geneid | 6295 |
---|---|
ensemblid | ENSG00000130561.17 |
hgncid | 10521 |
symbol | SAG |
name | S-antigen visual arrestin |
refseq_nuc | NM_000541.5 |
refseq_prot | NP_000532.2 |
ensembl_nuc | ENST00000409110.6 |
ensembl_prot | ENSP00000386444.1 |
mane_status | MANE Select |
chr | chr2 |
start | 233307816 |
end | 233347055 |
strand | + |
ver | v1.2 |
region | chr2:233307816-233347055 |
region5000 | chr2:233302816-233352055 |
regionname0 | SAG_chr2_233307816_233347055 |
regionname5000 | SAG_chr2_233302816_233352055 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 405 | 202 | 52 | 44 | 86 | 7 | 11 | 68 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0002 | 0/0 | 405 | 102 | 8 | 18 | 59 | 5 | 12 | 43 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003 | 0/0 | 405 | 29 | 16 | 6 | 5 | 0 | 2 | 5 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0004 | 0/0 | 405 | 22 | 6 | 0 | 12 | 0 | 4 | 12 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0005 | 0/0 | 405 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0006 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0007 | 0/0 | 405 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0008 | 0/0 | 405 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0009 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0010 | 0/0 | 405 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0011 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0012 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0013 | 0/0 | 405 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1218 | 170 | 33 | 40 | 81 | 4 | 10 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0002 | 0/0 | 1218 | 97 | 5 | 18 | 58 | 5 | 11 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0003 | 0/0 | 1218 | 25 | 13 | 3 | 5 | 3 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0004 | 0/0 | 1218 | 22 | 6 | 0 | 12 | 0 | 4 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0005 | 0/0 | 1218 | 19 | 9 | 4 | 4 | 0 | 2 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0006 | 0/0 | 1218 | 6 | 6 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0007 | 0/0 | 1218 | 5 | 3 | 0 | 1 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0008 | 0/0 | 1218 | 5 | 5 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0009 | 0/0 | 1218 | 4 | 4 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0010 | 0/0 | 1218 | 4 | 3 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0011 | 0/0 | 1218 | 2 | 0 | 2 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0012 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0013 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0014 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0015 | 0/0 | 1218 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0016 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0017 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0018 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0019 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
c0020 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 379 | 346 | 90 | 62 | 153 | 12 | 28 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
t0002 | 0/1 | 379 | 10 | 0 | 6 | 3 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
t0003 | 0/0 | 379 | 7 | 0 | 2 | 4 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
t0004 | 0/0 | 379 | 2 | 0 | 0 | 1 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
t0005 | 0/0 | 379 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
t0006 | 0/0 | 379 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
t0007 | 0/0 | 379 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1218 | 170 | 33 | 40 | 81 | 4 | 10 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0003 | 0/0 | 1218 | 25 | 13 | 3 | 5 | 3 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0006 | 0/0 | 1218 | 6 | 6 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0019 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0002c0002 | 0/0 | 1218 | 97 | 5 | 18 | 58 | 5 | 11 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0002c0007 | 0/0 | 1218 | 5 | 3 | 0 | 1 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0005 | 0/0 | 1218 | 19 | 9 | 4 | 4 | 0 | 2 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0009 | 0/0 | 1218 | 4 | 4 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0010 | 0/0 | 1218 | 4 | 3 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0011 | 0/0 | 1218 | 2 | 0 | 2 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0004c0004 | 0/0 | 1218 | 22 | 6 | 0 | 12 | 0 | 4 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0005c0008 | 0/0 | 1218 | 5 | 5 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0006c0020 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0007c0015 | 0/0 | 1218 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0008c0014 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0009c0013 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0010c0012 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0011c0018 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0012c0016 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0013c0017 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1596 | 154 | 31 | 32 | 77 | 4 | 9 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0001t0002 | 0/1 | 1596 | 10 | 0 | 6 | 3 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0001t0003 | 0/0 | 1596 | 3 | 0 | 2 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0001t0005 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0001t0006 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0001t0007 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0003t0001 | 0/0 | 1596 | 21 | 13 | 3 | 1 | 3 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0003t0003 | 0/0 | 1596 | 4 | 0 | 0 | 4 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0006t0001 | 0/0 | 1596 | 6 | 6 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0001c0019t0001 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0002c0002t0001 | 0/0 | 1596 | 96 | 5 | 18 | 57 | 5 | 11 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0002c0002t0004 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0002c0007t0001 | 0/0 | 1596 | 5 | 3 | 0 | 1 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0005t0001 | 0/0 | 1596 | 19 | 9 | 4 | 4 | 0 | 2 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0009t0001 | 0/0 | 1596 | 4 | 4 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0010t0001 | 0/0 | 1596 | 4 | 3 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0003c0011t0001 | 0/0 | 1596 | 2 | 0 | 2 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0004c0004t0001 | 0/0 | 1596 | 21 | 6 | 0 | 12 | 0 | 3 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0004c0004t0004 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0005c0008t0001 | 0/0 | 1596 | 5 | 5 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0006c0020t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0007c0015t0001 | 0/0 | 1596 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0008c0014t0001 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0009c0013t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0010c0012t0001 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0011c0018t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0012c0016t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
a0013c0017t0001 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | copy fasta | chr2 | 233302816 | 233352055 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0006t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0006t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0006t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0006t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0001c0019t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0002t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0007t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0007t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0002c0007t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0009t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0009t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0009t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0009t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0010t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0010t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0010t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0010t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0011t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0003c0011t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0004c0004t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0005c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0005c0008t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0005c0008t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0005c0008t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0005c0008t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0006c0020t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0007c0015t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0008c0014t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0009c0013t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0010c0012t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0011c0018t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0012c0016t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
a0013c0017t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0003 | t0001 | g0087 | EUR | GBR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0158 | EUR | GBR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0168 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0089 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0296 | EUR | FIN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | CHS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0295 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG00741 | hp2 | a0003 | c0011 | t0001 | g0151 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01106 | hp2 | a0001 | c0019 | t0001 | g0165 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01175 | hp2 | a0010 | c0012 | t0001 | g0005 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01261 | hp1 | a0003 | c0011 | t0001 | g0162 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0088 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0326 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01433 | hp2 | a0003 | c0005 | t0001 | g0251 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01496 | hp1 | a0008 | c0014 | t0001 | g0142 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0166 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01934 | hp2 | a0003 | c0005 | t0001 | g0190 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01981 | hp1 | a0003 | c0005 | t0001 | g0273 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0341 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02055 | hp1 | a0013 | c0017 | t0001 | g0304 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0347 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0346 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02145 | hp1 | a0003 | c0009 | t0001 | g0320 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | CDX | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02257 | hp1 | a0003 | c0010 | t0001 | g0081 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02258 | hp1 | a0003 | c0009 | t0001 | g0285 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02258 | hp2 | a0006 | c0020 | t0001 | g0143 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02300 | hp2 | a0003 | c0005 | t0001 | g0197 | AMR | PEL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02572 | hp2 | a0004 | c0004 | t0001 | g0181 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02622 | hp2 | a0002 | c0007 | t0001 | g0079 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02717 | hp1 | a0005 | c0008 | t0001 | g0104 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0301 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02818 | hp1 | a0004 | c0004 | t0001 | g0004 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02818 | hp2 | a0005 | c0008 | t0001 | g0069 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02896 | hp1 | a0004 | c0004 | t0001 | g0327 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02897 | hp2 | a0004 | c0004 | t0001 | g0328 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02922 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02922 | hp2 | a0001 | c0006 | t0001 | g0291 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02965 | hp1 | a0003 | c0005 | t0001 | g0288 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02965 | hp2 | a0002 | c0007 | t0001 | g0067 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02970 | hp1 | a0005 | c0008 | t0001 | g0070 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02970 | hp2 | a0002 | c0007 | t0001 | g0076 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02976 | hp1 | a0003 | c0009 | t0001 | g0074 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02976 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03098 | hp2 | a0011 | c0018 | t0001 | g0187 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0117 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03130 | hp2 | a0004 | c0004 | t0001 | g0004 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03139 | hp1 | a0005 | c0008 | t0001 | g0072 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03209 | hp1 | a0003 | c0010 | t0001 | g0098 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03239 | hp1 | a0004 | c0004 | t0001 | g0133 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0329 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03453 | hp1 | a0003 | c0005 | t0001 | g0321 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03453 | hp2 | a0001 | c0006 | t0001 | g0118 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03486 | hp2 | a0003 | c0005 | t0001 | g0322 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03490 | hp2 | a0004 | c0004 | t0004 | g0299 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03516 | hp2 | a0001 | c0006 | t0001 | g0297 | AFR | ESN | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03540 | hp2 | a0004 | c0004 | t0001 | g0126 | AFR | GWD | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03579 | hp1 | a0012 | c0016 | t0001 | g0129 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03669 | hp1 | a0007 | c0015 | t0001 | g0051 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03669 | hp2 | a0003 | c0005 | t0001 | g0303 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0330 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03704 | hp2 | a0004 | c0004 | t0001 | g0131 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0086 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0344 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04184 | hp2 | a0003 | c0005 | t0001 | g0033 | SAS | BEB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG04228 | hp2 | a0004 | c0004 | t0001 | g0132 | SAS | STU | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18522 | hp1 | a0003 | c0005 | t0001 | g0286 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18522 | hp2 | a0001 | c0006 | t0001 | g0284 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18906 | hp2 | a0001 | c0006 | t0001 | g0114 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18940 | hp2 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18944 | hp1 | a0004 | c0004 | t0001 | g0134 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18944 | hp2 | a0003 | c0005 | t0001 | g0193 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18948 | hp2 | a0002 | c0002 | t0004 | g0352 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0263 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18959 | hp2 | a0004 | c0004 | t0001 | g0102 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18966 | hp1 | a0004 | c0004 | t0001 | g0135 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18967 | hp1 | a0004 | c0004 | t0001 | g0300 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18968 | hp1 | a0003 | c0010 | t0001 | g0294 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18968 | hp2 | a0004 | c0004 | t0001 | g0130 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18971 | hp1 | a0003 | c0005 | t0001 | g0194 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18977 | hp2 | a0004 | c0004 | t0001 | g0137 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18981 | hp2 | a0004 | c0004 | t0001 | g0128 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18984 | hp1 | a0003 | c0005 | t0001 | g0306 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18989 | hp1 | a0004 | c0004 | t0001 | g0139 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18997 | hp1 | a0001 | c0003 | t0003 | g0082 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19011 | hp2 | a0001 | c0003 | t0003 | g0083 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19030 | hp1 | a0003 | c0010 | t0001 | g0062 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19043 | hp1 | a0009 | c0013 | t0001 | g0290 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19056 | hp2 | a0004 | c0004 | t0001 | g0125 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19059 | hp1 | a0004 | c0004 | t0001 | g0127 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19059 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19081 | hp2 | a0004 | c0004 | t0001 | g0136 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19086 | hp1 | a0002 | c0007 | t0001 | g0066 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19088 | hp2 | a0003 | c0005 | t0001 | g0305 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19089 | hp2 | a0004 | c0004 | t0001 | g0138 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA19240 | hp2 | a0003 | c0005 | t0001 | g0287 | AFR | YRI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20129 | hp1 | a0003 | c0005 | t0001 | g0289 | AFR | ASW | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0180 | EUR | TSI | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20905 | hp2 | a0002 | c0007 | t0001 | g0085 | SAS | GIH | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03471 | hp1 | a0003 | c0009 | t0001 | g0293 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA20300 | hp2 | a0003 | c0005 | t0001 | g0292 | AFR | USA | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA21309 | hp1 | a0005 | c0008 | t0001 | g0071 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0229 | REF | REF | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0281 | REF | REF | SAG_chr2_233302816_233352055 | SAG | chr2 | 233302816 | 233352055 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:233309224
