Item | Value |
---|---|
geneid | 64844 |
ensemblid | ENSG00000136536.15 |
hgncid | 17393 |
symbol | MARCHF7 |
name | membrane associated ring-CH-type finger 7 |
refseq_nuc | NM_001282805.2 |
refseq_prot | NP_001269734.1 |
ensembl_nuc | ENST00000409175.6 |
ensembl_prot | ENSP00000386830.1 |
mane_status | MANE Select |
chr | chr2 |
start | 159712506 |
end | 159771027 |
strand | + |
ver | v1.2 |
region | chr2:159712506-159771027 |
region5000 | chr2:159707506-159776027 |
regionname0 | MARCHF7_chr2_159712506_159771027 |
regionname5000 | MARCHF7_chr2_159707506_159776027 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 704 | 295 | 70 | 49 | 145 | 10 | 20 | 116 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002 | 0/0 | 704 | 28 | 0 | 0 | 28 | 0 | 0 | 22 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0003 | 0/1 | 704 | 11 | 0 | 5 | 4 | 0 | 1 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0004 | 0/0 | 704 | 9 | 3 | 1 | 0 | 3 | 2 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0005 | 0/0 | 704 | 8 | 0 | 7 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0006 | 0/0 | 704 | 6 | 3 | 0 | 2 | 0 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0007 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0008 | 0/0 | 704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0009 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0010 | 0/0 | 704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0011 | 0/0 | 704 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0012 | 0/0 | 704 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0013 | 0/0 | 704 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2115 | 102 | 32 | 12 | 44 | 4 | 10 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0002 | 0/0 | 2115 | 102 | 1 | 31 | 63 | 3 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0003 | 1/0 | 2115 | 47 | 2 | 1 | 38 | 2 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0004 | 0/0 | 2115 | 42 | 35 | 5 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0005 | 0/0 | 2115 | 28 | 0 | 0 | 28 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0006 | 0/1 | 2115 | 11 | 0 | 5 | 4 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0007 | 0/0 | 2115 | 9 | 3 | 1 | 0 | 3 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0008 | 0/0 | 2115 | 7 | 0 | 6 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0009 | 0/0 | 2115 | 6 | 3 | 0 | 2 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0010 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0011 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0012 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0013 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0014 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0015 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0016 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0017 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0018 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
c0019 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3929 | 87 | 1 | 31 | 48 | 3 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0002 | 0/0 | 3930 | 70 | 6 | 11 | 39 | 4 | 10 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0003 | 0/0 | 3933 | 42 | 2 | 7 | 32 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0004 | 1/0 | 3929 | 36 | 2 | 1 | 26 | 2 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0005 | 0/0 | 3929 | 14 | 13 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0006 | 0/0 | 3930 | 14 | 14 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0007 | 0/0 | 3929 | 11 | 0 | 0 | 11 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0008 | 0/0 | 3932 | 10 | 9 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0009 | 0/0 | 3933 | 10 | 5 | 0 | 3 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0010 | 0/1 | 3930 | 10 | 0 | 5 | 3 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0011 | 0/0 | 3931 | 9 | 3 | 1 | 0 | 3 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0012 | 0/0 | 3930 | 6 | 6 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0013 | 0/0 | 3932 | 4 | 2 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0014 | 0/0 | 3931 | 4 | 4 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0015 | 0/0 | 3932 | 3 | 0 | 0 | 1 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0016 | 0/0 | 3930 | 3 | 0 | 0 | 3 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0017 | 0/0 | 3935 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0018 | 0/0 | 3938 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0019 | 0/0 | 3929 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0020 | 0/0 | 3930 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0021 | 0/0 | 3929 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0022 | 0/0 | 3932 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0023 | 0/0 | 3926 | 2 | 0 | 0 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0024 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0025 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0026 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0027 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0028 | 0/0 | 3940 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0029 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0030 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0031 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0032 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0033 | 0/0 | 3931 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0034 | 0/0 | 3931 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0035 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0036 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0037 | 0/0 | 3937 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0038 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0039 | 0/0 | 3881 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
t0040 | 0/0 | 3926 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2115 | 102 | 32 | 12 | 44 | 4 | 10 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0002 | 0/0 | 2115 | 102 | 1 | 31 | 63 | 3 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003 | 1/0 | 2115 | 47 | 2 | 1 | 38 | 2 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004 | 0/0 | 2115 | 42 | 35 | 5 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0011 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0014 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002c0005 | 0/0 | 2115 | 28 | 0 | 0 | 28 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0003c0006 | 0/1 | 2115 | 11 | 0 | 5 | 4 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0004c0007 | 0/0 | 2115 | 9 | 3 | 1 | 0 | 3 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0005c0008 | 0/0 | 2115 | 7 | 0 | 6 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0005c0017 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0006c0009 | 0/0 | 2115 | 6 | 3 | 0 | 2 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0007c0019 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0008c0015 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0009c0013 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0010c0012 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0011c0016 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0012c0018 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0013c0010 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6044 | 68 | 6 | 11 | 39 | 3 | 9 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0006 | 0/0 | 6044 | 14 | 14 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0012 | 0/0 | 6044 | 6 | 6 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0014 | 0/0 | 6045 | 3 | 3 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0015 | 0/0 | 6046 | 3 | 0 | 0 | 1 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0016 | 0/0 | 6044 | 3 | 0 | 0 | 3 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0020 | 0/0 | 6044 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0029 | 0/0 | 6044 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0033 | 0/0 | 6045 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0001t0038 | 0/0 | 6044 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0002t0001 | 0/0 | 6043 | 86 | 1 | 31 | 47 | 3 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0002t0007 | 0/0 | 6043 | 11 | 0 | 0 | 11 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0002t0019 | 0/0 | 6043 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0002t0021 | 0/0 | 6043 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0002t0034 | 0/0 | 6045 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0003 | 0/0 | 6047 | 9 | 0 | 0 | 9 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0004 | 1/0 | 6043 | 33 | 2 | 1 | 24 | 2 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0024 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0027 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0030 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0031 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0003t0032 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0003 | 0/0 | 6047 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0005 | 0/0 | 6043 | 14 | 13 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0008 | 0/0 | 6046 | 10 | 9 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0009 | 0/0 | 6047 | 4 | 4 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0013 | 0/0 | 6046 | 4 | 2 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0018 | 0/0 | 6052 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0022 | 0/0 | 6046 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0023 | 0/0 | 6040 | 2 | 0 | 0 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0028 | 0/0 | 6054 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0037 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0004t0040 | 0/0 | 6040 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0011t0002 | 0/0 | 6044 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0001c0014t0002 | 0/0 | 6044 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002c0005t0003 | 0/0 | 6047 | 23 | 0 | 0 | 23 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002c0005t0009 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002c0005t0017 | 0/0 | 6049 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002c0005t0025 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0002c0005t0026 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0003c0006t0010 | 0/1 | 6044 | 10 | 0 | 5 | 3 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0003c0006t0039 | 0/0 | 5995 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0004c0007t0011 | 0/0 | 6045 | 9 | 3 | 1 | 0 | 3 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0005c0008t0003 | 0/0 | 6047 | 7 | 0 | 6 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0005c0017t0003 | 0/0 | 6047 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0006c0009t0009 | 0/0 | 6047 | 4 | 1 | 0 | 2 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0006c0009t0035 | 0/0 | 6047 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0006c0009t0036 | 0/0 | 6049 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0007c0019t0018 | 0/0 | 6052 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0008c0015t0009 | 0/0 | 6047 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0009c0013t0014 | 0/0 | 6045 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0010c0012t0004 | 0/0 | 6043 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0011c0016t0001 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0012c0018t0004 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
a0013c0010t0004 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | copy fasta | chr2 | 159707506 | 159776027 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0014g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0014g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0015g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0015g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0015g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0016g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0016g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0016g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0020g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0029g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0033g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0038g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0019g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0019g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0021g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0021g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0034g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0024g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0027g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0030g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0031g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0032g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0013g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0013g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0018g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0022g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0022g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0023g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0028g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0037g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0040g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0011t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0014t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0017g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0025g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0026g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0039g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0013 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0017t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0035g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0036g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0007c0019t0018g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0008c0015t0009g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0009c0013t0014g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0010c0012t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0011c0016t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0012c0018t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0013c0010t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0004 | g0192 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0148 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0147 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00280 | hp1 | a0004 | c0007 | t0011 | g0013 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00280 | hp2 | a0001 | c0001 | t0015 | g0295 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0090 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00323 | hp2 | a0001 | c0011 | t0002 | g0264 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00408 | hp2 | a0002 | c0005 | t0003 | g0045 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00438 | hp1 | a0006 | c0009 | t0009 | g0036 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00544 | hp1 | a0012 | c0018 | t0004 | g0188 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00558 | hp1 | a0001 | c0003 | t0004 | g0200 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00597 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00597 | hp2 | a0002 | c0005 | t0003 | g0061 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00609 | hp1 | a0001 | c0003 | t0004 | g0198 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00639 | hp1 | a0001 | c0004 | t0008 | g0312 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00735 | hp1 | a0003 | c0006 | t0010 | g0166 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00738 | hp1 | a0005 | c0008 | t0003 | g0066 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01074 | hp2 | a0004 | c0007 | t0011 | g0172 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01106 | hp2 | a0001 | c0001 | t0029 | g0265 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01168 | hp1 | a0001 | c0004 | t0013 | g0027 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01169 | hp2 | a0001 | c0004 | t0013 | g0027 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01175 | hp2 | a0001 | c0003 | t0004 | g0194 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01257 | hp2 | a0003 | c0006 | t0010 | g0012 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01258 | hp2 | a0003 | c0006 | t0010 | g0012 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01261 | hp2 | a0001 | c0004 | t0005 | g0213 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01358 | hp2 | a0003 | c0006 | t0010 | g0164 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01361 | hp2 | a0001 | c0004 | t0040 | g0211 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01433 | hp1 | a0005 | c0008 | t0003 | g0063 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01515 | hp2 | a0005 | c0008 | t0003 | g0062 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01516 | hp1 | a0001 | c0003 | t0004 | g0029 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01516 | hp2 | a0004 | c0007 | t0011 | g0173 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01517 | hp2 | a0004 | c0007 | t0011 | g0174 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01934 | hp2 | a0005 | c0008 | t0003 | g0048 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01952 | hp1 | a0005 | c0017 | t0003 | g0049 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01975 | hp2 | a0005 | c0008 | t0003 | g0047 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0079 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0223 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02055 | hp2 | a0001 | c0004 | t0005 | g0222 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02071 | hp1 | a0001 | c0003 | t0003 | g0084 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02080 | hp1 | a0002 | c0005 | t0009 | g0089 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02080 | hp2 | a0001 | c0003 | t0004 | g0191 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02083 | hp1 | a0002 | c0005 | t0003 | g0055 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0082 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02135 | hp1 | a0003 | c0006 | t0010 | g0163 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02135 | hp2 | a0002 | c0005 | t0003 | g0054 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0305 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02145 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | CDX | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02155 | hp2 | a0002 | c0005 | t0003 | g0044 | EAS | CDX | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02257 | hp2 | a0001 | c0004 | t0008 | g0026 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02258 | hp1 | a0006 | c0009 | t0036 | g0039 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02258 | hp2 | a0001 | c0004 | t0005 | g0018 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02273 | hp2 | a0005 | c0008 | t0003 | g0046 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02280 | hp1 | a0006 | c0009 | t0035 | g0037 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02293 | hp1 | a0005 | c0008 | t0003 | g0050 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02300 | hp1 | a0003 | c0006 | t0010 | g0168 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02451 | hp1 | a0001 | c0004 | t0009 | g0077 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02451 | hp2 | a0009 | c0013 | t0014 | g0301 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02572 | hp2 | a0001 | c0004 | t0013 | g0309 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02615 | hp2 | a0001 | c0004 | t0005 | g0220 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02622 | hp2 | a0001 | c0004 | t0008 | g0316 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0240 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02630 | hp2 | a0001 | c0004 | t0022 | g0313 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02647 | hp1 | a0001 | c0001 | t0020 | g0169 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02647 | hp2 | a0001 | c0004 | t0009 | g0078 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02717 | hp1 | a0001 | c0001 | t0020 | g0170 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02717 | hp2 | a0001 | c0004 | t0005 | g0212 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02738 | hp2 | a0004 | c0007 | t0011 | g0177 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02809 | hp1 | a0001 | c0004 | t0013 | g0310 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02809 | hp2 | a0004 | c0007 | t0011 | g0171 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02895 | hp1 | a0001 | c0004 | t0005 | g0219 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0246 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02896 | hp1 | a0001 | c0004 | t0005 | g0218 