geneid | 2571 |
---|---|
ensemblid | ENSG00000128683.14 |
hgncid | 4092 |
symbol | GAD1 |
name | glutamate decarboxylase 1 |
refseq_nuc | NM_000817.3 |
refseq_prot | NP_000808.2 |
ensembl_nuc | ENST00000358196.8 |
ensembl_prot | ENSP00000350928.3 |
mane_status | MANE Select |
chr | chr2 |
start | 170816887 |
end | 170861151 |
strand | + |
ver | v1.2 |
region | chr2:170816887-170861151 |
region5000 | chr2:170811887-170866151 |
regionname0 | GAD1_chr2_170816887_170861151 |
regionname5000 | GAD1_chr2_170811887_170866151 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 594 | 379 | 69 | 67 | 184 | 15 | 42 | 144 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002 | 0/0 | 594 | 23 | 23 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0003 | 0/0 | 594 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0004 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0005 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0006 | 0/0 | 594 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0007 | 0/0 | 594 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0008 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1785 | 207 | 43 | 40 | 86 | 9 | 27 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0002 | 0/0 | 1785 | 153 | 11 | 25 | 96 | 6 | 15 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0003 | 0/0 | 1785 | 17 | 17 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0004 | 0/0 | 1785 | 16 | 14 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0005 | 0/0 | 1785 | 6 | 6 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0006 | 0/0 | 1785 | 5 | 0 | 0 | 5 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0007 | 0/0 | 1785 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0008 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0009 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0010 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0011 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0012 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
c0013 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1495 | 209 | 63 | 37 | 80 | 10 | 19 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0002 | 1/0 | 1495 | 89 | 5 | 10 | 58 | 2 | 13 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0003 | 0/1 | 1495 | 75 | 0 | 12 | 50 | 3 | 9 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0004 | 0/0 | 1495 | 7 | 7 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0005 | 0/0 | 1495 | 7 | 7 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0006 | 0/0 | 1495 | 6 | 6 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0007 | 0/0 | 1495 | 4 | 0 | 4 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0008 | 0/0 | 1495 | 4 | 0 | 3 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0009 | 0/0 | 1495 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0010 | 0/0 | 1495 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0011 | 0/0 | 1495 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0012 | 0/0 | 1495 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0013 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0014 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0015 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0016 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0017 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
t0018 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0365 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1785 | 207 | 43 | 40 | 86 | 9 | 27 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002 | 0/0 | 1785 | 153 | 11 | 25 | 96 | 6 | 15 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0004 | 0/0 | 1785 | 16 | 14 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0007 | 0/0 | 1785 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0013 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0003 | 0/0 | 1785 | 17 | 17 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0005 | 0/0 | 1785 | 6 | 6 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0003c0006 | 0/0 | 1785 | 5 | 0 | 0 | 5 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0004c0008 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0005c0010 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0006c0011 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0007c0012 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0008c0009 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3279 | 50 | 24 | 11 | 8 | 3 | 4 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0002 | 1/0 | 3279 | 60 | 5 | 9 | 30 | 2 | 13 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0003 | 0/1 | 3279 | 73 | 0 | 12 | 48 | 3 | 9 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0004 | 0/0 | 3279 | 7 | 7 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0006 | 0/0 | 3279 | 5 | 5 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0007 | 0/0 | 3279 | 3 | 0 | 3 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0008 | 0/0 | 3279 | 4 | 0 | 3 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0010 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0011 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0012 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0015 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0001t0018 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002t0001 | 0/0 | 3279 | 126 | 10 | 24 | 71 | 6 | 15 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002t0002 | 0/0 | 3279 | 22 | 0 | 1 | 21 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002t0006 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002t0009 | 0/0 | 3279 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002t0016 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0002t0017 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0004t0001 | 0/0 | 3279 | 16 | 14 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0007t0002 | 0/0 | 3279 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0001c0013t0001 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0003t0001 | 0/0 | 3279 | 14 | 14 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0003t0005 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0003t0013 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0003t0014 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0002c0005t0005 | 0/0 | 3279 | 6 | 6 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0003c0006t0002 | 0/0 | 3279 | 5 | 0 | 0 | 5 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0004c0008t0001 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0005c0010t0003 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0006c0011t0007 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0007c0012t0001 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
a0008c0009t0003 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | copy fasta | chr2 | 170811887 | 170866151 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0365 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0003g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0006g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0007g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0008g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0008g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0008g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0010g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0011g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0012g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0015g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0001t0018g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0001 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0009g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0009g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0002t0017g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0004t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0007t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0007t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0001c0013t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0003t0014g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0005t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0005t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0005t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0005t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0005t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0002c0005t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0003c0006t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0003c0006t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0003c0006t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0003c0006t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0003c0006t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0004c0008t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0005c0010t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0006c0011t0007g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0007c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
a0008c0009t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0011 | g0245 | EUR | GBR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0147 | EUR | GBR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0209 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0231 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0093 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00408 | hp1 | a0003 | c0006 | t0002 | g0083 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00423 | hp1 | a0001 | c0002 | t0016 | g0007 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0379 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0281 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0316 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0357 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0305 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0386 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0239 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01346 | hp1 | a0001 | c0001 | t0012 | g0335 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0334 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0149 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01516 | hp1 | a0007 | c0012 | t0001 | g0179 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0366 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0363 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0250 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01928 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01943 | hp1 | a0001 | c0001 | t0010 | g0384 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0383 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0331 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0307 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02040 | hp1 | a0003 | c0006 | t0002 | g0124 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0332 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02074 | hp2 | a0004 | c0008 | t0001 | g0027 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02132 | hp1 | a0005 | c0010 | t0003 | g0301 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02148 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02258 | hp1 | a0002 | c0005 | t0005 | g0165 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0361 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02300 | hp2 | a0006 | c0011 | t0007 | g0385 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0382 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0249 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0251 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02622 | hp1 | a0002 | c0003 | t0005 | g0327 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0375 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0115 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0374 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02723 | hp1 | a0002 | c0003 | t0013 | g0217 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0370 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0364 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02809 | hp2 | a0001 | c0013 | t0001 | g0117 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02818 | hp1 | a0001 | c0001 | t0018 | g0278 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0368 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0116 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0176 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0280 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0220 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0329 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02970 | hp2 | a0001 | c0004 | t0001 | g0175 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0260 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0349 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03130 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0118 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0259 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03225 | hp2 | a0002 | c0003 | t0014 | g0381 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0214 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0378 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0376 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0284 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0313 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0185 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0380 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0338 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03927 | hp2 | a0001 | c0001 | t0008 | g0297 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0337 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0360 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18522 | hp2 | a0002 | c0005 | t0005 | g0169 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CHB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CHB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0377 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18941 | hp1 | a0001 | c0007 | t0002 | g0202 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18942 | hp1 | a0003 | c0006 | t0002 | g0082 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18949 | hp2 | a0001 | c0002 | t0017 | g0114 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0371 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18957 | hp1 | a0001 | c0002 | t0009 | g0141 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18969 | hp1 | a0001 | c0007 | t0002 | g0158 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18975 | hp2 | a0003 | c0006 | t0002 | g0078 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18995 | hp1 | a0008 | c0009 | t0003 | g0248 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19043 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19066 | hp2 | a0001 | c0002 | t0009 | g0006 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19085 | hp1 | a0003 | c0006 | t0002 | g0177 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19240 | hp1 | a0002 | c0003 | t0001 | g0344 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA19240 | hp2 | a0002 | c0005 | t0005 | g0168 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0367 | AFR | ASW | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0240 | AFR | ASW | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0146 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0195 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | GIH | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | GIH | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02109 | hp2 | a0002 | c0005 | t0005 | g0186 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02559 | hp1 | a0002 | c0005 | t0005 | g0167 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0252 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG06807 | hp1 | a0002 | c0005 | t0005 | g0166 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0365 | REF | REF | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0319 | REF | REF | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170818671
|
C | A | 1 | a0003 | 5 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.80C>A | p.Thr27Lys | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/17 | 305/3279 | 80/1785 | 27/594 | chr2 | 170818671 | ||
chr2:170829576
|
G | A | 1 | a0008 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.247G>A | p.Asp83Asn | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/17 | 472/3279 | 247/1785 | 83/594 | chr2 | 170829576 | ||
chr2:170829597
|
C | T | 1 | a0004 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.268C>T | p.Arg90Cys | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/17 | 493/3279 | 268/1785 | 90/594 | chr2 | 170829597 | ||
chr2:170844088
|
A | C | 1 | a0007 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.682A>C | p.Ile228Leu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/17 | 907/3279 | 682/1785 | 228/594 | chr2 | 170844088 | ||
chr2:170845769
|