|
C | T | 1 | a0006 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.35C>T | p.Pro12Leu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/16 | 270/1596 | 35/1218 | 12/405 | chr2 | 233309224 | ||
chr2:233320674
|
A | G | 4 | a0004a0011a0012others(1): Show | 25 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(22): Show |
missense_variant | MODERATE | c.226A>G | p.Ile76Val | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 461/1596 | 226/1218 | 76/405 | chr2 | 233320674 | ||
chr2:233320698
|
C | T | 1 | a0005 | 5 | HG02717.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.250C>T | p.Arg84Cys | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 485/1596 | 250/1218 | 84/405 | chr2 | 233320698 | ||
chr2:233320749
|
G | A | 1 | a0010 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.301G>A | p.Ala101Thr | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 536/1596 | 301/1218 | 101/405 | chr2 | 233320749 | ||
chr2:233327173
|
C | A | 1 | a0009 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.488C>A | p.Ala163Asp | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/16 | 723/1596 | 488/1218 | 163/405 | chr2 | 233327173 | ||
chr2:233327196
|
A | G | 1 | a0007 | 1 | HG03669.hp1 | missense_variant&splice_region_variant | MODERATE | c.511A>G | p.Lys171Glu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/16 | 746/1596 | 511/1218 | 171/405 | chr2 | 233327196 | ||
chr2:233342315
|
C | T | 1 | a0011 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1091C>T | p.Pro364Leu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/16 | 1326/1596 | 1091/1218 | 364/405 | chr2 | 233342315 | ||
chr2:233346826
|
G | A | 1 | a0008 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1132G>A | p.Val378Ile | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 1367/1596 | 1132/1218 | 378/405 | chr2 | 233346826 | ||
chr2:233346901
|
G | A | 6 | a0002a0006a0007others(3): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
missense_variant | MODERATE | c.1207G>A | p.Val403Ile | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 1442/1596 | 1207/1218 | 403/405 | chr2 | 233346901 | ||
chr2:233346902
|
T | C | 4 | a0003a0004a0009others(1): Show | 53 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(50): Show |
missense_variant | MODERATE | c.1208T>C | p.Val403Ala | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 1443/1596 | 1208/1218 | 403/405 | chr2 | 233346902 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:233320649
|
C | T | 2 | a0001c0019a0003c0011 | 3 | HG00741.hp2 HG01106.hp2 HG01261.hp1 |
synonymous_variant | LOW | c.201C>T | p.Cys67Cys | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 436/1596 | 201/1218 | 67/405 | chr2 | 233320649 | ||
chr2:233320679
|
C | T | 1 | a0005c0008 | 5 | HG02717.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.231C>T | p.Asp77Asp | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 466/1596 | 231/1218 | 77/405 | chr2 | 233320679 | ||
chr2:233320769
|
G | C | 2 | a0001c0006a0003c0009 | 10 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
synonymous_variant | LOW | c.321G>C | p.Leu107Leu | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/16 | 556/1596 | 321/1218 | 107/405 | chr2 | 233320769 | ||
chr2:233327174
|
C | T | 3 | a0001c0003a0002c0007a0003c0010 | 34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
synonymous_variant | LOW | c.489C>T | p.Ala163Ala | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/16 | 724/1596 | 489/1218 | 163/405 | chr2 | 233327174 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:233307828
|
C | G | 1 | a0001c0001t0007 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-223C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/16 | 1362 | chr2 | 233307828 | |||||
chr2:233307949
|
T | C | 1 | a0001c0001t0005 | 1 | NA19002.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/16 | 1241 | chr2 | 233307949 | |||||
chr2:233307982
|
G | A | 1 | a0001c0001t0006 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/16 | 1208 | chr2 | 233307982 | |||||
chr2:233346919
|
C | T | 2 | a0001c0001t0002a0001c0001t0005 | 11 | HG00621.hp1 HG00735.hp2 HG01168.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 7 | chr2 | 233346919 | |||||
chr2:233347001
|
C | T | 2 | a0001c0001t0003a0001c0003t0003 | 7 | HG00639.hp1 HG01346.hp2 HG03688.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 89 | chr2 | 233347001 | |||||
chr2:233347002
|
G | A | 2 | a0002c0002t0004a0004c0004t0004 | 2 | HG03490.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*90G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 16/16 | 90 | chr2 | 233347002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:233308081
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-29+59G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308081 | ||||||
chr2:233308220
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-29+198G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308220 | ||||||
chr2:233308271
|
G | A | 34 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 34 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-29+249G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308271 | ||||||
chr2:233308276
|
A | G | 1 | a0001c0001t0001g0356 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-29+254A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308276 | ||||||
chr2:233308296
|
C | CA | 10 | a0001c0001t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(7): Show | 10 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29+281dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 233308296 | |||||
chr2:233308394
|
G | A | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+372G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308394 | ||||||
chr2:233308399
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-29+377C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308399 | ||||||
chr2:233308406
|
G | A | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-29+384G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308406 | ||||||
chr2:233308548
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(5): Show | 8 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+526T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308548 | ||||||
chr2:233308575
|
T | C | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29+553T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308575 | ||||||
chr2:233308603
|
T | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.-28-559T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308603 | ||||||
chr2:233308800
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-362G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308800 | ||||||
chr2:233308811
|
C | T | 1 | a0001c0001t0001g0354 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-28-351C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308811 | ||||||
chr2:233308816
|
A | G | 24 | a0001c0003t0001g0346a0002c0002t0001g0010a0002c0002t0001g0331others(21): Show | 25 | HG00558.hp1 HG00673.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-28-346A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308816 | ||||||
chr2:233308817
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-28-345C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233308817 | ||||||
chr2:233309033
|
C | G | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-28-129C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233309033 | ||||||
chr2:233309036
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-28-126G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233309036 | ||||||
chr2:233309092
|
T | G | 1 | a0004c0004t0001g0102 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-28-70T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 1/15 | chr2 | 233309092 | ||||||
chr2:233309299
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.75+35T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309299 | ||||||
chr2:233309451
|
C | T | 1 | a0002c0002t0001g0353 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.75+187C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309451 | ||||||
chr2:233309466
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.75+202G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309466 | ||||||
chr2:233309535
|
C | T | 3 | a0002c0002t0001g0001a0002c0002t0001g0329a0002c0002t0001g0330 | 6 | HG01069.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+271C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309535 | ||||||
chr2:233309595
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.75+331A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309595 | ||||||
chr2:233309895
|
C | T | 1 | a0003c0010t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+631C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309895 | ||||||
chr2:233309978
|
A | G | 2 | a0004c0004t0001g0327a0004c0004t0001g0328 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+714A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233309978 | ||||||
chr2:233310087
|
A | G | 4 | a0001c0001t0001g0099a0001c0003t0001g0326a0002c0007t0001g0066others(1): Show | 4 | HG01358.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+823A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310087 | ||||||
chr2:233310185
|
G | A | 1 | a0005c0008t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75+921G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310185 | ||||||
chr2:233310196
|
G | A | 4 | a0001c0001t0001g0099a0001c0003t0001g0326a0002c0007t0001g0066others(1): Show | 4 | HG01358.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+932G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310196 | ||||||
chr2:233310241
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.75+977T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310241 | ||||||
chr2:233310391
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0356others(4): Show | 7 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1127T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310391 | ||||||
chr2:233310501
|
T | C | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+1237T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310501 | ||||||
chr2:233310506
|
C | CT | 44 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0043others(41): Show | 44 | HG01109.hp2 HG01358.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.75+1263dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310506 | |||||
chr2:233310506
|
C | CTT | 8 | a0001c0001t0001g0047a0001c0001t0001g0065a0001c0001t0001g0099others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+1262_75+1263dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310506 | |||||
chr2:233310506
|
CT | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0068others(16): Show | 19 | HG01168.hp1 HG01257.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+1263delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310506 | |||||
chr2:233310556
|
C | CTGGAG | 3 | a0002c0002t0001g0001a0002c0002t0001g0329a0002c0002t0001g0330 | 6 | HG01069.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1295_75+1299dup others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233310556 | |||||
chr2:233310684
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.75+1420T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310684 | ||||||
chr2:233310863
|
C | T | 1 | a0004c0004t0004g0299 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+1599C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310863 | ||||||
chr2:233310928
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.75+1664C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310928 | ||||||
chr2:233310953
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.75+1689G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310953 | ||||||
chr2:233310994
|
C | T | 2 | a0001c0006t0001g0114a0001c0006t0001g0297 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75+1730C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233310994 | ||||||
chr2:233311306
|
G | A | 5 | a0001c0003t0001g0002a0001c0003t0001g0077a0001c0003t0001g0078others(2): Show | 6 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+2042G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311306 | ||||||
chr2:233311386
|
C | T | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+2122C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311386 | ||||||
chr2:233311511
|
C | T | 43 | a0001c0001t0001g0099a0001c0003t0001g0002a0001c0003t0001g0075others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.75+2247C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311511 | ||||||
chr2:233311589
|
G | T | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+2325G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311589 | ||||||
chr2:233311595
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(5): Show | 8 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+2331G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311595 | ||||||
chr2:233311782
|
C | G | 2 | a0004c0004t0001g0327a0004c0004t0001g0328 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+2518C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233311782 | ||||||
chr2:233312083
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.75+2819G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312083 | ||||||
chr2:233312105
|
A | G | 1 | a0001c0006t0001g0284 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+2841A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312105 | ||||||
chr2:233312215
|
C | G | 2 | a0004c0004t0001g0327a0004c0004t0001g0328 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+2951C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312215 | ||||||
chr2:233312285
|
A | T | 13 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+3021A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312285 | ||||||
chr2:233312546
|
C | T | 62 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0059others(59): Show | 63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.75+3282C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312546 | ||||||
chr2:233312655
|
A | G | 10 | a0001c0001t0001g0048a0002c0002t0001g0049a0002c0002t0001g0050others(7): Show | 10 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+3391A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312655 | ||||||
chr2:233312657
|
C | T | 2 | a0001c0003t0001g0295a0001c0003t0001g0296 | 2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.75+3393C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312657 | ||||||
chr2:233312703
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(5): Show | 8 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-3372C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233312703 | ||||||
chr2:233313041
|
T | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0059others(58): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.76-3034T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313041 | ||||||
chr2:233313099
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-2976C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313099 | ||||||
chr2:233313289
|