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02896 | hp2 | a0001 | c0004 | t0008 | g0025 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0242 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02897 | hp2 | a0001 | c0004 | t0008 | g0025 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0210 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02965 | hp1 | a0001 | c0001 | t0014 | g0300 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02965 | hp2 | a0004 | c0007 | t0011 | g0176 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02970 | hp1 | a0001 | c0004 | t0005 | g0214 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0247 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03041 | hp2 | a0001 | c0004 | t0008 | g0026 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03098 | hp1 | a0001 | c0004 | t0008 | g0308 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03139 | hp2 | a0001 | c0004 | t0008 | g0311 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03195 | hp1 | a0006 | c0009 | t0009 | g0038 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0245 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03209 | hp1 | a0001 | c0001 | t0033 | g0160 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03209 | hp2 | a0004 | c0007 | t0011 | g0175 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03225 | hp1 | a0001 | c0004 | t0008 | g0315 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03225 | hp2 | a0001 | c0004 | t0037 | g0217 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03239 | hp2 | a0010 | c0012 | t0004 | g0207 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03453 | hp2 | a0001 | c0004 | t0003 | g0065 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03491 | hp1 | a0001 | c0003 | t0004 | g0181 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03492 | hp2 | a0001 | c0003 | t0004 | g0180 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03516 | hp1 | a0001 | c0004 | t0005 | g0215 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0299 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03540 | hp2 | a0001 | c0003 | t0004 | g0224 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03579 | hp1 | a0001 | c0004 | t0003 | g0052 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03579 | hp2 | a0001 | c0004 | t0005 | g0221 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03654 | hp1 | a0006 | c0009 | t0009 | g0040 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03654 | hp2 | a0001 | c0004 | t0023 | g0017 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03704 | hp2 | a0001 | c0014 | t0002 | g0259 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03710 | hp2 | a0008 | c0015 | t0009 | g0306 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03834 | hp2 | a0001 | c0004 | t0023 | g0017 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03927 | hp2 | a0001 | c0003 | t0004 | g0183 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04199 | hp1 | a0003 | c0006 | t0010 | g0165 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04199 | hp2 | a0001 | c0001 | t0015 | g0278 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04204 | hp2 | a0004 | c0007 | t0011 | g0013 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18612 | hp1 | a0001 | c0002 | t0019 | g0110 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18612 | hp2 | a0001 | c0003 | t0024 | g0203 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18747 | hp1 | a0001 | c0003 | t0032 | g0014 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18940 | hp2 | a0001 | c0003 | t0004 | g0197 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18942 | hp1 | a0001 | c0003 | t0004 | g0208 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18942 | hp2 | a0001 | c0001 | t0016 | g0256 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18943 | hp1 | a0001 | c0003 | t0003 | g0076 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18944 | hp1 | a0001 | c0003 | t0027 | g0206 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18944 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18946 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18948 | hp2 | a0002 | c0005 | t0003 | g0068 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18950 | hp1 | a0001 | c0002 | t0007 | g0008 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18950 | hp2 | a0001 | c0003 | t0004 | g0201 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18951 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18953 | hp1 | a0001 | c0001 | t0015 | g0318 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18953 | hp2 | a0001 | c0003 | t0004 | g0202 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18954 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18954 | hp2 | a0001 | c0003 | t0003 | g0085 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18957 | hp2 | a0002 | c0005 | t0003 | g0005 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18960 | hp1 | a0001 | c0002 | t0007 | g0127 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18960 | hp2 | a0002 | c0005 | t0003 | g0057 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18961 | hp1 | a0002 | c0005 | t0026 | g0056 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18961 | hp2 | a0003 | c0006 | t0010 | g0162 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18962 | hp2 | a0013 | c0010 | t0004 | g0015 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18964 | hp1 | a0011 | c0016 | t0001 | g0102 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18964 | hp2 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18965 | hp1 | a0001 | c0002 | t0007 | g0116 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18965 | hp2 | a0001 | c0003 | t0004 | g0187 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18968 | hp1 | a0001 | c0002 | t0021 | g0096 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18968 | hp2 | a0001 | c0003 | t0004 | g0186 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18969 | hp2 | a0001 | c0003 | t0004 | g0184 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18970 | hp1 | a0002 | c0005 | t0003 | g0059 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18972 | hp1 | a0001 | c0003 | t0004 | g0178 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18973 | hp1 | a0002 | c0005 | t0025 | g0051 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18977 | hp1 | a0002 | c0005 | t0003 | g0071 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18978 | hp1 | a0001 | c0002 | t0007 | g0008 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18979 | hp1 | a0001 | c0003 | t0004 | g0195 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18980 | hp1 | a0001 | c0001 | t0016 | g0258 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18980 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18981 | hp2 | a0001 | c0003 | t0004 | g0196 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18983 | hp2 | a0001 | c0003 | t0030 | g0205 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18985 | hp1 | a0002 | c0005 | t0003 | g0064 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18987 | hp1 | a0002 | c0005 | t0003 | g0033 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18989 | hp1 | a0002 | c0005 | t0003 | g0042 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18989 | hp2 | a0001 | c0003 | t0004 | g0204 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18990 | hp2 | a0001 | c0003 | t0003 | g0081 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18994 | hp2 | a0001 | c0003 | t0004 | g0199 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18998 | hp2 | a0002 | c0005 | t0003 | g0060 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18999 | hp2 | a0001 | c0002 | t0019 | g0152 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19000 | hp2 | a0001 | c0002 | t0007 | g0117 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19003 | hp2 | a0002 | c0005 | t0003 | g0074 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19004 | hp2 | a0002 | c0005 | t0017 | g0005 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19005 | hp1 | a0002 | c0005 | t0003 | g0072 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19006 | hp2 | a0001 | c0003 | t0004 | g0209 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19030 | hp1 | a0001 | c0004 | t0022 | g0314 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19043 | hp1 | a0001 | c0004 | t0005 | g0018 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19043 | hp2 | a0001 | c0004 | t0005 | g0028 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19055 | hp2 | a0001 | c0002 | t0034 | g0099 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19058 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19058 | hp2 | a0001 | c0003 | t0003 | g0083 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19060 | hp2 | a0002 | c0005 | t0003 | g0067 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19064 | hp1 | a0002 | c0005 | t0017 | g0070 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19066 | hp1 | a0002 | c0005 | t0003 | g0043 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19066 | hp2 | a0001 | c0003 | t0004 | g0015 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19068 | hp1 | a0001 | c0003 | t0004 | g0193 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19070 | hp1 | a0002 | c0005 | t0003 | g0053 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19070 | hp2 | a0003 | c0006 | t0010 | g0011 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19074 | hp2 | a0001 | c0003 | t0004 | g0189 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19076 | hp2 | a0001 | c0002 | t0007 | g0108 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19078 | hp1 | a0001 | c0003 | t0031 | g0185 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19078 | hp2 | a0002 | c0005 | t0003 | g0073 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19081 | hp1 | a0001 | c0001 | t0016 | g0257 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19082 | hp1 | a0006 | c0009 | t0009 | g0041 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19084 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19084 | hp2 | a0001 | c0003 | t0004 | g0190 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19085 | hp1 | a0002 | c0005 | t0003 | g0069 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19087 | hp2 | a0002 | c0005 | t0003 | g0058 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19088 | hp1 | a0001 | c0002 | t0021 | g0101 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19088 | hp2 | a0002 | c0005 | t0003 | g0075 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19090 | hp2 | a0001 | c0003 | t0004 | g0182 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19091 | hp2 | a0003 | c0006 | t0039 | g0011 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19240 | hp1 | a0001 | c0004 | t0018 | g0225 | AFR | YRI | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19240 | hp2 | a0001 | c0004 | t0005 | g0216 | AFR | YRI | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA20129 | hp1 | a0001 | c0004 | t0009 | g0034 | AFR | ASW | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA20129 | hp2 | a0001 | c0004 | t0028 | g0227 | AFR | ASW | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03471 | hp1 | a0001 | c0004 | t0009 | g0035 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0241 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG06807 | hp1 | a0001 | c0004 | t0008 | g0307 | AFR | USA | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | USA | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18955 | hp2 | a0001 | c0001 | t0038 | g0275 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0243 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA21309 | hp2 | a0007 | c0019 | t0018 | g0226 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
homoSapiens_chm13v2 | hp1 | a0003 | c0006 | t0010 | g0167 | REF | REF | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0004 | g0179 | REF | REF | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159729057
|
T | C | 1 | a0013 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.35T>C | p.Ile12Thr | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/12 | 278/6043 | 35/2115 | 12/704 | chr2 | 159729057 | ||
chr2:159743206
|
C | G | 1 | a0003 | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
missense_variant | MODERATE | c.299C>G | p.Thr100Ser | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/12 | 542/6043 | 299/2115 | 100/704 | chr2 | 159743206 | ||
chr2:159743209
|
C | T | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.302C>T | p.Thr101Ile | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/12 | 545/6043 | 302/2115 | 101/704 | chr2 | 159743209 | ||
chr2:159747861
|
A | G | 1 | a0012 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.571A>G | p.Met191Val | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 814/6043 | 571/2115 | 191/704 | chr2 | 159747861 | ||
chr2:159747868
|
C | T | 2 | a0002a0005 | 36 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(33): Show |
missense_variant | MODERATE | c.578C>T | p.Thr193Ile | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 821/6043 | 578/2115 | 193/704 | chr2 | 159747868 | ||
chr2:159748003
|
C | T | 2 | a0006a0008 | 7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
missense_variant | MODERATE | c.713C>T | p.Thr238Met | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 956/6043 | 713/2115 | 238/704 | chr2 | 159748003 | ||
chr2:159748030
|
G | A | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.740G>A | p.Ser247Asn | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 983/6043 | 740/2115 | 247/704 | chr2 | 159748030 | ||
chr2:159748183
|
G | C | 1 | a0011 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.893G>C | p.Arg298Thr | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1136/6043 | 893/2115 | 298/704 | chr2 | 159748183 | ||
chr2:159748257
|
G | A | 1 | a0005 | 8 | HG00738.hp1 HG01433.hp1 HG01515.hp2 others(5): Show |
missense_variant | MODERATE | c.967G>A | p.Ala323Thr | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1210/6043 | 967/2115 | 323/704 | chr2 | 159748257 | ||
chr2:159748425
|
G | A | 1 | a0004 | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
missense_variant | MODERATE | c.1135G>A | p.Gly379Ser | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1378/6043 | 1135/2115 | 379/704 | chr2 | 159748425 | ||
chr2:159748498
|
G | C | 1 | a0009 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1208G>C | p.Arg403Pro | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1451/6043 | 1208/2115 | 403/704 | chr2 | 159748498 | ||
chr2:159748615
|
G | A | 1 | a0010 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1325G>A | p.Gly442Glu | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1568/6043 | 1325/2115 | 442/704 | chr2 | 159748615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159743084
|
G | A | 1 | a0001c0011 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.177G>A | p.Ala59Ala | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/12 | 420/6043 | 177/2115 | 59/704 | chr2 | 159743084 | ||
chr2:159747941
|
C | T | 2 | a0001c0002a0011c0016 | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
synonymous_variant | LOW | c.651C>T | p.Asp217Asp | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 894/6043 | 651/2115 | 217/704 | chr2 | 159747941 | ||
chr2:159748301
|
C | T | 4 | a0001c0001a0001c0011a0001c0014others(1): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
synonymous_variant | LOW | c.1011C>T | p.Pro337Pro | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1254/6043 | 1011/2115 | 337/704 | chr2 | 159748301 | ||
chr2:159748655
|
C | T | 1 | a0001c0014 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1365C>T | p.Ser455Ser | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1608/6043 | 1365/2115 | 455/704 | chr2 | 159748655 | ||
chr2:159748757
|
T | C | 15 | a0001c0001a0001c0002a0001c0004others(12): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
synonymous_variant | LOW | c.1467T>C | p.Pro489Pro | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1710/6043 | 1467/2115 | 489/704 | chr2 | 159748757 | ||
chr2:159752543
|
A | G | 1 | a0005c0017 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.1755A>G | p.Lys585Lys | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/12 | 1998/6043 | 1755/2115 | 585/704 | chr2 | 159752543 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159712509
|
T | G | 9 | a0001c0003t0003a0001c0003t0024a0001c0004t0003others(6): Show | 47 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-240T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/12 | 16514 | chr2 | 159712509 | |||||
chr2:159712556
|
C | G | 1 | a0001c0001t0016 | 3 | NA18942.hp2 NA18980.hp1 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-193C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/12 | 16467 | chr2 | 159712556 | |||||
chr2:159715750
|
T | A | 1 | a0001c0003t0027 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/12 | 13273 | chr2 | 159715750 | |||||
chr2:159767565
|
A | G | 1 | a0002c0005t0026 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 223 | chr2 | 159767565 | |||||
chr2:159767736
|
ACTT | A | 2 | a0001c0004t0023a0001c0004t0040 | 3 | HG01361.hp2 HG03654.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*395_*397delCTT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 395 | chr2 | 159767736 | |||||
chr2:159767848
|
G | A | 3 | a0001c0004t0018a0001c0004t0028a0007c0019t0018 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*506G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 506 | chr2 | 159767848 | |||||
chr2:159767872
|
A | T | 1 | a0001c0004t0022 | 2 | HG02630.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*530A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 530 | chr2 | 159767872 | |||||
chr2:159768178
|
T | G | 2 | a0001c0004t0008a0001c0004t0022 | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*836T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 836 | chr2 | 159768178 | |||||
chr2:159768239
|
C | CT | 2 | a0003c0006t0010a0003c0006t0039 | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*902dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 903 | INFO_REALIGN_3_PRIME | chr2 | 159768239 | ||||
chr2:159768331
|
G | A | 1 | a0001c0001t0029 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*989G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 989 | chr2 | 159768331 | |||||
chr2:159768368
|
C | G | 1 | a0001c0002t0007 | 11 | NA18944.hp2 NA18950.hp1 NA18951.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1026C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1026 | chr2 | 159768368 | |||||
chr2:159768606
|
G | T | 1 | a0001c0001t0038 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1264 | chr2 | 159768606 | |||||
chr2:159769026
|
T | C | 1 | a0001c0003t0030 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1684 | chr2 | 159769026 | |||||
chr2:159769092
|
G | C | 1 | a0001c0003t0031 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1750 | chr2 | 159769092 | |||||
chr2:159769216
|
C | G | 7 | a0001c0001t0002a0001c0001t0015a0001c0001t0016others(4): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1874C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1874 | chr2 | 159769216 | |||||
chr2:159769330
|
T | C | 3 | a0001c0004t0008a0001c0004t0013a0001c0004t0022 | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1988T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1988 | chr2 | 159769330 | |||||
chr2:159769381
|
G | T | 1 | a0002c0005t0025 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2039G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2039 | chr2 | 159769381 | |||||
chr2:159769469
|
C | G | 1 | a0001c0001t0012 | 6 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2127C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2127 | chr2 | 159769469 | |||||
chr2:159769581
|
G | T | 1 | a0001c0002t0021 | 2 | NA18968.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2239G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2239 | chr2 | 159769581 | |||||
chr2:159769641
|
A | G | 46 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(43): Show | 323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*2299A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2299 | chr2 | 159769641 | |||||
chr2:159769643
|
C | CAT | 17 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(14): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2315_*2316dupTA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | ||||
chr2:159769643
|
C | CATAT | 15 | a0001c0001t0015a0001c0003t0003a0001c0004t0003others(12): Show | 60 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2313_*2316dupTATA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | ||||
chr2:159769643
|
C | CATATAT | 3 | a0001c0004t0028a0002c0005t0017a0006c0009t0036 | 4 | HG02258.hp1 NA19004.hp2 NA19064.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2311_*2316dupTATA others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | ||||
chr2:159769643
|
C | CATATATA others(3): Show |
1 | a0001c0004t0037 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2307_*2316dupTATA others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | ||||