A | T | 1 | a0006 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.931A>T | p.Ile311Leu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 9/17 | 1156/3279 | 931/1785 | 311/594 | chr2 | 170845769 | ||
chr2:170846058
|
C | G | 1 | a0005 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.997C>G | p.Gln333Glu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/17 | 1222/3279 | 997/1785 | 333/594 | chr2 | 170846058 | ||
chr2:170858877
|
G | A | 1 | a0002 | 23 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(20): Show |
missense_variant | MODERATE | c.1595G>A | p.Arg532Gln | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/17 | 1820/3279 | 1595/1785 | 532/594 | chr2 | 170858877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170822115
|
T | C | 4 | a0001c0002a0001c0007a0002c0005others(1): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
synonymous_variant | LOW | c.111T>C | p.His37His | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/17 | 336/3279 | 111/1785 | 37/594 | chr2 | 170822115 | ||
chr2:170829578
|
C | T | 1 | a0001c0013 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.249C>T | p.Asp83Asp | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/17 | 474/3279 | 249/1785 | 83/594 | chr2 | 170829578 | ||
chr2:170852729
|
C | T | 1 | a0001c0007 | 2 | NA18941.hp1 NA18969.hp1 |
synonymous_variant | LOW | c.1200C>T | p.Thr400Thr | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/17 | 1425/3279 | 1200/1785 | 400/594 | chr2 | 170852729 | ||
chr2:170857054
|
C | T | 2 | a0001c0004a0001c0013 | 17 | HG00733.hp2 HG01261.hp2 HG01891.hp1 others(14): Show |
synonymous_variant | LOW | c.1450C>T | p.Leu484Leu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/17 | 1675/3279 | 1450/1785 | 484/594 | chr2 | 170857054 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170816954
|
G | A | 3 | a0001c0001t0007a0001c0001t0010a0006c0011t0007 | 5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-158G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/17 | 1638 | chr2 | 170816954 | |||||
chr2:170816965
|
G | A | 6 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(3): Show | 81 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-147G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/17 | 1627 | chr2 | 170816965 | |||||
chr2:170818553
|
A | C | 1 | a0001c0001t0018 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/17 | 39 | chr2 | 170818553 | |||||
chr2:170859949
|
A | G | 3 | a0001c0001t0007a0001c0001t0012a0006c0011t0007 | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*67A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 67 | chr2 | 170859949 | |||||
chr2:170860124
|
A | C | 1 | a0001c0002t0009 | 2 | NA18957.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*242A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 242 | chr2 | 170860124 | |||||
chr2:170860124
|
A | G | 1 | a0001c0002t0017 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 242 | chr2 | 170860124 | |||||
chr2:170860293
|
G | A | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*411G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 411 | chr2 | 170860293 | |||||
chr2:170860307
|
T | C | 1 | a0002c0003t0013 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*425T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 425 | chr2 | 170860307 | |||||
chr2:170860395
|
C | T | 2 | a0001c0001t0006a0001c0002t0006 | 6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 513 | chr2 | 170860395 | |||||
chr2:170860582
|
C | T | 2 | a0002c0003t0005a0002c0005t0005 | 7 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*700C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 700 | chr2 | 170860582 | |||||
chr2:170860666
|
G | A | 1 | a0002c0003t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 784 | chr2 | 170860666 | |||||
chr2:170860685
|
T | C | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*803T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 803 | chr2 | 170860685 | |||||
chr2:170860872
|
G | A | 1 | a0001c0002t0016 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*990G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 990 | chr2 | 170860872 | |||||
chr2:170860890
|
C | T | 1 | a0001c0001t0004 | 7 | HG01884.hp2 HG02630.hp2 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1008C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 1008 | chr2 | 170860890 | |||||
chr2:170861087
|
G | A | 1 | a0001c0001t0011 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 1205 | chr2 | 170861087 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170817122
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-64+74G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817122 | ||||||
chr2:170817202
|
C | G | 1 | a0001c0001t0003g0386 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-64+154C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817202 | ||||||
chr2:170817225
|
A | AC | 39 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0238others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-64+190dupC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACC | 46 | a0001c0001t0001g0184a0001c0001t0001g0211a0001c0001t0001g0219others(43): Show | 48 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-64+189_-64+190dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACCC | 56 | a0001c0001t0001g0010a0001c0001t0001g0172a0001c0001t0001g0178others(53): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-64+188_-64+190dup others(3): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACCCC | 40 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0121others(37): Show | 44 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-64+187_-64+190dup others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACCCCC | 36 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0001g0089others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.-64+186_-64+190dup others(5): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACCCCCC | 22 | a0001c0001t0001g0063a0001c0001t0002g0057a0001c0001t0002g0058others(19): Show | 22 | HG00609.hp2 HG01109.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-64+185_-64+190dup others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACCCCCCC | 17 | a0001c0001t0001g0038a0001c0001t0002g0039a0001c0001t0002g0040others(14): Show | 17 | HG01081.hp2 HG01361.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.-64+184_-64+190dup others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | ACCCCCCC others(3): Show |
1 | a0001c0001t0002g0024 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-64+181_-64+190dup others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817225
|
A | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0010g0384others(1): Show | 5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-64+177A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817225 | ||||||
chr2:170817225
|
AC | A | 45 | a0001c0001t0001g0022a0001c0001t0001g0345a0001c0001t0001g0351others(42): Show | 49 | HG00438.hp1 HG00733.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.-64+190delC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | |||||
chr2:170817234
|
C | A | 2 | a0001c0001t0001g0022a0002c0003t0001g0023 | 2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-64+186C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817234 | ||||||
chr2:170817251
|
A | C | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0010g0384others(1): Show | 5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-64+203A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817251 | ||||||
chr2:170817342
|
G | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0010g0384others(1): Show | 5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-64+294G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817342 | ||||||
chr2:170817441
|
C | T | 1 | a0001c0002t0001g0183 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-64+393C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817441 | ||||||
chr2:170817494
|
G | T | 1 | a0001c0002t0001g0343 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-64+446G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817494 | ||||||
chr2:170817588
|
C | G | 78 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(75): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-64+540C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817588 | ||||||
chr2:170817602
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-64+554G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817602 | ||||||
chr2:170817822
|
T | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG01069.hp2 HG01975.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-63-707T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817822 | ||||||
chr2:170817937
|
C | A | 1 | a0001c0001t0002g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-63-592C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817937 | ||||||
chr2:170818031
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-63-498C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818031 | ||||||
chr2:170818068
|
T | G | 1 | a0001c0002t0001g0137 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-63-461T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818068 | ||||||
chr2:170818090
|
C | G | 4 | a0001c0001t0001g0221a0001c0001t0002g0226a0001c0001t0002g0227others(1): Show | 4 | HG03486.hp1 NA18950.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-63-439C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818090 | ||||||
chr2:170818159
|
A | C | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-63-370A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818159 | ||||||
chr2:170818186
|
T | C | 247 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(244): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-63-343T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818186 | ||||||
chr2:170818198
|
C | A | 1 | a0001c0001t0002g0337 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-63-331C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818198 | ||||||
chr2:170818392
|
G | A | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0265 | 3 | NA18950.hp1 NA19054.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-63-137G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818392 | ||||||
chr2:170818433
|
T | A | 1 | a0001c0002t0001g0343 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-63-96T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818433 | ||||||
chr2:170818805
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.82+132C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170818805 | ||||||
chr2:170818871
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(241): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.82+198A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170818871 | ||||||
chr2:170819228
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82+555C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819228 | ||||||
chr2:170819289
|
GAGAA | G | 3 | a0001c0002t0001g0037a0001c0002t0001g0056a0001c0002t0017g0114 | 3 | NA18949.hp2 NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.82+618_82+621delGA others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819289 | |||||
chr2:170819291
|
G | GAAAT | 76 | a0001c0001t0001g0022a0001c0001t0001g0310a0001c0001t0001g0312others(73): Show | 79 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.82+640_82+643dupAA others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | |||||
chr2:170819291
|
G | GAAATAAA others(1): Show |
7 | a0001c0001t0001g0241a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+636_82+643dupAA others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | |||||
chr2:170819291
|
G | GAAATAAA others(5): Show |
2 | a0001c0001t0001g0279a0001c0001t0015g0280 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82+632_82+643dupAA others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | |||||
chr2:170819291
|
GAAAT | G | 234 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(231): Show | 252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.82+640_82+643delAA others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | |||||
chr2:170819291
|
GAAATAAA others(1): Show |
G | 3 | a0001c0001t0003g0261a0001c0001t0003g0334a0001c0001t0012g0335 | 3 | HG01106.hp1 HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.82+636_82+643delAA others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | |||||
chr2:170819291
|
GAAATAAA others(5): Show |
G | 1 | a0001c0002t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82+632_82+643delAA others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | |||||
chr2:170819355
|
A | C | 2 | a0001c0001t0001g0022a0002c0003t0001g0023 | 2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+682A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819355 | ||||||
chr2:170819479
|
A | G | 2 | a0001c0002t0001g0055a0001c0002t0001g0072 | 2 | NA19010.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.82+806A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819479 | ||||||
chr2:170819485
|
G | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0026others(48): Show | 53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+812G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819485 | ||||||
chr2:170819499
|
C | T | 1 | a0001c0001t0018g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82+826C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819499 | ||||||
chr2:170819629
|
T | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0075 | 2 | HG01070.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.82+956T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819629 | ||||||
chr2:170819712
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.82+1039G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819712 | ||||||
chr2:170819955
|
T | TC | 97 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0006others(94): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.82+1285dupC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819955 | |||||
chr2:170819959
|
G | T | 1 | a0001c0001t0002g0096 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.82+1286G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819959 | ||||||
chr2:170820008
|
G | C | 1 | a0001c0002t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82+1335G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820008 | ||||||
chr2:170820074
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82+1401G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820074 | ||||||
chr2:170820191
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.82+1518G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820191 | ||||||
chr2:170820255
|
C | T | 8 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0211others(5): Show | 8 | HG01069.hp2 HG01975.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+1582C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820255 | ||||||
chr2:170820258
|
C | T | 51 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0026others(48): Show | 53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+1585C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820258 | ||||||
chr2:170820262
|
G | A | 4 | a0001c0001t0001g0241a0001c0004t0001g0239a0001c0004t0001g0240others(1): Show | 4 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1589G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820262 | ||||||
chr2:170820289
|
A | C | 55 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0010g0384others(52): Show | 58 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.82+1616A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820289 | ||||||
chr2:170820322
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.82+1649C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820322 | ||||||
chr2:170820441
|
G | A | 8 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0211others(5): Show | 8 | HG01069.hp2 HG01975.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-1646G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820441 | ||||||
chr2:170820688
|
G | T | 1 | a0001c0002t0001g0183 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.83-1399G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820688 | ||||||
chr2:170820713
|
C | A | 148 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0004others(145): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.83-1374C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820713 | ||||||
chr2:170821213
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.83-874T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821213 | ||||||
chr2:170821225
|
T | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | NA18966.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.83-862T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821225 | ||||||
chr2:170821235
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.83-852G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821235 | ||||||
chr2:170821242
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0010g0384a0001c0002t0001g0136others(1): Show | 5 | HG01928.hp1 HG01943.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-845C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821242 | ||||||