G | T | 27 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.76-2786G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313289 | ||||||
chr2:233313383
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.76-2692G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313383 | ||||||
chr2:233313457
|
G | A | 2 | a0004c0004t0001g0327a0004c0004t0001g0328 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.76-2618G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313457 | ||||||
chr2:233313515
|
A | AT | 63 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0059others(60): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.76-2547dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313515 | |||||
chr2:233313715
|
CT | C | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(121): Show | 127 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.76-2337delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313715 | |||||
chr2:233313715
|
CTT | C | 171 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(168): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.76-2338_76-2337del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313715 | |||||
chr2:233313715
|
CTTT | C | 57 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(54): Show | 59 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.76-2339_76-2337del others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233313715 | |||||
chr2:233313719
|
T | G | 1 | a0002c0002t0001g0106 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.76-2356T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313719 | ||||||
chr2:233313809
|
T | C | 3 | a0001c0001t0003g0121a0001c0001t0003g0122a0002c0002t0001g0123 | 3 | HG01346.hp2 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.76-2266T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233313809 | ||||||
chr2:233314040
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.76-2035C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314040 | ||||||
chr2:233314221
|
C | CA | 53 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(50): Show | 54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.76-1839dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233314221 | |||||
chr2:233314221
|
C | CAAA | 17 | a0001c0006t0001g0117a0001c0006t0001g0118a0001c0006t0001g0284others(14): Show | 18 | HG02258.hp1 HG02922.hp1 HG02922.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-1841_76-1839dup others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233314221 | |||||
chr2:233314221
|
C | CAAAA | 9 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG01109.hp2 HG02145.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-1842_76-1839dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233314221 | |||||
chr2:233314249
|
G | T | 6 | a0001c0001t0001g0048a0002c0002t0001g0053a0002c0002t0001g0054others(3): Show | 6 | HG00621.hp2 NA18991.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-1826G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314249 | ||||||
chr2:233314338
|
C | T | 18 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(15): Show | 19 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-1737C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314338 | ||||||
chr2:233314631
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.76-1444C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314631 | ||||||
chr2:233314689
|
T | C | 29 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(26): Show | 30 | HG01109.hp2 HG01358.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-1386T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314689 | ||||||
chr2:233314694
|
C | T | 2 | a0001c0006t0001g0114a0001c0006t0001g0297 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.76-1381C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233314694 | ||||||
chr2:233315191
|
G | A | 25 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(22): Show | 25 | HG01109.hp2 HG01358.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.76-884G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315191 | ||||||
chr2:233315191
|
GTGGCTT | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(6): Show | 9 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-882_76-877delGG others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315191 | |||||
chr2:233315201
|
G | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(6): Show | 9 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-874G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315201 | ||||||
chr2:233315203
|
CT | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(6): Show | 9 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-871delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315203 | ||||||
chr2:233315234
|
T | G | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.76-841T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315234 | ||||||
chr2:233315240
|
G | A | 20 | a0004c0004t0001g0004a0004c0004t0001g0102a0004c0004t0001g0125others(17): Show | 21 | HG02717.hp1 HG02818.hp1 HG03130.hp2 others(18): Show |
intron_variant | MODIFIER | c.76-835G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315240 | ||||||
chr2:233315281
|
C | CT | 44 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0274others(41): Show | 44 | HG00423.hp1 HG00621.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.76-765dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | |||||
chr2:233315281
|
C | CTT | 10 | a0001c0001t0001g0073a0001c0001t0001g0099a0001c0001t0001g0356others(7): Show | 10 | HG01891.hp2 HG03225.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-766_76-765dupTT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | |||||
chr2:233315281
|
CT | C | 119 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(116): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.76-765delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | |||||
chr2:233315281
|
CTT | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0060others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-766_76-765delTT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | |||||
chr2:233315281
|
CTTTTTTT others(2): Show |
C | 31 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(28): Show | 33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.76-773_76-765delTT others(7): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | |||||
chr2:233315281
|
CTTTTTTT others(9): Show |
C | 13 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-780_76-765delTT others(14): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315281 | |||||
chr2:233315411
|
A | G | 1 | a0001c0003t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.76-664A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315411 | ||||||
chr2:233315481
|
C | T | 34 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 34 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-594C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315481 | ||||||
chr2:233315500
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(7): Show | 10 | HG01891.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-575C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315500 | ||||||
chr2:233315706
|
C | CT | 32 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0073others(29): Show | 33 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-355dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233315706 | |||||
chr2:233315726
|
G | A | 1 | a0001c0001t0001g0323 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.76-349G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315726 | ||||||
chr2:233315740
|
T | C | 8 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-335T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315740 | ||||||
chr2:233315744
|
C | T | 5 | a0002c0002t0001g0120a0002c0002t0001g0177a0002c0002t0001g0178others(2): Show | 5 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-331C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315744 | ||||||
chr2:233315809
|
T | A | 1 | a0001c0001t0001g0354 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.76-266T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315809 | ||||||
chr2:233315826
|
T | C | 154 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0048others(151): Show | 161 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.76-249T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315826 | ||||||
chr2:233315989
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.76-86C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315989 | ||||||
chr2:233315991
|
C | T | 14 | a0001c0003t0001g0086a0001c0003t0001g0087a0001c0003t0001g0088others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-84C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315991 | ||||||
chr2:233315997
|
G | C | 37 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(34): Show | 37 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.76-78G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233315997 | ||||||
chr2:233316004
|
GCTGGTTT others(13): Show |
G | 2 | a0001c0006t0001g0114a0001c0006t0001g0297 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.76-68_76-49delGGTT others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 233316004 | |||||
chr2:233316035
|
C | T | 17 | a0004c0004t0001g0102a0004c0004t0001g0125a0004c0004t0001g0127others(14): Show | 17 | HG03239.hp1 HG03490.hp2 HG03579.hp1 others(14): Show |
intron_variant | MODIFIER | c.76-40C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233316035 | ||||||
chr2:233316048
|
T | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.76-27T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 2/15 | chr2 | 233316048 | ||||||
chr2:233316239
|
G | A | 1 | a0002c0002t0001g0332 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.136+104G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316239 | ||||||
chr2:233316380
|
T | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(3): Show | 6 | NA18941.hp2 NA18942.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+245T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316380 | ||||||
chr2:233316557
|
C | T | 4 | a0001c0006t0001g0291a0003c0009t0001g0285a0003c0009t0001g0293others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+422C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316557 | ||||||
chr2:233316581
|
G | A | 20 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(17): Show | 20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.136+446G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316581 | ||||||
chr2:233316622
|
T | C | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136+487T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233316622 | ||||||
chr2:233317018
|
C | T | 1 | a0002c0002t0001g0173 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.136+883C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317018 | ||||||
chr2:233317035
|
T | C | 69 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(66): Show | 70 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.136+900T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317035 | ||||||
chr2:233317217
|
C | T | 31 | a0001c0006t0001g0114a0001c0006t0001g0291a0001c0006t0001g0297others(28): Show | 32 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.136+1082C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317217 | ||||||
chr2:233317394
|
T | C | 4 | a0001c0006t0001g0117a0001c0006t0001g0118a0001c0006t0001g0284others(1): Show | 5 | HG02922.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1259T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317394 | ||||||
chr2:233317396
|
G | A | 1 | a0002c0007t0001g0076 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.136+1261G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317396 | ||||||
chr2:233317484
|
C | T | 6 | a0001c0006t0001g0114a0001c0006t0001g0291a0001c0006t0001g0297others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-1267C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317484 | ||||||
chr2:233317655
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.137-1096G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317655 | ||||||
chr2:233317689
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.137-1062G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317689 | ||||||
chr2:233317714
|
T | C | 4 | a0001c0003t0001g0086a0001c0003t0001g0087a0001c0003t0001g0088others(1): Show | 4 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-1037T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317714 | ||||||
chr2:233317723
|
A | T | 3 | a0004c0004t0001g0125a0004c0004t0001g0137a0004c0004t0001g0300 | 3 | NA18967.hp1 NA18977.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.137-1028A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317723 | ||||||
chr2:233317793
|
CTA | C | 5 | a0002c0007t0001g0066a0002c0007t0001g0067a0003c0005t0001g0288others(2): Show | 5 | HG02965.hp1 HG02965.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-954_137-953del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 233317793 | |||||
chr2:233317830
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137-921T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317830 | ||||||
chr2:233317924
|
C | A | 1 | a0002c0002t0001g0198 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.137-827C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317924 | ||||||
chr2:233317945
|
G | A | 6 | a0001c0006t0001g0114a0001c0006t0001g0291a0001c0006t0001g0297others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-806G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233317945 | ||||||
chr2:233318074
|
G | A | 240 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(237): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.137-677G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318074 | ||||||
chr2:233318128
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.137-623C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318128 | ||||||
chr2:233318133
|
C | T | 11 | a0001c0003t0001g0346a0002c0002t0001g0010a0002c0002t0001g0340others(8): Show | 12 | HG00673.hp1 HG02040.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.137-618C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318133 | ||||||
chr2:233318208
|
A | G | 11 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(8): Show | 12 | HG02145.hp1 HG02258.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-543A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318208 | ||||||
chr2:233318243
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.137-508C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318243 | ||||||
chr2:233318296
|
T | C | 4 | a0001c0006t0001g0117a0001c0006t0001g0118a0001c0006t0001g0284others(1): Show | 5 | HG02922.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-455T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318296 | ||||||
chr2:233318331
|
A | AT | 26 | a0002c0002t0001g0111a0002c0002t0001g0172a0004c0004t0001g0004others(23): Show | 27 | HG02055.hp1 HG02155.hp2 HG02572.hp2 others(24): Show |
intron_variant | MODIFIER | c.137-408dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 233318331 | |||||
chr2:233318341
|
T | G | 14 | a0001c0001t0001g0216a0001c0006t0001g0114a0001c0006t0001g0117others(11): Show | 15 | HG00438.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-410T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318341 | ||||||
chr2:233318401
|
T | A | 151 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0144others(148): Show | 159 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.137-350T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318401 | ||||||
chr2:233318453
|
G | T | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.137-298G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318453 | ||||||
chr2:233318467
|
G | C | 35 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0006t0001g0117others(32): Show | 37 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.137-284G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318467 | ||||||
chr2:233318472
|
G | A | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.137-279G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 3/15 | chr2 | 233318472 | ||||||
chr2:233318820
|
G | A | 13 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.181+25G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233318820 | ||||||
chr2:233318834
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | NA18952.hp2 NA18956.hp1 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+39G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233318834 | ||||||
chr2:233318877
|
A | G | 241 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(238): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.181+82A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233318877 | ||||||
chr2:233319047
|
