geneid | 2744 |
---|---|
ensemblid | ENSG00000115419.14 |
hgncid | 4331 |
symbol | GLS |
name | glutaminase |
refseq_nuc | NM_014905.5 |
refseq_prot | NP_055720.3 |
ensembl_nuc | ENST00000320717.8 |
ensembl_prot | ENSP00000317379.3 |
mane_status | MANE Select |
chr | chr2 |
start | 190880821 |
end | 190965552 |
strand | + |
ver | v1.2 |
region | chr2:190880821-190965552 |
region5000 | chr2:190875821-190970552 |
regionname0 | GLS_chr2_190880821_190965552 |
regionname5000 | GLS_chr2_190875821_190970552 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 669 | 367 | 84 | 64 | 171 | 16 | 30 | 137 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0002 | 0/0 | 669 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0003 | 0/0 | 669 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0004 | 0/0 | 669 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0005 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0006 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0007 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2010 | 346 | 78 | 63 | 159 | 16 | 28 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0002 | 0/0 | 2010 | 12 | 0 | 1 | 11 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0003 | 0/0 | 2010 | 6 | 0 | 0 | 6 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0004 | 0/0 | 2010 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0005 | 0/0 | 2010 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0006 | 0/0 | 2010 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0007 | 0/0 | 2010 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0008 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0009 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0010 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0011 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0012 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
c0013 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2804 | 81 | 7 | 10 | 54 | 4 | 6 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0002 | 0/1 | 2825 | 38 | 1 | 3 | 26 | 2 | 5 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0003 | 0/0 | 2825 | 31 | 5 | 10 | 15 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0004 | 0/0 | 2831 | 27 | 1 | 5 | 15 | 4 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0005 | 0/0 | 2828 | 21 | 1 | 9 | 6 | 1 | 4 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0006 | 0/0 | 2828 | 19 | 1 | 6 | 10 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0007 | 0/0 | 2809 | 12 | 0 | 1 | 11 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0008 | 0/0 | 2812 | 11 | 10 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0009 | 0/0 | 2828 | 10 | 5 | 1 | 3 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0010 | 0/0 | 2834 | 9 | 1 | 4 | 2 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0011 | 0/0 | 2813 | 7 | 1 | 4 | 0 | 1 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0012 | 0/0 | 2825 | 7 | 5 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0013 | 0/0 | 2825 | 6 | 0 | 0 | 2 | 0 | 4 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0014 | 0/0 | 2807 | 4 | 0 | 4 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0015 | 0/0 | 2822 | 4 | 0 | 0 | 4 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0016 | 0/0 | 2822 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0017 | 0/0 | 2820 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0018 | 0/0 | 2828 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0019 | 1/0 | 2831 | 4 | 1 | 1 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0020 | 0/0 | 2831 | 4 | 0 | 0 | 4 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0021 | 0/0 | 2837 | 4 | 3 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0022 | 0/0 | 2837 | 4 | 1 | 1 | 1 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0023 | 0/0 | 2804 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0024 | 0/0 | 2807 | 3 | 3 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0025 | 0/0 | 2819 | 3 | 3 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0026 | 0/0 | 2804 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0027 | 0/0 | 2813 | 2 | 1 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0028 | 0/0 | 2812 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0029 | 0/0 | 2825 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0030 | 0/0 | 2828 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0031 | 0/0 | 2834 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0032 | 0/0 | 2849 | 2 | 1 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0033 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0034 | 0/0 | 2811 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0035 | 0/0 | 2798 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0036 | 0/0 | 2798 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0037 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0038 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0039 | 0/0 | 2830 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0040 | 0/0 | 2807 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0041 | 0/0 | 2810 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0042 | 0/0 | 2809 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0043 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0044 | 0/0 | 2816 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0045 | 0/0 | 2815 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0046 | 0/0 | 2816 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0047 | 0/0 | 2816 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0048 | 0/0 | 2820 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0049 | 0/0 | 2821 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0050 | 0/0 | 2818 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0051 | 0/0 | 2822 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0052 | 0/0 | 2823 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0053 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0054 | 0/0 | 2822 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0055 | 0/0 | 2828 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0056 | 0/0 | 2827 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0057 | 0/0 | 2828 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0058 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0059 | 0/0 | 2827 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0060 | 0/0 | 2828 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0061 | 0/0 | 2828 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0062 | 0/0 | 2828 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0063 | 0/0 | 2832 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0064 | 0/0 | 2831 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0065 | 0/0 | 2831 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0066 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0067 | 0/0 | 2837 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0068 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0069 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0070 | 0/0 | 2849 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0071 | 0/0 | 2852 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0072 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0073 | 0/0 | 2825 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
t0074 | 0/0 | 2828 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0002 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0314 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2010 | 346 | 78 | 63 | 159 | 16 | 28 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0002 | 0/0 | 2010 | 12 | 0 | 1 | 11 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0004 | 0/0 | 2010 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0005 | 0/0 | 2010 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0008 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0009 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0012 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0002c0003 | 0/0 | 2010 | 6 | 0 | 0 | 6 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0003c0007 | 0/0 | 2010 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0004c0006 | 0/0 | 2010 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0005c0010 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0006c0011 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0007c0013 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4813 | 74 | 6 | 8 | 50 | 4 | 6 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0002 | 0/1 | 4834 | 36 | 1 | 3 | 26 | 2 | 3 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0003 | 0/0 | 4834 | 31 | 5 | 10 | 15 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0004 | 0/0 | 4840 | 27 | 1 | 5 | 15 | 4 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0005 | 0/0 | 4837 | 21 | 1 | 9 | 6 | 1 | 4 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0006 | 0/0 | 4837 | 19 | 1 | 6 | 10 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0008 | 0/0 | 4821 | 11 | 10 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0009 | 0/0 | 4837 | 10 | 5 | 1 | 3 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0010 | 0/0 | 4843 | 9 | 1 | 4 | 2 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0011 | 0/0 | 4822 | 7 | 1 | 4 | 0 | 1 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0012 | 0/0 | 4834 | 7 | 5 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0013 | 0/0 | 4834 | 4 | 0 | 0 | 2 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0014 | 0/0 | 4816 | 4 | 0 | 4 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0015 | 0/0 | 4831 | 4 | 0 | 0 | 4 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0016 | 0/0 | 4831 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0018 | 0/0 | 4837 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0019 | 1/0 | 4840 | 4 | 1 | 1 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0020 | 0/0 | 4840 | 4 | 0 | 0 | 4 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0021 | 0/0 | 4846 | 4 | 3 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0022 | 0/0 | 4846 | 4 | 1 | 1 | 1 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0024 | 0/0 | 4816 | 3 | 3 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0025 | 0/0 | 4828 | 3 | 3 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0026 | 0/0 | 4813 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0027 | 0/0 | 4822 | 2 | 1 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0028 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0029 | 0/0 | 4834 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0030 | 0/0 | 4837 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0031 | 0/0 | 4843 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0032 | 0/0 | 4858 | 2 | 1 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0033 | 0/0 | 4813 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0034 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0035 | 0/0 | 4807 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0036 | 0/0 | 4807 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0038 | 0/0 | 4813 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0039 | 0/0 | 4839 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0040 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0041 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0043 | 0/0 | 4823 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0044 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0045 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0046 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0047 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0048 | 0/0 | 4829 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0049 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0050 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0051 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0052 | 0/0 | 4832 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0053 | 0/0 | 4835 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0054 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0055 | 0/0 | 4837 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0056 | 0/0 | 4836 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0057 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0058 | 0/0 | 4838 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0059 | 0/0 | 4836 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0060 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0061 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0062 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0064 | 0/0 | 4840 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0065 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0067 | 0/0 | 4846 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0068 | 0/0 | 4852 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0069 | 0/0 | 4854 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0070 | 0/0 | 4858 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0071 | 0/0 | 4861 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0072 | 0/0 | 4906 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0073 | 0/0 | 4834 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0001t0074 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0002t0007 | 0/0 | 4818 | 12 | 0 | 1 | 11 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0004t0017 | 0/0 | 4829 | 4 | 4 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0005t0013 | 0/0 | 4834 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0008t0066 | 0/0 | 4838 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0009t0001 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0001c0012t0037 | 0/0 | 4813 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0002c0003t0001 | 0/0 | 4813 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0002c0003t0023 | 0/0 | 4813 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0003c0007t0002 | 0/0 | 4834 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0004c0006t0001 | 0/0 | 4813 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0005c0010t0042 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0006c0011t0063 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
a0007c0013t0001 | 0/0 | 4813 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | copy fasta | chr2 | 190875821 | 190970552 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0009g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0012g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0013g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0013g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0013g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0014g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0014g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0014g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0015g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0015g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0015g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0016g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0016g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0018g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0019g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0019g0314 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0019g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0019g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0020g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0020g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0020g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0020g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0021g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0021g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0021g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0021g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0022g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0022g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0022g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0024g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0024g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0025g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0025g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0026g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0027g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0027g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0028g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0028g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0029g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0030g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0031g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0031g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0032g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0032g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0033g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0034g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0035g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0036g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0038g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0039g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0040g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0041g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0043g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0044g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0045g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0046g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0047g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0048g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0049g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0050g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0051g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0052g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0053g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0054g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0055g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0056g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0057g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0058g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0059g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0060g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0061g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0062g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0064g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0065g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0067g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0068g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0069g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0070g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0071g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0072g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0073g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0001t0074g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0002t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0004t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0004t0017g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0004t0017g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0004t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0005t0013g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0005t0013g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0008t0066g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0009t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0001c0012t0037g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0002c0003t0023g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0002c0003t0023g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0002c0003t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0003c0007t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0004c0006t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0005c0010t0042g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0006c0011t0063g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
a0007c0013t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0233 | EUR | GBR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | GBR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00280 | hp1 | a0001 | c0001 | t0022 | g0242 | EUR | FIN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0333 | EUR | FIN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0092 | EUR | FIN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00323 | hp2 | a0001 | c0001 | t0074 | g0213 | EUR | FIN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00408 | hp1 | a0001 | c0001 | t0070 | g0313 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00438 | hp2 | a0001 | c0001 | t0055 | g0061 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00558 | hp2 | a0001 | c0001 | t0041 | g0065 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00597 | hp2 | a0001 | c0001 | t0013 | g0110 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00639 | hp1 | a0001 | c0001 | t0036 | g0081 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00673 | hp2 | a0001 | c0001 | t0071 | g0125 | EAS | CHS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00738 | hp1 | a0001 | c0001 | t0014 | g0247 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00738 | hp2 | a0001 | c0001 | t0039 | g0180 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG00741 | hp2 | a0004 | c0006 | t0001 | g0022 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01069 | hp1 | a0001 | c0001 | t0014 | g0243 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0074 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01070 | hp1 | a0001 | c0001 | t0026 | g0007 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01070 | hp2 | a0001 | c0001 | t0022 | g0123 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0075 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01071 | hp2 | a0001 | c0001 | t0026 | g0007 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0206 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01074 | hp2 | a0004 | c0006 | t0001 | g0022 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01099 | hp2 | a0001 | c0001 | t0010 | g0222 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0225 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01106 | hp2 | a0001 | c0001 | t0009 | g0334 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0282 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0079 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0249 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01192 | hp1 | a0001 | c0001 | t0019 | g0327 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01192 | hp2 | a0001 | c0001 | t0069 | g0070 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0254 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01257 | hp1 | a0001 | c0002 | t0007 | g0270 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01257 | hp2 | a0001 | c0001 | t0011 | g0095 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01258 | hp2 | a0001 | c0001 | t0011 | g0096 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0218 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01346 | hp2 | a0001 | c0001 | t0011 | g0097 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0248 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0230 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01496 | hp1 | a0001 | c0001 | t0035 | g0331 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0252 | EUR | IBS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0239 | EUR | IBS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0253 | EUR | IBS | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01884 | hp1 | a0001 | c0001 | t0049 | g0336 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01884 | hp2 | a0001 | c0001 | t0032 | g0126 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01978 | hp2 | a0001 | c0001 | t0014 | g0244 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0082 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0085 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02027 | hp2 | a0001 | c0009 | t0001 | g0130 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02040 | hp1 | a0001 | c0001 | t0045 | g0288 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02040 | hp2 | a0001 | c0001 | t0031 | g0098 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02055 | hp1 | a0001 | c0001 | t0022 | g0217 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02056 | hp2 | a0001 | c0001 | t0020 | g0060 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02071 | hp1 | a0001 | c0001 | t0051 | g0113 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02083 | hp1 | a0001 | c0002 | t0007 | g0269 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02145 | hp1 | a0001 | c0001 | t0033 | g0175 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02145 | hp2 | a0001 | c0001 | t0021 | g0129 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | CDX | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02165 | hp2 | a0001 | c0001 | t0065 | g0229 | EAS | CDX | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0325 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02258 | hp1 | a0001 | c0001 | t0024 | g0264 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0141 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02280 | hp1 | a0001 | c0004 | t0017 | g0037 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02280 | hp2 | a0001 | c0001 | t0053 | g0332 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02300 | hp2 | a0001 | c0001 | t0011 | g0053 | AMR | PEL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02451 | hp1 | a0001 | c0001 | t0009 | g0312 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02602 | hp1 | a0001 | c0001 | t0010 | g0221 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02602 | hp2 | a0001 | c0001 | t0013 | g0108 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02615 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02622 | hp1 | a0001 | c0001 | t0028 | g0343 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02622 | hp2 | a0001 | c0001 | t0048 | g0136 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02630 | hp1 | a0001 | c0001 | t0025 | g0029 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02630 | hp2 | a0001 | c0001 | t0064 | g0120 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02647 | hp2 | a0001 | c0001 | t0068 | g0138 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0067 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02698 | hp1 | a0001 | c0001 | t0027 | g0263 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02698 | hp2 | a0001 | c0001 | t0019 | g0039 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0197 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02809 | hp2 | a0001 | c0004 | t0017 | g0035 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02886 | hp1 | a0001 | c0001 | t0058 | g0311 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0195 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02895 | hp2 | a0001 | c0001 | t0057 | g0316 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02896 | hp1 | a0001 | c0001 | t0016 | g0203 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02896 | hp2 | a0001 | c0012 | t0037 | g0245 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02897 | hp2 | a0001 | c0001 | t0027 | g0202 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02922 | hp2 | a0001 | c0001 | t0024 | g0193 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02965 | hp1 | a0001 | c0001 | t0021 | g0127 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02970 | hp1 | a0001 | c0001 | t0052 | g0114 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0341 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02976 | hp1 | a0001 | c0001 | t0016 | g0018 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02976 | hp2 | a0001 | c0001 | t0062 | g0337 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0224 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03041 | hp1 | a0001 | c0001 | t0029 | g0001 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0133 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0265 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0328 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03139 | hp1 | a0001 | c0001 | t0018 | g0140 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03195 | hp1 | a0006 | c0011 | t0063 | g0345 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03195 | hp2 | a0007 | c0013 | t0001 | g0132 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03453 | hp2 | a0001 | c0001 | t0025 | g0029 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0329 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03486 | hp2 | a0001 | c0001 | t0029 | g0001 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03490 | hp2 | a0001 | c0001 | t0010 | g0209 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0111 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03491 | hp2 | a0003 | c0007 | t0002 | g0023 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03492 | hp1 | a0003 | c0007 | t0002 | g0023 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0135 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03516 | hp2 | a0001 | c0001 | t0025 | g0338 | AFR | ESN | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03540 | hp1 | a0001 | c0001 | t0050 | g0121 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03579 | hp1 | a0001 | c0001 | t0018 | g0139 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03579 | hp2 | a0001 | c0004 | t0017 | g0038 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03654 | hp2 | a0001 | c0005 | t0013 | g0106 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03669 | hp2 | a0001 | c0001 | t0061 | g0112 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03704 | hp1 | a0001 | c0001 | t0011 | g0094 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03704 | hp2 | a0001 | c0001 | t0060 | g0122 | SAS | PJL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | BEB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | BEB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0339 | SAS | BEB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0216 | SAS | BEB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04199 | hp1 | a0001 | c0001 | t0059 | g0289 | SAS | STU | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | STU | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04204 | hp1 | a0001 | c0005 | t0013 | g0107 | SAS | STU | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0211 | SAS | STU | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0057 | SAS | STU | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0215 | SAS | STU | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0196 | AFR | YRI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18522 | hp2 | a0001 | c0001 | t0019 | g0315 | AFR | YRI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18939 | hp2 | a0001 | c0001 | t0020 | g0099 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18949 | hp2 | a0001 | c0001 | t0030 | g0172 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18950 | hp2 | a0001 | c0002 | t0007 | g0279 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18952 | hp1 | a0001 | c0001 | t0021 | g0286 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18953 | hp2 | a0001 | c0002 | t0007 | g0271 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18954 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18954 | hp2 | a0001 | c0001 | t0047 | g0237 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18956 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18961 | hp2 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18966 | hp1 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18967 | hp1 | a0001 | c0002 | t0007 | g0276 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18968 | hp2 | a0001 | c0001 | t0020 | g0100 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18970 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18970 | hp2 | a0002 | c0003 | t0023 | g0152 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18978 | hp2 | a0002 | c0003 | t0023 | g0281 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18980 | hp1 | a0001 | c0001 | t0067 | g0304 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18981 | hp2 | a0001 | c0001 | t0009 | g0310 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18984 | hp2 | a0001 | c0001 | t0015 | g0025 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18985 | hp1 | a0001 | c0001 | t0020 | g0101 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18986 | hp1 | a0002 | c0003 | t0023 | g0151 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18988 | hp2 | a0001 | c0001 | t0030 | g0003 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0293 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18989 | hp2 | a0001 | c0001 | t0012 | g0231 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18990 | hp1 | a0001 | c0001 | t0031 | g0102 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18993 | hp1 | a0001 | c0002 | t0007 | g0280 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18995 | hp1 | a0001 | c0001 | t0022 | g0227 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18998 | hp1 | a0001 | c0002 | t0007 | g0272 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18999 | hp2 | a0001 | c0001 | t0015 | g0025 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19000 | hp1 | a0001 | c0002 | t0007 | g0277 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19005 | hp1 | a0001 | c0002 | t0007 | g0278 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19006 | hp1 | a0001 | c0001 | t0009 | g0298 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19006 | hp2 | a0001 | c0001 | t0046 | g0046 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19007 | hp1 | a0001 | c0001 | t0073 | g0118 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19009 | hp2 | a0001 | c0001 | t0015 | g0303 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19010 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19030 | hp1 | a0001 | c0001 | t0038 | g0032 | AFR | LWK | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | LWK | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19043 | hp2 | a0001 | c0001 | t0044 | g0342 | AFR | LWK | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19054 | hp1 | a0001 | c0001 | t0009 | g0330 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19054 | hp2 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19057 | hp2 | a0001 | c0002 | t0007 | g0274 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19058 | hp1 | a0001 | c0001 | t0054 | g0044 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19059 | hp2 | a0005 | c0010 | t0042 | g0262 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19062 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19066 | hp2 | a0001 | c0001 | t0015 | g0305 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19068 | hp1 | a0001 | c0001 | t0013 | g0109 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19072 | hp1 | a0001 | c0001 | t0040 | g0161 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19077 | hp1 | a0001 | c0002 | t0007 | g0275 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19080 | hp1 | a0001 | c0002 | t0007 | g0273 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19089 | hp2 | a0001 | c0001 | t0034 | g0261 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | YRI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA19240 | hp2 | a0001 | c0001 | t0016 | g0018 | AFR | YRI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0292 | AFR | ASW | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20129 | hp2 | a0001 | c0001 | t0021 | g0128 | AFR | ASW | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20752 | hp1 | a0001 | c0001 | t0032 | g0068 | EUR | TSI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | TSI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20805 | hp1 | a0001 | c0001 | t0009 | g0318 | EUR | TSI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01123 | hp1 | a0001 | c0001 | t0014 | g0246 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02109 | hp2 | a0001 | c0001 | t0028 | g0344 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02486 | hp1 | a0001 | c0001 | t0056 | g0340 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02486 | hp2 | a0001 | c0008 | t0066 | g0036 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02559 | hp1 | a0001 | c0001 | t0018 | g0001 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | ACB | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03471 | hp1 | a0001 | c0001 | t0072 | g0137 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | MSL | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG06807 | hp1 | a0001 | c0001 | t0043 | g0030 | AFR | USA | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
HG06807 | hp2 | a0001 | c0001 | t0016 | g0119 | AFR | USA | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA20300 | hp2 | a0001 | c0004 | t0017 | g0034 | AFR | USA | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA21309 | hp1 | a0001 | c0001 | t0010 | g0207 | AFR | LWK | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0084 | REF | REF | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0019 | g0314 | REF | REF | GLS_chr2_190875821_190970552 | GLS | chr2 | 190875821 | 190970552 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190881209
|
G | T | 1 | a0007 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.125G>T | p.Gly42Val | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 389/4840 | 125/2010 | 42/669 | chr2 | 190881209 | ||
chr2:190881350
|
A | C | 1 | a0002 | 6 | NA18954.hp1 NA18970.hp2 NA18978.hp2 others(3): Show |
missense_variant | MODERATE | c.266A>C | p.His89Pro | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 530/4840 | 266/2010 | 89/669 | chr2 | 190881350 | ||
chr2:190927351
|
G | T | 1 | a0006 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1294G>T | p.Ala432Ser | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/18 | 1558/4840 | 1294/2010 | 432/669 | chr2 | 190927351 | ||
chr2:190927354
|
A | G | 1 | a0003 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.1297A>G | p.Thr433Ala | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/18 | 1561/4840 | 1297/2010 | 433/669 | chr2 | 190927354 | ||
chr2:190954588
|
G | T | 1 | a0005 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1717G>T | p.Ala573Ser | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 16/18 | 1981/4840 | 1717/2010 | 573/669 | chr2 | 190954588 | ||
chr2:190954589
|
C | G | 1 | a0005 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1718C>G | p.Ala573Gly | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 16/18 | 1982/4840 | 1718/2010 | 573/669 | chr2 | 190954589 | ||
chr2:190962889
|
T | C | 1 | a0004 | 2 | HG00741.hp2 HG01074.hp2 |
missense_variant | MODERATE | c.1913T>C | p.Ile638Thr | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 2177/4840 | 1913/2010 | 638/669 | chr2 | 190962889 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190881219
|
C | A | 1 | a0001c0005 | 2 | HG03654.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.135C>A | p.Ala45Ala | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 399/4840 | 135/2010 | 45/669 | chr2 | 190881219 | ||
chr2:190895180
|
T | C | 1 | a0001c0008 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.415T>C | p.Leu139Leu | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 2/18 | 679/4840 | 415/2010 | 139/669 | chr2 | 190895180 | ||
chr2:190901967
|
A | G | 2 | a0001c0004a0001c0008 | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.756A>G | p.Gln252Gln | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/18 | 1020/4840 | 756/2010 | 252/669 | chr2 | 190901967 | ||
chr2:190905127
|
G | A | 1 | a0001c0009 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.939G>A | p.Pro313Pro | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/18 | 1203/4840 | 939/2010 | 313/669 | chr2 | 190905127 | ||
chr2:190924563
|
C | T | 1 | a0001c0012 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.1218C>T | p.Asp406Asp | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/18 | 1482/4840 | 1218/2010 | 406/669 | chr2 | 190924563 | ||
chr2:190953597
|
A | C | 1 | a0001c0002 | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
synonymous_variant | LOW | c.1683A>C | p.Ala561Ala | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/18 | 1947/4840 | 1683/2010 | 561/669 | chr2 | 190953597 | ||
chr2:190954590
|
T | C | 1 | a0005c0010 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.1719T>C | p.Ala573Ala | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 16/18 | 1983/4840 | 1719/2010 | 573/669 | chr2 | 190954590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190880821
|
A | G | 1 | a0001c0001t0074 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-264A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 264 | chr2 | 190880821 | |||||
chr2:190880843
|
G | A | 1 | a0001c0001t0074 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-242G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 242 | chr2 | 190880843 | |||||
chr2:190880856
|
C | A | 1 | a0001c0001t0033 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-229C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 229 | chr2 | 190880856 | |||||
chr2:190880872
|
C | CGCA | 2 | a0001c0001t0010a0001c0001t0031 | 11 | HG01099.hp2 HG01106.hp1 HG01175.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-167_-165dupGCA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
C | CGCAGCA | 3 | a0001c0001t0021a0001c0001t0022a0001c0001t0067 | 9 | HG00280.hp1 HG01070.hp2 HG02055.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-170_-165dupGCAGCA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
C | CGCAGCAG others(5): Show |
1 | a0001c0001t0068 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-176_-165dupGCAGCA others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
C | CGCAGCAG others(11): Show |
2 | a0001c0001t0032a0001c0001t0070 | 3 | HG00408.hp1 HG01884.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-182_-165dupGCAGCA others(12): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
C | CGCAGCAG others(14): Show |
1 | a0001c0001t0071 | 1 | HG00673.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185_-165dupGCAGCA others(15): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
C | CGCAGCAG others(59): Show |
1 | a0001c0001t0072 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-165_-164insGCAGCA others(60): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCA | C | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(10): Show | 63 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-167_-165delGCA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCA | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(8): Show | 88 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(85): Show |
5_prime_UTR_variant | MODIFIER | c.-170_-165delGCAGCA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(2): Show |
C | 7 | a0001c0001t0015a0001c0001t0016a0001c0001t0048others(4): Show | 16 | HG01884.hp1 HG02071.hp1 HG02280.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-165delGCAGCA others(3): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(5): Show |
C | 1 | a0001c0001t0025 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-176_-165delGCAGCA others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(8): Show |
C | 6 | a0001c0001t0028a0001c0001t0043a0001c0001t0044others(3): Show | 7 | HG02040.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-179_-165delGCAGCA others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(11): Show |
C | 4 | a0001c0001t0008a0001c0001t0011a0001c0001t0027others(1): Show | 21 | HG00323.hp1 HG01257.hp2 HG01258.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-182_-165delGCAGCA others(12): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(14): Show |
C | 2 | a0001c0001t0041a0001c0002t0007 | 13 | HG00558.hp2 HG01257.hp1 HG02083.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-185_-165delGCAGCA others(15): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(17): Show |
C | 13 | a0001c0001t0001a0001c0001t0014a0001c0001t0024others(10): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-188_-165delGCAGCA others(18): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(20): Show |
C | 1 | a0001c0012t0037 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-191_-165delGCAGCA others(21): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880872
|
CGCAGCAG others(26): Show |
C | 2 | a0001c0001t0035a0001c0001t0036 | 2 | HG00639.hp1 HG01496.hp1 |
5_prime_UTR_variant | MODIFIER | c.-197_-165delGCAGCA others(27): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 165 | INFO_REALIGN_3_PRIME | chr2 | 190880872 | ||||
chr2:190880884
|
AGCAGCAG others(10): Show |
A | 1 | a0001c0001t0034 | 1 | NA19089.hp2 | 5_prime_UTR_variant | MODIFIER | c.-200_-184delGCAGCA others(11): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 184 | chr2 | 190880884 | |||||
chr2:190880889
|
C | T | 1 | a0001c0001t0073 | 1 | NA19007.hp1 | 5_prime_UTR_variant | MODIFIER | c.-196C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 196 | chr2 | 190880889 | |||||
chr2:190880920
|
A | AGCAGCAG others(7): Show |
1 | a0001c0001t0069 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-165_-164insGCAGCA others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | chr2 | 190880920 | |||||
chr2:190880921
|
C | A | 1 | a0001c0001t0069 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-164C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | 164 | chr2 | 190880921 | |||||
chr2:190881054
|
C | T | 2 | a0001c0004t0017a0001c0008t0066 | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | chr2 | 190881054 | ||||||
chr2:190881068
|
C | T | 1 | a0001c0001t0028 | 2 | HG02109.hp2 HG02622.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-17C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/18 | chr2 | 190881068 | ||||||
chr2:190963086
|
C | T | 1 | a0001c0001t0062 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 100 | chr2 | 190963086 | |||||
chr2:190963268
|
AT | A | 2 | a0001c0004t0017a0001c0008t0066 | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*285delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 285 | INFO_REALIGN_3_PRIME | chr2 | 190963268 | ||||
chr2:190963477
|
A | T | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(38): Show | 194 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*491A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 491 | chr2 | 190963477 | |||||
chr2:190963479
|
C | A | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(38): Show | 194 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*493C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 493 | chr2 | 190963479 | |||||
chr2:190963634
|
A | T | 1 | a0001c0001t0028 | 2 | HG02109.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*648A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 648 | chr2 | 190963634 | |||||
chr2:190963636
|
T | C | 1 | a0001c0001t0072 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 650 | chr2 | 190963636 | |||||
chr2:190963665
|
C | A | 1 | a0001c0001t0055 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 679 | chr2 | 190963665 | |||||
chr2:190963666
|
C | T | 1 | a0001c0001t0065 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*680C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 680 | chr2 | 190963666 | |||||
chr2:190963734
|
G | A | 1 | a0001c0001t0056 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*748G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 748 | chr2 | 190963734 | |||||
chr2:190963794
|
T | C | 3 | a0001c0004t0017a0001c0008t0066a0006c0011t0063 | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*808T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 808 | chr2 | 190963794 | |||||
chr2:190963870
|
A | G | 25 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(22): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*884A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 884 | chr2 | 190963870 | |||||
chr2:190963903
|
GT | G | 12 | a0001c0001t0028a0001c0001t0043a0001c0001t0045others(9): Show | 27 | HG01257.hp1 HG01884.hp1 HG02040.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*929delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 929 | INFO_REALIGN_3_PRIME | chr2 | 190963903 | ||||
chr2:190963960
|
A | G | 13 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(10): Show | 75 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*974A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 974 | chr2 | 190963960 | |||||
chr2:190964020
|
A | G | 2 | a0001c0001t0053a0001c0001t0058 | 2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1034A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1034 | chr2 | 190964020 | |||||
chr2:190964087
|
A | AT | 2 | a0001c0001t0028a0001c0001t0050 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1106dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1107 | INFO_REALIGN_3_PRIME | chr2 | 190964087 | ||||
chr2:190964403
|
AGTT | A | 14 | a0001c0001t0001a0001c0001t0026a0001c0001t0030others(11): Show | 94 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1421_*1423delGTT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1421 | INFO_REALIGN_3_PRIME | chr2 | 190964403 | ||||
chr2:190964428
|
CT | C | 7 | a0001c0001t0008a0001c0001t0043a0001c0001t0048others(4): Show | 20 | HG01261.hp2 HG02280.hp1 HG02486.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1451delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1451 | INFO_REALIGN_3_PRIME | chr2 | 190964428 | ||||
chr2:190964627
|
C | G | 9 | a0001c0001t0013a0001c0001t0014a0001c0001t0025others(6): Show | 18 | HG00597.hp2 HG00738.hp1 HG01069.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1641C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1641 | chr2 | 190964627 | |||||
chr2:190964655
|
T | C | 1 | a0001c0001t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1669T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1669 | chr2 | 190964655 | |||||
chr2:190964686
|
C | G | 14 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(11): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1700C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1700 | chr2 | 190964686 | |||||