chr2:170821578
|
C | T | 1 | a0002c0003t0001g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-509C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821578 | ||||||
chr2:170821582
|
C | G | 1 | a0001c0002t0001g0210 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.83-505C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821582 | ||||||
chr2:170821759
|
G | A | 3 | a0001c0001t0007g0020a0001c0001t0010g0384a0006c0011t0007g0385 | 4 | HG01928.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-328G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821759 | ||||||
chr2:170821869
|
C | T | 240 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(237): Show | 258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.83-218C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821869 | ||||||
chr2:170822059
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83-28G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170822059 | ||||||
chr2:170822155
|
T | C | 2 | a0001c0002t0001g0037a0001c0002t0001g0056 | 2 | NA18982.hp1 NA18987.hp1 |
splice_region_variant&intron_variant | LOW | c.145+6T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822155 | ||||||
chr2:170822373
|
A | G | 9 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0211others(6): Show | 9 | HG01069.hp2 HG01975.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+224A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822373 | ||||||
chr2:170822446
|
C | T | 1 | a0001c0002t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.145+297C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822446 | ||||||
chr2:170822641
|
C | T | 1 | a0002c0003t0014g0381 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.145+492C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822641 | ||||||
chr2:170822810
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.145+661G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822810 | ||||||
chr2:170822819
|
G | C | 51 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0026others(48): Show | 53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.145+670G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822819 | ||||||
chr2:170823005
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(74): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.145+856G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823005 | ||||||
chr2:170823144
|
A | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0010g0384others(1): Show | 5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+995A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823144 | ||||||
chr2:170823145
|
G | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(76): Show | 83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+996G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823145 | ||||||
chr2:170823168
|
C | T | 2 | a0001c0002t0001g0113a0001c0002t0001g0209 | 2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.145+1019C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823168 | ||||||
chr2:170823174
|
A | G | 2 | a0001c0002t0001g0069a0001c0002t0001g0102 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.145+1025A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823174 | ||||||
chr2:170823202
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.145+1053G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823202 | ||||||
chr2:170823324
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+1175C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823324 | ||||||
chr2:170823532
|
A | G | 153 | a0001c0001t0001g0221a0001c0001t0007g0020a0001c0001t0007g0383others(150): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.145+1383A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823532 | ||||||
chr2:170823566
|
G | A | 7 | a0001c0002t0001g0026a0001c0002t0001g0042a0001c0002t0002g0025others(4): Show | 7 | HG02074.hp2 NA18945.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+1417G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823566 | ||||||
chr2:170823570
|
A | G | 153 | a0001c0001t0001g0221a0001c0001t0007g0020a0001c0001t0007g0383others(150): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.145+1421A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823570 | ||||||
chr2:170823698
|
T | C | 1 | a0001c0001t0018g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.145+1549T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823698 | ||||||
chr2:170823807
|
G | GA | 5 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0365others(2): Show | 7 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+1658_145+1659i others(3): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823807 | ||||||
chr2:170823808
|
G | A | 5 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0365others(2): Show | 7 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+1659G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823808 | ||||||
chr2:170823809
|
G | C | 1 | a0003c0006t0002g0078 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.145+1660G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823809 | ||||||
chr2:170824008
|
C | T | 1 | a0006c0011t0007g0385 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.145+1859C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824008 | ||||||
chr2:170824051
|
G | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0122others(96): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.145+1902G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824051 | ||||||
chr2:170824052
|
G | T | 99 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0122others(96): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.145+1903G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824052 | ||||||
chr2:170824077
|
C | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0122others(96): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.145+1928C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824077 | ||||||
chr2:170824205
|
C | T | 51 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0026others(48): Show | 53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.145+2056C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824205 | ||||||
chr2:170824378
|
T | TAC | 49 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0097others(46): Show | 50 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.145+2270_145+2271d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
T | TACAC | 21 | a0001c0001t0001g0038a0001c0001t0001g0222a0001c0001t0001g0279others(18): Show | 21 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.145+2268_145+2271d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0253a0001c0001t0002g0079a0001c0001t0004g0173others(1): Show | 4 | HG03195.hp1 HG03579.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+2264_145+2271d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0317 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.145+2262_145+2271d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
T | TACACACA others(5): Show |
1 | a0001c0004t0001g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.145+2260_145+2271d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
T | TACACACA others(9): Show |
1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145+2256_145+2271d others(18): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TAC | T | 43 | a0001c0001t0001g0022a0001c0001t0001g0219a0001c0001t0001g0328others(40): Show | 43 | HG00544.hp1 HG00597.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.145+2270_145+2271d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACAC | T | 50 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0333others(47): Show | 56 | HG00140.hp1 HG00733.hp1 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.145+2268_145+2271d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACACAC | T | 7 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(4): Show | 7 | HG02647.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+2266_145+2271d others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACACACA others(1): Show |
T | 12 | a0001c0001t0001g0241a0001c0004t0001g0220a0001c0004t0001g0239others(9): Show | 12 | HG00733.hp2 HG01261.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.145+2264_145+2271d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.145+2262_145+2271d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACACACA others(7): Show |
T | 12 | a0001c0001t0001g0063a0001c0001t0001g0172a0001c0001t0001g0211others(9): Show | 12 | HG00741.hp1 HG01069.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.145+2258_145+2271d others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACACACA others(9): Show |
T | 8 | a0001c0001t0001g0073a0001c0001t0007g0020a0001c0001t0007g0383others(5): Show | 9 | HG01243.hp2 HG01928.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+2256_145+2271d others(18): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824378
|
TACACACA others(11): Show |
T | 149 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0119others(146): Show | 165 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.145+2254_145+2271d others(20): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | |||||
chr2:170824417
|
ACAC | A | 5 | a0001c0001t0001g0354a0001c0001t0003g0244a0001c0001t0003g0334others(2): Show | 5 | HG00438.hp1 HG01346.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+2270_145+2272d others(5): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824417 | |||||
chr2:170824419
|
A | C | 1 | a0001c0002t0002g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.145+2270A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824419 | ||||||
chr2:170824419
|
AC | A | 4 | a0001c0001t0001g0370a0001c0001t0003g0254a0001c0001t0003g0290others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+2274delC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824419 | |||||
chr2:170824660
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0010g0384others(1): Show | 5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+2511C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824660 | ||||||
chr2:170824671
|
C | T | 1 | a0001c0002t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.145+2522C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824671 | ||||||
chr2:170824782
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.145+2633T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824782 | ||||||
chr2:170824929
|
C | CGT | 11 | a0001c0001t0003g0243a0001c0002t0001g0028a0001c0002t0001g0139others(8): Show | 11 | HG00408.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.145+2801_145+2802d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | |||||
chr2:170824929
|
C | CGTGT | 122 | a0001c0001t0001g0073a0001c0001t0003g0014a0001c0001t0003g0015others(119): Show | 129 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.145+2799_145+2802d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | |||||
chr2:170824929
|
C | CGTGTGT | 66 | a0001c0001t0001g0022a0001c0001t0001g0241a0001c0001t0001g0253others(63): Show | 67 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(64): Show |
intron_variant | MODIFIER | c.145+2797_145+2802d others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | |||||
chr2:170824929
|
C | CGTGTGTG others(1): Show |
72 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0089others(69): Show | 74 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.145+2795_145+2802d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | |||||
chr2:170824929
|
C | CGTGTGTG others(3): Show |
13 | a0001c0001t0001g0097a0001c0001t0001g0221a0001c0001t0002g0057others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+2793_145+2802d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | |||||
chr2:170824929
|
CGTGT | C | 10 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0211others(7): Show | 10 | HG01069.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.145+2799_145+2802d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | |||||
chr2:170825191
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+3042G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825191 | ||||||
chr2:170825473
|
A | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0084others(157): Show | 176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.145+3324A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825473 | ||||||
chr2:170825568
|
A | C | 4 | a0001c0001t0001g0336a0001c0001t0001g0362a0001c0001t0004g0314others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+3419A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825568 | ||||||
chr2:170825606
|
C | T | 4 | a0001c0002t0002g0036a0001c0002t0002g0050a0001c0002t0002g0051others(1): Show | 4 | HG00609.hp2 HG02083.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+3457C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825606 | ||||||
chr2:170825624
|
C | T | 73 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0089others(70): Show | 74 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.145+3475C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825624 | ||||||
chr2:170825676
|
A | G | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+3527A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825676 | ||||||
chr2:170825707
|
G | A | 11 | a0001c0002t0001g0006a0001c0002t0001g0104a0001c0002t0001g0105others(8): Show | 11 | HG00673.hp2 HG02135.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.145+3558G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825707 | ||||||
chr2:170825709
|
G | A | 43 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0211others(40): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.145+3560G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825709 | ||||||
chr2:170825734
|
G | A | 1 | a0001c0002t0001g0029 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.145+3585G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825734 | ||||||
chr2:170825829
|
C | T | 49 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0026others(46): Show | 51 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.146-3646C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825829 | ||||||
chr2:170825836
|
C | T | 3 | a0001c0001t0007g0020a0001c0001t0010g0384a0006c0011t0007g0385 | 4 | HG01928.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3639C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825836 | ||||||
chr2:170825894
|
G | T | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0262 | 3 | HG02683.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.146-3581G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825894 | ||||||
chr2:170825897
|
T | A | 1 | a0001c0002t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.146-3578T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825897 | ||||||
chr2:170825965
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.146-3510A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825965 | ||||||
chr2:170826230
|
C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0084others(104): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.146-3245C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826230 | ||||||
chr2:170826276
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.146-3199G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826276 | ||||||
chr2:170826289
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0084others(99): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.146-3186G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826289 | ||||||
chr2:170826314
|
C | A | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-3161C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826314 | ||||||
chr2:170826332
|
C | T | 3 | a0001c0002t0001g0037a0001c0002t0001g0056a0001c0002t0017g0114 | 3 | NA18949.hp2 NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.146-3143C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826332 | ||||||
chr2:170826517
|
G | A | 43 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0001g0211others(40): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.146-2958G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826517 | ||||||
chr2:170826567
|
C | CA | 159 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0063others(156): Show | 175 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.146-2891dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170826567 | |||||
chr2:170826567
|
C | CAA | 70 | a0001c0001t0001g0038a0001c0001t0001g0089a0001c0001t0001g0097others(67): Show | 71 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.146-2892_146-2891d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170826567 | |||||
chr2:170826567
|
CA | C | 8 | a0001c0001t0001g0352a0001c0001t0002g0377a0001c0001t0003g0309others(5): Show | 8 | HG01943.hp2 HG01975.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.146-2891delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170826567 | |||||
chr2:170826597
|
C | T | 264 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(261): Show | 283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.146-2878C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826597 | ||||||
chr2:170826601
|