C | T | 96 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0154others(93): Show | 102 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.181+252C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319047 | ||||||
chr2:233319048
|
G | A | 1 | a0001c0003t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.181+253G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319048 | ||||||
chr2:233319053
|
C | T | 36 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0006t0001g0114others(33): Show | 37 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.181+258C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319053 | ||||||
chr2:233319065
|
C | G | 10 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+270C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319065 | ||||||
chr2:233319067
|
C | T | 10 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+272C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319067 | ||||||
chr2:233319290
|
T | TG | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(240): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.181+500dupG | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 233319290 | |||||
chr2:233319359
|
G | A | 13 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.181+564G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319359 | ||||||
chr2:233319584
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.181+789G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319584 | ||||||
chr2:233319591
|
G | GA | 134 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(131): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.181+796_181+797ins others(1): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319591 | ||||||
chr2:233319848
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.182-782C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319848 | ||||||
chr2:233319928
|
C | T | 1 | a0003c0005t0001g0306 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.182-702C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319928 | ||||||
chr2:233319957
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.182-673C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233319957 | ||||||
chr2:233320012
|
C | A | 11 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(8): Show | 11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.182-618C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320012 | ||||||
chr2:233320012
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.182-618C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320012 | ||||||
chr2:233320091
|
G | A | 2 | a0001c0003t0001g0295a0001c0003t0001g0296 | 2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.182-539G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320091 | ||||||
chr2:233320284
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.182-346C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320284 | ||||||
chr2:233320300
|
A | G | 24 | a0004c0004t0001g0004a0004c0004t0001g0102a0004c0004t0001g0125others(21): Show | 25 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(22): Show |
intron_variant | MODIFIER | c.182-330A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320300 | ||||||
chr2:233320339
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0099a0001c0001t0001g0217 | 3 | HG01361.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.182-291G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320339 | ||||||
chr2:233320437
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.182-193C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320437 | ||||||
chr2:233320454
|
G | C | 1 | a0002c0002t0001g0333 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.182-176G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320454 | ||||||
chr2:233320556
|
G | A | 2 | a0002c0002t0001g0146a0002c0002t0001g0147 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.182-74G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320556 | ||||||
chr2:233320568
|
G | A | 11 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(8): Show | 11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.182-62G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320568 | ||||||
chr2:233320617
|
A | G | 1 | a0002c0007t0001g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.182-13A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 4/15 | chr2 | 233320617 | ||||||
chr2:233320834
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0031others(2): Show | 5 | HG01168.hp1 HG01255.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+11C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233320834 | ||||||
chr2:233320892
|
G | GGAAAGGG others(9): Show |
1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.375+76_375+77insAT others(14): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233320892 | |||||
chr2:233320915
|
T | C | 2 | a0001c0006t0001g0114a0001c0006t0001g0297 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.375+92T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233320915 | ||||||
chr2:233321012
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.375+189C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321012 | ||||||
chr2:233321280
|
T | G | 32 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.375+457T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321280 | ||||||
chr2:233321307
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.375+484C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321307 | ||||||
chr2:233321308
|
G | A | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.375+485G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321308 | ||||||
chr2:233321520
|
C | G | 1 | a0004c0004t0001g0125 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.375+697C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321520 | ||||||
chr2:233321888
|
G | A | 9 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.376-1058G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321888 | ||||||
chr2:233321914
|
C | T | 2 | a0002c0002t0001g0338a0002c0002t0001g0339 | 2 | HG00558.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.376-1032C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321914 | ||||||
chr2:233321950
|
T | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(60): Show | 64 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.376-996T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233321950 | ||||||
chr2:233321986
|
T | TAC | 19 | a0001c0001t0001g0048a0001c0001t0001g0191a0001c0001t0001g0210others(16): Show | 20 | HG00735.hp2 HG01192.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.376-910_376-909dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
T | TACAC | 12 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0124others(9): Show | 13 | HG00621.hp1 HG01358.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.376-912_376-909dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TAC | T | 44 | a0001c0001t0001g0073a0001c0001t0001g0099a0001c0001t0001g0103others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.376-910_376-909del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACAC | T | 30 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0001g0248others(27): Show | 30 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.376-912_376-909del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACAC | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0201a0001c0001t0001g0255others(11): Show | 16 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-914_376-909del others(6): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0256a0001c0001t0001g0356a0001c0003t0003g0082others(8): Show | 11 | HG00609.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.376-916_376-909del others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(3): Show |
T | 5 | a0001c0003t0001g0089a0002c0002t0001g0335a0002c0002t0001g0336others(2): Show | 5 | HG00280.hp2 HG02965.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-918_376-909del others(10): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(5): Show |
T | 11 | a0001c0001t0001g0150a0001c0003t0001g0326a0001c0003t0003g0263others(8): Show | 11 | HG01358.hp2 HG01978.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.376-920_376-909del others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(7): Show |
T | 83 | a0001c0001t0001g0144a0001c0001t0001g0154a0001c0001t0001g0159others(80): Show | 89 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.376-922_376-909del others(14): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(9): Show |
T | 3 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0168 | 3 | HG00280.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.376-924_376-909del others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(11): Show |
T | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0257others(21): Show | 25 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.376-926_376-909del others(18): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(13): Show |
T | 19 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.376-928_376-909del others(20): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233321986
|
TACACACA others(15): Show |
T | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 40 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.376-930_376-909del others(22): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233321986 | |||||
chr2:233322026
|
C | T | 2 | a0002c0002t0001g0169a0002c0002t0001g0170 | 2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.376-920C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322026 | ||||||
chr2:233322030
|
C | T | 1 | a0002c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.376-916C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322030 | ||||||
chr2:233322038
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.376-908T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322038 | ||||||
chr2:233322055
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.376-891C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322055 | ||||||
chr2:233322111
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.376-835C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322111 | ||||||
chr2:233322173
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0099 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.376-773G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322173 | ||||||
chr2:233322185
|
C | CA | 32 | a0001c0001t0001g0064a0001c0001t0001g0100a0001c0001t0001g0115others(29): Show | 32 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.376-737dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | |||||
chr2:233322185
|
CA | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(61): Show | 65 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.376-737delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | |||||
chr2:233322185
|
CAA | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0298others(11): Show | 14 | HG01081.hp2 HG01256.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.376-738_376-737del others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | |||||
chr2:233322185
|
CAAA | C | 18 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(15): Show | 19 | HG00738.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.376-739_376-737del others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | |||||
chr2:233322185
|
CAAAA | C | 6 | a0001c0003t0001g0086a0001c0003t0001g0087a0001c0003t0001g0088others(3): Show | 6 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-740_376-737del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 233322185 | |||||
chr2:233322332
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.376-614C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322332 | ||||||
chr2:233322372
|
G | C | 94 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(91): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.376-574G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322372 | ||||||
chr2:233322392
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.376-554G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322392 | ||||||
chr2:233322406
|
A | T | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-540A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322406 | ||||||
chr2:233322409
|
C | A | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-537C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322409 | ||||||
chr2:233322410
|
T | A | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-536T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322410 | ||||||
chr2:233322412
|
T | G | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-534T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322412 | ||||||
chr2:233322413
|
C | A | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-533C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322413 | ||||||
chr2:233322416
|
A | T | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-530A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322416 | ||||||
chr2:233322417
|
A | G | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-529A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322417 | ||||||
chr2:233322608
|
C | T | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-338C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322608 | ||||||
chr2:233322610
|
G | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0003c0005t0001g0003others(8): Show | 12 | HG02647.hp2 HG02922.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.376-336G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322610 | ||||||
chr2:233322681
|
A | G | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-265A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322681 | ||||||
chr2:233322688
|
C | A | 29 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(26): Show | 30 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.376-258C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322688 | ||||||
chr2:233322702
|
T | A | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-244T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322702 | ||||||
chr2:233322703
|
C | T | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-243C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322703 | ||||||
chr2:233322707
|
C | A | 1 | a0004c0004t0001g0127 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.376-239C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322707 | ||||||
chr2:233322755
|
A | G | 4 | a0001c0003t0001g0086a0001c0003t0001g0087a0001c0003t0001g0088others(1): Show | 4 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-191A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322755 | ||||||
chr2:233322796
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.376-150T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 5/15 | chr2 | 233322796 | ||||||
chr2:233323110
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.435+105G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323110 | ||||||
chr2:233323380
|
T | C | 13 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.435+375T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323380 | ||||||
chr2:233323382
|
A | T | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.435+377A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323382 | ||||||
chr2:233323675
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.435+670A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323675 | ||||||
chr2:233323750
|
C | A | 1 | a0002c0002t0001g0341 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.435+745C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323750 | ||||||
chr2:233323765
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0275 | 2 | NA18992.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.435+760C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323765 | ||||||
chr2:233323813
|
C | T | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435+808C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233323813 | ||||||
chr2:233324076
|
T | G | 157 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(154): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.435+1071T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324076 | ||||||
chr2:233324213
|
G | A | 1 | a0004c0004t0001g0004 | 2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.435+1208G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324213 | ||||||
chr2:233324274
|
A | C | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(240): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.435+1269A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324274 | ||||||
chr2:233324373
|
A | G | 63 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(60): Show | 64 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.435+1368A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324373 | ||||||
chr2:233324420
|
A | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.435+1415A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324420 | ||||||
chr2:233324584