chr2:190964748
|
T | C | 1 | a0006c0011t0063 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1762T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1762 | chr2 | 190964748 | |||||
chr2:190964788
|
AAATC | A | 2 | a0001c0001t0028a0001c0001t0050 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1809_*1812delTCAA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1809 | INFO_REALIGN_3_PRIME | chr2 | 190964788 | ||||
chr2:190964917
|
T | TAACCATT others(18): Show |
1 | a0001c0001t0039 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1932_*1956dupAACC others(21): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 1957 | INFO_REALIGN_3_PRIME | chr2 | 190964917 | ||||
chr2:190965040
|
C | T | 1 | a0001c0001t0026 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2054C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 2054 | chr2 | 190965040 | |||||
chr2:190965051
|
C | T | 13 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(10): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2065C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 2065 | chr2 | 190965051 | |||||
chr2:190965111
|
T | C | 1 | a0002c0003t0023 | 3 | NA18970.hp2 NA18978.hp2 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2125T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 2125 | chr2 | 190965111 | |||||
chr2:190965532
|
A | C | 1 | a0001c0001t0039 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 2546 | chr2 | 190965532 | |||||
chr2:190965548
|
A | G | 1 | a0001c0001t0074 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2562A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 18/18 | 2562 | chr2 | 190965548 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:190881493
|
G | A | 1 | a0001c0001t0043g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.386+23G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881493 | ||||||
chr2:190881502
|
G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0033others(2): Show | 7 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+32G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881502 | ||||||
chr2:190881507
|
T | G | 75 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(72): Show | 77 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.386+37T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881507 | ||||||
chr2:190881559
|
A | C | 1 | a0001c0001t0001g0346 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.386+89A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881559 | ||||||
chr2:190881757
|
C | T | 69 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(66): Show | 71 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.386+287C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881757 | ||||||
chr2:190881800
|
C | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.386+330C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881800 | ||||||
chr2:190881827
|
G | C | 1 | a0001c0001t0005g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.386+357G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881827 | ||||||
chr2:190881834
|
C | G | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.386+364C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881834 | ||||||
chr2:190881851
|
A | G | 1 | a0001c0001t0019g0039 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.386+381A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881851 | ||||||
chr2:190881984
|
G | A | 8 | a0001c0001t0013g0108a0001c0001t0013g0109a0001c0001t0013g0110others(5): Show | 8 | HG00597.hp2 HG02071.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.386+514G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190881984 | ||||||
chr2:190882022
|
G | T | 74 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(71): Show | 76 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.386+552G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190882022 | ||||||
chr2:190882129
|
G | A | 1 | a0001c0001t0052g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.386+659G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190882129 | ||||||
chr2:190882338
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.386+868T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190882338 | ||||||
chr2:190882422
|
C | G | 1 | a0001c0001t0056g0340 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.386+952C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190882422 | ||||||
chr2:190882504
|
A | G | 1 | a0001c0001t0005g0339 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.386+1034A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190882504 | ||||||
chr2:190883118
|
CAG | C | 3 | a0001c0001t0025g0029a0001c0001t0025g0338a0001c0001t0062g0337 | 4 | HG02630.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+1649_386+1650d others(4): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190883118 | ||||||
chr2:190883132
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0038g0032 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.386+1662T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190883132 | ||||||
chr2:190883689
|
T | A | 1 | a0001c0001t0003g0040 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.386+2219T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190883689 | ||||||
chr2:190883715
|
T | C | 1 | a0001c0001t0011g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.386+2245T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190883715 | ||||||
chr2:190884000
|
G | A | 2 | a0001c0001t0005g0105a0001c0001t0005g0117 | 2 | HG02015.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.386+2530G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884000 | ||||||
chr2:190884157
|
T | C | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.386+2687T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884157 | ||||||
chr2:190884309
|
A | C | 69 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(66): Show | 71 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.386+2839A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884309 | ||||||
chr2:190884402
|
T | C | 1 | a0001c0001t0073g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.386+2932T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884402 | ||||||
chr2:190884453
|
C | G | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.386+2983C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884453 | ||||||
chr2:190884618
|
T | A | 1 | a0001c0001t0062g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.386+3148T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884618 | ||||||
chr2:190884747
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(299): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.386+3277T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884747 | ||||||
chr2:190884806
|
CAAT | C | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+3337_386+3339d others(5): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884806 | ||||||
chr2:190884817
|
C | G | 72 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.386+3347C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884817 | ||||||
chr2:190884817
|
C | T | 1 | a0002c0003t0001g0293 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.386+3347C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884817 | ||||||
chr2:190884979
|
T | C | 72 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.386+3509T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190884979 | ||||||
chr2:190885197
|
A | AT | 68 | a0001c0001t0002g0042a0001c0001t0002g0071a0001c0001t0002g0072others(65): Show | 70 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.386+3739dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190885197 | |||||
chr2:190885284
|
C | T | 1 | a0001c0001t0062g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.386+3814C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190885284 | ||||||
chr2:190885287
|
G | C | 1 | a0001c0001t0016g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.386+3817G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190885287 | ||||||
chr2:190885474
|
G | C | 1 | a0001c0001t0064g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.386+4004G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190885474 | ||||||
chr2:190885703
|
CAT | C | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.386+4236_386+4237d others(4): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190885703 | |||||
chr2:190885795
|
A | T | 1 | a0001c0001t0012g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.386+4325A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190885795 | ||||||
chr2:190885860
|
A | T | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.386+4390A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190885860 | ||||||
chr2:190885869
|
TTTTA | T | 11 | a0001c0001t0005g0282a0001c0001t0005g0290a0001c0001t0005g0339others(8): Show | 11 | HG01109.hp1 HG02040.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.386+4415_386+4418d others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190885869 | |||||
chr2:190885948
|
A | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+4478A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190885948 | ||||||
chr2:190886010
|
CT | C | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+4542delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190886010 | |||||
chr2:190886439
|
A | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+4969A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190886439 | ||||||
chr2:190886517
|
AG | A | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.386+5048delG | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190886517 | ||||||
chr2:190886706
|
A | G | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.386+5236A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190886706 | ||||||
chr2:190886784
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.386+5314C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190886784 | ||||||
chr2:190886903
|
G | A | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.386+5433G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190886903 | ||||||
chr2:190886916
|
CA | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(294): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.386+5463delA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190886916 | |||||
chr2:190886995
|
A | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.386+5525A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190886995 | ||||||
chr2:190887109
|
CT | C | 4 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0046g0046others(1): Show | 4 | NA19006.hp2 NA19058.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+5642delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190887109 | |||||
chr2:190887184
|
A | G | 1 | a0001c0001t0004g0267 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.386+5714A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190887184 | ||||||
chr2:190887224
|
G | A | 1 | a0001c0001t0032g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.386+5754G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190887224 | ||||||
chr2:190887229
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.386+5759A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190887229 | ||||||
chr2:190887457
|
A | G | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.386+5987A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190887457 | ||||||
chr2:190887601
|
C | A | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(297): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.386+6131C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190887601 | ||||||
chr2:190887890
|
G | A | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.386+6420G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190887890 | ||||||
chr2:190888089
|
G | A | 3 | a0001c0001t0025g0029a0001c0001t0025g0338a0001c0001t0062g0337 | 4 | HG02630.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+6619G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888089 | ||||||
chr2:190888153
|
G | C | 1 | a0001c0001t0002g0294 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.386+6683G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888153 | ||||||
chr2:190888251
|
G | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.386+6781G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888251 | ||||||
chr2:190888563
|
T | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.387-6589T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888563 | ||||||
chr2:190888606
|
A | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-6546A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888606 | ||||||
chr2:190888729
|
T | G | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.387-6423T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888729 | ||||||
chr2:190888730
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.387-6422G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888730 | ||||||
chr2:190888731
|
A | T | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.387-6421A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888731 | ||||||
chr2:190888815
|
A | G | 2 | a0001c0001t0024g0264a0001c0001t0024g0265 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.387-6337A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190888815 | ||||||
chr2:190889077
|
A | G | 1 | a0001c0001t0027g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.387-6075A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889077 | ||||||
chr2:190889294
|
A | G | 2 | a0001c0001t0002g0333a0001c0001t0009g0334 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.387-5858A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889294 | ||||||
chr2:190889344
|
T | C | 3 | a0001c0001t0025g0029a0001c0001t0025g0338a0001c0001t0062g0337 | 4 | HG02630.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.387-5808T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889344 | ||||||
chr2:190889450
|
A | G | 14 | a0001c0001t0034g0261a0001c0002t0007g0269a0001c0002t0007g0270others(11): Show | 14 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.387-5702A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889450 | ||||||
chr2:190889594
|
T | C | 1 | a0001c0009t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.387-5558T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889594 | ||||||
chr2:190889738
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.387-5414C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889738 | ||||||
chr2:190889861
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.387-5291C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190889861 | ||||||
chr2:190890055
|
G | A | 1 | a0003c0007t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.387-5097G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890055 | ||||||
chr2:190890066
|
T | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(298): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.387-5086T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890066 | ||||||
chr2:190890095
|
C | T | 1 | a0001c0001t0056g0340 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.387-5057C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890095 | ||||||
chr2:190890124
|
T | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-5028T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890124 | ||||||
chr2:190890136
|
G | T | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-5016G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890136 | ||||||
chr2:190890163
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.387-4989A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890163 | ||||||
chr2:190890695
|
C | A | 9 | a0001c0001t0003g0008a0001c0001t0003g0040a0001c0001t0003g0041others(6): Show | 10 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.387-4457C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890695 | ||||||
chr2:190890780
|
T | C | 1 | a0001c0002t0007g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.387-4372T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890780 | ||||||
chr2:190890884
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.387-4268G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890884 | ||||||
chr2:190890894
|
A | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(298): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.387-4258A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890894 | ||||||
chr2:190890901
|
A | G | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.387-4251A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890901 | ||||||
chr2:190890902
|
G | A | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.387-4250G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190890902 | ||||||
chr2:190891031
|
A | AT | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(274): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.387-4111dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190891031 | |||||
chr2:190891031
|
A | ATTT | 14 | a0001c0001t0034g0261a0001c0002t0007g0269a0001c0002t0007g0270others(11): Show | 14 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.387-4113_387-4111d others(5): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190891031 | |||||
chr2:190891080
|
AT | A | 3 | a0001c0001t0043g0030a0001c0001t0048g0136a0001c0001t0052g0114 | 3 | HG02622.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.387-4067delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190891080 | |||||
chr2:190891098
|
A | T | 1 | a0001c0001t0006g0103 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.387-4054A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891098 | ||||||
chr2:190891377
|
G | A | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-3775G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891377 | ||||||
chr2:190891468
|
TA | T | 6 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0346others(3): Show | 7 | HG00673.hp2 HG00741.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-3672delA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190891468 | |||||
chr2:190891567
|
A | C | 1 | a0001c0001t0002g0294 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.387-3585A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891567 | ||||||
chr2:190891647
|
G | A | 1 | a0001c0001t0048g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.387-3505G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891647 | ||||||
chr2:190891675
|
A | G | 88 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.387-3477A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891675 | ||||||
chr2:190891698
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.387-3454T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891698 | ||||||
chr2:190891936
|
A | T | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.387-3216A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891936 | ||||||
chr2:190891992
|
A | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-3160A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190891992 | ||||||
chr2:190892091
|
AC | A | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-3060delC | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892091 | ||||||
chr2:190892104
|
T | A | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.387-3048T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892104 | ||||||
chr2:190892197
|
T | A | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.387-2955T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892197 | ||||||
chr2:190892239
|
G | C | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.387-2913G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892239 | ||||||
chr2:190892245
|
C | G | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.387-2907C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892245 | ||||||
chr2:190892271
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.387-2881C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892271 | ||||||
chr2:190892351
|
C | G | 5 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0255others(2): Show | 5 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-2801C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892351 | ||||||
chr2:190892577
|
G | A | 1 | a0001c0001t0006g0054 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.387-2575G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892577 | ||||||
chr2:190892757
|
G | A | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-2395G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892757 | ||||||
chr2:190892906
|
C | T | 1 | a0001c0001t0006g0052 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.387-2246C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892906 | ||||||
chr2:190892939
|
A | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-2213A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892939 | ||||||
chr2:190892965
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.387-2187G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190892965 | ||||||
chr2:190893031
|
A | G | 1 | a0001c0001t0005g0251 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.387-2121A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893031 | ||||||
chr2:190893191
|
A | G | 5 | a0001c0001t0008g0011a0001c0001t0008g0133a0001c0001t0008g0134others(2): Show | 6 | HG01261.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.387-1961A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893191 | ||||||
chr2:190893442
|
A | G | 4 | a0001c0001t0020g0099a0001c0001t0020g0100a0001c0001t0020g0101others(1): Show | 4 | NA18939.hp2 NA18968.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-1710A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893442 | ||||||
chr2:190893616
|
C | T | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.387-1536C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893616 | ||||||
chr2:190893630
|
C | G | 21 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(18): Show | 24 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.387-1522C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893630 | ||||||
chr2:190893635
|
G | A | 21 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(18): Show | 24 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.387-1517G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893635 | ||||||
chr2:190893638
|
T | C | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-1514T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893638 | ||||||
chr2:190893690
|
A | G | 6 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-1462A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893690 | ||||||
chr2:190893730
|
G | A | 6 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-1422G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893730 | ||||||
chr2:190893784
|
C | T | 1 | a0001c0001t0038g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.387-1368C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893784 | ||||||
chr2:190893904
|
T | G | 10 | a0001c0001t0008g0011a0001c0001t0008g0017a0001c0001t0008g0133others(7): Show | 12 | HG01261.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-1248T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893904 | ||||||
chr2:190893915
|
C | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.387-1237C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190893915 | ||||||
chr2:190894042
|
T | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(274): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.387-1110T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894042 | ||||||
chr2:190894127
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.387-1025T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894127 | ||||||
chr2:190894234
|
C | T | 1 | a0001c0001t0031g0098 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.387-918C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894234 | ||||||
chr2:190894343
|
G | T | 5 | a0001c0001t0011g0053a0001c0001t0011g0094a0001c0001t0011g0095others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.387-809G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894343 | ||||||
chr2:190894347
|
GT | G | 188 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(185): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.387-798delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190894347 | |||||
chr2:190894467
|
G | A | 1 | a0001c0001t0016g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.387-685G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894467 | ||||||
chr2:190894482
|
C | T | 1 | a0001c0001t0011g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.387-670C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894482 | ||||||
chr2:190894575
|
G | C | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0346others(1): Show | 5 | HG00741.hp2 HG01074.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.387-577G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894575 | ||||||
chr2:190894805
|
G | A | 2 | a0001c0001t0043g0030a0001c0001t0048g0136 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.387-347G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894805 | ||||||
chr2:190894819
|
A | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.387-333A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894819 | ||||||