chr2:159769712
|
A | G | 1 | a0001c0004t0022 | 2 | HG02630.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2370A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2370 | chr2 | 159769712 | |||||
chr2:159769787
|
A | T | 1 | a0001c0004t0040 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2445A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2445 | chr2 | 159769787 | |||||
chr2:159769936
|
G | T | 1 | a0001c0003t0032 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2594G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2594 | chr2 | 159769936 | |||||
chr2:159770111
|
C | T | 8 | a0001c0002t0001a0001c0002t0007a0001c0002t0019others(5): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2769C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2769 | chr2 | 159770111 | |||||
chr2:159770120
|
C | T | 1 | a0001c0001t0033 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2778C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2778 | chr2 | 159770120 | |||||
chr2:159770126
|
AT | A | 17 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(14): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2792delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2792 | INFO_REALIGN_3_PRIME | chr2 | 159770126 | ||||
chr2:159770231
|
T | TATCA | 3 | a0001c0004t0018a0001c0004t0028a0007c0019t0018 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2892_*2895dupCAAT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2896 | INFO_REALIGN_3_PRIME | chr2 | 159770231 | ||||
chr2:159770355
|
G | A | 1 | a0006c0009t0035 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3013G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3013 | chr2 | 159770355 | |||||
chr2:159770360
|
GT | G | 4 | a0001c0004t0005a0001c0004t0023a0001c0004t0037others(1): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3020delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3020 | INFO_REALIGN_3_PRIME | chr2 | 159770360 | ||||
chr2:159770373
|
T | TATCA | 3 | a0001c0004t0008a0001c0004t0013a0001c0004t0022 | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3032_*3035dupATCA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3036 | INFO_REALIGN_3_PRIME | chr2 | 159770373 | ||||
chr2:159770387
|
T | C | 8 | a0001c0002t0001a0001c0002t0007a0001c0002t0019others(5): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3045T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3045 | chr2 | 159770387 | |||||
chr2:159770469
|
G | A | 6 | a0001c0002t0001a0001c0002t0007a0001c0002t0019others(3): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3127G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3127 | chr2 | 159770469 | |||||
chr2:159770539
|
GATAATTG others(27): Show |
G | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3199_*3232delTAAT others(30): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3199 | INFO_REALIGN_3_PRIME | chr2 | 159770539 | ||||
chr2:159770579
|
T | G | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3237T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3237 | chr2 | 159770579 | |||||
chr2:159770582
|
T | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3240T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3240 | chr2 | 159770582 | |||||
chr2:159770583
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3241T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3241 | chr2 | 159770583 | |||||
chr2:159770642
|
G | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3300G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3300 | chr2 | 159770642 | |||||
chr2:159770657
|
C | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3315C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3315 | chr2 | 159770657 | |||||
chr2:159770658
|
A | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3316A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3316 | chr2 | 159770658 | |||||
chr2:159770659
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3317T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3317 | chr2 | 159770659 | |||||
chr2:159770661
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3319T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3319 | chr2 | 159770661 | |||||
chr2:159770663
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3321T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3321 | chr2 | 159770663 | |||||
chr2:159770667
|
C | CT | 3 | a0001c0004t0018a0001c0004t0028a0007c0019t0018 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3326dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3327 | INFO_REALIGN_3_PRIME | chr2 | 159770667 | ||||
chr2:159770669
|
G | T | 3 | a0001c0004t0018a0001c0004t0028a0007c0019t0018 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3327G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3327 | chr2 | 159770669 | |||||
chr2:159770677
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3335T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3335 | chr2 | 159770677 | |||||
chr2:159770679
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3337T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3337 | chr2 | 159770679 | |||||
chr2:159770683
|
TTTAGATA others(8): Show |
T | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3344_*3358delAGAT others(11): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3344 | INFO_REALIGN_3_PRIME | chr2 | 159770683 | ||||
chr2:159770701
|
G | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3359G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3359 | chr2 | 159770701 | |||||
chr2:159770705
|
T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3363T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3363 | chr2 | 159770705 | |||||
chr2:159770706
|
A | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3364A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3364 | chr2 | 159770706 | |||||
chr2:159770771
|
A | C | 1 | a0001c0002t0019 | 2 | NA18612.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3429A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3429 | chr2 | 159770771 | |||||
chr2:159770806
|
C | G | 12 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(9): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3464C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3464 | chr2 | 159770806 | |||||
chr2:159770903
|
T | G | 1 | a0004c0007t0011 | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3561T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3561 | chr2 | 159770903 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159712765
|
C | T | 108 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(105): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-143+159C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712765 | ||||||
chr2:159712834
|
G | T | 3 | a0001c0004t0018g0225a0001c0004t0028g0227a0007c0019t0018g0226 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-143+228G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712834 | ||||||
chr2:159712943
|
A | C | 1 | a0001c0001t0002g0325 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-143+337A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712943 | ||||||
chr2:159712953
|
T | C | 1 | a0001c0004t0005g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-143+347T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712953 | ||||||
chr2:159712991
|
G | A | 1 | a0001c0003t0004g0029 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-143+385G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712991 | ||||||
chr2:159713059
|
G | C | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032 | 3 | HG00735.hp2 HG01258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-143+453G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713059 | ||||||
chr2:159713138
|
T | C | 59 | a0001c0003t0003g0076a0001c0003t0003g0079a0001c0003t0003g0080others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-143+532T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713138 | ||||||
chr2:159713180
|
A | G | 10 | a0001c0001t0002g0003a0001c0001t0002g0317a0001c0001t0002g0319others(7): Show | 14 | HG00408.hp1 HG00544.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.-143+574A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713180 | ||||||
chr2:159713311
|
C | G | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-143+705C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713311 | ||||||
chr2:159713522
|
T | C | 192 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(189): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-143+916T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713522 | ||||||
chr2:159713620
|
T | C | 1 | a0001c0002t0001g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-142-937T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713620 | ||||||
chr2:159713919
|
G | GT | 8 | a0001c0003t0003g0079a0001c0003t0003g0080a0001c0003t0003g0081others(5): Show | 8 | HG00597.hp1 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-142-631dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 159713919 | |||||
chr2:159714056
|
G | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-501G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714056 | ||||||
chr2:159714113
|
A | G | 2 | a0001c0003t0004g0223a0001c0003t0004g0224 | 2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-142-444A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714113 | ||||||
chr2:159714117
|
A | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-142-440A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714117 | ||||||
chr2:159714171
|
A | G | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-142-386A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714171 | ||||||
chr2:159714220
|
T | A | 4 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(1): Show | 6 | HG02257.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-337T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714220 | ||||||
chr2:159714408
|
T | C | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-142-149T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714408 | ||||||
chr2:159714504
|
A | G | 1 | a0001c0001t0006g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-142-53A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714504 | ||||||
chr2:159714599
|
G | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
splice_donor_variant&intron_variant | HIGH | c.-101+1G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714599 | ||||||
chr2:159714758
|
C | T | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-101+160C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714758 | ||||||
chr2:159714798
|
A | G | 1 | a0001c0001t0002g0024 | 2 | HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-101+200A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714798 | ||||||
chr2:159714826
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-101+228C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714826 | ||||||
chr2:159714844
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-101+246G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714844 | ||||||
chr2:159715034
|
C | T | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-101+436C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715034 | ||||||
chr2:159715161
|
A | G | 1 | a0001c0002t0001g0161 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-100-520A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715161 | ||||||
chr2:159715198
|
A | G | 124 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(121): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-100-483A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715198 | ||||||
chr2:159715272
|
ATCT | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-100-407_-100-405d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 159715272 | |||||
chr2:159715343
|
A | G | 2 | a0003c0006t0010g0012a0003c0006t0010g0168 | 3 | HG01257.hp2 HG01258.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-100-338A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715343 | ||||||
chr2:159715365
|
G | A | 19 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(16): Show | 20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-100-316G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715365 | ||||||
chr2:159715370
|
T | C | 1 | a0004c0007t0011g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-100-311T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715370 | ||||||
chr2:159715385
|
G | C | 1 | a0001c0003t0004g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-100-296G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715385 | ||||||
chr2:159715493
|
C | G | 1 | a0001c0002t0001g0157 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-100-188C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715493 | ||||||
chr2:159715822
|
A | G | 1 | a0004c0007t0011g0177 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-15+56A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159715822 | ||||||
chr2:159715992
|
T | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+226T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159715992 | ||||||
chr2:159716008
|
G | A | 93 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(90): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-15+242G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716008 | ||||||
chr2:159716033
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+267A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716033 | ||||||
chr2:159716089
|
ATATTTT | A | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+325_-15+330del others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716089 | |||||
chr2:159716138
|
C | CT | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+380dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716138 | |||||
chr2:159716207
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+441A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716207 | ||||||
chr2:159716266
|
A | AT | 115 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(112): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-15+511dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716266 | |||||
chr2:159716326
|
T | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+560T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716326 | ||||||
chr2:159716400
|
G | A | 1 | a0001c0004t0005g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+634G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716400 | ||||||
chr2:159716424
|
A | T | 2 | a0001c0002t0001g0155a0001c0002t0001g0156 | 2 | NA18984.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-15+658A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716424 | ||||||
chr2:159716631
|
A | G | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+865A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716631 | ||||||
chr2:159716643
|
CA | C | 98 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(95): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+888delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716643 | |||||
chr2:159716715
|
A | G | 2 | a0001c0004t0009g0077a0001c0004t0009g0078 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-15+949A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716715 | ||||||
chr2:159716866
|
A | G | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-15+1100A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716866 | ||||||
chr2:159716905
|
G | C | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+1139G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716905 | ||||||
chr2:159716940
|
T | G | 1 | a0001c0001t0002g0249 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+1174T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716940 | ||||||
chr2:159717089
|
G | A | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+1323G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717089 | ||||||
chr2:159717195
|
ATT | A | 69 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(66): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-15+1430_-15+1431d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717195 | ||||||
chr2:159717220
|
G | C | 1 | a0001c0004t0023g0017 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-15+1454G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717220 | ||||||
chr2:159717260
|
C | T | 2 | a0001c0002t0001g0153a0001c0002t0001g0154 | 2 | NA18977.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-15+1494C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717260 | ||||||
chr2:159717462
|
A | G | 2 | a0001c0004t0005g0221a0001c0004t0005g0222 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+1696A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717462 | ||||||
chr2:159717520
|
CTT | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+1756_-15+1757d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159717520 | |||||
chr2:159717613
|
A | T | 124 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(121): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+1847A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717613 | ||||||
chr2:159717614
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+1848G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717614 | ||||||
chr2:159717628
|
T | TGTAAACC others(45): Show |
1 | a0001c0002t0019g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-15+1880_-15+1881i others(54): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159717628 | |||||
chr2:159717857
|
G | T | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+2091G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717857 | ||||||
chr2:159718016
|
G | C | 2 | a0001c0002t0001g0090a0001c0002t0001g0091 | 2 | HG00323.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-15+2250G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718016 | ||||||
chr2:159718037
|
A | G | 1 | a0001c0004t0005g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+2271A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718037 | ||||||
chr2:159718201
|
A | G | 1 | a0001c0001t0002g0298 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-15+2435A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718201 | ||||||
chr2:159718239
|
T | C | 4 | a0003c0006t0010g0011a0003c0006t0010g0162a0003c0006t0010g0163others(1): Show | 4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+2473T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718239 | ||||||
chr2:159718715
|
A | G | 86 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(83): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-15+2949A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718715 | ||||||
chr2:159718845
|
T | C | 288 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(285): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.-15+3079T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718845 | ||||||
chr2:159719065
|
C | T | 2 | a0001c0003t0004g0208a0001c0003t0004g0209 | 2 | NA18942.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-15+3299C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719065 | ||||||
chr2:159719099
|
C | T | 1 | a0010c0012t0004g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+3333C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719099 | ||||||
chr2:159719122
|
G | A | 2 | a0001c0004t0009g0077a0001c0004t0009g0078 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-15+3356G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719122 | ||||||
chr2:159719165
|
A | C | 1 | a0001c0001t0002g0249 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+3399A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719165 | ||||||
chr2:159719274
|
C | A | 98 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(95): Show | 110 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.-15+3508C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719274 | ||||||
chr2:159719413
|
CCTGAAAG others(5): Show |
C | 6 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(3): Show | 7 | HG01257.hp2 HG01258.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+3649_-15+3660d others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159719413 | |||||
chr2:159719647
|
A | G | 94 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(91): Show | 104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-15+3881A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719647 | ||||||
chr2:159719653
|
C | T | 37 | a0001c0004t0003g0052a0001c0004t0003g0065a0002c0005t0003g0005others(34): Show | 37 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+3887C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719653 | ||||||
chr2:159719708
|
C | G | 1 | a0001c0002t0001g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-15+3942C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719708 | ||||||
chr2:159719770
|
G | A | 60 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(57): Show | 69 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.-15+4004G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719770 | ||||||
chr2:159719954
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-15+4188G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719954 | ||||||