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0040others(1): Show | 4 | HG00423.hp2 HG02080.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1579G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324584 | ||||||
chr2:233324589
|
C | G | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(240): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.435+1584C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324589 | ||||||
chr2:233324601
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.435+1596G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324601 | ||||||
chr2:233324607
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.435+1602G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324607 | ||||||
chr2:233324609
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0040others(1): Show | 4 | HG00423.hp2 HG02080.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1604A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324609 | ||||||
chr2:233324681
|
C | T | 9 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+1676C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324681 | ||||||
chr2:233324682
|
G | A | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435+1677G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324682 | ||||||
chr2:233324711
|
G | C | 1 | a0001c0003t0001g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435+1706G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324711 | ||||||
chr2:233324845
|
G | A | 180 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(177): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.435+1840G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324845 | ||||||
chr2:233324870
|
G | A | 61 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(58): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.435+1865G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324870 | ||||||
chr2:233324947
|
A | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.435+1942A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324947 | ||||||
chr2:233324968
|
G | A | 3 | a0001c0006t0001g0117a0001c0006t0001g0118a0001c0006t0001g0284 | 3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.435+1963G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233324968 | ||||||
chr2:233325019
|
A | G | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435+2014A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325019 | ||||||
chr2:233325095
|
G | A | 1 | a0001c0003t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.436-2026G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325095 | ||||||
chr2:233325203
|
C | CA | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.436-1900dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325203 | |||||
chr2:233325203
|
C | CAA | 23 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(20): Show | 24 | HG02572.hp2 HG02818.hp1 HG02896.hp1 others(21): Show |
intron_variant | MODIFIER | c.436-1901_436-1900d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325203 | |||||
chr2:233325203
|
CA | C | 101 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0159others(98): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.436-1900delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325203 | |||||
chr2:233325237
|
A | G | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-1884A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325237 | ||||||
chr2:233325299
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | NA18948.hp1 NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.436-1822T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325299 | ||||||
chr2:233325351
|
A | G | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436-1770A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325351 | ||||||
chr2:233325354
|
T | TA | 147 | a0001c0001t0001g0011a0001c0001t0001g0058a0001c0001t0001g0059others(144): Show | 154 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.436-1752dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325354 | |||||
chr2:233325354
|
T | TAA | 27 | a0001c0001t0001g0012a0001c0001t0001g0298a0002c0002t0001g0182others(24): Show | 28 | HG01256.hp1 HG02055.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.436-1753_436-1752d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325354 | |||||
chr2:233325354
|
T | TAAA | 36 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 36 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.436-1754_436-1752d others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233325354 | |||||
chr2:233325458
|
C | CAT | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(240): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.436-1663_436-1662i others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325458 | ||||||
chr2:233325546
|
C | T | 5 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0292others(2): Show | 5 | HG03453.hp1 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-1575C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325546 | ||||||
chr2:233325730
|
G | A | 32 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(29): Show | 33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.436-1391G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325730 | ||||||
chr2:233325785
|
C | T | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.436-1336C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325785 | ||||||
chr2:233325892
|
C | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 39 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.436-1229C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325892 | ||||||
chr2:233325898
|
C | T | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436-1223C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325898 | ||||||
chr2:233325980
|
A | G | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(240): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.436-1141A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233325980 | ||||||
chr2:233326009
|
GA | G | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-1111delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326009 | ||||||
chr2:233326033
|
T | C | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.436-1088T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326033 | ||||||
chr2:233326069
|
G | A | 1 | a0002c0002t0001g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.436-1052G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326069 | ||||||
chr2:233326077
|
C | T | 3 | a0001c0003t0001g0346a0002c0007t0001g0066a0002c0007t0001g0067 | 3 | HG02129.hp2 HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.436-1044C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326077 | ||||||
chr2:233326090
|
T | C | 2 | a0011c0018t0001g0187a0013c0017t0001g0304 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.436-1031T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326090 | ||||||
chr2:233326112
|
G | A | 186 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(183): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.436-1009G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326112 | ||||||
chr2:233326182
|
G | A | 181 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(178): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.436-939G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326182 | ||||||
chr2:233326199
|
C | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.436-922C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326199 | ||||||
chr2:233326210
|
G | A | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-911G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326210 | ||||||
chr2:233326276
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-845C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326276 | ||||||
chr2:233326313
|
G | A | 96 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0154others(93): Show | 102 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.436-808G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326313 | ||||||
chr2:233326418
|
C | T | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0144others(116): Show | 126 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.436-703C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326418 | ||||||
chr2:233326508
|
T | C | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.436-613T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326508 | ||||||
chr2:233326533
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA18948.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.436-588C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326533 | ||||||
chr2:233326584
|
T | G | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436-537T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326584 | ||||||
chr2:233326586
|
C | CA | 52 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 53 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.436-517dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233326586 | |||||
chr2:233326586
|
C | CAA | 6 | a0004c0004t0001g0127a0004c0004t0001g0128a0004c0004t0001g0138others(3): Show | 6 | HG02055.hp1 HG02572.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-518_436-517dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233326586 | |||||
chr2:233326586
|
CA | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0185a0001c0003t0001g0097others(3): Show | 6 | HG02129.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-517delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 233326586 | |||||
chr2:233326616
|
G | T | 33 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.436-505G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326616 | ||||||
chr2:233326656
|
T | C | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.436-465T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326656 | ||||||
chr2:233326697
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.436-424A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326697 | ||||||
chr2:233326714
|
C | A | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0144others(116): Show | 126 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.436-407C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326714 | ||||||
chr2:233326808
|
A | G | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.436-313A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326808 | ||||||
chr2:233326824
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.436-297A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326824 | ||||||
chr2:233326898
|
C | CT | 8 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0288others(5): Show | 8 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.436-223_436-222ins others(1): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233326898 | ||||||
chr2:233327085
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.436-36G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233327085 | ||||||
chr2:233327091
|
C | T | 1 | a0003c0005t0001g0303 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.436-30C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233327091 | ||||||
chr2:233327103
|
G | C | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0144others(116): Show | 126 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.436-18G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 6/15 | chr2 | 233327103 | ||||||
chr2:233327255
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.512+58C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327255 | ||||||
chr2:233327255
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.512+58C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327255 | ||||||
chr2:233327434
|
G | A | 20 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(17): Show | 20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.512+237G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327434 | ||||||
chr2:233327464
|
G | GTTGT | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 40 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.512+290_512+293dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327464 | |||||
chr2:233327464
|
GTTGT | G | 5 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0292others(2): Show | 5 | HG03453.hp1 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+290_512+293del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327464 | |||||
chr2:233327535
|
C | CT | 24 | a0004c0004t0001g0004a0004c0004t0001g0102a0004c0004t0001g0125others(21): Show | 25 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(22): Show |
intron_variant | MODIFIER | c.512+346dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327535 | |||||
chr2:233327535
|
C | T | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.512+338C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327535 | ||||||
chr2:233327550
|
T | C | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.512+353T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327550 | ||||||
chr2:233327551
|
T | A | 62 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(59): Show | 63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.512+354T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327551 | ||||||
chr2:233327580
|
C | T | 1 | a0001c0001t0006g0301 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.512+383C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327580 | ||||||
chr2:233327612
|
G | A | 1 | a0001c0003t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.512+415G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327612 | ||||||
chr2:233327657
|
C | A | 2 | a0001c0003t0001g0346a0002c0007t0001g0066 | 2 | HG02129.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.512+460C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327657 | ||||||
chr2:233327688
|
G | A | 3 | a0001c0006t0001g0117a0001c0006t0001g0118a0001c0006t0001g0284 | 3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.512+491G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327688 | ||||||
chr2:233327709
|
A | AT | 50 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(47): Show | 51 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(48): Show |
intron_variant | MODIFIER | c.512+525dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233327709 | |||||
chr2:233327750
|
A | G | 1 | a0002c0002t0001g0199 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.512+553A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327750 | ||||||
chr2:233327781
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.512+584C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327781 | ||||||
chr2:233327868
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.513-610A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233327868 | ||||||
chr2:233328015
|
GT | G | 26 | a0001c0006t0001g0117a0003c0009t0001g0074a0004c0004t0001g0004others(23): Show | 27 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(24): Show |
intron_variant | MODIFIER | c.513-453delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 233328015 | |||||
chr2:233328042
|
C | T | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-436C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328042 | ||||||
chr2:233328054
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.513-424C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328054 | ||||||
chr2:233328065
|
C | T | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513-413C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328065 | ||||||
chr2:233328067
|
T | C | 125 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(122): Show | 127 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.513-411T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328067 | ||||||
chr2:233328076
|
T | C | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-402T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328076 | ||||||
chr2:233328208
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.513-270C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328208 | ||||||
chr2:233328215
|
T | C | 100 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(97): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.513-263T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328215 | ||||||
chr2:233328251
|
C | T | 2 | a0004c0004t0001g0327a0004c0004t0001g0328 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.513-227C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328251 | ||||||
chr2:233328299
|
C | T | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.513-179C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328299 | ||||||
chr2:233328305
|
C | T | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-173C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328305 | ||||||
chr2:233328309
|
G | A | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-169G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328309 | ||||||
chr2:233328319