chr2:190894827
|
A | C | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.387-325A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894827 | ||||||
chr2:190894838
|
G | A | 88 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.387-314G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894838 | ||||||
chr2:190894887
|
G | A | 2 | a0001c0001t0004g0252a0001c0001t0004g0253 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.387-265G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894887 | ||||||
chr2:190894898
|
A | G | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-254A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894898 | ||||||
chr2:190894951
|
AT | A | 85 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(82): Show | 89 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.387-193delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 190894951 | |||||
chr2:190894983
|
A | G | 1 | a0001c0001t0012g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.387-169A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894983 | ||||||
chr2:190894998
|
T | A | 1 | a0002c0003t0001g0144 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.387-154T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190894998 | ||||||
chr2:190895050
|
C | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.387-102C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190895050 | ||||||
chr2:190895095
|
A | C | 1 | a0001c0001t0005g0258 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.387-57A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 1/17 | chr2 | 190895095 | ||||||
chr2:190895299
|
A | C | 1 | a0001c0001t0053g0332 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.483+51A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 2/17 | chr2 | 190895299 | ||||||
chr2:190896534
|
T | C | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+809T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190896534 | ||||||
chr2:190896827
|
A | G | 6 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.605+1102A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190896827 | ||||||
chr2:190897031
|
C | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.605+1306C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897031 | ||||||
chr2:190897486
|
T | C | 2 | a0001c0001t0003g0055a0001c0001t0003g0056 | 2 | HG02132.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.605+1761T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897486 | ||||||
chr2:190897539
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.605+1814A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897539 | ||||||
chr2:190897761
|
A | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.605+2036A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897761 | ||||||
chr2:190897783
|
G | C | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.605+2058G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897783 | ||||||
chr2:190897872
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.605+2147T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897872 | ||||||
chr2:190897927
|
G | A | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.605+2202G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190897927 | ||||||
chr2:190898084
|
T | C | 1 | a0001c0001t0064g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.605+2359T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898084 | ||||||
chr2:190898308
|
T | A | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.606-2256T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898308 | ||||||
chr2:190898555
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0145 | 3 | NA18939.hp1 NA19064.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.606-2009T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898555 | ||||||
chr2:190898693
|
G | A | 5 | a0001c0001t0011g0053a0001c0001t0011g0094a0001c0001t0011g0095others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.606-1871G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898693 | ||||||
chr2:190898759
|
G | C | 88 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.606-1805G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898759 | ||||||
chr2:190898782
|
C | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.606-1782C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898782 | ||||||
chr2:190898838
|
G | A | 2 | a0001c0001t0043g0030a0001c0001t0048g0136 | 2 | HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.606-1726G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898838 | ||||||
chr2:190898859
|
C | G | 3 | a0001c0002t0007g0278a0001c0002t0007g0279a0001c0002t0007g0280 | 3 | NA18950.hp2 NA18993.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.606-1705C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898859 | ||||||
chr2:190898918
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.606-1646G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190898918 | ||||||
chr2:190899026
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.606-1538T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899026 | ||||||
chr2:190899067
|
T | C | 2 | a0001c0001t0003g0058a0001c0001t0006g0057 | 2 | HG01361.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.606-1497T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899067 | ||||||
chr2:190899235
|
A | G | 1 | a0001c0001t0064g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.606-1329A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899235 | ||||||
chr2:190899342
|
G | A | 87 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(84): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.606-1222G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899342 | ||||||
chr2:190899575
|
C | G | 11 | a0001c0001t0005g0019a0001c0001t0012g0019a0001c0001t0012g0199others(8): Show | 12 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.606-989C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899575 | ||||||
chr2:190899629
|
T | C | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.606-935T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899629 | ||||||
chr2:190899631
|
C | T | 1 | a0001c0001t0005g0124 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.606-933C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899631 | ||||||
chr2:190899669
|
G | T | 1 | a0003c0007t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.606-895G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899669 | ||||||
chr2:190899728
|
G | A | 2 | a0001c0001t0003g0059a0001c0001t0003g0104 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.606-836G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190899728 | ||||||
chr2:190899862
|
C | CT | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.606-696dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 190899862 | |||||
chr2:190900030
|
AAC | A | 88 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.606-532_606-531del others(2): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 190900030 | |||||
chr2:190900133
|
C | T | 1 | a0001c0001t0024g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.606-431C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190900133 | ||||||
chr2:190900332
|
A | G | 3 | a0001c0001t0025g0029a0001c0001t0025g0338a0001c0001t0062g0337 | 4 | HG02630.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.606-232A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190900332 | ||||||
chr2:190900366
|
C | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.606-198C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190900366 | ||||||
chr2:190900480
|
T | C | 116 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(113): Show | 122 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.606-84T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 3/17 | chr2 | 190900480 | ||||||
chr2:190900880
|
T | C | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.735+187T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190900880 | ||||||
chr2:190901067
|
A | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.735+374A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901067 | ||||||
chr2:190901205
|
C | T | 1 | a0001c0001t0035g0331 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.735+512C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901205 | ||||||
chr2:190901228
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.735+535A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901228 | ||||||
chr2:190901307
|
G | T | 1 | a0001c0001t0073g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.735+614G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901307 | ||||||
chr2:190901363
|
AG | A | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-583delG | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901363 | ||||||
chr2:190901487
|
G | A | 3 | a0001c0001t0043g0030a0001c0001t0048g0136a0001c0001t0052g0114 | 3 | HG02622.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.736-460G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901487 | ||||||
chr2:190901574
|
T | C | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-373T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901574 | ||||||
chr2:190901664
|
C | T | 1 | a0001c0001t0008g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.736-283C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901664 | ||||||
chr2:190901921
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.736-26T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 4/17 | chr2 | 190901921 | ||||||
chr2:190902116
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(6): Show | 12 | HG00408.hp2 HG02071.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.815+90A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902116 | ||||||
chr2:190902173
|
T | G | 73 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(70): Show | 75 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.815+147T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902173 | ||||||
chr2:190902272
|
A | G | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.815+246A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902272 | ||||||
chr2:190902486
|
A | G | 1 | a0001c0001t0031g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.815+460A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902486 | ||||||
chr2:190902492
|
G | C | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.815+466G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902492 | ||||||
chr2:190902514
|
A | T | 1 | a0001c0001t0004g0250 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.815+488A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902514 | ||||||
chr2:190902557
|
G | A | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.815+531G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902557 | ||||||
chr2:190902715
|
G | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.815+689G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902715 | ||||||
chr2:190902754
|
T | C | 6 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.815+728T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902754 | ||||||
chr2:190902857
|
A | G | 1 | a0001c0001t0051g0113 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.815+831A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902857 | ||||||
chr2:190902916
|
A | G | 1 | a0001c0001t0003g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.815+890A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902916 | ||||||
chr2:190902962
|
G | A | 1 | a0001c0001t0008g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.815+936G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190902962 | ||||||
chr2:190903060
|
A | T | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.815+1034A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903060 | ||||||
chr2:190903242
|
A | G | 1 | a0001c0001t0009g0330 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.815+1216A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903242 | ||||||
chr2:190903333
|
C | T | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.815+1307C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903333 | ||||||
chr2:190903590
|
A | G | 3 | a0001c0001t0009g0328a0001c0001t0009g0329a0001c0001t0019g0327 | 3 | HG01192.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.816-1414A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903590 | ||||||
chr2:190903638
|
A | G | 1 | a0001c0001t0008g0135 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.816-1366A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903638 | ||||||
chr2:190903804
|
T | G | 1 | a0001c0001t0002g0294 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.816-1200T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903804 | ||||||
chr2:190903953
|
G | C | 1 | a0001c0001t0009g0298 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.816-1051G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190903953 | ||||||
chr2:190904040
|
G | A | 1 | a0001c0001t0011g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.816-964G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904040 | ||||||
chr2:190904055
|
T | C | 1 | a0001c0001t0005g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.816-949T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904055 | ||||||
chr2:190904080
|
G | C | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-924G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904080 | ||||||
chr2:190904092
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.816-912T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904092 | ||||||
chr2:190904200
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.816-804A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904200 | ||||||
chr2:190904247
|
C | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.816-757C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904247 | ||||||
chr2:190904352
|
C | T | 2 | a0001c0001t0013g0111a0001c0001t0061g0112 | 2 | HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.816-652C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904352 | ||||||
chr2:190904450
|
C | T | 2 | a0001c0001t0005g0248a0001c0001t0010g0249 | 2 | HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.816-554C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904450 | ||||||
chr2:190904596
|
G | C | 1 | a0001c0001t0005g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.816-408G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904596 | ||||||
chr2:190904803
|
A | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.816-201A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904803 | ||||||
chr2:190904865
|
T | C | 21 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(18): Show | 24 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.816-139T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 5/17 | chr2 | 190904865 | ||||||
chr2:190905352
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG01123.hp2 HG01255.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.979+185G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190905352 | ||||||
chr2:190905375
|
A | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.979+208A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190905375 | ||||||
chr2:190905508
|
A | C | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+341A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190905508 | ||||||
chr2:190905509
|
G | C | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+342G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190905509 | ||||||
chr2:190905672
|
T | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+505T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190905672 | ||||||
chr2:190905887
|
T | G | 81 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(78): Show | 83 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.979+720T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190905887 | ||||||
chr2:190906016
|
A | T | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.979+849A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190906016 | ||||||
chr2:190906168
|
G | A | 115 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(112): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.979+1001G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190906168 | ||||||
chr2:190906694
|
C | T | 1 | a0001c0001t0025g0338 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979+1527C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190906694 | ||||||
chr2:190906726
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.979+1559A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190906726 | ||||||
chr2:190906831
|
A | C | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.979+1664A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190906831 | ||||||
chr2:190906907
|
A | G | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+1740A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190906907 | ||||||
chr2:190906931
|
GT | G | 8 | a0001c0001t0002g0294a0001c0001t0050g0121a0001c0004t0017g0034others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.979+1780delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190906931 | |||||
chr2:190907057
|
T | C | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.979+1890T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907057 | ||||||
chr2:190907149
|
C | T | 1 | a0001c0001t0006g0093 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.979+1982C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907149 | ||||||
chr2:190907166
|
T | C | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.979+1999T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907166 | ||||||
chr2:190907170
|
C | T | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.979+2003C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907170 | ||||||
chr2:190907243
|
G | GT | 87 | a0001c0001t0002g0326a0001c0001t0004g0004a0001c0001t0004g0005others(84): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.979+2091dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190907243 | |||||
chr2:190907266
|
G | A | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(297): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.979+2099G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907266 | ||||||
chr2:190907298
|
G | A | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(297): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.979+2131G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907298 | ||||||
chr2:190907299
|
T | C | 1 | a0001c0001t0020g0099 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.979+2132T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907299 | ||||||
chr2:190907316
|
G | A | 24 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0027others(21): Show | 28 | HG01433.hp1 HG01496.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.979+2149G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907316 | ||||||
chr2:190907319
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.979+2152G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907319 | ||||||
chr2:190907351
|
G | A | 1 | a0001c0001t0020g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.979+2184G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907351 | ||||||
chr2:190907382
|
C | T | 5 | a0001c0001t0008g0011a0001c0001t0008g0133a0001c0001t0008g0134others(2): Show | 6 | HG01261.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+2215C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907382 | ||||||
chr2:190907438
|
T | TAG | 4 | a0001c0001t0011g0053a0001c0001t0011g0095a0001c0001t0011g0096others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2275_979+2276d others(4): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190907438 | |||||
chr2:190907443
|
A | G | 9 | a0001c0001t0003g0008a0001c0001t0003g0040a0001c0001t0003g0041others(6): Show | 10 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.979+2276A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907443 | ||||||
chr2:190907625
|
T | TATTA | 5 | a0001c0001t0014g0243a0001c0001t0014g0244a0001c0001t0014g0246others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2460_979+2461i others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190907625 | |||||
chr2:190907644
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.979+2477T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907644 | ||||||
chr2:190907923
|
C | T | 1 | a0001c0001t0064g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.980-2340C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907923 | ||||||
chr2:190907980
|
A | G | 24 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(21): Show | 27 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.980-2283A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190907980 | ||||||
chr2:190908012
|
A | C | 1 | a0001c0001t0022g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.980-2251A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908012 | ||||||
chr2:190908060
|
T | A | 24 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(21): Show | 27 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.980-2203T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908060 | ||||||
chr2:190908378
|
T | C | 1 | a0001c0001t0024g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.980-1885T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908378 | ||||||
chr2:190908462
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.980-1801A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908462 | ||||||
chr2:190908894
|
A | G | 1 | a0001c0001t0009g0310 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.980-1369A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908894 | ||||||
chr2:190908921
|
ATTTAT | A | 6 | a0002c0003t0001g0144a0002c0003t0001g0153a0002c0003t0001g0293others(3): Show | 6 | NA18954.hp1 NA18970.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1341_980-1337d others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908921 | ||||||
chr2:190908925
|
A | G | 1 | a0001c0001t0005g0258 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.980-1338A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908925 | ||||||
chr2:190908927
|
G | A | 6 | a0002c0003t0001g0144a0002c0003t0001g0153a0002c0003t0001g0293others(3): Show | 6 | NA18954.hp1 NA18970.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1336G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908927 | ||||||
chr2:190908928
|
T | A | 6 | a0002c0003t0001g0144a0002c0003t0001g0153a0002c0003t0001g0293others(3): Show | 6 | NA18954.hp1 NA18970.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-1335T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190908928 | ||||||
chr2:190909053
|
TACTAATT others(3): Show |
T | 1 | a0001c0001t0027g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.980-1191_980-1182d others(12): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190909053 | |||||
chr2:190909151
|
G | A | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-1112G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909151 | ||||||
chr2:190909167
|
CA | C | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-1092delA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190909167 | |||||
chr2:190909180
|
A | G | 1 | a0001c0001t0001g0346 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.980-1083A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909180 | ||||||
chr2:190909215
|
A | AT | 87 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(84): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.980-1047dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr2 | 190909215 | |||||
chr2:190909306
|
A | G | 1 | a0001c0001t0004g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.980-957A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909306 | ||||||
chr2:190909330
|
A | G | 2 | a0001c0001t0024g0264a0001c0001t0024g0265 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-933A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909330 | ||||||
chr2:190909382
|
T | C | 115 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(112): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.980-881T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909382 | ||||||
chr2:190909404
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.980-859C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909404 | ||||||
chr2:190909475
|
C | A | 1 | a0001c0001t0058g0311 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.980-788C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909475 | ||||||
chr2:190909587
|
G | A | 1 | a0001c0001t0010g0209 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.980-676G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909587 | ||||||
chr2:190909639
|
T | G | 1 | a0001c0001t0071g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.980-624T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909639 | ||||||
chr2:190909834
|
G | A | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.980-429G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909834 | ||||||
chr2:190909884
|
A | C | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980-379A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909884 | ||||||
chr2:190909891
|