chr2:159720072
|
C | G | 53 | a0001c0004t0003g0052a0001c0004t0003g0065a0001c0004t0005g0028others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+4306C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720072 | ||||||
chr2:159720099
|
C | A | 2 | a0002c0005t0003g0042a0002c0005t0003g0043 | 2 | NA18989.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-15+4333C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720099 | ||||||
chr2:159720154
|
G | A | 1 | a0002c0005t0003g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-15+4388G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720154 | ||||||
chr2:159720171
|
A | G | 55 | a0001c0003t0003g0079a0001c0003t0003g0080a0001c0003t0003g0081others(52): Show | 55 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-15+4405A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720171 | ||||||
chr2:159720393
|
C | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-15+4627C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720393 | ||||||
chr2:159720422
|
A | G | 1 | a0001c0001t0002g0292 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-15+4656A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720422 | ||||||
chr2:159720499
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+4733A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720499 | ||||||
chr2:159720764
|
A | G | 3 | a0001c0004t0018g0225a0001c0004t0028g0227a0007c0019t0018g0226 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-15+4998A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720764 | ||||||
chr2:159720939
|
C | T | 6 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5173C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720939 | ||||||
chr2:159721018
|
C | T | 1 | a0001c0004t0005g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+5252C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721018 | ||||||
chr2:159721019
|
G | A | 1 | a0001c0001t0014g0299 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+5253G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721019 | ||||||
chr2:159721023
|
A | AT | 93 | a0001c0001t0002g0158a0001c0001t0002g0290a0001c0001t0002g0291others(90): Show | 94 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-15+5272dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159721023 | |||||
chr2:159721056
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+5290G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721056 | ||||||
chr2:159721309
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-15+5543T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721309 | ||||||
chr2:159721404
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-15+5638C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721404 | ||||||
chr2:159721641
|
C | G | 1 | a0001c0003t0004g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15+5875C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721641 | ||||||
chr2:159721671
|
T | A | 1 | a0001c0004t0040g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15+5905T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721671 | ||||||
chr2:159721783
|
C | T | 3 | a0001c0004t0013g0027a0001c0004t0013g0309a0001c0004t0013g0310 | 4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+6017C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721783 | ||||||
chr2:159721906
|
A | T | 53 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+6140A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721906 | ||||||
chr2:159722079
|
A | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-15+6313A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722079 | ||||||
chr2:159722162
|
A | G | 3 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0286 | 3 | HG01109.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-15+6396A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722162 | ||||||
chr2:159722361
|
C | T | 1 | a0009c0013t0014g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+6595C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722361 | ||||||
chr2:159722399
|
G | T | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-6610G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722399 | ||||||
chr2:159722467
|
G | A | 1 | a0006c0009t0009g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-14-6542G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722467 | ||||||
chr2:159722573
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-6436A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722573 | ||||||
chr2:159722617
|
G | C | 1 | a0001c0004t0009g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-14-6392G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722617 | ||||||
chr2:159722706
|
T | A | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-6303T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722706 | ||||||
chr2:159722878
|
C | T | 8 | a0001c0004t0005g0018a0001c0004t0005g0210a0001c0004t0005g0218others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-6131C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722878 | ||||||
chr2:159723067
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14-5942A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723067 | ||||||
chr2:159723165
|
C | T | 1 | a0001c0002t0001g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-14-5844C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723165 | ||||||
chr2:159723179
|
T | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-5830T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723179 | ||||||
chr2:159723286
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-14-5723G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723286 | ||||||
chr2:159723381
|
G | T | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-5628G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723381 | ||||||
chr2:159723451
|
G | C | 3 | a0001c0004t0018g0225a0001c0004t0028g0227a0007c0019t0018g0226 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-14-5558G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723451 | ||||||
chr2:159723514
|
C | T | 1 | a0001c0004t0028g0227 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-14-5495C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723514 | ||||||
chr2:159723540
|
C | T | 1 | a0001c0001t0002g0324 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-14-5469C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723540 | ||||||
chr2:159723570
|
A | G | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0001g0134 | 3 | NA18747.hp2 NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-14-5439A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723570 | ||||||
chr2:159723646
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-14-5363C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723646 | ||||||
chr2:159723653
|
C | T | 5 | a0001c0004t0009g0034a0001c0004t0009g0035a0001c0004t0018g0225others(2): Show | 5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-5356C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723653 | ||||||
chr2:159723654
|
T | C | 8 | a0001c0003t0003g0079a0001c0003t0003g0080a0001c0003t0003g0081others(5): Show | 8 | HG00597.hp1 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-5355T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723654 | ||||||
chr2:159723814
|
A | G | 1 | a0001c0002t0019g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-14-5195A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723814 | ||||||
chr2:159723861
|
A | G | 2 | a0001c0004t0009g0077a0001c0004t0009g0078 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-14-5148A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723861 | ||||||
chr2:159723876
|
C | CATGT | 61 | a0001c0003t0003g0076a0001c0003t0003g0079a0001c0003t0003g0080others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-14-5132_-14-5129d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159723876 | |||||
chr2:159723900
|
C | G | 281 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(278): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.-14-5109C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723900 | ||||||
chr2:159724088
|
G | T | 5 | a0001c0004t0009g0034a0001c0004t0009g0035a0001c0004t0018g0225others(2): Show | 5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-4921G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724088 | ||||||
chr2:159724216
|
G | T | 2 | a0001c0004t0009g0077a0001c0004t0009g0078 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-14-4793G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724216 | ||||||
chr2:159724225
|
G | A | 1 | a0001c0004t0008g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-4784G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724225 | ||||||
chr2:159724278
|
C | T | 1 | a0001c0002t0001g0131 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-14-4731C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724278 | ||||||
chr2:159724354
|
T | A | 1 | a0001c0004t0008g0312 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-14-4655T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724354 | ||||||
chr2:159724356
|
G | T | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-4653G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724356 | ||||||
chr2:159724480
|
A | T | 1 | a0001c0004t0009g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-4529A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724480 | ||||||
chr2:159724721
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-4288C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724721 | ||||||
chr2:159724790
|
G | A | 2 | a0001c0004t0022g0313a0001c0004t0022g0314 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-14-4219G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724790 | ||||||
chr2:159724868
|
TC | T | 10 | a0002c0005t0003g0033a0002c0005t0003g0067a0002c0005t0003g0068others(7): Show | 10 | NA18948.hp2 NA18977.hp1 NA18987.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-4138delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159724868 | |||||
chr2:159725288
|
C | T | 1 | a0001c0001t0006g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-14-3721C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725288 | ||||||
chr2:159725302
|
A | G | 1 | a0001c0004t0013g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-3707A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725302 | ||||||
chr2:159725454
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-14-3555T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725454 | ||||||
chr2:159725464
|
G | A | 1 | a0001c0002t0019g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-14-3545G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725464 | ||||||
chr2:159725509
|
C | T | 92 | a0001c0001t0002g0158a0001c0001t0002g0250a0001c0001t0002g0280others(89): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-14-3500C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725509 | ||||||
chr2:159725535
|
A | AT | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-3468dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159725535 | |||||
chr2:159725593
|
G | A | 1 | a0001c0004t0005g0212 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-3416G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725593 | ||||||
chr2:159725673
|
A | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-3336A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725673 | ||||||
chr2:159725685
|
C | T | 19 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(16): Show | 20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-3324C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725685 | ||||||
chr2:159725918
|
C | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-3091C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725918 | ||||||
chr2:159726103
|
G | T | 1 | a0001c0003t0027g0206 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14-2906G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726103 | ||||||
chr2:159726217
|
A | AGGTTT | 8 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0094others(5): Show | 10 | NA18968.hp1 NA18979.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-2791_-14-2787d others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726217 | |||||
chr2:159726218
|
G | GGTTTGGT others(3): Show |
1 | a0001c0002t0001g0093 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-14-2787_-14-2786i others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | |||||
chr2:159726218
|
GGTTTT | G | 116 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0009others(113): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-14-2735_-14-2731d others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | |||||
chr2:159726218
|
GGTTTTGT others(3): Show |
G | 76 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(73): Show | 78 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.-14-2740_-14-2731d others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | |||||
chr2:159726218
|
GGTTTTGT others(8): Show |
G | 87 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(84): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-14-2745_-14-2731d others(17): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | |||||
chr2:159726218
|
GGTTTTGT others(13): Show |
G | 18 | a0001c0001t0002g0323a0001c0004t0005g0028a0001c0004t0005g0212others(15): Show | 20 | HG00639.hp1 HG01261.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-2750_-14-2731d others(22): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | |||||
chr2:159726218
|
GGTTTTGT others(18): Show |
G | 7 | a0001c0001t0002g0277a0001c0001t0002g0279a0001c0001t0014g0159others(4): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-2755_-14-2731d others(27): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | |||||
chr2:159726223
|
T | G | 7 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0100others(4): Show | 7 | HG01071.hp1 HG01978.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-2786T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726223 | ||||||
chr2:159726228
|
T | G | 71 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0009others(68): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14-2781T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726228 | ||||||
chr2:159726233
|
T | G | 43 | a0001c0002t0001g0010a0001c0002t0001g0032a0001c0002t0001g0129others(40): Show | 44 | HG00438.hp1 HG00597.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-14-2776T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726233 | ||||||
chr2:159726238
|
T | G | 4 | a0001c0001t0002g0284a0001c0002t0001g0130a0002c0005t0003g0042others(1): Show | 4 | HG01109.hp2 NA18989.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2771T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726238 | ||||||
chr2:159726243
|
T | G | 1 | a0002c0005t0003g0075 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-14-2766T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726243 | ||||||
chr2:159726312
|
G | C | 53 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-14-2697G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726312 | ||||||
chr2:159726353
|
C | T | 1 | a0009c0013t0014g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-2656C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726353 | ||||||
chr2:159726363
|
C | T | 39 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(36): Show | 39 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-2646C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726363 | ||||||
chr2:159726365
|
C | A | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-14-2644C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726365 | ||||||
chr2:159726397
|
G | A | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-2612G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726397 | ||||||
chr2:159726497
|
T | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-2512T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726497 | ||||||
chr2:159726510
|
C | CCT | 9 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(6): Show | 10 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-2497_-14-2496d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726510 | |||||
chr2:159726551
|
C | T | 32 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(29): Show | 36 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.-14-2458C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726551 | ||||||
chr2:159726558
|
G | C | 1 | a0001c0003t0004g0182 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-14-2451G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726558 | ||||||
chr2:159726756
|
T | C | 1 | a0001c0002t0001g0097 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-14-2253T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726756 | ||||||
chr2:159727021
|
C | G | 1 | a0002c0005t0003g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-14-1988C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727021 | ||||||
chr2:159727095
|
A | G | 6 | a0001c0001t0002g0296a0001c0001t0002g0297a0001c0001t0015g0295others(3): Show | 6 | HG00280.hp2 HG01496.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1914A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727095 | ||||||
chr2:159727114
|
A | G | 2 | a0001c0001t0002g0291a0001c0001t0002g0304 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-14-1895A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727114 | ||||||
chr2:159727173
|
C | T | 47 | a0001c0004t0003g0052a0001c0004t0003g0065a0001c0004t0009g0077others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-1836C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727173 | ||||||
chr2:159727215
|
G | A | 1 | a0011c0016t0001g0102 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-14-1794G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727215 | ||||||
chr2:159727353
|
C | T | 2 | a0001c0001t0006g0019a0001c0001t0006g0237 | 3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-14-1656C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727353 | ||||||
chr2:159727537
|
G | A | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-1472G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727537 | ||||||
chr2:159727587
|
C | CA | 4 | a0001c0001t0002g0317a0001c0001t0006g0232a0001c0001t0006g0238others(1): Show | 4 | HG02109.hp2 HG03098.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-1421dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159727587 | |||||
chr2:159727589
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-1420G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727589 | ||||||
chr2:159727621
|
C | T | 124 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(121): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-1388C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727621 | ||||||
chr2:159727762
|
A | C | 69 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(66): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-14-1247A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727762 | ||||||
chr2:159727812
|
A | G | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-1197A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727812 | ||||||
chr2:159727836
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-1173G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727836 | ||||||
chr2:159728250
|
T | C | 124 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(121): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-759T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728250 | ||||||
chr2:159728284
|
A | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-725A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728284 | ||||||
chr2:159728314
|
A | G | 1 | a0009c0013t0014g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-695A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728314 | ||||||
chr2:159728408
|
A | G | 2 | a0001c0003t0004g0223a0001c0003t0004g0224 | 2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-14-601A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728408 | ||||||
chr2:159728480
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-529A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728480 | ||||||
chr2:159728533
|
A | C | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-476A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728533 | ||||||
chr2:159728724
|
A | T | 1 | a0004c0007t0011g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-14-285A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728724 | ||||||
chr2:159728887
|
G | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-122G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728887 | ||||||
chr2:159728966
|
C | A | 1 | a0001c0002t0001g0103 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-14-43C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728966 | ||||||
chr2:159728998
|
T | G | 5 | a0001c0004t0009g0034a0001c0004t0009g0035a0001c0004t0018g0225others(2): Show | 5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-11T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728998 | ||||||
chr2:159729229
|
C | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+54C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729229 | ||||||
chr2:159729349
|
T | A | 1 | a0001c0004t0005g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.153+174T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729349 | ||||||
chr2:159729445
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.153+270C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729445 | ||||||
chr2:159729491
|
C | T | 2 | a0001c0004t0009g0077a0001c0004t0009g0078 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.153+316C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729491 | ||||||
chr2:159729672
|
C | CA | 94 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(91): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.153+510dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159729672 | |||||
chr2:159729716
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+541G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729716 | ||||||
chr2:159729752
|
A | G | 124 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(121): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.153+577A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729752 | ||||||
chr2:159729799
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+624C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729799 | ||||||
chr2:159729926
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+751A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729926 | ||||||
chr2:159730569
|
G | A | 1 | a0001c0014t0002g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153+1394G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159730569 | ||||||
chr2:159730618
|
T | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+1443T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159730618 | ||||||
chr2:159730893
|
G | T | 1 | a0001c0003t0004g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.153+1718G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159730893 | ||||||
chr2:159730925
|
CTG | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+1752_153+1753d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159730925 | |||||
chr2:159731014
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+1839C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731014 | ||||||
chr2:159731038
|
A | T | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+1863A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731038 | ||||||
chr2:159731580
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.153+2405C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731580 | ||||||
chr2:159731583
|
C | T | 1 | a0001c0002t0001g0128 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.153+2408C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731583 | ||||||
chr2:159731622
|
C | T | 1 | a0003c0006t0010g0166 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.153+2447C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731622 | ||||||
chr2:159731686
|
G | A | 1 | a0008c0015t0009g0306 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.153+2511G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731686 | ||||||
chr2:159731740
|
G | A | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+2565G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731740 | ||||||
chr2:159731808
|
A | C | 53 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+2633A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731808 | ||||||
chr2:159731879
|
C | T | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+2704C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731879 | ||||||
chr2:159731894
|
G | C | 2 | a0001c0002t0001g0104a0001c0002t0001g0105 | 2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.153+2719G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731894 | ||||||
chr2:159731955
|
T | C | 1 | a0001c0004t0037g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+2780T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731955 | ||||||
chr2:159731973
|
G | A | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.153+2798G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731973 | ||||||
chr2:159731977
|
G | A | 1 | a0001c0004t0008g0307 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153+2802G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731977 | ||||||
chr2:159732082
|
C | T | 1 | a0001c0002t0001g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.153+2907C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732082 | ||||||
chr2:159732083
|
G | A | 1 | a0001c0001t0015g0318 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.153+2908G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732083 | ||||||
chr2:159732091
|
G | A | 2 | a0001c0002t0001g0104a0001c0002t0001g0105 | 2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.153+2916G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732091 | ||||||
chr2:159732266
|
T | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3091T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732266 | ||||||
chr2:159732298
|
A | T | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+3123A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732298 | ||||||
chr2:159732420
|
A | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3245A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732420 | ||||||
chr2:159732567
|
T | C | 1 | a0001c0001t0012g0240 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153+3392T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732567 | ||||||
chr2:159732587
|
G | A | 1 | a0002c0005t0003g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.153+3412G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732587 | ||||||
chr2:159732642
|
A | G | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+3467A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732642 | ||||||
chr2:159732659
|
C | T | 1 | a0001c0004t0009g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+3484C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732659 | ||||||
chr2:159732674
|
C | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3499C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732674 | ||||||
chr2:159732698
|
T | TA | 4 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(1): Show | 4 | HG02040.hp1 HG02083.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+3529dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159732698 | |||||
chr2:159732798
|
A | G | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.153+3623A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732798 | ||||||
chr2:159732814
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.153+3639C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732814 | ||||||
chr2:159732832
|
T | C | 124 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(121): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.153+3657T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732832 | ||||||
chr2:159732854
|
T | G | 1 | a0001c0002t0001g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.153+3679T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732854 | ||||||
chr2:159732869
|
T | C | 47 | a0001c0004t0003g0052a0001c0004t0003g0065a0001c0004t0009g0077others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.153+3694T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732869 | ||||||
chr2:159732981
|
C | A | 69 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(66): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.153+3806C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732981 | ||||||
chr2:159733005
|
A | C | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+3830A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733005 | ||||||
chr2:159733061
|
AGTTATAA others(1): Show |
A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3887_153+3894d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733061 | ||||||
chr2:159733062
|
G | T | 185 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(182): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.153+3887G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733062 | ||||||
chr2:159733072
|
T | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3897T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733072 | ||||||
chr2:159733099
|
CATT | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3931_153+3933d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733099 | |||||
chr2:159733266
|
T | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+4091T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733266 | ||||||
chr2:159733279
|
C | T | 3 | a0001c0004t0018g0225a0001c0004t0028g0227a0007c0019t0018g0226 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.153+4104C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733279 | ||||||
chr2:159733307
|
A | G | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.153+4132A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733307 | ||||||
chr2:159733547
|
A | AT | 7 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(4): Show | 8 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+4374dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733547 | |||||
chr2:159733549
|
T | TA | 171 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(168): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.153+4390dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733549 | |||||
chr2:159733549
|
T | TAA | 18 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(15): Show | 19 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.153+4389_153+4390d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733549 | |||||
chr2:159733550
|
A | T | 1 | a0004c0007t0011g0174 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.153+4375A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733550 | ||||||
chr2:159733569
|
T | C | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+4394T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733569 | ||||||
chr2:159734323
|
CT | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+5159delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734323 | |||||
chr2:159734351
|
C | T | 4 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(1): Show | 4 | NA18962.hp1 NA18994.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+5176C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734351 | ||||||
chr2:159734402
|
ATTAATTT | A | 26 | a0001c0002t0001g0001a0001c0002t0001g0009a0001c0002t0001g0010others(23): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.153+5232_153+5238d others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734402 | |||||
chr2:159734497
|
A | T | 1 | a0001c0002t0001g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.153+5322A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734497 | ||||||
chr2:159734685
|
A | G | 1 | a0001c0004t0009g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+5510A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734685 | ||||||
chr2:159734812
|
A | G | 1 | a0003c0006t0010g0012 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.153+5637A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734812 | ||||||
chr2:159734817
|
G | GA | 19 | a0001c0001t0002g0263a0001c0001t0002g0287a0001c0001t0002g0288others(16): Show | 19 | HG00438.hp2 HG00609.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+5661dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734817 | |||||
chr2:159734817
|
GAA | G | 52 | a0001c0004t0003g0052a0001c0004t0003g0065a0001c0004t0009g0034others(49): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+5660_153+5661d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734817 | |||||
chr2:159734856
|
A | T | 4 | a0001c0001t0002g0023a0001c0001t0002g0249a0001c0001t0002g0274others(1): Show | 5 | HG01943.hp1 NA18941.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+5681A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734856 | ||||||
chr2:159735028
|
A | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+5853A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735028 | ||||||
chr2:159735058
|
A | G | 2 | a0001c0001t0006g0235a0001c0001t0006g0236 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.153+5883A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735058 | ||||||
chr2:159735137
|
T | G | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.153+5962T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735137 | ||||||
chr2:159735240
|
A | G | 10 | a0002c0005t0003g0033a0002c0005t0003g0067a0002c0005t0003g0068others(7): Show | 10 | NA18948.hp2 NA18977.hp1 NA18987.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+6065A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735240 | ||||||
chr2:159735307
|
G | A | 5 | a0005c0008t0003g0046a0005c0008t0003g0047a0005c0008t0003g0048others(2): Show | 5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+6132G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735307 | ||||||
chr2:159735336
|
A | G | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+6161A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735336 | ||||||
chr2:159735454
|
A | G | 1 | a0009c0013t0014g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153+6279A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735454 | ||||||
chr2:159735535
|
A | T | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+6360A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735535 | ||||||
chr2:159735601
|
A | G | 2 | a0001c0001t0002g0024a0001c0001t0002g0273 | 3 | HG00558.hp2 HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.153+6426A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735601 | ||||||
chr2:159735614
|
T | TC | 3 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0236 | 3 | HG02486.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.153+6439_153+6440i others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735614 | ||||||
chr2:159735699
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+6524A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735699 | ||||||
chr2:159735925
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0002g0262 | 2 | HG02083.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.153+6750C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735925 | ||||||
chr2:159736179
|
G | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6882G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736179 | ||||||
chr2:159736378
|
C | T | 7 | a0006c0009t0009g0036a0006c0009t0009g0038a0006c0009t0009g0040others(4): Show | 7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-6683C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736378 | ||||||
chr2:159736428
|
C | T | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.154-6633C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736428 | ||||||
chr2:159736603
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6458G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736603 | ||||||
chr2:159736687
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6374A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736687 | ||||||
chr2:159736806
|
A | T | 327 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(324): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.154-6255A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736806 | ||||||
chr2:159736959
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6102A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736959 | ||||||
chr2:159737015
|
A | G | 4 | a0006c0009t0009g0036a0006c0009t0009g0040a0006c0009t0009g0041others(1): Show | 4 | HG00438.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-6046A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737015 | ||||||
chr2:159737054
|
A | C | 1 | a0001c0001t0002g0321 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.154-6007A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737054 | ||||||
chr2:159737264
|
T | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-5797T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737264 | ||||||
chr2:159737535
|
G | T | 1 | a0001c0003t0004g0199 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.154-5526G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737535 | ||||||
chr2:159737626
|
A | C | 1 | a0001c0001t0002g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.154-5435A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737626 | ||||||
chr2:159737649
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-5412A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737649 | ||||||
chr2:159737697
|
A | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-5364A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737697 | ||||||
chr2:159737718
|
G | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-5343G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737718 | ||||||
chr2:159737795
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.154-5266A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737795 | ||||||
chr2:159737987
|
G | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-5074G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737987 | ||||||
chr2:159737995
|
A | G | 1 | a0001c0004t0009g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154-5066A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737995 | ||||||
chr2:159738016
|
A | G | 47 | a0001c0003t0003g0076a0001c0003t0003g0079a0001c0003t0003g0080others(44): Show | 47 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.154-5045A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738016 | ||||||
chr2:159738067
|
G | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.154-4994G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738067 | ||||||
chr2:159738264
|
C | T | 7 | a0006c0009t0009g0036a0006c0009t0009g0038a0006c0009t0009g0040others(4): Show | 7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-4797C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738264 | ||||||
chr2:159738338
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-4723G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738338 | ||||||
chr2:159738372
|
A | G | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-4689A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738372 | ||||||
chr2:159738380
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-4681A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738380 | ||||||
chr2:159738418
|
C | A | 6 | a0003c0006t0010g0012a0003c0006t0010g0164a0003c0006t0010g0165others(3): Show | 7 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-4643C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738418 | ||||||
chr2:159738451
|
G | A | 99 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(96): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.154-4610G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738451 | ||||||
chr2:159738496
|
C | T | 1 | a0004c0007t0011g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-4565C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738496 | ||||||
chr2:159738616
|
G | A | 132 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(129): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.154-4445G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738616 | ||||||
chr2:159738714
|
A | G | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-4347A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738714 | ||||||
chr2:159738811
|
C | T | 3 | a0004c0007t0011g0171a0004c0007t0011g0175a0004c0007t0011g0176 | 3 | HG02809.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.154-4250C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738811 | ||||||
chr2:159738922
|
C | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-4139C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738922 | ||||||
chr2:159738954
|
T | C | 289 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(286): Show | 323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.154-4107T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738954 | ||||||
chr2:159739109
|
G | A | 2 | a0001c0002t0001g0088a0001c0002t0007g0108 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.154-3952G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739109 | ||||||
chr2:159739199
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-3862A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739199 | ||||||
chr2:159739287
|
C | T | 1 | a0001c0002t0019g0152 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.154-3774C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739287 | ||||||
chr2:159739373
|
C | T | 5 | a0001c0004t0009g0034a0001c0004t0009g0035a0001c0004t0018g0225others(2): Show | 5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-3688C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739373 | ||||||
chr2:159739392
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-3669A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739392 | ||||||
chr2:159739459
|
A | T | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-3602A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739459 | ||||||
chr2:159739532
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.154-3529A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739532 | ||||||
chr2:159739654
|
C | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.154-3407C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739654 | ||||||
chr2:159739669
|
A | G | 3 | a0006c0009t0009g0038a0006c0009t0035g0037a0006c0009t0036g0039 | 3 | HG02258.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.154-3392A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739669 | ||||||
chr2:159739832
|
TAAC | T | 3 | a0001c0004t0013g0027a0001c0004t0013g0309a0001c0004t0013g0310 | 4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-3226_154-3224d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159739832 | |||||
chr2:159739883
|
G | A | 94 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(91): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.154-3178G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739883 | ||||||
chr2:159740088
|
G | T | 1 | a0004c0007t0011g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.154-2973G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740088 | ||||||
chr2:159740189
|
T | A | 8 | a0001c0003t0004g0182a0001c0003t0004g0184a0001c0003t0004g0186others(5): Show | 8 | HG03239.hp2 NA18942.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-2872T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740189 | ||||||
chr2:159740204
|
A | G | 61 | a0001c0003t0003g0076a0001c0003t0003g0079a0001c0003t0003g0080others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.154-2857A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740204 | ||||||
chr2:159740423
|
G | C | 1 | a0001c0001t0002g0274 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.154-2638G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740423 | ||||||
chr2:159740907
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-2154G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740907 | ||||||
chr2:159740916
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-2145G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740916 | ||||||
chr2:159741029
|
A | G | 3 | a0001c0001t0014g0299a0001c0001t0014g0300a0009c0013t0014g0301 | 3 | HG02451.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.154-2032A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741029 | ||||||
chr2:159741144
|
G | T | 1 | a0001c0002t0001g0126 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.154-1917G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741144 | ||||||
chr2:159741412
|
T | C | 2 | a0001c0004t0009g0034a0001c0004t0009g0035 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.154-1649T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741412 | ||||||
chr2:159741459
|
A | ATCT | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-1600_154-1598d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159741459 | |||||
chr2:159741467
|
C | T | 48 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.154-1594C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741467 | ||||||
chr2:159741690
|
T | C | 1 | a0001c0001t0014g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.154-1371T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741690 | ||||||
chr2:159741796
|
A | T | 2 | a0002c0005t0003g0042a0002c0005t0003g0043 | 2 | NA18989.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.154-1265A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741796 | ||||||
chr2:159741891
|
C | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-1170C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741891 | ||||||
chr2:159741912
|
C | CTG | 4 | a0004c0007t0011g0013a0004c0007t0011g0172a0004c0007t0011g0173others(1): Show | 5 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-1137_154-1136d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159741912 | |||||
chr2:159741914
|
G | C | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-1147G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741914 | ||||||
chr2:159742254
|
T | G | 4 | a0001c0003t0004g0189a0001c0003t0004g0190a0001c0003t0004g0191others(1): Show | 4 | HG00544.hp1 HG02080.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-807T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742254 | ||||||
chr2:159742257
|
T | G | 53 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.154-804T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742257 | ||||||
chr2:159742433
|
A | G | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-628A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742433 | ||||||
chr2:159742505
|
G | A | 2 | a0001c0003t0004g0180a0001c0003t0004g0181 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.154-556G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742505 | ||||||
chr2:159742548
|
T | TA | 26 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(23): Show | 27 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-504dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159742548 | |||||
chr2:159742548
|
T | TAA | 69 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(66): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.154-505_154-504dup others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159742548 | |||||
chr2:159742565
|
C | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-496C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742565 | ||||||
chr2:159742569
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-492G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742569 | ||||||
chr2:159742670
|
A | C | 53 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.154-391A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742670 | ||||||
chr2:159742704
|
C | T | 2 | a0001c0001t0006g0235a0001c0001t0006g0236 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.154-357C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742704 | ||||||
chr2:159742763
|
CCT | C | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-297_154-296del others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742763 | ||||||
chr2:159742928
|
C | T | 1 | a0001c0001t0012g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.154-133C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742928 | ||||||
chr2:159742936
|
CAAAA | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-116_154-113del others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159742936 | |||||
chr2:159742982
|
A | G | 48 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.154-79A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742982 | ||||||
chr2:159743446
|
T | C | 1 | a0001c0001t0033g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.346+193T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743446 | ||||||
chr2:159743663
|
G | T | 1 | a0003c0006t0010g0163 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.346+410G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743663 | ||||||
chr2:159743682
|
T | C | 1 | a0001c0004t0008g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.346+429T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743682 | ||||||
chr2:159743691
|
G | A | 2 | a0001c0002t0001g0097a0001c0002t0034g0099 | 2 | NA19055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.346+438G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743691 | ||||||
chr2:159743737
|
CA | C | 174 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0009others(171): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.346+497delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743737 | |||||
chr2:159743747
|
A | AAG | 92 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(89): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.346+495_346+496ins others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743747 | |||||
chr2:159743749
|
A | AGAG | 3 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289 | 3 | HG02280.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.346+496_346+497ins others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743749 | ||||||
chr2:159743749
|
A | G | 92 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(89): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.346+496A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743749 | ||||||
chr2:159743869
|
A | G | 2 | a0001c0004t0009g0034a0001c0004t0009g0035 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.346+616A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743869 | ||||||
chr2:159743903
|
G | A | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.346+650G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743903 | ||||||
chr2:159743927
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+674A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743927 | ||||||
chr2:159743966
|
TAGG | T | 4 | a0003c0006t0010g0011a0003c0006t0010g0162a0003c0006t0010g0163others(1): Show | 4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+716_346+718del others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743966 | |||||
chr2:159743974
|
C | CT | 47 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0088others(44): Show | 52 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.346+751dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTT | 11 | a0001c0002t0001g0007a0001c0002t0001g0100a0001c0002t0001g0107others(8): Show | 12 | HG00609.hp2 HG00673.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+750_346+751dup others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTTT | 7 | a0001c0002t0001g0032a0001c0002t0001g0123a0001c0002t0001g0129others(4): Show | 7 | HG00639.hp2 HG02818.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+749_346+751dup others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTTTT | 6 | a0001c0002t0001g0031a0001c0002t0001g0090a0001c0002t0001g0091others(3): Show | 6 | HG00323.hp1 HG01258.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+748_346+751dup others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTTTTTTT others(1): Show |
5 | a0001c0002t0001g0010a0001c0002t0001g0147a0001c0002t0001g0148others(2): Show | 6 | HG00099.hp2 HG00140.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+744_346+751dup others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTTTTTTT others(4): Show |
1 | a0007c0019t0018g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+741_346+751dup others(11): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTTTTTTT others(11): Show |
1 | a0001c0004t0009g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346+734_346+751dup others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
C | CTTTTTTT others(17): Show |
1 | a0001c0004t0009g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+728_346+751dup others(24): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743974
|
CT | C | 11 | a0001c0003t0003g0079a0001c0003t0003g0081a0001c0003t0003g0086others(8): Show | 11 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+751delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | |||||
chr2:159743990
|
TTTTTTTT others(8): Show |
T | 7 | a0001c0002t0001g0001a0001c0002t0001g0087a0001c0002t0001g0138others(4): Show | 13 | HG00738.hp2 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+738_346+752del others(15): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743990 | ||||||
chr2:159744000
|
TTTTTG | T | 46 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0023others(43): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.346+748_346+752del others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744000 | ||||||
chr2:159744001
|
TTTTG | T | 16 | a0001c0001t0002g0251a0001c0001t0002g0263a0001c0001t0002g0284others(13): Show | 16 | HG00741.hp1 HG01109.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+749_346+752del others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744001 | ||||||
chr2:159744002
|
TTTG | T | 68 | a0001c0001t0002g0021a0001c0001t0002g0024a0001c0001t0002g0158others(65): Show | 74 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.346+750_346+752del others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744002 | ||||||
chr2:159744003
|
TTG | T | 41 | a0001c0001t0002g0262a0001c0001t0002g0268a0001c0001t0002g0269others(38): Show | 43 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.346+751_346+752del others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744003 | ||||||
chr2:159744004
|
TG | T | 16 | a0001c0001t0002g0022a0001c0001t0002g0302a0001c0004t0005g0216others(13): Show | 18 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+753delG | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159744004 | |||||
chr2:159744005
|
G | T | 85 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.346+752G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744005 | ||||||
chr2:159744009
|
A | C | 1 | a0001c0001t0015g0318 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.346+756A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744009 | ||||||
chr2:159744018
|
C | T | 1 | a0002c0005t0003g0064 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.346+765C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744018 | ||||||
chr2:159744113
|
A | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+860A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744113 | ||||||
chr2:159744133
|
G | A | 3 | a0001c0003t0003g0076a0002c0005t0009g0089a0002c0005t0025g0051 | 3 | HG02080.hp1 NA18943.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.346+880G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744133 | ||||||
chr2:159744199
|
G | A | 1 | a0003c0006t0010g0167 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.346+946G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744199 | ||||||
chr2:159744235
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+982A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744235 | ||||||
chr2:159744239
|
C | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.346+986C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744239 | ||||||
chr2:159744268
|
G | A | 14 | a0001c0004t0005g0028a0001c0004t0008g0025a0001c0004t0008g0026others(11): Show | 17 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+1015G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744268 | ||||||
chr2:159744278
|
G | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+1025G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744278 | ||||||
chr2:159744301
|
A | G | 53 | a0001c0003t0003g0076a0001c0004t0003g0052a0001c0004t0003g0065others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.346+1048A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744301 | ||||||
chr2:159744392
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+1139A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744392 | ||||||
chr2:159744469
|
A | G | 5 | a0001c0004t0009g0034a0001c0004t0009g0035a0001c0004t0018g0225others(2): Show | 5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1216A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744469 | ||||||
chr2:159744496
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+1243A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744496 | ||||||
chr2:159744563
|
A | G | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.347-1207A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744563 | ||||||
chr2:159744925
|
A | G | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-845A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744925 | ||||||
chr2:159745015
|
A | G | 61 | a0001c0003t0003g0076a0001c0003t0003g0079a0001c0003t0003g0080others(58): Show | 61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.347-755A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745015 | ||||||
chr2:159745028
|
T | C | 2 | a0001c0004t0003g0052a0001c0004t0003g0065 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.347-742T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745028 | ||||||
chr2:159745060
|
C | T | 2 | a0001c0001t0006g0019a0001c0001t0006g0237 | 3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.347-710C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745060 | ||||||
chr2:159745173
|
A | T | 29 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(26): Show | 34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.347-597A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745173 | ||||||
chr2:159745240
|
C | T | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.347-530C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745240 | ||||||
chr2:159745278
|
A | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-492A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745278 | ||||||
chr2:159745359
|
G | A | 228 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(225): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.347-411G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745359 | ||||||
chr2:159745377
|
C | T | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-393C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745377 | ||||||
chr2:159745389
|
C | G | 1 | a0001c0001t0016g0258 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.347-381C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745389 | ||||||
chr2:159745397
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-373G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745397 | ||||||
chr2:159745420
|
C | T | 7 | a0001c0001t0002g0020a0001c0001t0002g0254a0001c0001t0002g0255others(4): Show | 8 | HG01071.hp2 HG01081.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-350C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745420 | ||||||
chr2:159745458
|
C | T | 1 | a0001c0001t0015g0318 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.347-312C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745458 | ||||||
chr2:159745467
|
C | T | 13 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0112others(10): Show | 13 | HG04184.hp1 NA18747.hp2 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-303C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745467 | ||||||
chr2:159745484
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-286A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745484 | ||||||
chr2:159745613
|
G | A | 1 | a0001c0002t0001g0114 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.347-157G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745613 | ||||||
chr2:159745747
|
A | G | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.347-23A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745747 | ||||||
chr2:159746186
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+249C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746186 | ||||||
chr2:159746300
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+363A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746300 | ||||||
chr2:159746370
|
T | G | 1 | a0001c0004t0005g0214 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514+433T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746370 | ||||||
chr2:159746452
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+515G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746452 | ||||||
chr2:159746548
|
T | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+611T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746548 | ||||||
chr2:159747084
|
A | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.515-721A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747084 | ||||||
chr2:159747128
|
C | T | 2 | a0004c0007t0011g0173a0004c0007t0011g0174 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.515-677C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747128 | ||||||
chr2:159747270
|
C | A | 4 | a0006c0009t0009g0036a0006c0009t0009g0040a0006c0009t0009g0041others(1): Show | 4 | HG00438.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-535C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747270 | ||||||
chr2:159747477
|
A | T | 1 | a0001c0004t0013g0027 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.515-328A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747477 | ||||||
chr2:159748949
|
A | C | 1 | a0001c0001t0002g0324 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1613+46A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748949 | ||||||
chr2:159748959
|
C | T | 3 | a0001c0004t0018g0225a0001c0004t0028g0227a0007c0019t0018g0226 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1613+56C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748959 | ||||||
chr2:159748973
|
C | CT | 15 | a0001c0001t0020g0170a0001c0004t0005g0018a0001c0004t0005g0028others(12): Show | 17 | HG01261.hp2 HG01361.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1613+74dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159748973 | |||||
chr2:159748973
|
C | CTT | 4 | a0001c0001t0020g0169a0001c0004t0005g0215a0001c0004t0005g0216others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+73_1613+74dup others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159748973 | |||||
chr2:159748973
|
CTTTTCTT others(1): Show |
C | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613+75_1613+82del others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159748973 | |||||
chr2:159748977
|
TC | T | 148 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(145): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1613+75delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748977 | ||||||
chr2:159748978
|