C | T | 3 | a0001c0001t0007g0020a0001c0001t0010g0384a0006c0011t0007g0385 | 4 | HG01928.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2874C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826601 | ||||||
chr2:170826657
|
G | A | 1 | a0001c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.146-2818G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826657 | ||||||
chr2:170826682
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0005 | 4 | NA18980.hp2 NA18986.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2793A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826682 | ||||||
chr2:170826824
|
A | T | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146-2651A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826824 | ||||||
chr2:170826916
|
C | T | 1 | a0001c0001t0003g0018 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.146-2559C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826916 | ||||||
chr2:170826965
|
A | G | 1 | a0001c0002t0001g0112 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.146-2510A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826965 | ||||||
chr2:170827158
|
G | A | 47 | a0001c0001t0003g0303a0001c0001t0003g0330a0001c0002t0001g0004others(44): Show | 49 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.146-2317G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827158 | ||||||
chr2:170827193
|
C | G | 2 | a0001c0001t0003g0325a0001c0001t0003g0326 | 2 | HG00597.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.146-2282C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827193 | ||||||
chr2:170827230
|
G | A | 1 | a0001c0001t0003g0302 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.146-2245G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827230 | ||||||
chr2:170827248
|
C | A | 51 | a0001c0001t0003g0303a0001c0001t0003g0330a0001c0002t0001g0004others(48): Show | 53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.146-2227C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827248 | ||||||
chr2:170827257
|
C | T | 1 | a0002c0003t0001g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146-2218C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827257 | ||||||
chr2:170827272
|
C | T | 8 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0244others(5): Show | 8 | HG02602.hp1 HG02738.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-2203C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827272 | ||||||
chr2:170827455
|
C | T | 4 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0274others(1): Show | 4 | NA18952.hp2 NA18962.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2020C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827455 | ||||||
chr2:170827456
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0211a0001c0001t0001g0238others(1): Show | 4 | HG02109.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2019G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827456 | ||||||
chr2:170827522
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0018g0278 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.146-1953T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827522 | ||||||
chr2:170827530
|
C | T | 1 | a0002c0003t0001g0313 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.146-1945C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827530 | ||||||
chr2:170827554
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.146-1921C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827554 | ||||||
chr2:170827565
|
G | T | 12 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0220others(9): Show | 12 | HG00733.hp2 HG01261.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.146-1910G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827565 | ||||||
chr2:170827687
|
T | C | 2 | a0001c0002t0001g0042a0004c0008t0001g0027 | 2 | HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.146-1788T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827687 | ||||||
chr2:170827777
|
C | T | 1 | a0001c0002t0002g0103 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.146-1698C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827777 | ||||||
chr2:170827780
|
A | G | 1 | a0001c0001t0003g0286 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.146-1695A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827780 | ||||||
chr2:170827834
|
T | C | 4 | a0001c0001t0018g0278a0001c0002t0001g0139a0002c0003t0001g0313others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1641T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827834 | ||||||
chr2:170827873
|
T | G | 316 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(313): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.146-1602T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827873 | ||||||
chr2:170827905
|
G | C | 1 | a0001c0001t0002g0377 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.146-1570G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827905 | ||||||
chr2:170827990
|
G | A | 8 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0004t0001g0220others(5): Show | 8 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.146-1485G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827990 | ||||||
chr2:170828028
|
A | C | 387 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0022others(384): Show | 411 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.146-1447A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828028 | ||||||
chr2:170828043
|
ATCCTCAC others(31): Show |
A | 148 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0073others(145): Show | 154 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.146-1384_146-1347d others(40): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828043 | |||||
chr2:170828057
|
T | C | 52 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0184others(49): Show | 54 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.146-1418T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828057 | ||||||
chr2:170828067
|
GTCCTCCC others(54): Show |
G | 1 | a0001c0001t0001g0310 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146-1384_146-1324d others(63): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828067 | |||||
chr2:170828085
|
TCACCCCT others(311): Show |
T | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1384_146-1067d others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828085 | |||||
chr2:170828087
|
AC | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(223): Show | 244 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.146-1384delC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828087 | |||||
chr2:170828090
|
CCTCCTCC others(8): Show |
C | 6 | a0001c0001t0003g0291a0001c0001t0006g0256a0001c0001t0006g0257others(3): Show | 6 | HG01884.hp1 HG02132.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-1384_146-1370d others(17): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828090 | ||||||
chr2:170828098
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(223): Show | 244 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.146-1377T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828098 | ||||||
chr2:170828105
|
G | GTCCTCAC others(2): Show |
173 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(170): Show | 188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.146-1365_146-1364i others(11): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | |||||
chr2:170828105
|
G | GTCCTCAC others(25): Show |
46 | a0001c0001t0001g0184a0001c0001t0003g0296a0001c0001t0003g0303others(43): Show | 48 | HG00438.hp2 HG00609.hp2 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.146-1365_146-1364i others(34): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | |||||
chr2:170828105
|
G | GTCCTCAC others(140): Show |
4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-1365_146-1364i others(149): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | |||||
chr2:170828105
|
G | GTCCTCAC others(853): Show |
1 | a0001c0001t0004g0375 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.146-1365_146-1364i others(862): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | |||||
chr2:170828108
|
C | CTCACCCT others(306): Show |
2 | a0001c0001t0001g0119a0001c0001t0001g0121 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.146-1365_146-1364i others(315): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828108 | |||||
chr2:170828138
|
T | A | 1 | a0001c0001t0004g0375 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.146-1337T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828138 | ||||||
chr2:170828140
|
C | A | 1 | a0001c0001t0002g0317 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.146-1335C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828140 | ||||||
chr2:170828147
|
C | CACCCTCC others(39): Show |
2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | NA18986.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.146-1305_146-1304i others(48): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828147 | |||||
chr2:170828147
|
C | CACCCTCC others(16): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0263others(1): Show | 4 | HG00544.hp2 HG00621.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1306_146-1305i others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828147 | |||||
chr2:170828147
|
C | T | 50 | a0001c0001t0001g0184a0001c0001t0001g0241a0001c0001t0003g0296others(47): Show | 52 | HG00438.hp2 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.146-1328C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828147 | ||||||
chr2:170828154
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0121 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.146-1321C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828154 | ||||||
chr2:170828171
|
G | A | 25 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0001g0310others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.146-1304G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828171 | ||||||
chr2:170828176
|
CCT | C | 60 | a0001c0001t0001g0178a0001c0001t0002g0005a0001c0001t0002g0024others(57): Show | 63 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.146-1292_146-1291d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828176 | |||||
chr2:170828180
|
T | C | 25 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0001g0310others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.146-1295T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828180 | ||||||
chr2:170828194
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0003g0291a0001c0001t0008g0316others(1): Show | 4 | HG01109.hp2 HG02132.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1281A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828194 | ||||||
chr2:170828196
|
CT | C | 24 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0002g0039others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.146-1278delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828196 | ||||||
chr2:170828197
|
TCTCCTCT others(17): Show |
T | 43 | a0001c0001t0001g0089a0001c0001t0001g0228a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.146-1270_146-1247d others(26): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828197 | |||||
chr2:170828202
|
T | TCCCTCTG others(14): Show |
19 | a0001c0001t0001g0127a0001c0001t0002g0039a0001c0001t0002g0057others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.146-1272_146-1271i others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828202 | |||||
chr2:170828204
|
T | C | 1 | a0001c0001t0008g0297 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-1271T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828204 | ||||||
chr2:170828212
|
A | ATCCTCAC others(3): Show |
1 | a0001c0001t0002g0005 | 2 | NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.146-1257_146-1248d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828212 | |||||
chr2:170828212
|
A | G | 23 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0002g0039others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.146-1263A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828212 | ||||||
chr2:170828221
|
C | T | 22 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0002g0039others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.146-1254C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828221 | ||||||
chr2:170828222
|
CTCCTCTT others(7): Show |
C | 61 | a0001c0001t0001g0178a0001c0001t0002g0024a0001c0001t0002g0040others(58): Show | 63 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.146-1247_146-1234d others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828222 | |||||
chr2:170828228
|
T | C | 1 | a0001c0001t0008g0297 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-1247T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828228 | ||||||
chr2:170828229
|
T | C | 27 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0002g0005others(24): Show | 28 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-1246T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828229 | ||||||
chr2:170828235
|
T | TATCCTCA others(3): Show |
21 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0002g0039others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-1240_146-1239i others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828235 | ||||||
chr2:170828236
|
G | A | 1 | a0002c0003t0001g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.146-1239G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828236 | ||||||
chr2:170828236
|
G | C | 21 | a0001c0001t0001g0127a0001c0001t0001g0253a0001c0001t0002g0039others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-1239G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828236 | ||||||
chr2:170828236
|
G | GTCCTCAC others(71): Show |
1 | a0001c0001t0008g0297 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-1230_146-1229i others(80): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828236 | |||||
chr2:170828252
|
T | C | 1 | a0001c0001t0002g0005 | 2 | NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.146-1223T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828252 | ||||||
chr2:170828276
|
T | TTCCCTCT others(16): Show |
5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-1190_146-1189i others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828276 | |||||
chr2:170828276
|
T | TTCCCTCT others(16): Show |
50 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0184others(47): Show | 52 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.146-1190_146-1189i others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828276 | |||||
chr2:170828276
|
T | TTCCCTCT others(17): Show |
12 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(9): Show | 13 | HG01346.hp1 HG01891.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.146-1190_146-1189i others(26): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828276 | |||||
chr2:170828286
|
T | C | 4 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1189T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828286 | ||||||
chr2:170828296
|
C | CTCCTCCC others(59): Show |
4 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1154_146-1153i others(68): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828296 | |||||
chr2:170828299
|
C | CTCCCTCT others(16): Show |
4 | a0001c0002t0001g0002a0001c0002t0001g0109a0001c0002t0001g0112others(1): Show | 6 | NA18945.hp2 NA18980.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1162_146-1140d others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828299 | |||||
chr2:170828322
|
T | TTCCCTCT others(13): Show |
1 | a0001c0001t0003g0302 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.146-1139_146-1120d others(22): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828322 | |||||
chr2:170828349
|
T | C | 1 | a0001c0002t0001g0205 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.146-1126T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828349 | ||||||
chr2:170828365
|
T | TTCCCTCT others(39): Show |
1 | a0001c0001t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-1089_146-1044d others(48): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828365 | |||||
chr2:170828380
|
TCACCCTC others(16): Show |
T | 6 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0309others(3): Show | 6 | HG01167.hp1 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1072_146-1050d others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828380 | |||||
chr2:170828383
|
C | T | 63 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0184others(60): Show | 65 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.146-1092C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828383 | ||||||
chr2:170828431
|
C | G | 1 | a0001c0002t0001g0170 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.146-1044C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828431 | ||||||
chr2:170828446
|
G | A | 5 | a0001c0001t0001g0345a0001c0001t0001g0354a0001c0002t0001g0139others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-1029G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828446 | ||||||
chr2:170828447
|
C | T | 4 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1028C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828447 | ||||||