A | G | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980-372A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909891 | ||||||
chr2:190909907
|
A | G | 2 | a0001c0001t0004g0252a0001c0001t0004g0253 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.980-356A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190909907 | ||||||
chr2:190910030
|
T | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.980-233T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190910030 | ||||||
chr2:190910037
|
C | T | 68 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(65): Show | 72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.980-226C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190910037 | ||||||
chr2:190910054
|
T | A | 1 | a0001c0001t0002g0300 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.980-209T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190910054 | ||||||
chr2:190910151
|
A | G | 1 | a0001c0001t0002g0297 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.980-112A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 6/17 | chr2 | 190910151 | ||||||
chr2:190910357
|
C | CT | 7 | a0001c0001t0005g0290a0001c0001t0016g0119a0001c0004t0017g0034others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038+47dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190910357 | |||||
chr2:190910457
|
A | G | 4 | a0001c0001t0004g0021a0001c0001t0004g0240a0001c0001t0005g0021others(1): Show | 4 | HG00733.hp1 HG01243.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+136A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190910457 | ||||||
chr2:190910645
|
C | T | 1 | a0001c0001t0059g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1038+324C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190910645 | ||||||
chr2:190910745
|
A | G | 1 | a0001c0001t0004g0238 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1038+424A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190910745 | ||||||
chr2:190910962
|
G | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(274): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.1038+641G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190910962 | ||||||
chr2:190910984
|
A | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+663A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190910984 | ||||||
chr2:190911033
|
T | C | 2 | a0001c0001t0009g0312a0001c0001t0009g0325 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1038+712T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911033 | ||||||
chr2:190911043
|
G | A | 1 | a0001c0001t0070g0313 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1038+722G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911043 | ||||||
chr2:190911308
|
C | G | 10 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0042others(7): Show | 12 | HG01496.hp1 NA18940.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+987C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911308 | ||||||
chr2:190911524
|
C | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+1203C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911524 | ||||||
chr2:190911635
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1038+1314A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911635 | ||||||
chr2:190911763
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1038+1442T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911763 | ||||||
chr2:190911783
|
T | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1038+1462T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911783 | ||||||
chr2:190911893
|
C | T | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1038+1572C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911893 | ||||||
chr2:190911904
|
A | T | 1 | a0001c0001t0047g0237 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1038+1583A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911904 | ||||||
chr2:190911921
|
T | A | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1038+1600T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190911921 | ||||||
chr2:190912000
|
G | A | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+1679G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912000 | ||||||
chr2:190912346
|
C | CT | 10 | a0001c0001t0001g0031a0001c0001t0001g0185a0001c0001t0002g0335others(7): Show | 10 | HG00323.hp2 HG01167.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+2044dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190912346 | |||||
chr2:190912346
|
C | CTT | 78 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(75): Show | 83 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1038+2043_1038+204 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190912346 | |||||
chr2:190912346
|
CT | C | 86 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(83): Show | 89 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1038+2044delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190912346 | |||||
chr2:190912448
|
C | G | 2 | a0001c0001t0014g0246a0001c0001t0014g0247 | 2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1038+2127C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912448 | ||||||
chr2:190912572
|
G | A | 1 | a0001c0001t0005g0214 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1038+2251G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912572 | ||||||
chr2:190912577
|
A | G | 1 | a0001c0001t0048g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1038+2256A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912577 | ||||||
chr2:190912589
|
A | G | 95 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(92): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1038+2268A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912589 | ||||||
chr2:190912617
|
A | G | 1 | a0001c0001t0020g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1038+2296A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912617 | ||||||
chr2:190912810
|
A | G | 2 | a0002c0003t0001g0144a0002c0003t0001g0153 | 2 | NA18954.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1038+2489A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912810 | ||||||
chr2:190912829
|
G | A | 4 | a0001c0001t0020g0099a0001c0001t0020g0100a0001c0001t0020g0101others(1): Show | 4 | NA18939.hp2 NA18968.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+2508G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190912829 | ||||||
chr2:190913042
|
AT | A | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(295): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1038+2732delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190913042 | |||||
chr2:190913573
|
A | T | 1 | a0001c0001t0064g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1038+3252A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190913573 | ||||||
chr2:190913688
|
AG | A | 6 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+3369delG | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190913688 | |||||
chr2:190913888
|
C | T | 10 | a0001c0001t0002g0028a0001c0001t0002g0319a0001c0001t0002g0320others(7): Show | 11 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.1038+3567C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190913888 | ||||||
chr2:190914242
|
G | A | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1038+3921G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914242 | ||||||
chr2:190914270
|
T | C | 1 | a0001c0001t0053g0332 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1038+3949T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914270 | ||||||
chr2:190914359
|
T | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0260 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1038+4038T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914359 | ||||||
chr2:190914605
|
A | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+4284A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914605 | ||||||
chr2:190914611
|
C | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1038+4290C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914611 | ||||||
chr2:190914701
|
C | G | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1038+4380C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914701 | ||||||
chr2:190914954
|
C | T | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+4633C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914954 | ||||||
chr2:190914979
|
T | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+4658T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190914979 | ||||||
chr2:190915028
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1038+4707T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915028 | ||||||
chr2:190915030
|
T | TTTTTC | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+4713_1038+471 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190915030 | |||||
chr2:190915140
|
G | A | 2 | a0001c0001t0024g0264a0001c0001t0024g0265 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038+4819G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915140 | ||||||
chr2:190915152
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1038+4831G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915152 | ||||||
chr2:190915157
|
A | AT | 6 | a0001c0001t0002g0088a0001c0001t0002g0309a0001c0001t0003g0087others(3): Show | 6 | HG03017.hp2 HG04199.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+4852dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190915157 | |||||
chr2:190915388
|
T | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+5067T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915388 | ||||||
chr2:190915538
|
T | C | 1 | a0001c0001t0055g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1038+5217T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915538 | ||||||
chr2:190915695
|
A | T | 1 | a0001c0001t0005g0124 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1039-5329A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915695 | ||||||
chr2:190915772
|
A | G | 19 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(16): Show | 22 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039-5252A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915772 | ||||||
chr2:190915833
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1039-5191G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915833 | ||||||
chr2:190915902
|
C | G | 1 | a0001c0001t0064g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1039-5122C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190915902 | ||||||
chr2:190916014
|
T | G | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1039-5010T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916014 | ||||||
chr2:190916075
|
G | A | 1 | a0001c0001t0024g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1039-4949G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916075 | ||||||
chr2:190916256
|
C | A | 2 | a0001c0001t0003g0062a0001c0001t0003g0091 | 2 | NA18955.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1039-4768C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916256 | ||||||
chr2:190916437
|
G | A | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039-4587G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916437 | ||||||
chr2:190916443
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1039-4581A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916443 | ||||||
chr2:190916689
|
A | G | 1 | a0001c0001t0043g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1039-4335A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916689 | ||||||
chr2:190916994
|
G | A | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1039-4030G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190916994 | ||||||
chr2:190917042
|
G | A | 115 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(112): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1039-3982G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190917042 | ||||||
chr2:190917734
|
A | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-3290A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190917734 | ||||||
chr2:190917804
|
TC | T | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-3219delC | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190917804 | ||||||
chr2:190917866
|
A | G | 3 | a0001c0001t0043g0030a0001c0001t0048g0136a0001c0001t0052g0114 | 3 | HG02622.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1039-3158A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190917866 | ||||||
chr2:190917992
|
T | G | 1 | a0001c0001t0012g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1039-3032T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190917992 | ||||||
chr2:190917998
|
C | A | 1 | a0001c0001t0005g0282 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1039-3026C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190917998 | ||||||
chr2:190918058
|
T | G | 1 | a0001c0001t0010g0254 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039-2966T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918058 | ||||||
chr2:190918071
|
G | A | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-2953G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918071 | ||||||
chr2:190918139
|
C | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1039-2885C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918139 | ||||||
chr2:190918180
|
T | G | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1039-2844T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918180 | ||||||
chr2:190918293
|
C | G | 1 | a0001c0001t0004g0234 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1039-2731C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918293 | ||||||
chr2:190918339
|
T | C | 2 | a0001c0001t0068g0138a0001c0001t0072g0137 | 2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-2685T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918339 | ||||||
chr2:190918374
|
T | C | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1039-2650T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918374 | ||||||
chr2:190918408
|
G | A | 1 | a0001c0001t0004g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1039-2616G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918408 | ||||||
chr2:190918436
|
T | C | 1 | a0001c0001t0005g0214 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1039-2588T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918436 | ||||||
chr2:190918450
|
G | A | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1039-2574G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918450 | ||||||
chr2:190918620
|
A | G | 1 | a0001c0001t0010g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1039-2404A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918620 | ||||||
chr2:190918734
|
T | C | 1 | a0001c0001t0004g0250 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1039-2290T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918734 | ||||||
chr2:190918748
|
T | G | 3 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285 | 3 | NA18956.hp2 NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1039-2276T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918748 | ||||||
chr2:190918848
|
G | A | 1 | a0001c0001t0008g0011 | 2 | HG01261.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1039-2176G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918848 | ||||||
chr2:190918864
|
A | G | 1 | a0001c0001t0046g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1039-2160A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918864 | ||||||
chr2:190918882
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1039-2142A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918882 | ||||||
chr2:190918909
|
AACATTTA others(22): Show |
A | 1 | a0001c0001t0004g0233 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1039-2113_1039-208 others(33): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190918909 | |||||
chr2:190918937
|
A | T | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1039-2087A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918937 | ||||||
chr2:190918949
|
C | A | 2 | a0001c0001t0003g0058a0001c0001t0006g0057 | 2 | HG01361.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1039-2075C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190918949 | ||||||
chr2:190919066
|
GAA | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(78): Show | 92 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.1039-1954_1039-195 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 190919066 | |||||
chr2:190919261
|
C | G | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-1763C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190919261 | ||||||
chr2:190919341
|
T | C | 1 | a0001c0001t0006g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1039-1683T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190919341 | ||||||
chr2:190919364
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1039-1660C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190919364 | ||||||
chr2:190919787
|
T | C | 2 | a0001c0005t0013g0106a0001c0005t0013g0107 | 2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1039-1237T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190919787 | ||||||
chr2:190920049
|
A | G | 94 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(91): Show | 100 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1039-975A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920049 | ||||||
chr2:190920075
|
G | T | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039-949G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920075 | ||||||
chr2:190920427
|
A | T | 1 | a0001c0001t0005g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1039-597A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920427 | ||||||
chr2:190920590
|
A | G | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1039-434A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920590 | ||||||
chr2:190920689
|
T | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1039-335T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920689 | ||||||
chr2:190920905
|
A | G | 1 | a0001c0001t0024g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1039-119A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920905 | ||||||
chr2:190920950
|
A | G | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1039-74A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190920950 | ||||||
chr2:190921000
|
T | C | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-24T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 7/17 | chr2 | 190921000 | ||||||
chr2:190921452
|
T | G | 1 | a0001c0001t0002g0299 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1130+249T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190921452 | ||||||
chr2:190921517
|
A | G | 1 | a0001c0001t0059g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1130+314A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190921517 | ||||||
chr2:190921659
|
T | C | 1 | a0001c0001t0010g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1130+456T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190921659 | ||||||
chr2:190921780
|
A | C | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1130+577A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190921780 | ||||||
chr2:190922008
|
G | A | 1 | a0001c0001t0013g0111 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1130+805G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190922008 | ||||||
chr2:190922115
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1130+912G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190922115 | ||||||
chr2:190922142
|
T | C | 80 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(77): Show | 85 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1130+939T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190922142 | ||||||
chr2:190922663
|
C | T | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131-1254C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190922663 | ||||||
chr2:190922755
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0259 | 2 | NA19070.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1131-1162A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190922755 | ||||||
chr2:190922856
|
C | T | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-1061C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190922856 | ||||||
chr2:190923038
|
C | T | 80 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(77): Show | 82 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1131-879C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923038 | ||||||
chr2:190923053
|
A | T | 81 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(78): Show | 83 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1131-864A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923053 | ||||||
chr2:190923169
|
A | G | 1 | a0001c0001t0014g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1131-748A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923169 | ||||||
chr2:190923353
|
G | T | 4 | a0001c0001t0021g0127a0001c0001t0021g0128a0001c0001t0021g0129others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131-564G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923353 | ||||||
chr2:190923691
|
G | A | 107 | a0001c0001t0002g0306a0001c0001t0004g0004a0001c0001t0004g0005others(104): Show | 113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1131-226G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923691 | ||||||
chr2:190923756
|
A | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0039g0180 | 3 | HG00639.hp2 HG00738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1131-161A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923756 | ||||||
chr2:190923794
|
C | T | 1 | a0001c0001t0012g0231 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1131-123C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923794 | ||||||
chr2:190923836
|
C | T | 1 | a0001c0001t0056g0340 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1131-81C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 9/17 | chr2 | 190923836 | ||||||
chr2:190924203
|
T | A | 1 | a0002c0003t0001g0293 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1197+220T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 10/17 | chr2 | 190924203 | ||||||
chr2:190924366
|
T | TA | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1198-176dupA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 190924366 | |||||
chr2:190924478
|
A | G | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1198-65A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 10/17 | chr2 | 190924478 | ||||||
chr2:190924480
|
A | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1198-63A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 10/17 | chr2 | 190924480 | ||||||
chr2:190924501
|
C | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1198-42C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 10/17 | chr2 | 190924501 | ||||||
chr2:190924533
|
G | T | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-10G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 10/17 | chr2 | 190924533 | ||||||
chr2:190924797
|
C | T | 78 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(75): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1248+204C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190924797 | ||||||
chr2:190924892
|
C | T | 1 | a0001c0001t0010g0209 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1248+299C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190924892 | ||||||
chr2:190924945
|
A | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1248+352A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190924945 | ||||||
chr2:190925064
|
A | G | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1248+471A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925064 | ||||||
chr2:190925071
|
A | T | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1248+478A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925071 | ||||||
chr2:190925146
|
G | T | 1 | a0001c0001t0013g0111 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1248+553G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925146 | ||||||
chr2:190925181
|
G | A | 6 | a0001c0001t0004g0216a0001c0001t0005g0206a0001c0001t0005g0215others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248+588G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925181 | ||||||
chr2:190925271
|
A | G | 2 | a0001c0001t0002g0333a0001c0001t0009g0334 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1248+678A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925271 | ||||||
chr2:190925842
|
C | G | 1 | a0001c0001t0006g0086 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1248+1249C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925842 | ||||||
chr2:190925885
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1248+1292A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190925885 | ||||||
chr2:190926148
|
C | T | 1 | a0001c0012t0037g0245 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1249-1158C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190926148 | ||||||
chr2:190926221
|
T | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1249-1085T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190926221 | ||||||
chr2:190926735
|