C | T | 121 | a0001c0001t0002g0158a0001c0001t0002g0262a0001c0001t0002g0263others(118): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1613+75C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748978 | ||||||
chr2:159748980
|
T | C | 3 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0236 | 3 | HG02486.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1613+77T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748980 | ||||||
chr2:159748987
|
T | C | 86 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(83): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1613+84T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748987 | ||||||
chr2:159749002
|
G | A | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613+99G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749002 | ||||||
chr2:159749005
|
G | T | 1 | a0001c0004t0008g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1613+102G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749005 | ||||||
chr2:159749013
|
C | G | 3 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289 | 3 | HG02280.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1613+110C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749013 | ||||||
chr2:159749104
|
G | A | 1 | a0002c0005t0003g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1613+201G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749104 | ||||||
chr2:159749272
|
C | T | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1613+369C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749272 | ||||||
chr2:159749349
|
T | G | 96 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(93): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1613+446T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749349 | ||||||
chr2:159749349
|
T | TG | 5 | a0001c0004t0009g0034a0001c0004t0009g0035a0001c0004t0018g0225others(2): Show | 5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+446_1613+447i others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749349 | ||||||
chr2:159749367
|
G | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1613+464G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749367 | ||||||
chr2:159749567
|
C | T | 1 | a0001c0004t0005g0219 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1613+664C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749567 | ||||||
chr2:159749736
|
G | T | 1 | a0001c0004t0005g0214 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1613+833G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749736 | ||||||
chr2:159749737
|
C | CG | 37 | a0001c0002t0001g0087a0001c0002t0001g0105a0001c0002t0001g0111others(34): Show | 38 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1613+842dupG | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159749737 | |||||
chr2:159749740
|
G | C | 94 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(91): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1613+837G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749740 | ||||||
chr2:159749740
|
G | T | 1 | a0001c0001t0015g0318 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1613+837G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749740 | ||||||
chr2:159749744
|
G | T | 3 | a0001c0004t0009g0077a0001c0004t0009g0078a0005c0008t0003g0063 | 3 | HG01433.hp1 HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1613+841G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749744 | ||||||
chr2:159749745
|
GC | G | 92 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(89): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1613+843delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749745 | ||||||
chr2:159749746
|
C | G | 3 | a0001c0001t0002g0262a0001c0001t0002g0284a0001c0001t0002g0298 | 3 | HG01109.hp2 NA19000.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1613+843C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749746 | ||||||
chr2:159749789
|
T | C | 8 | a0001c0004t0005g0018a0001c0004t0005g0210a0001c0004t0005g0218others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613+886T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749789 | ||||||
chr2:159750056
|
A | G | 1 | a0001c0002t0001g0134 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1613+1153A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750056 | ||||||
chr2:159750143
|
C | A | 1 | a0001c0002t0001g0228 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1613+1240C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750143 | ||||||
chr2:159750249
|
C | T | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1613+1346C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750249 | ||||||
chr2:159750261
|
T | C | 280 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(277): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1613+1358T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750261 | ||||||
chr2:159750266
|
G | A | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1613+1363G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750266 | ||||||
chr2:159750355
|
T | A | 1 | a0001c0001t0006g0244 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1613+1452T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750355 | ||||||
chr2:159750523
|
CAAAATAA others(3): Show |
C | 1 | a0001c0001t0006g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1613+1638_1613+164 others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159750523 | |||||
chr2:159750608
|
G | A | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1613+1705G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750608 | ||||||
chr2:159750646
|
A | T | 60 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(57): Show | 69 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.1613+1743A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750646 | ||||||
chr2:159750649
|
A | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1613+1746A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750649 | ||||||
chr2:159750758
|
G | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1614-1644G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750758 | ||||||
chr2:159750773
|
TTA | T | 36 | a0002c0005t0003g0005a0002c0005t0003g0033a0002c0005t0003g0042others(33): Show | 36 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1614-1624_1614-162 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159750773 | |||||
chr2:159750855
|
G | A | 1 | a0001c0004t0005g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1614-1547G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750855 | ||||||
chr2:159750925
|
T | G | 1 | a0001c0004t0023g0017 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1614-1477T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750925 | ||||||
chr2:159750976
|
C | A | 3 | a0001c0004t0013g0027a0001c0004t0013g0309a0001c0004t0013g0310 | 4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614-1426C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750976 | ||||||
chr2:159751818
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1614-584G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159751818 | ||||||
chr2:159752008
|
C | T | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032 | 3 | HG00735.hp2 HG01258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1614-394C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159752008 | ||||||
chr2:159752111
|
A | G | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1614-291A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159752111 | ||||||
chr2:159752264
|
G | A | 1 | a0002c0005t0003g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1614-138G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159752264 | ||||||
chr2:159752651
|
T | C | 24 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(21): Show | 27 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1783+80T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159752651 | ||||||
chr2:159752947
|
C | T | 19 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(16): Show | 20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1783+376C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159752947 | ||||||
chr2:159753189
|
G | A | 3 | a0001c0001t0016g0256a0001c0001t0016g0257a0001c0001t0016g0258 | 3 | NA18942.hp2 NA18980.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1783+618G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753189 | ||||||
chr2:159753483
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1783+912G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753483 | ||||||
chr2:159753493
|
G | A | 4 | a0006c0009t0009g0036a0006c0009t0009g0040a0006c0009t0009g0041others(1): Show | 4 | HG00438.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1783+922G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753493 | ||||||
chr2:159753550
|
C | CA | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1783+992dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159753550 | |||||
chr2:159753550
|
CA | C | 97 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(94): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1783+992delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159753550 | |||||
chr2:159753644
|
A | G | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1783+1073A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753644 | ||||||
chr2:159753753
|
A | G | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1783+1182A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753753 | ||||||
chr2:159753869
|
G | A | 282 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(279): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1783+1298G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753869 | ||||||
chr2:159754047
|
A | C | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1783+1476A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754047 | ||||||
chr2:159754656
|
C | T | 1 | a0001c0001t0029g0265 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1783+2085C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754656 | ||||||
chr2:159754726
|
A | G | 1 | a0003c0006t0010g0166 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1783+2155A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754726 | ||||||
chr2:159754793
|
A | G | 7 | a0006c0009t0009g0036a0006c0009t0009g0038a0006c0009t0009g0040others(4): Show | 7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1783+2222A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754793 | ||||||
chr2:159754889
|
C | T | 13 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(10): Show | 16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1783+2318C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754889 | ||||||
chr2:159754940
|
A | G | 1 | a0001c0004t0008g0315 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1783+2369A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754940 | ||||||
chr2:159754966
|
G | A | 52 | a0001c0004t0003g0052a0001c0004t0003g0065a0001c0004t0009g0034others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1783+2395G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754966 | ||||||
chr2:159754972
|
A | T | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1783+2401A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754972 | ||||||
chr2:159754992
|
C | A | 1 | a0001c0004t0005g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1783+2421C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754992 | ||||||
chr2:159755192
|
C | T | 1 | a0001c0002t0007g0116 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1783+2621C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755192 | ||||||
chr2:159755232
|
C | T | 3 | a0001c0001t0006g0232a0001c0001t0006g0238a0001c0001t0006g0239 | 3 | HG02109.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1783+2661C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755232 | ||||||
chr2:159755297
|
TG | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1783+2728delG | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159755297 | |||||
chr2:159755339
|
T | C | 1 | a0001c0001t0002g0022 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1783+2768T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755339 | ||||||
chr2:159755501
|
C | G | 1 | a0005c0017t0003g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1783+2930C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755501 | ||||||
chr2:159755781
|
T | C | 54 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0004t0003g0052others(51): Show | 54 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1783+3210T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755781 | ||||||
chr2:159755852
|
T | C | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1783+3281T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755852 | ||||||
chr2:159756099
|
A | T | 5 | a0001c0004t0005g0212a0001c0004t0005g0213a0001c0004t0005g0214others(2): Show | 5 | HG01261.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1784-3127A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756099 | ||||||
chr2:159756189
|
A | G | 2 | a0006c0009t0009g0036a0006c0009t0009g0041 | 2 | HG00438.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1784-3037A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756189 | ||||||
chr2:159756494
|
C | G | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1784-2732C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756494 | ||||||
chr2:159756687
|
C | CA | 13 | a0001c0001t0002g0024a0001c0001t0002g0266a0001c0003t0003g0080others(10): Show | 14 | HG00544.hp1 HG00597.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1784-2512dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | |||||
chr2:159756687
|
CA | C | 56 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(53): Show | 65 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1784-2512delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | |||||
chr2:159756687
|
CAA | C | 26 | a0001c0001t0002g0274a0001c0001t0002g0290a0001c0001t0006g0232others(23): Show | 27 | HG00438.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1784-2513_1784-251 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | |||||
chr2:159756687
|
CAAA | C | 62 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(59): Show | 63 | HG00438.hp2 HG00597.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1784-2514_1784-251 others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | |||||
chr2:159756687
|
CAAAA | C | 30 | a0001c0001t0006g0233a0001c0001t0006g0234a0001c0001t0006g0244others(27): Show | 30 | HG00735.hp1 HG00735.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1784-2515_1784-251 others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | |||||
chr2:159756687
|
CAAAAA | C | 75 | a0001c0001t0006g0247a0001c0002t0001g0001a0001c0002t0001g0004others(72): Show | 93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1784-2516_1784-251 others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | |||||
chr2:159756707
|
AAAAAAAA others(1): Show |
A | 12 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0308others(9): Show | 15 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1784-2517_1784-251 others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756707 | |||||
chr2:159756714
|
A | C | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1784-2512A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756714 | ||||||
chr2:159756766
|
C | T | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1784-2460C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756766 | ||||||
chr2:159756820
|
CAA | C | 14 | a0001c0001t0002g0294a0001c0004t0008g0025a0001c0004t0008g0026others(11): Show | 17 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1784-2403_1784-240 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756820 | |||||
chr2:159756895
|
G | GTTTGTT | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1784-2321_1784-231 others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756895 | |||||
chr2:159756917
|
G | A | 10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1784-2309G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756917 | ||||||
chr2:159757114
|
C | T | 3 | a0001c0004t0018g0225a0001c0004t0028g0227a0007c0019t0018g0226 | 3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1784-2112C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757114 | ||||||
chr2:159757505
|
G | C | 1 | a0001c0002t0001g0130 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1784-1721G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757505 | ||||||
chr2:159757586
|
C | T | 2 | a0001c0001t0014g0159a0001c0001t0033g0160 | 2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1784-1640C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757586 | ||||||
chr2:159757743
|
C | T | 47 | a0001c0004t0003g0052a0001c0004t0003g0065a0001c0004t0009g0077others(44): Show | 47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1784-1483C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757743 | ||||||
chr2:159757781
|
A | G | 1 | a0001c0002t0001g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1784-1445A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757781 | ||||||
chr2:159757812
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0111a0001c0002t0001g0115 | 3 | NA18972.hp2 NA18985.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1784-1414C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757812 | ||||||
chr2:159757969
|
C | T | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1784-1257C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757969 | ||||||
chr2:159758165
|
T | C | 2 | a0002c0005t0003g0055a0002c0005t0026g0056 | 2 | HG02083.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1784-1061T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758165 | ||||||
chr2:159758247
|
A | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1784-979A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758247 | ||||||
chr2:159758354
|
T | A | 1 | a0001c0002t0001g0129 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1784-872T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758354 | ||||||
chr2:159758546
|
T | G | 4 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(1): Show | 4 | NA18962.hp1 NA18994.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784-680T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758546 | ||||||
chr2:159758549
|
G | C | 280 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(277): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1784-677G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758549 | ||||||
chr2:159758742
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1784-484C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758742 | ||||||
chr2:159759503
|
A | AT | 34 | a0001c0003t0003g0079a0001c0003t0003g0080a0001c0003t0003g0081others(31): Show | 34 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1893+181dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159759503 | |||||
chr2:159759503
|
AT | A | 96 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(93): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1893+181delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159759503 | |||||
chr2:159759721
|
A | G | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1893+386A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159759721 | ||||||
chr2:159759756
|
A | C | 1 | a0001c0001t0002g0274 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1893+421A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159759756 | ||||||
chr2:159759931
|
TACA | T | 8 | a0004c0007t0011g0013a0004c0007t0011g0171a0004c0007t0011g0172others(5): Show | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1893+598_1893+600d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159759931 | |||||
chr2:159759991
|
T | A | 1 | a0001c0004t0005g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1893+656T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159759991 | ||||||
chr2:159760362
|
C | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1893+1027C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760362 | ||||||
chr2:159760364
|
A | G | 1 | a0001c0001t0002g0253 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1893+1029A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760364 | ||||||
chr2:159760464
|
T | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1893+1129T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760464 | ||||||
chr2:159760598
|
TA | T | 3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283 | 3 | NA18966.hp2 NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1893+1266delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159760598 | |||||
chr2:159760708
|
C | CT | 155 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(152): Show | 165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1893+1379dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159760708 | |||||
chr2:159760715
|
G | T | 281 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(278): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1893+1380G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760715 | ||||||
chr2:159760724
|
T | C | 8 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0136others(5): Show | 10 | HG00099.hp2 HG00140.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1893+1389T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760724 | ||||||