chr2:170828448
|
G | A | 7 | a0001c0001t0002g0212a0001c0004t0001g0115a0001c0004t0001g0116others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1027G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828448 | ||||||
chr2:170828455
|
G | A | 1 | a0001c0004t0001g0249 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.146-1020G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828455 | ||||||
chr2:170828458
|
G | GTCCTCCC others(16): Show |
1 | a0001c0001t0001g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.146-973_146-951dup others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828458 | |||||
chr2:170828458
|
GTCCTCCC others(16): Show |
G | 156 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0130others(153): Show | 162 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.146-973_146-951del others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828458 | |||||
chr2:170828481
|
C | CTCCTCCC others(823): Show |
4 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-823_146-822ins others(830): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828481 | |||||
chr2:170828555
|
A | ACCTCTGC others(15): Show |
1 | a0001c0001t0001g0310 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146-902_146-881dup others(22): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828555 | |||||
chr2:170828619
|
G | GCCCTCCT others(16): Show |
1 | a0001c0002t0001g0200 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.146-822_146-800dup others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828619 | |||||
chr2:170828619
|
GCCCTCCT others(16): Show |
G | 82 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0178others(79): Show | 85 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.146-822_146-800del others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828619 | |||||
chr2:170828670
|
C | T | 1 | a0001c0002t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146-805C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828670 | ||||||
chr2:170828740
|
CCCTCTGC others(16): Show |
C | 1 | a0002c0003t0001g0367 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.146-720_146-698del others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828740 | |||||
chr2:170828831
|
T | C | 1 | a0002c0003t0001g0367 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.146-644T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828831 | ||||||
chr2:170828952
|
C | CTCCTCCC others(16): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0219 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146-513_146-491dup others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828952 | |||||
chr2:170828987
|
C | G | 76 | a0001c0001t0001g0127a0001c0001t0002g0005a0001c0001t0002g0024others(73): Show | 79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.146-488C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828987 | ||||||
chr2:170829006
|
T | C | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146-469T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170829006 | ||||||
chr2:170829007
|
C | T | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146-468C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170829007 | ||||||
chr2:170829188
|
A | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0219 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146-287A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170829188 | ||||||
chr2:170829681
|
T | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.304+48T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170829681 | ||||||
chr2:170829818
|
T | G | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+185T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170829818 | ||||||
chr2:170830049
|
C | T | 220 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0022others(217): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.304+416C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830049 | ||||||
chr2:170830486
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.305-464C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830486 | ||||||
chr2:170830812
|
T | C | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-138T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830812 | ||||||
chr2:170830839
|
C | A | 5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-111C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830839 | ||||||
chr2:170830913
|
G | C | 1 | a0001c0002t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.305-37G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830913 | ||||||
chr2:170831201
|
G | A | 1 | a0001c0004t0001g0260 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.547+9G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831201 | ||||||
chr2:170831275
|
T | G | 1 | a0001c0001t0001g0253 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.547+83T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831275 | ||||||
chr2:170831384
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.547+192G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831384 | ||||||
chr2:170831453
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.547+261G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831453 | ||||||
chr2:170831591
|
C | T | 1 | a0001c0002t0001g0105 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.547+399C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831591 | ||||||
chr2:170831594
|
A | ATG | 43 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0089others(40): Show | 44 | HG01081.hp1 HG01258.hp2 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.547+442_547+443dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
A | ATGTG | 69 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(66): Show | 70 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.547+440_547+443dup others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
A | ATGTGTG | 47 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0002g0005others(44): Show | 50 | HG00673.hp1 HG01081.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.547+438_547+443dup others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
A | ATGTGTGT others(1): Show |
15 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0061others(12): Show | 15 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.547+436_547+443dup others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
A | ATGTGTGT others(3): Show |
6 | a0001c0001t0002g0075a0001c0001t0002g0212a0001c0001t0002g0339others(3): Show | 6 | HG01070.hp1 HG02559.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+434_547+443dup others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0223 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.547+432_547+443dup others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
A | ATGTGTGT others(9): Show |
2 | a0001c0001t0002g0080a0002c0003t0001g0023 | 2 | HG03130.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.547+428_547+443dup others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
ATG | A | 58 | a0001c0001t0001g0022a0001c0001t0001g0362a0001c0001t0003g0016others(55): Show | 61 | HG00597.hp1 HG01168.hp1 HG01169.hp2 others(58): Show |
intron_variant | MODIFIER | c.547+442_547+443del others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
ATGTG | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0266a0001c0001t0003g0243others(1): Show | 4 | HG00408.hp2 HG01069.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.547+440_547+443del others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831594
|
ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.547+432_547+443del others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | |||||
chr2:170831628
|
GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0128others(1): Show | 4 | HG02027.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+438_547+445del others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831628 | |||||
chr2:170831634
|
G | A | 6 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+442G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831634 | ||||||
chr2:170831634
|
G | GTA | 4 | a0001c0002t0001g0012a0001c0002t0001g0149a0001c0002t0001g0231others(1): Show | 5 | HG00323.hp1 HG00621.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+447_547+448dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831634
|
G | GTGTGTA | 2 | a0001c0001t0001g0003a0001c0001t0001g0010 | 5 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.547+443_547+444ins others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831634
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0122 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.547+443_547+444ins others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831634
|
G | GTGTGTGT others(5): Show |
4 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0175others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+443_547+444ins others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831634
|
G | GTGTGTGT others(7): Show |
1 | a0001c0004t0001g0240 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.547+443_547+444ins others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831634
|
G | GTGTGTGT others(9): Show |
5 | a0001c0001t0001g0241a0001c0004t0001g0118a0001c0004t0001g0214others(2): Show | 5 | HG00733.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+443_547+444ins others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831634
|
G | GTGTGTGT others(11): Show |
1 | a0001c0004t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547+443_547+444ins others(18): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | |||||
chr2:170831636
|
A | G | 78 | a0001c0001t0001g0310a0001c0001t0002g0005a0001c0001t0002g0024others(75): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.547+444A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831636 | ||||||
chr2:170831682
|
TAATA | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0279a0001c0001t0007g0020others(3): Show | 7 | HG01099.hp1 HG01346.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+500_547+503del others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831682 | |||||
chr2:170831725
|
T | TAA | 23 | a0001c0001t0001g0241a0001c0001t0006g0256a0001c0001t0006g0257others(20): Show | 23 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.547+535_547+536dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831725 | |||||
chr2:170831759
|
AAATATTT others(6): Show |
A | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+579_547+591del others(13): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831759 | |||||
chr2:170831862
|
T | C | 2 | a0001c0001t0003g0291a0001c0001t0003g0373 | 2 | HG02132.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.547+670T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831862 | ||||||
chr2:170832083
|
C | G | 71 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0253others(68): Show | 76 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.547+891C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832083 | ||||||
chr2:170832083
|
C | T | 2 | a0001c0002t0002g0032a0001c0002t0002g0271 | 2 | HG02056.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.547+891C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832083 | ||||||
chr2:170832093
|
C | T | 5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+901C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832093 | ||||||
chr2:170832250
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.547+1058C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832250 | ||||||
chr2:170832257
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0070 | 2 | HG01255.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.547+1065T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832257 | ||||||
chr2:170832311
|
G | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1119G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832311 | ||||||
chr2:170832313
|
T | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1121T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832313 | ||||||
chr2:170832315
|
T | G | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1123T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832315 | ||||||
chr2:170832316
|
T | G | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1124T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832316 | ||||||
chr2:170832317
|
G | T | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1125G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832317 | ||||||
chr2:170832341
|
G | C | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1149G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832341 | ||||||
chr2:170832342
|
C | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1150C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832342 | ||||||
chr2:170832344
|
T | C | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1152T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832344 | ||||||
chr2:170832345
|
G | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1153G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832345 | ||||||
chr2:170832346
|
T | G | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1154T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832346 | ||||||
chr2:170832350
|
T | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1158T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832350 | ||||||
chr2:170832355
|
C | T | 17 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.547+1163C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832355 | ||||||
chr2:170832381
|
A | C | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1189A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832381 | ||||||
chr2:170832383
|
G | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1191G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832383 | ||||||
chr2:170832391
|
T | G | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1199T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832391 | ||||||
chr2:170832404
|
T | A | 1 | a0001c0002t0002g0067 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1212T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832404 | ||||||
chr2:170832651
|
TGC | T | 9 | a0001c0001t0001g0022a0001c0001t0002g0062a0001c0001t0002g0174others(6): Show | 9 | HG00323.hp1 HG01074.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.547+1472_547+1473d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832651 | |||||
chr2:170832653
|
C | T | 1 | a0001c0002t0001g0142 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.547+1461C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832653 | ||||||
chr2:170832656
|
GCGCGCGC others(5): Show |
G | 17 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.547+1466_547+1477d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832656 | |||||
chr2:170832658
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.547+1466G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832658 | ||||||
chr2:170832660
|
G | GCACA | 3 | a0001c0001t0001g0225a0001c0001t0003g0303a0001c0002t0001g0026 | 3 | HG00621.hp1 NA19084.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.547+1469_547+1470i others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | |||||
chr2:170832660
|
G | GCACACA | 22 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0264others(19): Show | 23 | HG00438.hp2 HG02074.hp2 HG03704.hp2 others(20): Show |
intron_variant | MODIFIER | c.547+1469_547+1470i others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | |||||
chr2:170832660
|
G | GCACACAC others(1): Show |
9 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0003g0330others(6): Show | 9 | HG00544.hp2 HG00609.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.547+1469_547+1470i others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | |||||
chr2:170832660
|
G | GCACACAC others(3): Show |
4 | a0001c0001t0001g0263a0001c0002t0002g0050a0001c0002t0002g0052others(1): Show | 4 | HG02083.hp1 NA18984.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+1469_547+1470i others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | |||||
chr2:170832660
|
GCGCGCAC others(3): Show |
G | 9 | a0001c0001t0001g0241a0001c0001t0002g0074a0001c0001t0002g0079others(6): Show | 9 | HG00673.hp1 HG00733.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.547+1470_547+1479d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | |||||
chr2:170832660
|
GCGCGCAC others(5): Show |
G | 67 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0040others(64): Show | 71 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.547+1470_547+1481d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | |||||
chr2:170832661
|
C | T | 2 | a0001c0002t0001g0156a0001c0002t0001g0195 | 2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.547+1469C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832661 | ||||||
chr2:170832662
|
G | A | 38 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(35): Show | 39 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.547+1470G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832662 | ||||||
chr2:170832662
|