T | C | 10 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0042others(7): Show | 12 | HG01496.hp1 NA18940.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1249-571T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190926735 | ||||||
chr2:190926782
|
C | T | 1 | a0001c0001t0005g0282 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1249-524C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190926782 | ||||||
chr2:190926808
|
A | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1249-498A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190926808 | ||||||
chr2:190926862
|
T | A | 3 | a0001c0001t0024g0193a0001c0001t0024g0264a0001c0001t0024g0265 | 3 | HG02258.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1249-444T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190926862 | ||||||
chr2:190927087
|
T | G | 1 | a0001c0001t0005g0339 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1249-219T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190927087 | ||||||
chr2:190927105
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1249-201T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 11/17 | chr2 | 190927105 | ||||||
chr2:190927503
|
A | ATT | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1425+24_1425+25dup others(2): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190927503 | |||||
chr2:190927673
|
G | T | 1 | a0001c0001t0028g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1425+191G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190927673 | ||||||
chr2:190927742
|
C | T | 1 | a0001c0001t0046g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1425+260C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190927742 | ||||||
chr2:190927744
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1425+262T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190927744 | ||||||
chr2:190927862
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0260 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1425+380T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190927862 | ||||||
chr2:190927960
|
T | A | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1425+478T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190927960 | ||||||
chr2:190927980
|
A | C | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1425+498A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190927980 | ||||||
chr2:190928121
|
G | A | 87 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(84): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1425+639G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190928121 | ||||||
chr2:190928288
|
T | TA | 8 | a0001c0001t0003g0009a0001c0001t0003g0062a0001c0001t0003g0063others(5): Show | 9 | NA18955.hp1 NA18960.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1425+807dupA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928288 | |||||
chr2:190928337
|
CT | C | 6 | a0001c0001t0001g0160a0001c0001t0002g0294a0001c0001t0002g0301others(3): Show | 6 | HG01070.hp2 HG02896.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1425+870delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928337 | |||||
chr2:190928554
|
C | T | 1 | a0001c0002t0007g0277 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1425+1072C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190928554 | ||||||
chr2:190928639
|
A | G | 2 | a0001c0001t0024g0264a0001c0001t0024g0265 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1425+1157A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190928639 | ||||||
chr2:190928708
|
C | CT | 105 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(102): Show | 111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1425+1241dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928708 | |||||
chr2:190928723
|
T | A | 3 | a0001c0001t0001g0148a0001c0001t0002g0333a0001c0001t0009g0334 | 3 | HG00280.hp2 HG01106.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1425+1241T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190928723 | ||||||
chr2:190928892
|
G | GT | 129 | a0001c0001t0001g0031a0001c0001t0001g0145a0001c0001t0001g0177others(126): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1425+1434dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928892 | |||||
chr2:190928892
|
G | GTT | 83 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(80): Show | 86 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1425+1433_1425+143 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928892 | |||||
chr2:190928892
|
G | GTTT | 12 | a0001c0001t0002g0084a0001c0001t0003g0040a0001c0001t0003g0050others(9): Show | 12 | HG01109.hp1 HG01261.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1425+1432_1425+143 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928892 | |||||
chr2:190928923
|
CTTGTT | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1425+1448_1425+145 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190928923 | |||||
chr2:190928999
|
A | C | 2 | a0002c0003t0001g0144a0002c0003t0001g0153 | 2 | NA18954.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1426-1438A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190928999 | ||||||
chr2:190929046
|
C | T | 2 | a0001c0002t0007g0275a0001c0002t0007g0277 | 2 | NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1426-1391C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929046 | ||||||
chr2:190929125
|
T | TAAACACA others(194): Show |
7 | a0001c0001t0004g0212a0001c0001t0004g0219a0001c0001t0004g0220others(4): Show | 7 | NA18947.hp2 NA18961.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1426-1311_1426-131 others(205): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190929125 | |||||
chr2:190929142
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1426-1295A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929142 | ||||||
chr2:190929163
|
T | C | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1426-1274T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929163 | ||||||
chr2:190929215
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 93 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.1426-1222G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929215 | ||||||
chr2:190929220
|
A | G | 1 | a0001c0001t0062g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1426-1217A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929220 | ||||||
chr2:190929310
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1426-1127G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929310 | ||||||
chr2:190929355
|
A | G | 1 | a0001c0001t0010g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1426-1082A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929355 | ||||||
chr2:190929474
|
AT | A | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1426-950delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190929474 | |||||
chr2:190929532
|
C | T | 2 | a0001c0001t0006g0083a0001c0001t0006g0103 | 2 | HG02080.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1426-905C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929532 | ||||||
chr2:190929546
|
T | C | 5 | a0001c0001t0001g0155a0001c0001t0001g0177a0001c0001t0001g0194others(2): Show | 5 | HG00597.hp1 NA18948.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.1426-891T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929546 | ||||||
chr2:190929573
|
G | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0142others(22): Show | 26 | HG02015.hp1 HG02135.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1426-864G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929573 | ||||||
chr2:190929765
|
C | T | 2 | a0002c0003t0001g0144a0002c0003t0001g0153 | 2 | NA18954.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1426-672C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929765 | ||||||
chr2:190929813
|
A | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426-624A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929813 | ||||||
chr2:190929919
|
C | T | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1426-518C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929919 | ||||||
chr2:190929940
|
C | T | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1426-497C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929940 | ||||||
chr2:190929970
|
C | A | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1426-467C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190929970 | ||||||
chr2:190930006
|
C | G | 2 | a0001c0001t0004g0255a0001c0001t0010g0254 | 2 | HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1426-431C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190930006 | ||||||
chr2:190930070
|
G | GT | 20 | a0001c0001t0001g0158a0001c0001t0003g0064a0001c0001t0005g0117others(17): Show | 20 | HG00597.hp2 HG01257.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.1426-353dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 190930070 | |||||
chr2:190930070
|
G | T | 3 | a0001c0001t0024g0193a0001c0001t0024g0264a0001c0001t0024g0265 | 3 | HG02258.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1426-367G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190930070 | ||||||
chr2:190930081
|
T | C | 1 | a0003c0007t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1426-356T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190930081 | ||||||
chr2:190930092
|
G | A | 1 | a0001c0001t0071g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1426-345G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 12/17 | chr2 | 190930092 | ||||||
chr2:190930700
|
C | T | 1 | a0001c0001t0036g0081 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1557+132C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 13/17 | chr2 | 190930700 | ||||||
chr2:190930820
|
G | C | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(297): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1557+252G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 13/17 | chr2 | 190930820 | ||||||
chr2:190931058
|
T | C | 3 | a0001c0002t0007g0270a0001c0002t0007g0271a0001c0002t0007g0276 | 3 | HG01257.hp1 NA18953.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1558-487T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 13/17 | chr2 | 190931058 | ||||||
chr2:190931148
|
C | A | 14 | a0001c0001t0003g0009a0001c0001t0003g0055a0001c0001t0003g0056others(11): Show | 15 | HG00438.hp2 HG02040.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1558-397C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 13/17 | chr2 | 190931148 | ||||||
chr2:190931306
|
G | A | 1 | a0001c0001t0005g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1558-239G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 13/17 | chr2 | 190931306 | ||||||
chr2:190931326
|
T | C | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1558-219T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 13/17 | chr2 | 190931326 | ||||||
chr2:190931645
|
A | C | 1 | a0001c0001t0005g0339 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.1650+8A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190931645 | ||||||
chr2:190931654
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0030g0003 | 3 | NA18952.hp2 NA18969.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1650+17T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190931654 | ||||||
chr2:190931716
|
T | A | 4 | a0001c0001t0003g0066a0001c0001t0006g0082a0001c0001t0006g0085others(1): Show | 4 | HG00558.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1650+79T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190931716 | ||||||
chr2:190931788
|
C | T | 1 | a0001c0001t0001g0015 | 2 | NA18981.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1650+151C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190931788 | ||||||
chr2:190932173
|
A | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1650+536A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190932173 | ||||||
chr2:190932246
|
A | G | 2 | a0001c0001t0005g0228a0001c0001t0008g0134 | 2 | HG02080.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1650+609A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190932246 | ||||||
chr2:190932320
|
C | T | 1 | a0007c0013t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1650+683C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190932320 | ||||||
chr2:190932440
|
T | C | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+803T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190932440 | ||||||
chr2:190932563
|
G | A | 7 | a0001c0001t0005g0019a0001c0001t0012g0019a0001c0001t0012g0199others(4): Show | 8 | HG02615.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+926G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190932563 | ||||||
chr2:190932653
|
A | G | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1650+1016A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190932653 | ||||||
chr2:190933442
|
T | A | 1 | a0001c0002t0007g0270 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1650+1805T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190933442 | ||||||
chr2:190933542
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1650+1905A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190933542 | ||||||
chr2:190933585
|
A | G | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1650+1948A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190933585 | ||||||
chr2:190933722
|
T | C | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+2085T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190933722 | ||||||
chr2:190933847
|
T | G | 1 | a0001c0001t0015g0303 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1650+2210T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190933847 | ||||||
chr2:190933983
|
A | C | 1 | a0001c0001t0057g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1650+2346A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190933983 | ||||||
chr2:190934649
|
C | T | 1 | a0001c0001t0002g0024 | 2 | NA18955.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1650+3012C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190934649 | ||||||
chr2:190934669
|
T | A | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650+3032T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190934669 | ||||||
chr2:190934773
|
T | G | 12 | a0001c0001t0002g0028a0001c0001t0002g0317a0001c0001t0002g0319others(9): Show | 13 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650+3136T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190934773 | ||||||
chr2:190934874
|
T | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1650+3237T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190934874 | ||||||
chr2:190934885
|
G | C | 1 | a0001c0001t0003g0091 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1650+3248G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190934885 | ||||||
chr2:190934935
|
A | G | 1 | a0001c0002t0007g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1650+3298A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190934935 | ||||||
chr2:190935080
|
C | A | 1 | a0001c0002t0007g0278 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1650+3443C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190935080 | ||||||
chr2:190935422
|
T | C | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+3785T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190935422 | ||||||
chr2:190935438
|
A | G | 1 | a0001c0001t0005g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1650+3801A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190935438 | ||||||
chr2:190935684
|
T | G | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1650+4047T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190935684 | ||||||
chr2:190935967
|
A | G | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+4330A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190935967 | ||||||
chr2:190935989
|
A | T | 1 | a0001c0001t0002g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650+4352A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190935989 | ||||||
chr2:190936171
|
A | T | 1 | a0001c0001t0005g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1650+4534A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936171 | ||||||
chr2:190936176
|
A | T | 1 | a0001c0001t0009g0334 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1650+4539A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936176 | ||||||
chr2:190936179
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1650+4542T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936179 | ||||||
chr2:190936325
|
T | G | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1650+4688T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936325 | ||||||
chr2:190936352
|
T | A | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1650+4715T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936352 | ||||||
chr2:190936353
|
A | T | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1650+4716A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936353 | ||||||
chr2:190936452
|
C | T | 16 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1650+4815C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936452 | ||||||
chr2:190936463
|
T | G | 12 | a0001c0001t0002g0028a0001c0001t0002g0317a0001c0001t0002g0319others(9): Show | 13 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650+4826T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936463 | ||||||
chr2:190936554
|
T | A | 1 | a0001c0001t0030g0172 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1650+4917T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936554 | ||||||
chr2:190936679
|
A | G | 11 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0042others(8): Show | 13 | HG01496.hp1 NA18940.hp2 NA18965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1650+5042A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936679 | ||||||
chr2:190936924
|
A | G | 1 | a0001c0001t0024g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1650+5287A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190936924 | ||||||
chr2:190937249
|
T | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1650+5612T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190937249 | ||||||
chr2:190937430
|
A | G | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+5793A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190937430 | ||||||
chr2:190937451
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1650+5814G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190937451 | ||||||
chr2:190937613
|
A | C | 1 | a0001c0001t0004g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1650+5976A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190937613 | ||||||
chr2:190937714
|
C | T | 1 | a0001c0001t0005g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1650+6077C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190937714 | ||||||
chr2:190937840
|
G | GT | 152 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(149): Show | 164 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1650+6220dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190937840 | |||||
chr2:190937840
|
G | GTT | 26 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0142others(23): Show | 27 | HG01109.hp2 HG02055.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.1650+6219_1650+622 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190937840 | |||||
chr2:190937840
|
GT | G | 6 | a0001c0001t0062g0337a0001c0004t0017g0034a0001c0004t0017g0035others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+6220delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190937840 | |||||
chr2:190937957
|
C | A | 84 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(81): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1650+6320C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190937957 | ||||||
chr2:190938056
|
A | AT | 3 | a0001c0001t0002g0084a0001c0001t0004g0004a0001c0001t0004g0241 | 5 | NA18942.hp1 NA18944.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+6426dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190938056 | |||||
chr2:190938082
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1650+6445A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938082 | ||||||
chr2:190938144
|
G | T | 1 | a0001c0001t0011g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1650+6507G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938144 | ||||||
chr2:190938280
|
G | T | 1 | a0001c0001t0006g0103 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1650+6643G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938280 | ||||||
chr2:190938293
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650+6656C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938293 | ||||||
chr2:190938333
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1650+6696C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938333 | ||||||
chr2:190938334
|
T | C | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1650+6697T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938334 | ||||||
chr2:190938335
|
G | T | 1 | a0001c0001t0002g0295 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1650+6698G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938335 | ||||||
chr2:190938500
|
T | A | 1 | a0001c0001t0004g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1650+6863T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938500 | ||||||
chr2:190938612
|
T | C | 1 | a0001c0001t0006g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1650+6975T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190938612 | ||||||
chr2:190939202
|
C | CT | 9 | a0001c0001t0001g0115a0001c0001t0001g0150a0001c0001t0001g0183others(6): Show | 9 | HG02027.hp2 HG02083.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650+7566dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190939202 | |||||
chr2:190939275
|
CTG | C | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650+7644_1650+764 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190939275 | |||||
chr2:190939306
|
C | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1650+7669C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939306 | ||||||
chr2:190939330
|
C | T | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+7693C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939330 | ||||||
chr2:190939383
|
C | G | 1 | a0001c0001t0035g0331 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1650+7746C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939383 | ||||||
chr2:190939386
|
A | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | NA18972.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1650+7749A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939386 | ||||||
chr2:190939436
|
G | C | 24 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(21): Show | 27 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.1650+7799G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939436 | ||||||
chr2:190939505
|
A | T | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1650+7868A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939505 | ||||||
chr2:190939556
|
T | TA | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+7923dupA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190939556 | |||||
chr2:190939691
|
A | G | 2 | a0001c0001t0024g0264a0001c0001t0024g0265 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1650+8054A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939691 | ||||||
chr2:190939786
|
T | C | 1 | a0001c0001t0014g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1650+8149T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939786 | ||||||
chr2:190939837
|
T | C | 1 | a0001c0001t0074g0213 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1650+8200T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939837 | ||||||
chr2:190939838
|
G | A | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1650+8201G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939838 | ||||||
chr2:190939838
|
G | C | 1 | a0001c0001t0021g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1650+8201G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939838 | ||||||
chr2:190939925
|
T | A | 1 | a0001c0012t0037g0245 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1650+8288T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939925 | ||||||
chr2:190939976
|
A | T | 1 | a0001c0001t0047g0237 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1650+8339A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190939976 | ||||||
chr2:190940011
|
C | T | 1 | a0001c0001t0018g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1650+8374C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190940011 | ||||||
chr2:190940012
|
G | A | 3 | a0001c0001t0047g0237a0001c0001t0068g0138a0001c0001t0072g0137 | 3 | HG02647.hp2 HG03471.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1650+8375G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190940012 | ||||||
chr2:190940329
|
G | A | 6 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+8692G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190940329 | ||||||
chr2:190940640
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1650+9003C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190940640 | ||||||
chr2:190940820
|
A | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1650+9183A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190940820 | ||||||
chr2:190940961
|
