | a0001c0001t0012g0044a0001c0001t0012g0046a0001c0001t0012g0047others(2): Show | 5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+967G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252757 | ||||||
chr6:169252813
|
T | C | 3 | a0001c0001t0001g0331a0001c0001t0014g0330a0001c0001t0035g0329 | 3 | HG03098.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23+911A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252813 | ||||||
chr6:169252891
|
T | C | 3 | a0001c0001t0001g0332a0001c0016t0005g0334a0001c0036t0001g0333 | 3 | HG01891.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-23+833A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169252891 | ||||||
chr6:169253011
|
G | A | 1 | a0001c0005t0005g0335 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-23+713C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169253011 | ||||||
chr6:169253016
|
G | A | 7 | a0001c0001t0001g0338a0001c0001t0003g0336a0001c0001t0003g0337others(4): Show | 7 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+708C>T | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169253016 | ||||||
chr6:169253166
|
C | T | 5 | a0001c0001t0004g0043a0001c0017t0002g0039a0001c0017t0002g0040others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+558G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169253166 | ||||||
chr6:169253240
|
C | T | 7 | a0001c0001t0003g0033a0001c0001t0003g0035a0001c0002t0020g0037others(4): Show | 8 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23+484G>A | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169253240 | ||||||
chr6:169253380
|
T | C | 1 | a0001c0015t0015g0343 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-23+344A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169253380 | ||||||
chr6:169253611
|
T | C | 1 | a0001c0001t0001g0344 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-23+113A>G | THBS2 | ENSG00000186340.17 | transcript | ENST00000617924.6 | protein_coding | 1/21 | chr6 | 169253611 |