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.513-159C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328319 | ||||||
chr2:233328340
|
G | C | 25 | a0003c0009t0001g0074a0004c0004t0001g0004a0004c0004t0001g0102others(22): Show | 26 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(23): Show |
intron_variant | MODIFIER | c.513-138G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328340 | ||||||
chr2:233328357
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.513-121C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328357 | ||||||
chr2:233328402
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.513-76A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 7/15 | chr2 | 233328402 | ||||||
chr2:233328671
|
A | T | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.648+58A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233328671 | ||||||
chr2:233328741
|
A | G | 120 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0144others(117): Show | 127 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.648+128A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233328741 | ||||||
chr2:233328813
|
C | T | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.648+200C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233328813 | ||||||
chr2:233329119
|
T | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.649-374T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | chr2 | 233329119 | ||||||
chr2:233329152
|
G | GC | 356 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(353): Show | 367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.649-339dupC | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 233329152 | |||||
chr2:233329254
|
AC | A | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-235delC | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 233329254 | |||||
chr2:233329608
|
T | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.733+31T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329608 | ||||||
chr2:233329724
|
C | T | 1 | a0001c0001t0001g0323 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.733+147C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329724 | ||||||
chr2:233329725
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0308 | 2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733+148G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329725 | ||||||
chr2:233329775
|
C | A | 1 | a0002c0002t0001g0340 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.733+198C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329775 | ||||||
chr2:233329791
|
T | A | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.733+214T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329791 | ||||||
chr2:233329936
|
A | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+359A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233329936 | ||||||
chr2:233330013
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.733+436G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330013 | ||||||
chr2:233330038
|
G | T | 1 | a0001c0003t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733+461G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330038 | ||||||
chr2:233330138
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.733+561A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330138 | ||||||
chr2:233330254
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.733+677A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330254 | ||||||
chr2:233330303
|
G | A | 15 | a0001c0003t0001g0086a0001c0003t0001g0087a0001c0003t0001g0088others(12): Show | 15 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.733+726G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330303 | ||||||
chr2:233330426
|
A | G | 20 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(17): Show | 20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.733+849A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330426 | ||||||
chr2:233330465
|
TTCCC | T | 41 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0046others(38): Show | 42 | HG00642.hp1 HG00741.hp2 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.733+898_733+901del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330465 | |||||
chr2:233330471
|
C | CCCTT | 3 | a0001c0003t0001g0097a0001c0019t0001g0165a0003c0005t0001g0033 | 3 | HG01106.hp2 HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.733+897_733+898ins others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330471
|
CCCTCCCT others(1): Show |
C | 77 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0020others(74): Show | 81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+898_733+905del others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330471
|
CCCTCCCT others(5): Show |
C | 62 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(59): Show | 63 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.733+898_733+909del others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330471
|
CCCTCCCT others(9): Show |
C | 23 | a0001c0001t0001g0031a0001c0001t0001g0265a0001c0001t0007g0063others(20): Show | 25 | HG00140.hp2 HG00558.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.733+898_733+913del others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330471
|
CCCTCCCT others(13): Show |
C | 6 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0044others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+898_733+917del others(20): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330471
|
CCCTCCCT others(17): Show |
C | 3 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0003t0001g0326 | 3 | HG01358.hp2 HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.733+898_733+921del others(24): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330471
|
CCCTCCCT others(25): Show |
C | 2 | a0001c0001t0001g0017a0001c0001t0001g0045 | 2 | NA18947.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.733+898_733+929del others(32): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330471 | |||||
chr2:233330475
|
C | CCCTT | 14 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0099others(11): Show | 15 | HG01099.hp2 HG01257.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.733+962_733+965dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | |||||
chr2:233330475
|
C | T | 17 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0061others(14): Show | 18 | HG01106.hp2 HG01978.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.733+898C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330475 | ||||||
chr2:233330475
|
CCCTT | C | 53 | a0001c0001t0001g0048a0001c0001t0001g0100a0001c0001t0001g0101others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.733+962_733+965del others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | |||||
chr2:233330475
|
CCCTTCCT others(1): Show |
C | 29 | a0001c0001t0001g0068a0001c0001t0001g0112a0001c0001t0001g0124others(26): Show | 29 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.733+958_733+965del others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | |||||
chr2:233330475
|
CCCTTCCT others(5): Show |
C | 9 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0201others(6): Show | 10 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+954_733+965del others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | |||||
chr2:233330475
|
CCCTTCCT others(9): Show |
C | 1 | a0001c0001t0001g0235 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.733+950_733+965del others(16): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 233330475 | |||||
chr2:233330479
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0308 | 2 | HG03225.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733+902T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330479 | ||||||
chr2:233330483
|
T | C | 5 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0002g0195others(2): Show | 5 | HG00735.hp2 HG01192.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.733+906T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330483 | ||||||
chr2:233330487
|
T | C | 4 | a0001c0001t0001g0245a0001c0001t0002g0175a0001c0001t0002g0221others(1): Show | 4 | HG01168.hp2 HG01943.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+910T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330487 | ||||||
chr2:233330491
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.733+914T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330491 | ||||||
chr2:233330675
|
C | T | 9 | a0001c0006t0001g0114a0001c0006t0001g0117a0001c0006t0001g0118others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-965C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330675 | ||||||
chr2:233330781
|
C | T | 5 | a0001c0003t0001g0090a0001c0003t0001g0092a0001c0003t0001g0093others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-859C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233330781 | ||||||
chr2:233331052
|
T | G | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.734-588T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331052 | ||||||
chr2:233331054
|
A | T | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.734-586A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331054 | ||||||
chr2:233331089
|
A | G | 33 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(30): Show | 34 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.734-551A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331089 | ||||||
chr2:233331195
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0262 | 2 | HG00609.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.734-445C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331195 | ||||||
chr2:233331265
|
C | T | 1 | a0002c0002t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.734-375C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331265 | ||||||
chr2:233331558
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.734-82C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331558 | ||||||
chr2:233331578
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.734-62A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 9/15 | chr2 | 233331578 | ||||||
chr2:233331776
|
G | A | 1 | a0005c0008t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806+64G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331776 | ||||||
chr2:233331822
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0099 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.806+110C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331822 | ||||||
chr2:233331932
|
A | T | 1 | a0003c0005t0001g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.806+220A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331932 | ||||||
chr2:233331933
|
T | C | 1 | a0002c0002t0001g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.806+221T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233331933 | ||||||
chr2:233332038
|
G | A | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.806+326G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332038 | ||||||
chr2:233332419
|
T | G | 1 | a0001c0001t0001g0275 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.806+707T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332419 | ||||||
chr2:233332452
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.806+740A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332452 | ||||||
chr2:233332646
|
A | C | 244 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(241): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.806+934A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332646 | ||||||
chr2:233332663
|
A | AT | 38 | a0001c0001t0001g0189a0001c0001t0001g0208a0001c0001t0001g0308others(35): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.806+966dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | |||||
chr2:233332663
|
A | ATT | 14 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(11): Show | 14 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.806+965_806+966dup others(2): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | |||||
chr2:233332663
|
A | ATTT | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 10 | HG01109.hp2 HG02074.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.806+964_806+966dup others(3): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | |||||
chr2:233332663
|
A | ATTTT | 114 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0154others(111): Show | 121 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.806+963_806+966dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | |||||
chr2:233332663
|
A | ATTTTT | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0002c0002t0001g0108others(3): Show | 6 | HG01175.hp1 HG02647.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+962_806+966dup others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 233332663 | |||||
chr2:233332863
|
A | G | 30 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(27): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.806+1151A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332863 | ||||||
chr2:233332944
|
T | C | 1 | a0002c0002t0001g0110 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.806+1232T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233332944 | ||||||
chr2:233333016
|
A | G | 38 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 38 | HG00323.hp1 HG00423.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.806+1304A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333016 | ||||||
chr2:233333048
|
A | G | 20 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(17): Show | 20 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.806+1336A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333048 | ||||||
chr2:233333116
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0045 | 3 | NA18947.hp2 NA18990.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.806+1404G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333116 | ||||||
chr2:233333444
|
C | T | 1 | a0002c0002t0001g0109 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.807-1518C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333444 | ||||||
chr2:233333617
|
C | G | 1 | a0001c0003t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.807-1345C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333617 | ||||||
chr2:233333701
|
C | T | 110 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0154others(107): Show | 116 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.807-1261C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333701 | ||||||
chr2:233333850
|
G | T | 1 | a0001c0001t0001g0189 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.807-1112G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333850 | ||||||
chr2:233333859
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.807-1103C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233333859 | ||||||
chr2:233334097
|
AG | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0201a0001c0001t0001g0278others(2): Show | 6 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-864delG | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334097 | ||||||
chr2:233334203
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-759C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334203 | ||||||
chr2:233334204
|
A | T | 1 | a0003c0005t0001g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.807-758A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334204 | ||||||
chr2:233334238
|
C | T | 2 | a0002c0007t0001g0066a0002c0007t0001g0067 | 2 | HG02965.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.807-724C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334238 | ||||||
chr2:233334313
|
G | C | 1 | a0002c0002t0001g0172 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.807-649G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334313 | ||||||
chr2:233334504
|
G | A | 81 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(78): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.807-458G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334504 | ||||||
chr2:233334594
|
C | T | 1 | a0002c0002t0001g0215 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.807-368C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334594 | ||||||
chr2:233334630
|
C | T | 6 | a0001c0006t0001g0114a0001c0006t0001g0291a0001c0006t0001g0297others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-332C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334630 | ||||||
chr2:233334676
|
T | C | 215 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(212): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.807-286T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334676 | ||||||
chr2:233334769
|
T | A | 1 | a0002c0002t0001g0108 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.807-193T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334769 | ||||||
chr2:233334792
|
C | T | 21 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(18): Show | 21 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.807-170C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334792 | ||||||