C | A | 3 | a0001c0001t0043g0030a0001c0001t0048g0136a0001c0001t0052g0114 | 3 | HG02622.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1650+9324C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190940961 | ||||||
chr2:190941081
|
A | G | 1 | a0001c0001t0013g0111 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1650+9444A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941081 | ||||||
chr2:190941127
|
A | T | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1650+9490A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941127 | ||||||
chr2:190941181
|
GTT | G | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1650+9546_1650+954 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190941181 | |||||
chr2:190941363
|
C | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650+9726C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941363 | ||||||
chr2:190941416
|
T | G | 2 | a0001c0001t0002g0297a0001c0001t0002g0299 | 2 | HG00642.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1650+9779T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941416 | ||||||
chr2:190941488
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1650+9851T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941488 | ||||||
chr2:190941538
|
TA | T | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1650+9908delA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190941538 | |||||
chr2:190941551
|
G | T | 6 | a0001c0001t0004g0216a0001c0001t0005g0206a0001c0001t0005g0215others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650+9914G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941551 | ||||||
chr2:190941569
|
A | AGAC | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(297): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1650+9932_1650+993 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941569 | ||||||
chr2:190941729
|
AAAG | A | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(297): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1650+10099_1650+10 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190941729 | |||||
chr2:190941746
|
C | T | 1 | a0007c0013t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1650+10109C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941746 | ||||||
chr2:190941906
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1650+10269C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941906 | ||||||
chr2:190941942
|
G | A | 2 | a0001c0001t0004g0005a0001c0001t0012g0005 | 3 | NA18949.hp1 NA18970.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1650+10305G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190941942 | ||||||
chr2:190942067
|
C | CT | 39 | a0001c0001t0001g0159a0001c0001t0002g0026a0001c0001t0002g0027others(36): Show | 44 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1650+10460dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTT | 21 | a0001c0001t0002g0071a0001c0001t0002g0084a0001c0001t0002g0300others(18): Show | 21 | HG00408.hp1 HG01099.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1650+10459_1650+10 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTT | 16 | a0001c0001t0002g0072a0001c0001t0002g0080a0001c0001t0002g0296others(13): Show | 16 | HG00099.hp2 HG00558.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1650+10458_1650+10 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTT | 22 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0047others(19): Show | 24 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1650+10457_1650+10 others(10): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTT | 19 | a0001c0001t0002g0322a0001c0001t0003g0040a0001c0001t0003g0041others(16): Show | 19 | HG00642.hp2 HG01109.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650+10456_1650+10 others(11): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTT | 9 | a0001c0001t0002g0323a0001c0001t0003g0078a0001c0001t0005g0228others(6): Show | 10 | HG01069.hp1 HG01123.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650+10455_1650+10 others(12): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT | 18 | a0001c0001t0003g0058a0001c0001t0004g0004a0001c0001t0004g0219others(15): Show | 20 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1650+10454_1650+10 others(13): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT others(1): Show |
30 | a0001c0001t0004g0005a0001c0001t0004g0208a0001c0001t0004g0210others(27): Show | 32 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1650+10453_1650+10 others(14): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT others(2): Show |
23 | a0001c0001t0004g0020a0001c0001t0004g0224a0001c0001t0004g0226others(20): Show | 24 | HG00099.hp1 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1650+10452_1650+10 others(15): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0004g0255a0001c0001t0005g0211a0001c0001t0005g0239others(3): Show | 6 | HG01175.hp1 HG01175.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+10451_1650+10 others(16): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0004g0021a0001c0001t0004g0240a0001c0001t0005g0021others(3): Show | 6 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+10450_1650+10 others(17): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0028g0343 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1650+10448_1650+10 others(19): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0028g0344 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650+10447_1650+10 others(20): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
CT | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(54): Show | 66 | HG00597.hp1 HG00639.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1650+10460delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
CTTTTTTT others(3): Show |
C | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1650+10451_1650+10 others(16): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0003g0055a0001c0001t0003g0056a0001c0001t0008g0133others(2): Show | 5 | HG02132.hp2 HG02572.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+10450_1650+10 others(17): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
CTTTTTTT others(5): Show |
C | 18 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(15): Show | 21 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1650+10449_1650+10 others(18): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942067
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0009g0330 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1650+10447_1650+10 others(20): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942067 | |||||
chr2:190942271
|
G | A | 1 | a0007c0013t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1650+10634G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942271 | ||||||
chr2:190942302
|
G | A | 1 | a0001c0001t0062g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1650+10665G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942302 | ||||||
chr2:190942311
|
A | T | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650+10674A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942311 | ||||||
chr2:190942315
|
C | T | 4 | a0002c0003t0001g0293a0002c0003t0023g0151a0002c0003t0023g0152others(1): Show | 4 | NA18970.hp2 NA18978.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1650+10678C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942315 | ||||||
chr2:190942440
|
G | A | 4 | a0001c0001t0003g0043a0001c0001t0003g0045a0001c0001t0046g0046others(1): Show | 4 | NA19006.hp2 NA19058.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1650+10803G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942440 | ||||||
chr2:190942583
|
T | C | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1650+10946T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942583 | ||||||
chr2:190942620
|
T | A | 69 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1651-10945T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942620 | ||||||
chr2:190942631
|
A | G | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1651-10934A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942631 | ||||||
chr2:190942633
|
C | T | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-10932C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942633 | ||||||
chr2:190942641
|
A | G | 1 | a0001c0001t0008g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1651-10924A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942641 | ||||||
chr2:190942727
|
A | G | 88 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1651-10838A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942727 | ||||||
chr2:190942789
|
T | C | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-10776T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942789 | ||||||
chr2:190942812
|
CAG | C | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0346others(1): Show | 5 | HG00741.hp2 HG01074.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-10751_1651-10 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190942812 | |||||
chr2:190942949
|
A | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-10616A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942949 | ||||||
chr2:190942998
|
A | G | 4 | a0001c0001t0006g0074a0001c0001t0006g0075a0001c0001t0006g0077others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-10567A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190942998 | ||||||
chr2:190943281
|
C | T | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-10284C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190943281 | ||||||
chr2:190943486
|
A | G | 10 | a0001c0001t0008g0011a0001c0001t0008g0017a0001c0001t0008g0133others(7): Show | 12 | HG01261.hp2 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-10079A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190943486 | ||||||
chr2:190943966
|
G | A | 1 | a0001c0001t0006g0085 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1651-9599G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190943966 | ||||||
chr2:190943983
|
T | C | 88 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(85): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1651-9582T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190943983 | ||||||
chr2:190944054
|
T | G | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-9511T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944054 | ||||||
chr2:190944078
|
G | T | 1 | a0001c0001t0003g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1651-9487G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944078 | ||||||
chr2:190944109
|
A | G | 2 | a0001c0001t0005g0205a0001c0001t0065g0229 | 2 | HG02165.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1651-9456A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944109 | ||||||
chr2:190944157
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 97 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1651-9408T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944157 | ||||||
chr2:190944196
|
A | AT | 127 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0027others(124): Show | 137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1651-9357dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190944196 | |||||
chr2:190944418
|
G | C | 1 | a0001c0012t0037g0245 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1651-9147G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944418 | ||||||
chr2:190944560
|
T | C | 2 | a0001c0001t0004g0252a0001c0001t0004g0253 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1651-9005T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944560 | ||||||
chr2:190944744
|
C | T | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-8821C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944744 | ||||||
chr2:190944755
|
T | TA | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-8809dupA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190944755 | |||||
chr2:190944844
|
C | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 85 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1651-8721C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944844 | ||||||
chr2:190944845
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(298): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1651-8720A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190944845 | ||||||
chr2:190945070
|
A | ATAGT | 299 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(296): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1651-8494_1651-849 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190945070 | |||||
chr2:190945227
|
T | A | 4 | a0001c0001t0003g0010a0001c0001t0003g0069a0001c0001t0003g0090others(1): Show | 4 | HG02922.hp1 HG03471.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-8338T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190945227 | ||||||
chr2:190945497
|
C | CA | 3 | a0001c0001t0025g0029a0001c0001t0025g0338a0001c0001t0062g0337 | 4 | HG02630.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-8061dupA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190945497 | |||||
chr2:190945626
|
C | T | 1 | a0001c0001t0061g0112 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1651-7939C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190945626 | ||||||
chr2:190945664
|
C | CA | 6 | a0001c0001t0003g0010a0001c0001t0003g0059a0001c0001t0003g0069others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-7889dupA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190945664 | |||||
chr2:190945673
|
A | AAAAG | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-7888_1651-788 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190945673 | |||||
chr2:190945791
|
T | A | 2 | a0001c0001t0016g0203a0001c0001t0027g0202 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1651-7774T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190945791 | ||||||
chr2:190946024
|
T | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-7541T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190946024 | ||||||
chr2:190946056
|
C | T | 1 | a0001c0001t0006g0287 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1651-7509C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190946056 | ||||||
chr2:190946083
|
A | G | 1 | a0001c0001t0002g0028 | 2 | HG00558.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1651-7482A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190946083 | ||||||
chr2:190946105
|
A | C | 1 | a0001c0001t0004g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1651-7460A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190946105 | ||||||
chr2:190946170
|
A | G | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1651-7395A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190946170 | ||||||
chr2:190946265
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1651-7300A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190946265 | ||||||
chr2:190946633
|
GAAGTA | G | 69 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1651-6927_1651-692 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190946633 | |||||
chr2:190946970
|
TAAATA | T | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-6589_1651-658 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190946970 | |||||
chr2:190947082
|
C | T | 1 | a0001c0001t0010g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1651-6483C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947082 | ||||||
chr2:190947420
|
T | A | 4 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | NA18952.hp1 NA18956.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-6145T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947420 | ||||||
chr2:190947444
|
C | T | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1651-6121C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947444 | ||||||
chr2:190947495
|
T | C | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-6070T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947495 | ||||||
chr2:190947636
|
C | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-5929C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947636 | ||||||
chr2:190947722
|
A | G | 1 | a0001c0001t0003g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1651-5843A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947722 | ||||||
chr2:190947806
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0143a0001c0001t0001g0147others(10): Show | 16 | HG00741.hp2 HG01074.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1651-5759G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947806 | ||||||
chr2:190947832
|
A | G | 1 | a0001c0001t0005g0215 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1651-5733A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190947832 | ||||||
chr2:190948255
|
G | A | 2 | a0001c0001t0005g0105a0001c0001t0005g0117 | 2 | HG02015.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1651-5310G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190948255 | ||||||
chr2:190948257
|
C | A | 1 | a0001c0001t0062g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1651-5308C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190948257 | ||||||
chr2:190948367
|
A | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-5198A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190948367 | ||||||
chr2:190948392
|
C | T | 1 | a0001c0001t0072g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1651-5173C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190948392 | ||||||
chr2:190948557
|
T | A | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-5008T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190948557 | ||||||
chr2:190948813
|
A | G | 84 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(81): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1651-4752A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190948813 | ||||||
chr2:190949008
|
G | A | 13 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(10): Show | 14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1651-4557G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949008 | ||||||
chr2:190949090
|
T | TAAAGAG | 16 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1651-4473_1651-447 others(10): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190949090 | |||||
chr2:190949245
|
C | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1651-4320C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949245 | ||||||
chr2:190949307
|
T | A | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1651-4258T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949307 | ||||||
chr2:190949345
|
G | A | 3 | a0002c0003t0023g0151a0002c0003t0023g0152a0002c0003t0023g0281 | 3 | NA18970.hp2 NA18978.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1651-4220G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949345 | ||||||
chr2:190949406
|
T | G | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-4159T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949406 | ||||||
chr2:190949421
|
C | G | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-4144C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949421 | ||||||
chr2:190949474
|
G | A | 1 | a0001c0001t0010g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1651-4091G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949474 | ||||||
chr2:190949582
|
A | G | 1 | a0001c0001t0020g0101 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1651-3983A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949582 | ||||||
chr2:190949641
|
G | A | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-3924G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949641 | ||||||
chr2:190949882
|
T | C | 5 | a0001c0001t0014g0243a0001c0001t0014g0244a0001c0001t0014g0246others(2): Show | 5 | HG00738.hp1 HG01069.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-3683T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949882 | ||||||
chr2:190949966
|
T | C | 1 | a0001c0001t0004g0250 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1651-3599T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949966 | ||||||
chr2:190949985
|
TAACAA | T | 4 | a0001c0001t0008g0017a0001c0001t0008g0195a0001c0001t0008g0197others(1): Show | 5 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-3579_1651-357 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949985 | ||||||
chr2:190949994
|
A | AAT | 6 | a0001c0001t0008g0011a0001c0001t0008g0133a0001c0001t0008g0134others(3): Show | 7 | HG00323.hp2 HG01261.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1651-3556_1651-355 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190949994 | |||||
chr2:190949994
|
A | T | 7 | a0001c0001t0002g0301a0001c0001t0005g0019a0001c0001t0012g0019others(4): Show | 8 | HG02615.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-3571A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190949994 | ||||||
chr2:190950071
|
T | C | 4 | a0001c0001t0014g0243a0001c0001t0014g0244a0001c0001t0014g0246others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-3494T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950071 | ||||||
chr2:190950121
|
C | T | 4 | a0001c0001t0006g0074a0001c0001t0006g0075a0001c0001t0006g0077others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-3444C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950121 | ||||||
chr2:190950271
|
G | C | 1 | a0007c0013t0001g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1651-3294G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950271 | ||||||
chr2:190950312
|
A | C | 70 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-3253A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950312 | ||||||
chr2:190950326
|
C | T | 72 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(69): Show | 74 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-3239C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950326 | ||||||
chr2:190950371
|
G | A | 1 | a0001c0002t0007g0273 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1651-3194G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950371 | ||||||
chr2:190950380
|
G | A | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1651-3185G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950380 | ||||||
chr2:190950476
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1651-3089A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950476 | ||||||
chr2:190950596
|
C | T | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1651-2969C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950596 | ||||||
chr2:190950598
|
C | T | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1651-2967C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950598 | ||||||
chr2:190950613
|
A | AATT | 5 | a0001c0001t0008g0011a0001c0001t0008g0133a0001c0001t0008g0134others(2): Show | 6 | HG01261.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-2951_1651-295 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190950613 | |||||
chr2:190950648
|
T | C | 21 | a0001c0001t0005g0019a0001c0001t0008g0011a0001c0001t0008g0017others(18): Show | 24 | HG01261.hp2 HG02109.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.1651-2917T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950648 | ||||||
chr2:190950692
|
T | C | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-2873T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190950692 | ||||||
chr2:190951033
|
G | A | 2 | a0001c0001t0024g0264a0001c0001t0024g0265 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1651-2532G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951033 | ||||||
chr2:190951088
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1651-2477C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951088 | ||||||
chr2:190951140
|
G | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(271): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1651-2425G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951140 | ||||||
chr2:190951442
|
A | G | 1 | a0001c0001t0014g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1651-2123A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951442 | ||||||
chr2:190951535
|
G | A | 5 | a0001c0001t0006g0283a0001c0001t0006g0284a0001c0001t0006g0285others(2): Show | 5 | NA18952.hp1 NA18956.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-2030G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951535 | ||||||
chr2:190951694
|
G | A | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1651-1871G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951694 | ||||||
chr2:190951724
|
G | T | 1 | a0003c0007t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1651-1841G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951724 | ||||||
chr2:190951995
|
C | A | 1 | a0005c0010t0042g0262 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1651-1570C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951995 | ||||||
chr2:190951997
|
G | T | 1 | a0005c0010t0042g0262 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1651-1568G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190951997 | ||||||
chr2:190952195
|
C | T | 77 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(74): Show | 79 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1651-1370C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190952195 | ||||||
chr2:190952430
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1651-1135C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190952430 | ||||||
chr2:190952460
|