G | GCA | 17 | a0001c0001t0001g0312a0001c0001t0003g0288a0001c0001t0003g0334others(14): Show | 17 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
G | GCACA | 21 | a0001c0001t0001g0073a0001c0001t0001g0333a0001c0001t0001g0370others(18): Show | 24 | HG00544.hp1 HG00609.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
G | GCACACA | 15 | a0001c0001t0001g0063a0001c0001t0001g0184a0001c0001t0001g0320others(12): Show | 16 | HG01192.hp2 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
G | GCACACAC others(1): Show |
6 | a0001c0001t0003g0304a0001c0001t0003g0309a0001c0002t0001g0028others(3): Show | 6 | HG01943.hp2 HG02074.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
G | GCACACAC others(3): Show |
2 | a0001c0002t0001g0043a0001c0002t0001g0185 | 2 | HG01123.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.547+1471_547+1472i others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
GCGCA | G | 36 | a0001c0001t0001g0172a0001c0001t0001g0221a0001c0001t0002g0080others(33): Show | 39 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.547+1472_547+1475d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
GCGCACA | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(115): Show | 129 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.547+1472_547+1477d others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
GCGCACAC others(1): Show |
G | 5 | a0001c0001t0001g0328a0001c0001t0001g0374a0001c0001t0003g0247others(2): Show | 5 | HG00438.hp1 HG02132.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+1472_547+1479d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832662
|
GCGCACAC others(3): Show |
G | 2 | a0001c0001t0004g0375a0001c0002t0001g0164 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.547+1472_547+1481d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | |||||
chr2:170832664
|
G | A | 119 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0130others(116): Show | 125 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.547+1472G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832664 | ||||||
chr2:170832664
|
G | GCA | 3 | a0001c0001t0002g0218a0002c0003t0001g0376a0002c0003t0001g0378 | 3 | HG03516.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.547+1503_547+1504d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832664 | |||||
chr2:170832664
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.547+1493_547+1504d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832664 | |||||
chr2:170832672
|
A | G | 17 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.547+1480A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832672 | ||||||
chr2:170832691
|
C | G | 5 | a0001c0001t0002g0024a0001c0001t0002g0041a0001c0001t0002g0059others(2): Show | 5 | NA18941.hp2 NA18959.hp2 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.547+1499C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832691 | ||||||
chr2:170832853
|
G | A | 89 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(86): Show | 92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.547+1661G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832853 | ||||||
chr2:170832911
|
C | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(147): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.547+1719C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832911 | ||||||
chr2:170833013
|
G | C | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1821G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833013 | ||||||
chr2:170833126
|
C | G | 35 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0003g0014others(32): Show | 39 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.547+1934C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833126 | ||||||
chr2:170833210
|
G | T | 89 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(86): Show | 92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.547+2018G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833210 | ||||||
chr2:170833340
|
A | C | 94 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(91): Show | 98 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.547+2148A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833340 | ||||||
chr2:170833460
|
A | G | 89 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(86): Show | 92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.547+2268A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833460 | ||||||
chr2:170833603
|
C | T | 5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2411C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833603 | ||||||
chr2:170833611
|
T | C | 69 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0310others(66): Show | 74 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.547+2419T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833611 | ||||||
chr2:170833765
|
G | A | 67 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0040others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.547+2573G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833765 | ||||||
chr2:170833781
|
G | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2589G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833781 | ||||||
chr2:170833816
|
TG | T | 228 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0022others(225): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.547+2627delG | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170833816 | |||||
chr2:170833861
|
G | A | 1 | a0001c0001t0003g0290 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.547+2669G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833861 | ||||||
chr2:170833931
|
C | T | 1 | a0003c0006t0002g0124 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.547+2739C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833931 | ||||||
chr2:170833932
|
G | A | 3 | a0001c0002t0001g0037a0001c0002t0001g0069a0001c0002t0001g0102 | 3 | HG02647.hp2 HG03540.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.547+2740G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833932 | ||||||
chr2:170833954
|
T | C | 154 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(151): Show | 160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.547+2762T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833954 | ||||||
chr2:170834000
|
C | CA | 54 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(51): Show | 56 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.548-2780dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834000 | |||||
chr2:170834000
|
C | CAA | 6 | a0001c0001t0001g0241a0001c0002t0001g0274a0001c0004t0001g0214others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.548-2781_548-2780d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834000 | |||||
chr2:170834013
|
AG | A | 4 | a0001c0001t0002g0080a0001c0002t0002g0067a0001c0002t0002g0110others(1): Show | 4 | NA18959.hp1 NA18987.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-2779delG | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834013 | ||||||
chr2:170834014
|
G | A | 93 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(90): Show | 96 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.548-2779G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834014 | ||||||
chr2:170834221
|
C | T | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.548-2572C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834221 | ||||||
chr2:170834314
|
G | A | 67 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0040others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.548-2479G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834314 | ||||||
chr2:170834451
|
TAAAAG | T | 89 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(86): Show | 92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.548-2340_548-2336d others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834451 | |||||
chr2:170834571
|
C | T | 1 | a0001c0001t0003g0307 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.548-2222C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834571 | ||||||
chr2:170834592
|
T | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-2201T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834592 | ||||||
chr2:170834765
|
C | CT | 12 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0211others(9): Show | 13 | HG01928.hp1 HG01975.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.548-2011dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834765 | |||||
chr2:170834765
|
CT | C | 75 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(72): Show | 77 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.548-2011delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834765 | |||||
chr2:170834765
|
CTT | C | 65 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0040others(62): Show | 68 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.548-2012_548-2011d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834765 | |||||
chr2:170834824
|
G | A | 1 | a0001c0001t0008g0379 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.548-1969G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834824 | ||||||
chr2:170834825
|
C | A | 1 | a0001c0001t0008g0379 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.548-1968C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834825 | ||||||
chr2:170834987
|
G | C | 1 | a0001c0001t0002g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.548-1806G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834987 | ||||||
chr2:170835181
|
T | A | 13 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(10): Show | 13 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.548-1612T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835181 | ||||||
chr2:170835203
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.548-1590T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835203 | ||||||
chr2:170835204
|
A | T | 1 | a0001c0001t0002g0094 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.548-1589A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835204 | ||||||
chr2:170835213
|
T | A | 93 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(90): Show | 97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.548-1580T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835213 | ||||||
chr2:170835219
|
A | G | 89 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(86): Show | 92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.548-1574A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835219 | ||||||
chr2:170835279
|
T | C | 1 | a0001c0013t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.548-1514T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835279 | ||||||
chr2:170835292
|
A | T | 1 | a0001c0002t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.548-1501A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835292 | ||||||
chr2:170835314
|
T | C | 1 | a0001c0002t0001g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.548-1479T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835314 | ||||||
chr2:170835347
|
G | A | 93 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(90): Show | 97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.548-1446G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835347 | ||||||
chr2:170835417
|
A | G | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-1376A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835417 | ||||||
chr2:170835469
|
T | C | 7 | a0001c0001t0004g0173a0001c0001t0004g0213a0001c0001t0004g0284others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.548-1324T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835469 | ||||||
chr2:170835490
|
C | T | 1 | a0001c0002t0002g0103 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.548-1303C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835490 | ||||||
chr2:170835577
|
T | A | 5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-1216T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835577 | ||||||
chr2:170835779
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.548-1014A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835779 | ||||||
chr2:170835941
|
A | T | 1 | a0001c0002t0002g0032 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.548-852A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835941 | ||||||
chr2:170835978
|
G | A | 1 | a0001c0002t0001g0170 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.548-815G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835978 | ||||||
chr2:170836111
|
C | CT | 6 | a0001c0001t0002g0088a0001c0001t0003g0215a0001c0001t0006g0256others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-669dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170836111 | |||||
chr2:170836259
|
A | T | 4 | a0001c0002t0001g0055a0001c0002t0001g0065a0001c0002t0001g0066others(1): Show | 4 | HG02155.hp2 HG03704.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-534A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836259 | ||||||
chr2:170836302
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.548-491A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836302 | ||||||
chr2:170836314
|
T | C | 1 | a0001c0002t0001g0185 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.548-479T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836314 | ||||||
chr2:170836485
|
T | C | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-308T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836485 | ||||||
chr2:170836508
|
A | G | 1 | a0001c0001t0004g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.548-285A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836508 | ||||||
chr2:170836574
|
T | G | 1 | a0001c0002t0001g0209 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.548-219T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836574 | ||||||
chr2:170836945
|
A | C | 75 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(72): Show | 78 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.638+62A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170836945 | ||||||
chr2:170836987
|
T | C | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.638+104T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170836987 | ||||||
chr2:170837054
|
A | G | 1 | a0001c0004t0001g0364 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.638+171A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837054 | ||||||
chr2:170837129
|
C | G | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+246C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837129 | ||||||
chr2:170837198
|
G | C | 79 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(76): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.638+315G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837198 | ||||||
chr2:170837264
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.638+381T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837264 | ||||||
chr2:170837554
|
A | G | 5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+671A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837554 | ||||||
chr2:170837596
|
AG | A | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+717delG | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170837596 | |||||
chr2:170837655
|
T | G | 3 | a0001c0001t0002g0039a0001c0001t0002g0062a0001c0001t0008g0316 | 3 | HG01081.hp2 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.638+772T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837655 | ||||||
chr2:170837719
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.638+836T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837719 | ||||||
chr2:170838182
|
C | T | 1 | a0001c0001t0018g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+1299C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838182 | ||||||
chr2:170838560
|
A | G | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+1677A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838560 | ||||||
chr2:170838805
|
C | T | 6 | a0001c0002t0001g0029a0001c0002t0001g0045a0001c0002t0001g0048others(3): Show | 6 | NA18975.hp1 NA18983.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+1922C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838805 | ||||||
chr2:170838877
|
T | C | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+1994T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838877 | ||||||
chr2:170839006
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0238 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.638+2123A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839006 | ||||||
chr2:170839142
|
T | C | 1 | a0001c0001t0004g0375 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638+2259T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839142 | ||||||
chr2:170839149
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.638+2266G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839149 | ||||||
chr2:170839340
|
T | C | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2457T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839340 | ||||||
chr2:170839352
|
C | T | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+2469C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839352 | ||||||
chr2:170839613
|