chr2:233334806
|
C | A | 1 | a0004c0004t0001g0134 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.807-156C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334806 | ||||||
chr2:233334811
|
C | T | 8 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0288others(5): Show | 8 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.807-151C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334811 | ||||||
chr2:233334812
|
G | A | 10 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(7): Show | 10 | HG02074.hp2 HG02083.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.807-150G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334812 | ||||||
chr2:233334936
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0003c0009t0001g0285others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-26A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334936 | ||||||
chr2:233334937
|
A | G | 18 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.807-25A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 10/15 | chr2 | 233334937 | ||||||
chr2:233335191
|
C | T | 7 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0288others(4): Show | 7 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.944+92C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335191 | ||||||
chr2:233335231
|
T | C | 1 | a0003c0010t0001g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.944+132T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335231 | ||||||
chr2:233335242
|
G | C | 1 | a0002c0002t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.944+143G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335242 | ||||||
chr2:233335422
|
T | C | 1 | a0002c0002t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.944+323T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335422 | ||||||
chr2:233335464
|
G | A | 2 | a0002c0002t0001g0169a0002c0002t0001g0170 | 2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.944+365G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335464 | ||||||
chr2:233335558
|
G | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0006t0001g0114others(15): Show | 18 | HG02145.hp1 HG02258.hp1 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.944+459G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335558 | ||||||
chr2:233335575
|
G | GTTCA | 115 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(112): Show | 122 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.944+496_944+499dup others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233335575 | |||||
chr2:233335575
|
G | GTTCATTC others(1): Show |
6 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0288others(3): Show | 6 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.944+492_944+499dup others(8): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233335575 | |||||
chr2:233335672
|
C | T | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(174): Show | 185 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.944+573C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335672 | ||||||
chr2:233335749
|
G | A | 30 | a0003c0005t0001g0033a0003c0005t0001g0190a0003c0005t0001g0197others(27): Show | 31 | HG01433.hp2 HG01934.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.944+650G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335749 | ||||||
chr2:233335759
|
C | T | 7 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG02109.hp2 HG02622.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.944+660C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233335759 | ||||||
chr2:233336059
|
T | C | 13 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.944+960T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336059 | ||||||
chr2:233336103
|
A | C | 1 | a0004c0004t0001g0125 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.944+1004A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336103 | ||||||
chr2:233336228
|
G | A | 7 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0288others(4): Show | 7 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.944+1129G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336228 | ||||||
chr2:233336399
|
C | T | 1 | a0002c0002t0001g0164 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.944+1300C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336399 | ||||||
chr2:233336499
|
G | A | 19 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.944+1400G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336499 | ||||||
chr2:233336515
|
G | GA | 24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0099others(21): Show | 24 | HG00140.hp1 HG00280.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.944+1429dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233336515 | |||||
chr2:233336587
|
AT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0042a0001c0001t0001g0043others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.944+1491delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233336587 | |||||
chr2:233336738
|
G | A | 31 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 31 | HG00323.hp1 HG00423.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.944+1639G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336738 | ||||||
chr2:233336754
|
C | T | 11 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(8): Show | 11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.944+1655C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336754 | ||||||
chr2:233336786
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | NA18952.hp2 NA18956.hp1 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.944+1687C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336786 | ||||||
chr2:233336993
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.945-1683G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233336993 | ||||||
chr2:233337095
|
C | CA | 15 | a0001c0001t0001g0100a0001c0001t0001g0212a0001c0001t0001g0310others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.945-1567dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233337095 | |||||
chr2:233337095
|
CA | C | 118 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0073others(115): Show | 125 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.945-1567delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233337095 | |||||
chr2:233337234
|
A | G | 1 | a0002c0002t0001g0344 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.945-1442A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337234 | ||||||
chr2:233337247
|
AT | A | 212 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(209): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.945-1420delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 233337247 | |||||
chr2:233337250
|
T | G | 46 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0007g0063others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.945-1426T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337250 | ||||||
chr2:233337392
|
C | G | 32 | a0003c0005t0001g0033a0003c0005t0001g0190a0003c0005t0001g0197others(29): Show | 33 | HG01433.hp2 HG01934.hp2 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.945-1284C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337392 | ||||||
chr2:233337395
|
C | T | 1 | a0012c0016t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.945-1281C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337395 | ||||||
chr2:233337485
|
C | T | 1 | a0001c0003t0001g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.945-1191C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337485 | ||||||
chr2:233337491
|
C | G | 183 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(180): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.945-1185C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337491 | ||||||
chr2:233337579
|
T | C | 193 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(190): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.945-1097T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337579 | ||||||
chr2:233337618
|
C | T | 96 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(93): Show | 103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.945-1058C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337618 | ||||||
chr2:233337724
|
T | C | 139 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(136): Show | 147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.945-952T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337724 | ||||||
chr2:233337812
|
T | C | 96 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(93): Show | 103 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.945-864T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337812 | ||||||
chr2:233337857
|
C | T | 32 | a0003c0005t0001g0033a0003c0005t0001g0190a0003c0005t0001g0197others(29): Show | 33 | HG01433.hp2 HG01934.hp2 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.945-819C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337857 | ||||||
chr2:233337892
|
A | G | 2 | a0001c0003t0001g0295a0001c0003t0001g0296 | 2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.945-784A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337892 | ||||||
chr2:233337899
|
G | C | 1 | a0001c0003t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.945-777G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337899 | ||||||
chr2:233337902
|
C | T | 1 | a0001c0003t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.945-774C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337902 | ||||||
chr2:233337976
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.945-700C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233337976 | ||||||
chr2:233338152
|
G | A | 26 | a0001c0001t0001g0048a0001c0001t0001g0105a0001c0001t0001g0115others(23): Show | 26 | HG00438.hp2 HG00609.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.945-524G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338152 | ||||||
chr2:233338164
|
G | A | 1 | a0001c0003t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.945-512G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338164 | ||||||
chr2:233338299
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.945-377C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338299 | ||||||
chr2:233338348
|
A | G | 95 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(92): Show | 101 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.945-328A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338348 | ||||||
chr2:233338491
|
G | A | 3 | a0002c0002t0001g0119a0002c0002t0001g0177a0002c0002t0001g0178 | 3 | HG00733.hp1 HG00741.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.945-185G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338491 | ||||||
chr2:233338517
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.945-159C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338517 | ||||||
chr2:233338618
|
T | C | 1 | a0002c0002t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.945-58T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338618 | ||||||
chr2:233338619
|
C | T | 1 | a0002c0002t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.945-57C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338619 | ||||||
chr2:233338620
|
T | A | 1 | a0002c0002t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.945-56T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 11/15 | chr2 | 233338620 | ||||||
chr2:233338862
|
C | G | 35 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0007g0063others(32): Show | 36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1022+109C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233338862 | ||||||
chr2:233338981
|
T | C | 213 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(210): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1022+228T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233338981 | ||||||
chr2:233339278
|
G | A | 182 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(179): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1022+525G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339278 | ||||||
chr2:233339464
|
C | G | 182 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(179): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1022+711C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339464 | ||||||
chr2:233339537
|
G | GT | 32 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(29): Show | 33 | HG00621.hp2 HG00738.hp1 HG01978.hp2 others(30): Show |
intron_variant | MODIFIER | c.1022+803dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339537 | |||||
chr2:233339537
|
G | GTT | 18 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(15): Show | 18 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1022+802_1022+803d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339537 | |||||
chr2:233339537
|
GT | G | 89 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0061others(86): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1022+803delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339537 | |||||
chr2:233339542
|
T | G | 1 | a0001c0001t0006g0301 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1022+789T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339542 | ||||||
chr2:233339556
|
T | C | 94 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(91): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1022+803T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339556 | ||||||
chr2:233339557
|
C | G | 11 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(8): Show | 11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022+804C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339557 | ||||||
chr2:233339563
|
G | A | 1 | a0001c0003t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1022+810G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339563 | ||||||
chr2:233339700
|
ATC | A | 211 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(208): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1023-750_1023-749d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339700 | |||||
chr2:233339702
|
C | CTCACTCT others(8805): Show |
1 | a0005c0008t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1023-751_1023-750i others(8814): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339702 | |||||
chr2:233339851
|
C | T | 3 | a0003c0010t0001g0062a0003c0010t0001g0081a0003c0010t0001g0098 | 3 | HG02257.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1023-604C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339851 | ||||||
chr2:233339880
|
C | G | 1 | a0002c0007t0001g0066 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1023-575C>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339880 | ||||||
chr2:233339882
|
C | T | 1 | a0003c0005t0001g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1023-573C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339882 | ||||||
chr2:233339883
|
G | A | 94 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(91): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1023-572G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339883 | ||||||
chr2:233339901
|
G | A | 37 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(34): Show | 38 | HG01109.hp2 HG01433.hp2 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1023-554G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339901 | ||||||
chr2:233339964
|
C | CT | 128 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(125): Show | 135 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1023-481dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 233339964 | |||||
chr2:233339973
|
T | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG00323.hp1 HG01243.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1023-482T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339973 | ||||||
chr2:233339999
|
C | T | 46 | a0001c0001t0003g0121a0001c0001t0003g0122a0001c0001t0007g0063others(43): Show | 47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1023-456C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233339999 | ||||||
chr2:233340097
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1023-358C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340097 | ||||||
chr2:233340107
|
C | T | 37 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(34): Show | 38 | HG01109.hp2 HG01433.hp2 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.1023-348C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340107 | ||||||
chr2:233340209
|
G | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0006t0001g0114others(13): Show | 16 | HG02145.hp1 HG02647.hp2 HG02922.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023-246G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340209 | ||||||
chr2:233340362
|
T | C | 1 | a0003c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1023-93T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340362 | ||||||
chr2:233340436
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1023-19G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 12/15 | chr2 | 233340436 | ||||||