G | A | 1 | a0001c0001t0005g0290 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1651-1105G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190952460 | ||||||
chr2:190952689
|
C | T | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1651-876C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190952689 | ||||||
chr2:190952759
|
G | A | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-806G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190952759 | ||||||
chr2:190952973
|
A | C | 1 | a0001c0001t0035g0331 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1651-592A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190952973 | ||||||
chr2:190953093
|
G | T | 1 | a0003c0007t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1651-472G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190953093 | ||||||
chr2:190953101
|
T | A | 72 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(69): Show | 74 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1651-464T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190953101 | ||||||
chr2:190953320
|
A | G | 1 | a0001c0001t0049g0336 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1651-245A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190953320 | ||||||
chr2:190953339
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(293): Show | 318 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.1651-226T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190953339 | ||||||
chr2:190953409
|
T | A | 10 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0042others(7): Show | 12 | HG01496.hp1 NA18940.hp2 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-156T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190953409 | ||||||
chr2:190953454
|
C | T | 3 | a0001c0001t0043g0030a0001c0001t0048g0136a0001c0001t0052g0114 | 3 | HG02622.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1651-111C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | chr2 | 190953454 | ||||||
chr2:190953517
|
ATG | A | 4 | a0001c0001t0014g0243a0001c0001t0014g0244a0001c0001t0014g0246others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-44_1651-43del others(2): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 190953517 | |||||
chr2:190953950
|
A | ATG | 34 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0165others(31): Show | 34 | HG00597.hp2 HG01257.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.1712+369_1712+370d others(4): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | ATGTG | 36 | a0001c0001t0001g0184a0001c0001t0002g0024a0001c0001t0002g0296others(33): Show | 38 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1712+367_1712+370d others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | ATGTGTG | 20 | a0001c0001t0002g0301a0001c0001t0002g0307a0001c0001t0002g0322others(17): Show | 21 | HG01192.hp2 HG02004.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1712+365_1712+370d others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | ATGTGTGT others(1): Show |
14 | a0001c0001t0001g0192a0001c0001t0001g0260a0001c0001t0002g0026others(11): Show | 15 | HG01106.hp2 HG01496.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712+363_1712+370d others(10): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0002g0027a0001c0001t0009g0310 | 3 | NA18981.hp2 NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1712+361_1712+370d others(12): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0302a0001c0001t0003g0091 | 2 | NA18955.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1712+359_1712+370d others(14): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0308 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1712+357_1712+370d others(16): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
A | G | 1 | a0001c0004t0017g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1712+324A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | chr2 | 190953950 | ||||||
chr2:190953950
|
ATG | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 91 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1712+369_1712+370d others(4): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
ATGTG | A | 28 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0167others(25): Show | 28 | HG00738.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1712+367_1712+370d others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
ATGTGTG | A | 56 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0194others(53): Show | 61 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1712+365_1712+370d others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
ATGTGTGT others(3): Show |
A | 4 | a0001c0001t0005g0214a0001c0001t0012g0199a0001c0001t0025g0029others(1): Show | 5 | HG02027.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1712+361_1712+370d others(12): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
ATGTGTGT others(5): Show |
A | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1712+359_1712+370d others(14): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953950
|
ATGTGTGT others(9): Show |
A | 5 | a0001c0001t0001g0268a0001c0001t0004g0212a0001c0001t0028g0343others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1712+355_1712+370d others(18): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190953950 | |||||
chr2:190953986
|
G | A | 1 | a0001c0001t0057g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1712+360G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | chr2 | 190953986 | ||||||
chr2:190954052
|
C | G | 1 | a0001c0001t0003g0051 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1712+426C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | chr2 | 190954052 | ||||||
chr2:190954097
|
CT | C | 85 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(82): Show | 87 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1713-477delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190954097 | |||||
chr2:190954146
|
A | G | 2 | a0001c0001t0045g0288a0001c0001t0059g0289 | 2 | HG02040.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1713-438A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | chr2 | 190954146 | ||||||
chr2:190954313
|
A | G | 107 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(104): Show | 114 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1713-271A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | chr2 | 190954313 | ||||||
chr2:190954376
|
TA | T | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1713-200delA | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 190954376 | |||||
chr2:190954379
|
A | G | 1 | a0001c0002t0007g0276 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1713-205A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 15/17 | chr2 | 190954379 | ||||||
chr2:190954981
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1853+163C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190954981 | ||||||
chr2:190955122
|
AT | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1853+308delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190955122 | |||||
chr2:190955126
|
T | A | 3 | a0001c0001t0009g0341a0001c0001t0044g0342a0007c0013t0001g0132 | 3 | HG02970.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1853+308T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955126 | ||||||
chr2:190955135
|
A | T | 78 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(75): Show | 80 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1853+317A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955135 | ||||||
chr2:190955136
|
A | T | 83 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(80): Show | 85 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1853+318A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955136 | ||||||
chr2:190955137
|
T | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1853+319T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955137 | ||||||
chr2:190955142
|
A | T | 1 | a0001c0001t0006g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1853+324A>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955142 | ||||||
chr2:190955181
|
G | C | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1853+363G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955181 | ||||||
chr2:190955240
|
C | T | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1853+422C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955240 | ||||||
chr2:190955308
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1853+490G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955308 | ||||||
chr2:190955495
|
A | G | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1853+677A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955495 | ||||||
chr2:190955534
|
G | A | 1 | a0001c0001t0004g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1853+716G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955534 | ||||||
chr2:190955630
|
T | C | 1 | a0001c0001t0050g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1853+812T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955630 | ||||||
chr2:190955748
|
G | A | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1853+930G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955748 | ||||||
chr2:190955757
|
C | T | 1 | a0003c0007t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1853+939C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955757 | ||||||
chr2:190955805
|
G | A | 9 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1853+987G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955805 | ||||||
chr2:190955973
|
T | G | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1853+1155T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190955973 | ||||||
chr2:190956232
|
T | C | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1853+1414T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956232 | ||||||
chr2:190956449
|
C | T | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1853+1631C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956449 | ||||||
chr2:190956514
|
A | G | 1 | a0001c0001t0009g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1853+1696A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956514 | ||||||
chr2:190956644
|
T | A | 6 | a0001c0001t0003g0010a0001c0001t0003g0059a0001c0001t0003g0069others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1853+1826T>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956644 | ||||||
chr2:190956724
|
T | G | 1 | a0001c0001t0011g0097 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1853+1906T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956724 | ||||||
chr2:190956828
|
T | C | 1 | a0001c0002t0007g0274 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1853+2010T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956828 | ||||||
chr2:190956950
|
A | G | 1 | a0001c0001t0003g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1853+2132A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190956950 | ||||||
chr2:190957088
|
C | CCTTT | 73 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(70): Show | 75 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1853+2283_1853+228 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190957088 | |||||
chr2:190957215
|
C | T | 13 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0160others(10): Show | 13 | HG02135.hp2 HG02155.hp2 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.1853+2397C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957215 | ||||||
chr2:190957236
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1853+2418G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957236 | ||||||
chr2:190957263
|
T | C | 1 | a0001c0001t0062g0337 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1853+2445T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957263 | ||||||
chr2:190957438
|
T | C | 73 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(70): Show | 75 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1853+2620T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957438 | ||||||
chr2:190957628
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(291): Show | 316 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1853+2810G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957628 | ||||||
chr2:190957635
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1853+2817T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957635 | ||||||
chr2:190957707
|
G | A | 2 | a0001c0001t0003g0066a0001c0001t0006g0082 | 2 | HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1853+2889G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957707 | ||||||
chr2:190957721
|
A | G | 2 | a0001c0001t0002g0333a0001c0001t0009g0334 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1853+2903A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957721 | ||||||
chr2:190957866
|
T | C | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1853+3048T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957866 | ||||||
chr2:190957914
|
G | A | 1 | a0001c0001t0014g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1853+3096G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190957914 | ||||||
chr2:190958055
|
TAGGCTAT others(21): Show |
T | 1 | a0001c0009t0001g0130 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1853+3267_1853+329 others(32): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190958055 | |||||
chr2:190958290
|
A | C | 1 | a0001c0001t0003g0104 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1853+3472A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190958290 | ||||||
chr2:190958391
|
T | C | 1 | a0001c0001t0020g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1853+3573T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190958391 | ||||||
chr2:190958482
|
G | T | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1853+3664G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190958482 | ||||||
chr2:190958613
|
G | A | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0080others(2): Show | 5 | HG00099.hp2 HG01099.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1853+3795G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190958613 | ||||||
chr2:190958674
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0259 | 2 | NA19070.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1853+3856T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190958674 | ||||||
chr2:190958866
|
G | A | 14 | a0001c0001t0045g0288a0001c0001t0059g0289a0001c0002t0007g0269others(11): Show | 14 | HG01257.hp1 HG02040.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1854-3964G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190958866 | ||||||
chr2:190959243
|
C | CT | 8 | a0001c0001t0001g0159a0001c0001t0001g0266a0001c0001t0004g0250others(5): Show | 8 | HG01074.hp1 HG02622.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1854-3572dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190959243 | |||||
chr2:190959243
|
CT | C | 96 | a0001c0001t0001g0163a0001c0001t0003g0008a0001c0001t0003g0009others(93): Show | 99 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.1854-3572delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190959243 | |||||
chr2:190959462
|
T | G | 2 | a0001c0001t0025g0029a0001c0001t0025g0338 | 3 | HG02630.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1854-3368T>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190959462 | ||||||
chr2:190959565
|
G | A | 5 | a0001c0004t0017g0034a0001c0004t0017g0035a0001c0004t0017g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1854-3265G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190959565 | ||||||
chr2:190959641
|
G | C | 2 | a0001c0001t0045g0288a0001c0001t0059g0289 | 2 | HG02040.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1854-3189G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190959641 | ||||||
chr2:190959765
|
C | G | 1 | a0001c0004t0017g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1854-3065C>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190959765 | ||||||
chr2:190959848
|
A | C | 7 | a0001c0001t0018g0001a0001c0001t0018g0139a0001c0001t0018g0140others(4): Show | 8 | HG02258.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1854-2982A>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190959848 | ||||||
chr2:190959901
|
A | G | 5 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0255others(2): Show | 5 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1854-2929A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190959901 | ||||||
chr2:190960076
|
AATG | A | 13 | a0001c0001t0008g0011a0001c0001t0008g0017a0001c0001t0008g0133others(10): Show | 15 | HG01261.hp2 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1854-2750_1854-274 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960076 | |||||
chr2:190960324
|
T | C | 2 | a0001c0001t0028g0343a0001c0001t0028g0344 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1854-2506T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190960324 | ||||||
chr2:190960337
|
T | C | 174 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0003g0008others(171): Show | 185 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1854-2493T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190960337 | ||||||
chr2:190960359
|
A | AT | 84 | a0001c0001t0001g0031a0001c0001t0001g0143a0001c0001t0001g0159others(81): Show | 89 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1854-2449dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960359
|
A | ATT | 15 | a0001c0001t0009g0341a0001c0001t0013g0108a0001c0001t0013g0109others(12): Show | 15 | HG00597.hp2 HG01884.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1854-2450_1854-244 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960359
|
A | ATTT | 8 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0272others(5): Show | 8 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1854-2451_1854-244 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960359
|
A | ATTTT | 12 | a0001c0001t0008g0011a0001c0001t0008g0017a0001c0001t0008g0133others(9): Show | 14 | HG01261.hp2 HG02572.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1854-2452_1854-244 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960359
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0045g0288 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1854-2458_1854-244 others(14): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960359
|
AT | A | 24 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0173others(21): Show | 27 | HG00408.hp1 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1854-2449delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960359
|
ATTT | A | 7 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121others(4): Show | 7 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1854-2451_1854-244 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960359 | |||||
chr2:190960457
|
C | A | 12 | a0001c0002t0007g0269a0001c0002t0007g0270a0001c0002t0007g0271others(9): Show | 12 | HG01257.hp1 HG02083.hp1 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.1854-2373C>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190960457 | ||||||
chr2:190960461
|
C | T | 3 | a0001c0001t0003g0073a0001c0001t0003g0087a0001c0001t0036g0081 | 3 | HG00639.hp1 HG01256.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1854-2369C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190960461 | ||||||
chr2:190960466
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0089 | 2 | NA18960.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1854-2364G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190960466 | ||||||
chr2:190960539
|
A | ATTTATTT | 180 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(177): Show | 189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1854-2280_1854-227 others(11): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190960539 | |||||
chr2:190960595
|
C | T | 2 | a0001c0001t0009g0312a0001c0001t0009g0325 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1854-2235C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190960595 | ||||||
chr2:190961043
|
T | C | 177 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(174): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1854-1787T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961043 | ||||||
chr2:190961268
|
G | A | 1 | a0001c0001t0052g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1854-1562G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961268 | ||||||
chr2:190961355
|
G | A | 1 | a0001c0001t0010g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1854-1475G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961355 | ||||||
chr2:190961394
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1854-1436G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961394 | ||||||
chr2:190961577
|
T | C | 8 | a0001c0001t0006g0054a0001c0001t0006g0067a0001c0001t0020g0099others(5): Show | 8 | HG01192.hp2 HG02135.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1854-1253T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961577 | ||||||
chr2:190961656
|
A | G | 172 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(169): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1854-1174A>G | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961656 | ||||||
chr2:190961689
|
G | GT | 48 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0171others(45): Show | 52 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1854-1125dupT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961689
|
G | GTT | 21 | a0001c0001t0002g0297a0001c0001t0004g0210a0001c0001t0005g0215others(18): Show | 23 | HG02071.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1854-1126_1854-112 others(6): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961689
|
G | GTTT | 83 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(80): Show | 89 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1854-1127_1854-112 others(7): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961689
|
G | GTTTT | 9 | a0001c0001t0003g0089a0001c0001t0004g0224a0001c0001t0004g0250others(6): Show | 9 | HG00738.hp1 HG01069.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1854-1128_1854-112 others(8): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961689
|
G | GTTTTT | 54 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0040others(51): Show | 56 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1854-1129_1854-112 others(9): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961689
|
G | GTTTTTT | 17 | a0001c0001t0003g0010a0001c0001t0003g0059a0001c0001t0003g0090others(14): Show | 17 | HG00323.hp1 HG00438.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1854-1130_1854-112 others(10): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961689
|
G | T | 1 | a0001c0001t0003g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1854-1141G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961689 | ||||||
chr2:190961689
|
GT | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0147a0001c0001t0001g0173others(8): Show | 13 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1854-1125delT | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 190961689 | |||||
chr2:190961692
|
T | TG | 3 | a0001c0001t0028g0343a0001c0001t0028g0344a0001c0001t0050g0121 | 3 | HG02109.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1854-1138_1854-113 others(5): Show |
GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961692 | ||||||
chr2:190961706
|
G | A | 2 | a0001c0001t0009g0341a0001c0001t0044g0342 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1854-1124G>A | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961706 | ||||||
chr2:190961761
|
C | T | 73 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(70): Show | 75 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1854-1069C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961761 | ||||||
chr2:190961932
|
G | T | 1 | a0001c0001t0041g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1854-898G>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961932 | ||||||
chr2:190961969
|
T | C | 1 | a0001c0001t0010g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1854-861T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190961969 | ||||||
chr2:190962196
|
T | C | 1 | a0001c0001t0056g0340 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1854-634T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190962196 | ||||||
chr2:190962285
|
G | C | 113 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0020others(110): Show | 120 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1854-545G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190962285 | ||||||
chr2:190962388
|
T | C | 1 | a0006c0011t0063g0345 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1854-442T>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190962388 | ||||||
chr2:190962517
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1854-313C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190962517 | ||||||
chr2:190962802
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1854-28C>T | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190962802 | ||||||
chr2:190962822
|
G | C | 2 | a0001c0001t0009g0298a0001c0001t0067g0304 | 2 | NA18980.hp1 NA19006.hp1 |
splice_region_variant&intron_variant | LOW | c.1854-8G>C | GLS | ENSG00000115419.14 | transcript | ENST00000320717.8 | protein_coding | 17/17 | chr2 | 190962822 |