C | CA | 16 | a0001c0001t0001g0119a0001c0001t0001g0178a0001c0001t0003g0246others(13): Show | 16 | HG00597.hp2 HG02027.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.638+2747dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170839613 | |||||
chr2:170839613
|
CA | C | 6 | a0001c0001t0001g0370a0001c0001t0002g0039a0001c0001t0002g0181others(3): Show | 6 | HG01081.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.638+2747delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170839613 | |||||
chr2:170839633
|
T | A | 1 | a0001c0001t0018g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+2750T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839633 | ||||||
chr2:170839655
|
T | C | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2772T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839655 | ||||||
chr2:170839677
|
AT | A | 5 | a0001c0001t0001g0241a0001c0004t0001g0214a0001c0004t0001g0239others(2): Show | 5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+2795delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839677 | ||||||
chr2:170839679
|
ATTC | A | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2804_638+2806d others(5): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170839679 | |||||
chr2:170839696
|
C | T | 1 | a0001c0001t0003g0372 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.638+2813C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839696 | ||||||
chr2:170839721
|
G | C | 56 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(53): Show | 59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2838G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839721 | ||||||
chr2:170839962
|
T | C | 154 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(151): Show | 160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.638+3079T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839962 | ||||||
chr2:170840081
|
G | A | 6 | a0001c0002t0001g0029a0001c0002t0001g0045a0001c0002t0001g0048others(3): Show | 6 | NA18975.hp1 NA18983.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+3198G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840081 | ||||||
chr2:170840173
|
C | T | 46 | a0001c0001t0001g0089a0001c0001t0001g0228a0001c0001t0001g0266others(43): Show | 47 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.638+3290C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840173 | ||||||
chr2:170840189
|
G | A | 2 | a0001c0001t0003g0014a0001c0002t0001g0236 | 3 | NA18942.hp2 NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.638+3306G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840189 | ||||||
chr2:170840270
|
A | G | 150 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(147): Show | 155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.638+3387A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840270 | ||||||
chr2:170840508
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.639-3537C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840508 | ||||||
chr2:170840597
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0219 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.639-3448A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840597 | ||||||
chr2:170840643
|
A | G | 105 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(102): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.639-3402A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840643 | ||||||
chr2:170840658
|
A | AAGGGAGG others(5): Show |
1 | a0001c0001t0002g0342 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.639-3373_639-3362d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | |||||
chr2:170840658
|
A | AAGGGAGG others(14): Show |
4 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-3380_639-3379i others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | |||||
chr2:170840658
|
A | AAGGGAGG others(18): Show |
77 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(74): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.639-3380_639-3379i others(27): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | |||||
chr2:170840658
|
A | AAGGGAGG others(22): Show |
1 | a0001c0002t0002g0270 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.639-3380_639-3379i others(31): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | |||||
chr2:170840735
|
C | A | 2 | a0001c0001t0002g0317a0001c0001t0018g0278 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.639-3310C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840735 | ||||||
chr2:170841015
|
G | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-3030G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841015 | ||||||
chr2:170841054
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-2991C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841054 | ||||||
chr2:170841195
|
A | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(85): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.639-2850A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841195 | ||||||
chr2:170841285
|
T | C | 16 | a0001c0001t0001g0241a0001c0001t0007g0020a0001c0001t0007g0383others(13): Show | 17 | HG00733.hp2 HG01261.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.639-2760T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841285 | ||||||
chr2:170841531
|
T | C | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-2514T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841531 | ||||||
chr2:170841539
|
CAAAAT | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(85): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.639-2492_639-2488d others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170841539 | |||||
chr2:170841741
|
G | C | 16 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0075others(13): Show | 16 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.639-2304G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841741 | ||||||
chr2:170841836
|
A | G | 1 | a0001c0001t0018g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.639-2209A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841836 | ||||||
chr2:170842124
|
T | G | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0004g0375 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639-1921T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842124 | ||||||
chr2:170842162
|
T | C | 90 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(87): Show | 93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.639-1883T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842162 | ||||||
chr2:170842255
|
C | G | 1 | a0001c0001t0004g0375 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.639-1790C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842255 | ||||||
chr2:170842309
|
C | T | 6 | a0001c0001t0004g0173a0001c0001t0004g0213a0001c0001t0004g0284others(3): Show | 6 | HG01884.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-1736C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842309 | ||||||
chr2:170842664
|
C | T | 1 | a0001c0002t0017g0114 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.639-1381C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842664 | ||||||
chr2:170842808
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639-1237T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842808 | ||||||
chr2:170842889
|
T | A | 83 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(80): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.639-1156T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842889 | ||||||
chr2:170842896
|
T | C | 1 | a0001c0001t0003g0247 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.639-1149T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842896 | ||||||
chr2:170843047
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.639-998G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843047 | ||||||
chr2:170843182
|
C | T | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.639-863C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843182 | ||||||
chr2:170843612
|
C | A | 7 | a0001c0002t0001g0170a0001c0002t0001g0191a0001c0002t0001g0192others(4): Show | 7 | HG00621.hp2 HG02056.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.639-433C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843612 | ||||||
chr2:170843619
|
C | CT | 8 | a0001c0001t0001g0225a0001c0001t0001g0320a0001c0001t0001g0354others(5): Show | 9 | HG00621.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.639-408dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170843619 | |||||
chr2:170843619
|
CT | C | 111 | a0001c0001t0001g0022a0001c0001t0001g0182a0001c0001t0001g0219others(108): Show | 114 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.639-408delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170843619 | |||||
chr2:170843619
|
CTT | C | 7 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0262others(4): Show | 8 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-409_639-408del others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170843619 | |||||
chr2:170843849
|
C | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(76): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.639-196C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843849 | ||||||
chr2:170844036
|
C | A | 1 | a0001c0001t0003g0021 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.639-9C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170844036 | ||||||
chr2:170844159
|
T | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | splice_donor_variant&intron_variant | HIGH | c.751+2T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844159 | ||||||
chr2:170844219
|
G | A | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.751+62G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844219 | ||||||
chr2:170844248
|
A | AT | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+99dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 170844248 | |||||
chr2:170844291
|
G | C | 1 | a0001c0002t0001g0099 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.751+134G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844291 | ||||||
chr2:170844298
|
A | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751+141A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844298 | ||||||
chr2:170844394
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0073 | 2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.751+237T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844394 | ||||||
chr2:170844407
|
C | CT | 15 | a0001c0001t0003g0282a0001c0001t0003g0294a0001c0001t0003g0323others(12): Show | 15 | HG00280.hp1 HG00621.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.751+269dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 170844407 | |||||
chr2:170844407
|
CT | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(84): Show | 91 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.751+269delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 170844407 | |||||
chr2:170844425
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.751+268T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844425 | ||||||
chr2:170844426
|
T | G | 1 | a0007c0012t0001g0179 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.751+269T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844426 | ||||||
chr2:170844506
|
T | C | 1 | a0001c0001t0003g0321 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.751+349T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844506 | ||||||
chr2:170845220
|
C | T | 2 | a0001c0002t0001g0037a0001c0002t0001g0056 | 2 | NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.752-286C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845220 | ||||||
chr2:170845253
|
G | C | 1 | a0001c0001t0003g0300 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.752-253G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845253 | ||||||
chr2:170845254
|
C | G | 154 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(151): Show | 160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.752-252C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845254 | ||||||
chr2:170845276
|
C | T | 1 | a0001c0001t0003g0348 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.752-230C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845276 | ||||||
chr2:170845655
|
G | GT | 3 | a0001c0001t0003g0015a0001c0001t0003g0365a0001c0001t0003g0366 | 4 | HG01516.hp2 HG01517.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+40dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 170845655 | |||||
chr2:170845665
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0370 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.868-41G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 8/16 | chr2 | 170845665 | ||||||
chr2:170845970
|
C | T | 105 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(102): Show | 109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.948-39C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 9/16 | chr2 | 170845970 | ||||||
chr2:170846075
|
G | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+12G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846075 | ||||||
chr2:170846362
|
G | A | 1 | a0001c0002t0006g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1002+299G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846362 | ||||||
chr2:170846368
|
T | C | 1 | a0002c0003t0001g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1002+305T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846368 | ||||||
chr2:170846450
|
G | A | 71 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0040others(68): Show | 74 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1002+387G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846450 | ||||||
chr2:170846831
|
C | A | 10 | a0001c0001t0001g0229a0001c0001t0003g0215a0001c0001t0003g0244others(7): Show | 12 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1002+768C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846831 | ||||||
chr2:170847010
|
A | T | 1 | a0001c0001t0002g0096 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1003-666A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847010 | ||||||
chr2:170847110
|
C | A | 1 | a0001c0002t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1003-566C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847110 | ||||||
chr2:170847167
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003-509C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847167 | ||||||
chr2:170847174
|
A | G | 1 | a0001c0002t0001g0033 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1003-502A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847174 | ||||||
chr2:170847406
|
A | ACAGAATT others(321): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0219 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1003-259_1003-258i others(330): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 170847406 | |||||
chr2:170847875
|
G | A | 1 | a0001c0001t0003g0017 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1119+83G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170847875 | ||||||
chr2:170847886
|
C | G | 1 | a0007c0012t0001g0179 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1119+94C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170847886 | ||||||
chr2:170848009
|
C | T | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+217C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848009 | ||||||
chr2:170848259
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1119+467C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848259 | ||||||
chr2:170848436
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1119+644G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848436 | ||||||
chr2:170848454
|
G | A | 1 | a0001c0001t0002g0377 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1119+662G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848454 | ||||||
chr2:170848456
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1119+664C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848456 | ||||||
chr2:170848496
|
C | CA | 61 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0178others(58): Show | 64 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1119+720dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 170848496 | |||||
chr2:170848496
|
C | T | 1 | a0001c0001t0001g0370 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1119+704C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848496 | ||||||
chr2:170848507
|
A | G | 1 | a0002c0003t0001g0368 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1119+715A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848507 | ||||||
chr2:170848647
|
AT | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(87): Show | 102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1120-628delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 170848647 | |||||
chr2:170848936
|
C | T | 4 | a0002c0003t0001g0019a0002c0003t0001g0361a0002c0003t0001g0376others(1): Show | 5 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-350C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848936 | ||||||
chr2:170849355
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG01074.hp1 | splice_region_variant&intron_variant | LOW | c.1184+5C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849355 | ||||||