chr2:233340551
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1046+73G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340551 | ||||||
chr2:233340618
|
G | A | 11 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(8): Show | 11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+140G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340618 | ||||||
chr2:233340739
|
C | T | 94 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(91): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1046+261C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340739 | ||||||
chr2:233340751
|
T | TTG | 62 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0310others(59): Show | 63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1046+291_1046+292d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233340751 | |||||
chr2:233340751
|
TTG | T | 130 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(127): Show | 137 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1046+291_1046+292d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233340751 | |||||
chr2:233340809
|
T | C | 1 | a0002c0007t0001g0076 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1046+331T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340809 | ||||||
chr2:233340925
|
C | T | 11 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0052others(8): Show | 11 | HG00621.hp2 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1046+447C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233340925 | ||||||
chr2:233341034
|
G | A | 14 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1046+556G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341034 | ||||||
chr2:233341089
|
T | C | 131 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(128): Show | 138 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1046+611T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341089 | ||||||
chr2:233341132
|
G | A | 7 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0288others(4): Show | 7 | HG02965.hp1 HG03453.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046+654G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341132 | ||||||
chr2:233341265
|
T | A | 15 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0310others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046+787T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341265 | ||||||
chr2:233341275
|
C | A | 63 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0310others(60): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1046+797C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341275 | ||||||
chr2:233341378
|
G | A | 5 | a0001c0003t0001g0090a0001c0003t0001g0092a0001c0003t0001g0093others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047-893G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341378 | ||||||
chr2:233341836
|
A | G | 94 | a0001c0001t0001g0159a0001c0001t0001g0171a0001c0001t0001g0302others(91): Show | 100 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1047-435A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341836 | ||||||
chr2:233341866
|
C | A | 1 | a0002c0002t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1047-405C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233341866 | ||||||
chr2:233342123
|
C | CA | 144 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0100others(141): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1047-131dupA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233342123 | |||||
chr2:233342123
|
C | CAA | 10 | a0001c0003t0001g0077a0001c0003t0001g0078a0001c0003t0003g0084others(7): Show | 10 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1047-132_1047-131d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 233342123 | |||||
chr2:233342258
|
T | C | 15 | a0001c0001t0001g0100a0001c0001t0001g0310a0001c0001t0001g0311others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047-13T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 13/15 | chr2 | 233342258 | ||||||
chr2:233342410
|
G | A | 1 | a0002c0002t0001g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1102+84G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342410 | ||||||
chr2:233342481
|
A | G | 1 | a0001c0001t0006g0301 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1102+155A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342481 | ||||||
chr2:233342550
|
TA | T | 5 | a0001c0003t0001g0090a0001c0003t0001g0092a0001c0003t0001g0093others(2): Show | 5 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1102+225delA | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342550 | ||||||
chr2:233342676
|
T | G | 142 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0060others(139): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1102+350T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342676 | ||||||
chr2:233342715
|
G | C | 1 | a0003c0005t0001g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1102+389G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342715 | ||||||
chr2:233342762
|
A | AT | 30 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0048others(27): Show | 30 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1102+451dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233342762 | |||||
chr2:233342790
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1102+464C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342790 | ||||||
chr2:233342804
|
G | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1102+478G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342804 | ||||||
chr2:233342827
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1102+501A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233342827 | ||||||
chr2:233343063
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1102+737T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343063 | ||||||
chr2:233343069
|
T | G | 9 | a0003c0010t0001g0294a0004c0004t0001g0125a0004c0004t0001g0128others(6): Show | 9 | NA18944.hp1 NA18966.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.1102+743T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343069 | ||||||
chr2:233343077
|
T | G | 1 | a0001c0003t0001g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1102+751T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343077 | ||||||
chr2:233343077
|
T | TG | 11 | a0001c0001t0001g0154a0002c0002t0001g0005a0002c0002t0001g0034others(8): Show | 11 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102+755dupG | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343077 | |||||
chr2:233343081
|
G | GT | 132 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(129): Show | 134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1102+777dupT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | |||||
chr2:233343081
|
G | GTT | 27 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0024others(24): Show | 27 | HG00423.hp2 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1102+776_1102+777d others(4): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | |||||
chr2:233343081
|
G | GTTT | 7 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0053others(4): Show | 7 | HG02083.hp1 HG02132.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1102+775_1102+777d others(5): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | |||||
chr2:233343081
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0045 | 2 | HG02647.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1102+755G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343081 | ||||||
chr2:233343081
|
GT | G | 11 | a0001c0003t0001g0002a0001c0003t0001g0075a0001c0003t0001g0077others(8): Show | 12 | HG02080.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102+777delT | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | |||||
chr2:233343081
|
GTTTTT | G | 40 | a0001c0001t0001g0073a0003c0005t0001g0033a0003c0005t0001g0190others(37): Show | 41 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.1102+773_1102+777d others(7): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233343081 | |||||
chr2:233343082
|
T | G | 70 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(67): Show | 76 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1102+756T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343082 | ||||||
chr2:233343083
|
T | G | 5 | a0002c0002t0001g0036a0002c0002t0001g0108a0002c0002t0001g0204others(2): Show | 5 | HG02080.hp1 NA18945.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+757T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343083 | ||||||
chr2:233343236
|
C | A | 1 | a0002c0002t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1102+910C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343236 | ||||||
chr2:233343261
|
G | T | 211 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(208): Show | 220 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1102+935G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343261 | ||||||
chr2:233343372
|
G | A | 2 | a0003c0010t0001g0062a0003c0010t0001g0081 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1102+1046G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343372 | ||||||
chr2:233343378
|
C | T | 4 | a0001c0006t0001g0114a0001c0006t0001g0297a0003c0009t0001g0074others(1): Show | 4 | HG02145.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102+1052C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343378 | ||||||
chr2:233343903
|
T | C | 2 | a0003c0005t0001g0288a0009c0013t0001g0290 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1102+1577T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343903 | ||||||
chr2:233343912
|
C | T | 1 | a0001c0003t0001g0326 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1102+1586C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343912 | ||||||
chr2:233343971
|
A | G | 4 | a0002c0002t0001g0036a0002c0007t0001g0066a0002c0007t0001g0067others(1): Show | 4 | HG02080.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102+1645A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233343971 | ||||||
chr2:233344228
|
T | A | 1 | a0003c0005t0001g0033 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1102+1902T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344228 | ||||||
chr2:233344240
|
G | A | 1 | a0003c0005t0001g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1102+1914G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344240 | ||||||
chr2:233344257
|
G | A | 83 | a0001c0001t0001g0011a0001c0001t0001g0058a0001c0001t0001g0060others(80): Show | 85 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.1102+1931G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344257 | ||||||
chr2:233344264
|
G | A | 91 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(88): Show | 98 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1102+1938G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344264 | ||||||
chr2:233344318
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1102+1992G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344318 | ||||||
chr2:233344339
|
T | G | 33 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(30): Show | 34 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1102+2013T>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344339 | ||||||
chr2:233344438
|
T | C | 1 | a0001c0001t0006g0301 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1103-1965T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344438 | ||||||
chr2:233344450
|
C | T | 2 | a0001c0003t0003g0083a0001c0003t0003g0084 | 2 | NA18940.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1103-1953C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344450 | ||||||
chr2:233344467
|
G | A | 1 | a0003c0005t0001g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1103-1936G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344467 | ||||||
chr2:233344503
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1103-1900C>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344503 | ||||||
chr2:233344505
|
A | G | 1 | a0002c0002t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1103-1898A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344505 | ||||||
chr2:233344666
|
A | C | 1 | a0002c0002t0001g0341 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1103-1737A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344666 | ||||||
chr2:233344723
|
G | A | 1 | a0001c0001t0006g0301 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1103-1680G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344723 | ||||||
chr2:233344951
|
A | C | 112 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0100others(109): Show | 119 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1103-1452A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233344951 | ||||||
chr2:233345001
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1103-1402T>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345001 | ||||||
chr2:233345041
|
C | T | 1 | a0001c0003t0001g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1103-1362C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345041 | ||||||
chr2:233345316
|
G | C | 54 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0006t0001g0114others(51): Show | 55 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.1103-1087G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345316 | ||||||
chr2:233345419
|
A | G | 50 | a0001c0001t0001g0011a0001c0001t0001g0073a0003c0005t0001g0033others(47): Show | 51 | HG00741.hp2 HG01261.hp1 HG01433.hp2 others(48): Show |
intron_variant | MODIFIER | c.1103-984A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345419 | ||||||
chr2:233345585
|
G | A | 33 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(30): Show | 34 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1103-818G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345585 | ||||||
chr2:233345628
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1103-775G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233345628 | ||||||
chr2:233346000
|
A | G | 5 | a0003c0005t0001g0286a0003c0005t0001g0287a0003c0005t0001g0292others(2): Show | 5 | HG03453.hp1 HG03486.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-403A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346000 | ||||||
chr2:233346054
|
G | T | 3 | a0001c0006t0001g0117a0001c0006t0001g0118a0001c0006t0001g0284 | 3 | HG03130.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1103-349G>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346054 | ||||||
chr2:233346061
|
G | A | 33 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(30): Show | 34 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1103-342G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346061 | ||||||
chr2:233346130
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1103-273G>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346130 | ||||||
chr2:233346164
|
T | TAATAAAA others(3): Show |
101 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(98): Show | 107 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1103-234_1103-225d others(12): Show |
SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 233346164 | |||||
chr2:233346179
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1103-224T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346179 | ||||||
chr2:233346244
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1103-159C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346244 | ||||||
chr2:233346276
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1103-127T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 14/15 | chr2 | 233346276 | ||||||
chr2:233346499
|
A | C | 49 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0034others(46): Show | 53 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1112+87A>C | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346499 | ||||||
chr2:233346499
|
A | G | 1 | a0002c0002t0001g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1112+87A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346499 | ||||||
chr2:233346578
|
G | A | 2 | a0001c0006t0001g0114a0001c0006t0001g0297 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1112+166G>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346578 | ||||||
chr2:233346587
|
C | T | 1 | a0001c0003t0001g0346 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1112+175C>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346587 | ||||||
chr2:233346625
|
T | A | 1 | a0001c0001t0001g0021 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1113-182T>A | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346625 | ||||||
chr2:233346698
|
A | G | 1 | a0002c0007t0001g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1113-109A>G | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346698 | ||||||
chr2:233346732
|
A | T | 1 | a0001c0001t0001g0021 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1113-75A>T | SAG | ENSG00000130561.17 | transcript | ENST00000409110.6 | protein_coding | 15/15 | chr2 | 233346732 |