chr2:159760820
|
T | A | 1 | a0002c0005t0003g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1893+1485T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760820 | ||||||
chr2:159760957
|
G | C | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1893+1622G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760957 | ||||||
chr2:159761020
|
C | T | 1 | a0001c0002t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1893+1685C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761020 | ||||||
chr2:159761027
|
A | AT | 66 | a0001c0001t0002g0271a0001c0001t0014g0299a0001c0001t0014g0300others(63): Show | 67 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1893+1709dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761027 | |||||
chr2:159761027
|
AT | A | 6 | a0001c0001t0002g0274a0001c0002t0001g0112a0001c0002t0001g0145others(3): Show | 6 | HG01168.hp2 HG01943.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1893+1709delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761027 | |||||
chr2:159761270
|
C | T | 1 | a0001c0004t0040g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1894-1610C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761270 | ||||||
chr2:159761326
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1894-1554G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761326 | ||||||
chr2:159761371
|
A | G | 1 | a0001c0001t0002g0280 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1894-1509A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761371 | ||||||
chr2:159761406
|
C | CT | 12 | a0001c0003t0004g0187a0001c0003t0004g0197a0001c0003t0004g0223others(9): Show | 13 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1894-1449dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
C | CTT | 7 | a0001c0004t0005g0028a0001c0004t0005g0212a0001c0004t0005g0213others(4): Show | 8 | HG01261.hp2 HG01361.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894-1450_1894-144 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
C | CTTT | 11 | a0001c0004t0005g0215a0001c0004t0008g0025a0001c0004t0008g0026others(8): Show | 14 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1894-1451_1894-144 others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
C | CTTTT | 25 | a0001c0002t0001g0092a0001c0002t0001g0098a0001c0002t0001g0103others(22): Show | 27 | HG00280.hp1 HG00735.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1894-1452_1894-144 others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
C | CTTTTT | 57 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(54): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1894-1453_1894-144 others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
C | CTTTTTT | 23 | a0001c0002t0001g0030a0001c0002t0001g0032a0001c0002t0001g0088others(20): Show | 28 | HG00673.hp1 HG00735.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1894-1454_1894-144 others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
CT | C | 6 | a0001c0003t0004g0195a0001c0003t0004g0208a0001c0004t0009g0078others(3): Show | 6 | HG02080.hp1 HG02647.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1894-1449delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
CTT | C | 51 | a0001c0003t0003g0076a0001c0003t0003g0079a0001c0003t0003g0080others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1894-1450_1894-144 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
CTTT | C | 6 | a0001c0003t0003g0082a0001c0004t0018g0225a0001c0004t0028g0227others(3): Show | 6 | HG02132.hp1 HG02280.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894-1451_1894-144 others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
CTTTTT | C | 24 | a0001c0001t0002g0263a0001c0001t0002g0270a0001c0001t0002g0290others(21): Show | 25 | HG02056.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1894-1453_1894-144 others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761406
|
CTTTTTT | C | 67 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(64): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1894-1454_1894-144 others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | |||||
chr2:159761537
|
C | CCCAAGTA others(1): Show |
10 | a0003c0006t0010g0011a0003c0006t0010g0012a0003c0006t0010g0162others(7): Show | 11 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1894-1341_1894-133 others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761537 | |||||
chr2:159761574
|
C | A | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1894-1306C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761574 | ||||||
chr2:159761611
|
C | T | 2 | a0001c0004t0009g0077a0001c0004t0009g0078 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1894-1269C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761611 | ||||||
chr2:159761777
|
A | G | 1 | a0001c0004t0008g0312 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1894-1103A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761777 | ||||||
chr2:159761875
|
A | G | 86 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(83): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1894-1005A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761875 | ||||||
chr2:159762064
|
A | G | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1894-816A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762064 | ||||||
chr2:159762095
|
T | C | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1894-785T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762095 | ||||||
chr2:159762444
|
T | C | 2 | a0001c0004t0009g0034a0001c0004t0009g0035 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1894-436T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762444 | ||||||
chr2:159762477
|
A | C | 1 | a0001c0002t0001g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1894-403A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762477 | ||||||
chr2:159762558
|
T | A | 1 | a0009c0013t0014g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1894-322T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762558 | ||||||
chr2:159762595
|
T | A | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1894-285T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762595 | ||||||
chr2:159762719
|
A | G | 2 | a0001c0001t0014g0299a0001c0001t0014g0300 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1894-161A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762719 | ||||||
chr2:159762722
|
T | G | 281 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(278): Show | 315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1894-158T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762722 | ||||||
chr2:159762775
|
A | G | 1 | a0001c0003t0004g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1894-105A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762775 | ||||||
chr2:159762793
|
A | G | 19 | a0001c0001t0006g0019a0001c0001t0006g0232a0001c0001t0006g0233others(16): Show | 20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1894-87A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762793 | ||||||
chr2:159763109
|
A | C | 2 | a0005c0008t0003g0062a0005c0008t0003g0063 | 2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2007+116A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763109 | ||||||
chr2:159763383
|
T | A | 1 | a0001c0001t0002g0274 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2007+390T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763383 | ||||||
chr2:159763734
|
TC | T | 4 | a0001c0002t0001g0092a0001c0002t0001g0103a0001c0002t0001g0111others(1): Show | 4 | NA18972.hp2 NA18985.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007+742delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763734 | ||||||
chr2:159763853
|
C | T | 2 | a0001c0001t0014g0299a0001c0001t0014g0300 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2008-773C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763853 | ||||||
chr2:159764211
|
T | G | 1 | a0001c0001t0002g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2008-415T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764211 | ||||||
chr2:159764212
|
T | TGTGTGTG others(6): Show |
2 | a0001c0003t0003g0076a0001c0004t0003g0052 | 2 | HG03579.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2008-414_2008-413i others(15): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764212 | ||||||
chr2:159764212
|
T | TTG | 8 | a0001c0001t0002g0255a0001c0001t0002g0267a0001c0001t0002g0269others(5): Show | 8 | HG02280.hp2 HG02300.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2008-371_2008-370d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
T | TTGTG | 18 | a0001c0001t0002g0270a0001c0001t0002g0272a0001c0001t0002g0273others(15): Show | 20 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.2008-373_2008-370d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
T | TTGTGTG | 2 | a0001c0001t0002g0020a0001c0001t0014g0300 | 3 | HG01081.hp1 HG02965.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2008-375_2008-370d others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
T | TTGTGTGT others(1): Show |
4 | a0001c0001t0002g0263a0001c0001t0014g0299a0001c0004t0022g0314others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2008-377_2008-370d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
TTG | T | 29 | a0001c0001t0002g0250a0001c0001t0002g0251a0001c0001t0002g0252others(26): Show | 31 | HG00140.hp2 HG01074.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.2008-371_2008-370d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
TTGTG | T | 19 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(16): Show | 20 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2008-373_2008-370d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
TTGTGTG | T | 16 | a0001c0001t0002g0003a0001c0001t0002g0317a0001c0001t0002g0319others(13): Show | 20 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.2008-375_2008-370d others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
TTGTGTGT others(1): Show |
T | 5 | a0001c0001t0014g0159a0001c0002t0001g0095a0001c0002t0001g0103others(2): Show | 5 | HG00673.hp1 HG01943.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2008-377_2008-370d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
TTGTGTGT others(3): Show |
T | 78 | a0001c0001t0002g0324a0001c0001t0033g0160a0001c0002t0001g0001others(75): Show | 95 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2008-379_2008-370d others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764212
|
TTGTGTGT others(5): Show |
T | 4 | a0001c0002t0001g0088a0001c0002t0001g0109a0001c0002t0001g0155others(1): Show | 4 | NA18990.hp1 NA19054.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008-381_2008-370d others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | |||||
chr2:159764241
|
T | TGTGC | 4 | a0003c0006t0010g0011a0003c0006t0010g0162a0003c0006t0010g0163others(1): Show | 4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2008-382_2008-381i others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764241 | |||||
chr2:159764251
|
T | C | 1 | a0008c0015t0009g0306 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2008-375T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764251 | ||||||
chr2:159764253
|
T | C | 3 | a0001c0004t0018g0225a0002c0005t0009g0089a0008c0015t0009g0306 | 3 | HG02080.hp1 HG03710.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2008-373T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764253 | ||||||
chr2:159764255
|
T | C | 40 | a0001c0003t0003g0079a0001c0003t0003g0080a0001c0003t0003g0081others(37): Show | 42 | HG00280.hp1 HG00558.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2008-371T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764255 | ||||||
chr2:159764255
|
T | TGC | 22 | a0001c0003t0003g0083a0001c0003t0003g0086a0001c0003t0004g0014others(19): Show | 23 | HG00099.hp1 HG00597.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2008-364_2008-363d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGCGC | 3 | a0001c0003t0004g0195a0001c0003t0004g0197a0007c0019t0018g0226 | 3 | NA18940.hp2 NA18979.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2008-366_2008-363d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGCGCGCG others(1): Show |
4 | a0001c0004t0003g0052a0005c0008t0003g0046a0005c0008t0003g0050others(1): Show | 4 | HG01433.hp1 HG02273.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008-370_2008-363d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGC | 3 | a0001c0004t0005g0213a0001c0004t0005g0219a0012c0018t0004g0188 | 3 | HG00544.hp1 HG01261.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGCGC | 3 | a0001c0004t0009g0034a0001c0004t0009g0035a0006c0009t0035g0037 | 3 | HG02280.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGCGCG others(5): Show |
1 | a0006c0009t0009g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGCGCG others(7): Show |
1 | a0005c0008t0003g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGCGCG others(9): Show |
1 | a0005c0017t0003g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGCG others(3): Show |
3 | a0002c0005t0003g0068a0002c0005t0026g0056a0006c0009t0009g0038 | 3 | HG03195.hp1 NA18948.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(5): Show |
2 | a0002c0005t0003g0042a0002c0005t0003g0057 | 2 | NA18960.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(7): Show |
2 | a0002c0005t0003g0059a0005c0008t0003g0047 | 2 | HG01975.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(5): Show |
1 | a0002c0005t0003g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(7): Show |
2 | a0002c0005t0003g0054a0002c0005t0003g0075 | 2 | HG02135.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(9): Show |
3 | a0002c0005t0003g0064a0005c0008t0003g0048a0005c0008t0003g0062 | 3 | HG01515.hp2 HG01934.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(7): Show |
1 | a0006c0009t0036g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(9): Show |
7 | a0002c0005t0003g0005a0002c0005t0003g0053a0002c0005t0003g0067others(4): Show | 7 | NA18957.hp2 NA18977.hp1 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.2008-370_2008-369i others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(11): Show |
1 | a0002c0005t0003g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2008-370_2008-369i others(20): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(11): Show |
4 | a0002c0005t0003g0058a0002c0005t0003g0072a0002c0005t0003g0073others(1): Show | 4 | NA18973.hp1 NA19005.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.2008-370_2008-369i others(20): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(13): Show |
5 | a0002c0005t0003g0033a0002c0005t0003g0045a0002c0005t0003g0060others(2): Show | 5 | HG00408.hp2 NA18987.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2008-370_2008-369i others(22): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(15): Show |
2 | a0002c0005t0003g0061a0006c0009t0009g0036 | 2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(24): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764255
|
T | TGTGTGTG others(21): Show |
1 | a0001c0004t0003g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2008-370_2008-369i others(30): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | |||||
chr2:159764257
|
C | CGT | 6 | a0001c0004t0005g0018a0001c0004t0005g0210a0001c0004t0005g0218others(3): Show | 7 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2008-368_2008-367i others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764257 | |||||
chr2:159764257
|
C | T | 2 | a0001c0004t0005g0219a0001c0004t0037g0217 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2008-369C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764257 | ||||||
chr2:159764258
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2008-368G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764258 | ||||||
chr2:159764337
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2008-289G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764337 | ||||||
chr2:159764747
|
A | G | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2056+73A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159764747 | ||||||
chr2:159764843
|
G | GT | 189 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(186): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2056+180dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159764843 | |||||
chr2:159764901
|
C | CT | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2056+237dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159764901 | |||||
chr2:159764911
|
T | C | 10 | a0001c0004t0008g0025a0001c0004t0008g0026a0001c0004t0008g0307others(7): Show | 12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2056+237T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159764911 | ||||||
chr2:159764919
|
A | C | 1 | a0001c0001t0006g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2056+245A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159764919 | ||||||
chr2:159765002
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2056+328A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765002 | ||||||
chr2:159765102
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2056+428T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765102 | ||||||
chr2:159765206
|
G | GTT | 89 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(86): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2056+540_2056+541d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159765206 | |||||
chr2:159765206
|
G | GTTT | 6 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2056+539_2056+541d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159765206 | |||||
chr2:159765228
|
G | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2056+554G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765228 | ||||||
chr2:159765413
|
T | G | 24 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(21): Show | 27 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.2056+739T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765413 | ||||||
chr2:159765414
|
G | A | 3 | a0001c0004t0013g0027a0001c0004t0013g0309a0001c0004t0013g0310 | 4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2056+740G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765414 | ||||||
chr2:159765617
|
C | G | 1 | a0001c0002t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2056+943C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765617 | ||||||
chr2:159765662
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2056+988T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765662 | ||||||
chr2:159765854
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2056+1180C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765854 | ||||||
chr2:159766057
|
CAT | C | 16 | a0001c0004t0005g0018a0001c0004t0005g0028a0001c0004t0005g0210others(13): Show | 18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2057-1226_2057-122 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766057 | ||||||
chr2:159766119
|
G | C | 100 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(97): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.2057-1165G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766119 | ||||||
chr2:159766119
|
G | T | 4 | a0003c0006t0010g0011a0003c0006t0010g0162a0003c0006t0010g0163others(1): Show | 4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2057-1165G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766119 | ||||||
chr2:159766385
|
G | T | 1 | a0009c0013t0014g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2057-899G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766385 | ||||||
chr2:159766450
|
C | T | 96 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0006others(93): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2057-834C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766450 | ||||||
chr2:159766855
|
C | T | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2057-429C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766855 | ||||||
chr2:159767019
|
C | CTTGAACC others(118): Show |
1 | a0001c0001t0033g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2057-250_2057-249i others(127): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159767019 | |||||
chr2:159767019
|
C | CTTGAACC others(120): Show |
1 | a0001c0001t0014g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2057-250_2057-249i others(129): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159767019 | |||||
chr2:159767041
|
T | A | 2 | a0001c0001t0020g0169a0001c0001t0020g0170 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2057-243T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767041 | ||||||
chr2:159767079
|
G | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0021others(92): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2057-205G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767079 | ||||||
chr2:159767089
|
G | A | 6 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2057-195G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767089 | ||||||
chr2:159767240
|
T | A | 1 | a0001c0002t0001g0122 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2057-44T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767240 |