chr2:170849669
|
T | C | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+319T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849669 | ||||||
chr2:170849677
|
T | C | 1 | a0001c0001t0001g0354 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1184+327T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849677 | ||||||
chr2:170849737
|
A | T | 83 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(80): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1184+387A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849737 | ||||||
chr2:170850036
|
G | A | 2 | a0001c0001t0003g0346a0001c0002t0001g0028 | 2 | NA18990.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1184+686G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850036 | ||||||
chr2:170850269
|
C | T | 1 | a0001c0004t0001g0281 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1184+919C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850269 | ||||||
chr2:170850275
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0003g0247others(4): Show | 7 | HG00597.hp2 HG01981.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184+925A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850275 | ||||||
chr2:170850487
|
G | C | 1 | a0001c0004t0001g0220 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1184+1137G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850487 | ||||||
chr2:170850585
|
G | T | 1 | a0002c0003t0005g0327 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1184+1235G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850585 | ||||||
chr2:170850619
|
A | G | 1 | a0001c0002t0001g0237 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1184+1269A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850619 | ||||||
chr2:170850733
|
A | C | 83 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(80): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1184+1383A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850733 | ||||||
chr2:170850839
|
C | A | 1 | a0001c0001t0003g0372 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1184+1489C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850839 | ||||||
chr2:170851024
|
G | GA | 11 | a0001c0001t0001g0241a0001c0004t0001g0115a0001c0004t0001g0116others(8): Show | 11 | HG00733.hp2 HG01261.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1185-1680dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 170851024 | |||||
chr2:170851024
|
GA | G | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-1680delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 170851024 | |||||
chr2:170851376
|
C | A | 4 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0208others(1): Show | 4 | HG01081.hp1 HG02735.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-1338C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851376 | ||||||
chr2:170851384
|
T | C | 1 | a0001c0002t0001g0028 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1185-1330T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851384 | ||||||
chr2:170851537
|
A | G | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-1177A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851537 | ||||||
chr2:170851590
|
G | A | 42 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0310others(39): Show | 46 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1185-1124G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851590 | ||||||
chr2:170852289
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1185-425A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852289 | ||||||
chr2:170852331
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1185-383G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852331 | ||||||
chr2:170852474
|
T | C | 7 | a0002c0003t0001g0378a0002c0005t0005g0165a0002c0005t0005g0166others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-240T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852474 | ||||||
chr2:170852505
|
G | T | 1 | a0001c0002t0001g0210 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1185-209G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852505 | ||||||
chr2:170852550
|
C | T | 3 | a0001c0002t0001g0069a0001c0002t0001g0102a0001c0002t0002g0036 | 3 | HG02647.hp2 HG03540.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1185-164C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852550 | ||||||
chr2:170852861
|
G | T | 1 | a0001c0001t0004g0375 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1263+69G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852861 | ||||||
chr2:170852920
|
A | G | 112 | a0001c0001t0001g0241a0001c0001t0002g0005a0001c0001t0002g0024others(109): Show | 116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1263+128A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852920 | ||||||
chr2:170852937
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1263+145C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852937 | ||||||
chr2:170852997
|
T | C | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+205T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852997 | ||||||
chr2:170853011
|
G | A | 49 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0040others(46): Show | 52 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1263+219G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853011 | ||||||
chr2:170853174
|
T | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0211a0001c0001t0001g0238others(1): Show | 4 | HG02109.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+382T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853174 | ||||||
chr2:170853443
|
T | A | 1 | a0001c0001t0003g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1264-430T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853443 | ||||||
chr2:170853489
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-384C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853489 | ||||||
chr2:170853490
|
G | A | 1 | a0001c0001t0004g0284 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1264-383G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853490 | ||||||
chr2:170853633
|
G | C | 1 | a0001c0001t0003g0288 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1264-240G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853633 | ||||||
chr2:170854044
|
A | G | 2 | a0002c0003t0001g0313a0002c0003t0001g0332 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1413+22A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854044 | ||||||
chr2:170854298
|
T | C | 2 | a0002c0003t0001g0313a0002c0003t0001g0332 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1413+276T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854298 | ||||||
chr2:170854330
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1413+308A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854330 | ||||||
chr2:170854353
|
A | T | 2 | a0001c0001t0001g0038a0001c0002t0001g0277 | 2 | HG01243.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1413+331A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854353 | ||||||
chr2:170854393
|
A | C | 1 | a0001c0001t0002g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1413+371A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854393 | ||||||
chr2:170854397
|
C | CT | 28 | a0001c0001t0001g0038a0001c0001t0001g0182a0001c0001t0001g0184others(25): Show | 28 | HG00597.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1413+396dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170854397 | |||||
chr2:170854397
|
CT | C | 30 | a0001c0001t0001g0241a0001c0001t0001g0370a0001c0001t0002g0087others(27): Show | 31 | HG00733.hp2 HG01261.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.1413+396delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170854397 | |||||
chr2:170854652
|
A | C | 1 | a0001c0001t0002g0341 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1413+630A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854652 | ||||||
chr2:170854701
|
G | A | 1 | a0002c0003t0001g0382 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1413+679G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854701 | ||||||
chr2:170855075
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1413+1053A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855075 | ||||||
chr2:170855098
|
TCTAA | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0333a0001c0001t0003g0386others(1): Show | 4 | HG01255.hp1 HG02055.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1413+1082_1413+108 others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855098 | |||||
chr2:170855112
|
AAAC | A | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413+1096_1413+109 others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855112 | |||||
chr2:170855209
|
CT | C | 14 | a0001c0001t0001g0130a0001c0001t0002g0040a0001c0001t0002g0087others(11): Show | 15 | HG01074.hp1 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1413+1205delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855209 | |||||
chr2:170855271
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413+1249C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855271 | ||||||
chr2:170855346
|
T | A | 1 | a0001c0001t0003g0302 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1413+1324T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855346 | ||||||
chr2:170855540
|
T | C | 2 | a0001c0001t0001g0345a0001c0001t0001g0354 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1414-1478T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855540 | ||||||
chr2:170855585
|
T | C | 7 | a0001c0004t0001g0220a0001c0004t0001g0249a0001c0004t0001g0250others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414-1433T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855585 | ||||||
chr2:170855649
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1414-1369C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855649 | ||||||
chr2:170855673
|
G | A | 97 | a0001c0001t0001g0241a0001c0001t0001g0253a0001c0001t0002g0005others(94): Show | 101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1414-1345G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855673 | ||||||
chr2:170855872
|
C | CA | 57 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0178others(54): Show | 61 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1414-1123dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | |||||
chr2:170855872
|
CA | C | 64 | a0001c0001t0001g0263a0001c0001t0002g0005a0001c0001t0002g0024others(61): Show | 66 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-1123delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | |||||
chr2:170855872
|
CAA | C | 22 | a0001c0001t0001g0253a0001c0001t0002g0040a0001c0001t0002g0087others(19): Show | 23 | HG00733.hp2 HG01261.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1414-1124_1414-112 others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | |||||
chr2:170855872
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0003g0292a0007c0012t0001g0179 | 2 | HG01516.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1414-1134_1414-112 others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | |||||
chr2:170855872
|
CAAAAAAA others(6): Show |
C | 158 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0038others(155): Show | 171 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1414-1135_1414-112 others(17): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | |||||
chr2:170855925
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1414-1093C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855925 | ||||||
chr2:170855926
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1414-1092G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855926 | ||||||
chr2:170856055
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1414-963A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856055 | ||||||
chr2:170856069
|
T | G | 1 | a0001c0001t0002g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1414-949T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856069 | ||||||
chr2:170856094
|
G | T | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-924G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856094 | ||||||
chr2:170856164
|
T | C | 4 | a0001c0001t0007g0020a0001c0001t0007g0383a0001c0001t0012g0335others(1): Show | 5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-854T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856164 | ||||||
chr2:170856178
|
C | G | 94 | a0001c0001t0001g0241a0001c0001t0001g0253a0001c0001t0002g0005others(91): Show | 97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1414-840C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856178 | ||||||
chr2:170856211
|
C | T | 1 | a0001c0002t0001g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1414-807C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856211 | ||||||
chr2:170856386
|
T | C | 1 | a0001c0002t0001g0030 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1414-632T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856386 | ||||||
chr2:170856634
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1414-384T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856634 | ||||||
chr2:170856641
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1414-377A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856641 | ||||||
chr2:170856766
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | NA18966.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1414-252C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856766 | ||||||
chr2:170856798
|
T | C | 2 | a0001c0002t0001g0069a0001c0002t0001g0102 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1414-220T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856798 | ||||||
chr2:170857456
|
G | T | 1 | a0001c0002t0001g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1521+331G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857456 | ||||||
chr2:170857532
|
G | T | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0004g0375 | 3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1521+407G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857532 | ||||||
chr2:170857569
|
G | C | 40 | a0001c0001t0001g0089a0001c0001t0001g0228a0001c0001t0001g0266others(37): Show | 41 | HG00408.hp2 HG00597.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1521+444G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857569 | ||||||
chr2:170857589
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1521+464A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857589 | ||||||
chr2:170857625
|
C | T | 1 | a0001c0001t0003g0355 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1521+500C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857625 | ||||||
chr2:170857936
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1521+811T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857936 | ||||||
chr2:170857946
|
T | C | 6 | a0001c0004t0001g0115a0001c0004t0001g0116a0001c0004t0001g0118others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521+821T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857946 | ||||||
chr2:170858010
|
C | A | 3 | a0001c0002t0001g0012a0001c0002t0001g0149a0001c0002t0001g0231 | 4 | HG00323.hp1 HG00738.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522-794C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858010 | ||||||
chr2:170858039
|
CCA | C | 34 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0003g0014others(31): Show | 38 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1522-764_1522-763d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858039 | ||||||
chr2:170858323
|
T | G | 1 | a0001c0001t0002g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1522-481T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858323 | ||||||
chr2:170858340
|
C | A | 6 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1522-464C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858340 | ||||||
chr2:170858556
|
T | G | 17 | a0001c0001t0002g0039a0001c0001t0002g0062a0001c0001t0002g0080others(14): Show | 17 | HG00609.hp2 HG01081.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1522-248T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858556 | ||||||
chr2:170858572
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1522-232G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858572 | ||||||
chr2:170858623
|
C | G | 97 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0039others(94): Show | 101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1522-181C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858623 | ||||||
chr2:170859252
|
T | C | 6 | a0001c0001t0006g0256a0001c0001t0006g0257a0001c0001t0006g0258others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1611+359T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/16 | chr2 | 170859252 | ||||||
chr2:170859476
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1612-233A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/16 | chr2 | 170859476 | ||||||
chr2:170859610
|
A | G | 24 | a0001c0001t0001g0351a0001c0001t0001g0352a0002c0003t0001g0019others(21): Show | 25 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1612-99A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/16 | chr2 | 170859610 |