geneid | 2006 |
---|---|
ensemblid | ENSG00000049540.19 |
hgncid | 3327 |
symbol | ELN |
name | elastin |
refseq_nuc | NM_000501.4 |
refseq_prot | NP_000492.2 |
ensembl_nuc | ENST00000252034.12 |
ensembl_prot | ENSP00000252034.7 |
mane_status | MANE Select |
chr | chr7 |
start | 74028173 |
end | 74069907 |
strand | + |
ver | v1.2 |
region | chr7:74028173-74069907 |
region5000 | chr7:74023173-74074907 |
regionname0 | ELN_chr7_74028173_74069907 |
regionname5000 | ELN_chr7_74023173_74074907 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 724 | 280 | 63 | 44 | 139 | 5 | 29 | 95 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002 | 0/0 | 724 | 56 | 9 | 15 | 17 | 8 | 7 | 11 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0003 | 0/0 | 724 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0004 | 0/0 | 724 | 6 | 1 | 2 | 0 | 1 | 2 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0005 | 0/0 | 724 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0006 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0007 | 0/0 | 724 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0008 | 0/0 | 724 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0009 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0010 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0011 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0012 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0013 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0014 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0015 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0016 | 0/0 | 728 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0017 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2175 | 276 | 63 | 44 | 137 | 5 | 27 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0002 | 0/0 | 2175 | 52 | 6 | 15 | 17 | 8 | 6 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0003 | 0/0 | 2175 | 7 | 0 | 0 | 7 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0004 | 0/0 | 2175 | 6 | 1 | 2 | 0 | 1 | 2 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0005 | 0/0 | 2175 | 3 | 3 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0006 | 0/0 | 2175 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0007 | 0/0 | 2175 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0008 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0009 | 0/0 | 2175 | 2 | 1 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0010 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0011 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0012 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0013 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0014 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0015 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0016 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0017 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0018 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0019 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0020 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0021 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0022 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
c0023 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1223 | 262 | 39 | 55 | 135 | 8 | 25 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0002 | 0/0 | 1224 | 31 | 9 | 3 | 14 | 2 | 3 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0003 | 0/0 | 1224 | 29 | 4 | 4 | 11 | 2 | 8 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0004 | 0/0 | 1224 | 22 | 21 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0005 | 0/0 | 1223 | 18 | 4 | 1 | 9 | 2 | 2 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0006 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0007 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0008 | 0/0 | 1223 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
t0009 | 0/0 | 1223 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2175 | 276 | 63 | 44 | 137 | 5 | 27 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0016 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0017 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0018 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0020 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002 | 0/0 | 2175 | 52 | 6 | 15 | 17 | 8 | 6 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0005 | 0/0 | 2175 | 3 | 3 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0015 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0003c0003 | 0/0 | 2175 | 7 | 0 | 0 | 7 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0004c0004 | 0/0 | 2175 | 6 | 1 | 2 | 0 | 1 | 2 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0005c0009 | 0/0 | 2175 | 2 | 1 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0006c0008 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0007c0007 | 0/0 | 2175 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0008c0006 | 0/0 | 2175 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0009c0010 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0010c0023 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0011c0012 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0012c0021 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0013c0022 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0014c0019 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0015c0014 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0016c0013 | 0/0 | 2187 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0017c0011 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3397 | 202 | 31 | 40 | 109 | 4 | 18 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0002 | 0/0 | 3398 | 19 | 7 | 1 | 9 | 1 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0003 | 0/0 | 3398 | 18 | 1 | 1 | 10 | 0 | 6 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0004 | 0/0 | 3398 | 19 | 18 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0005 | 0/0 | 3397 | 15 | 4 | 1 | 8 | 0 | 2 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0006 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0007 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0001t0009 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0016t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0017t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0018t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0001c0020t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002t0001 | 0/0 | 3397 | 38 | 4 | 14 | 13 | 4 | 3 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002t0002 | 0/0 | 3398 | 7 | 0 | 1 | 3 | 1 | 2 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002t0003 | 0/0 | 3398 | 3 | 0 | 0 | 1 | 1 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002t0004 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002t0005 | 0/0 | 3397 | 2 | 0 | 0 | 0 | 2 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0002t0008 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0005t0001 | 0/0 | 3397 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0005t0002 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0002c0015t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0003c0003t0001 | 0/0 | 3397 | 5 | 0 | 0 | 5 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0003c0003t0002 | 0/0 | 3398 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0004c0004t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0004c0004t0003 | 0/0 | 3398 | 5 | 1 | 2 | 0 | 1 | 1 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0005c0009t0001 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0005c0009t0002 | 0/0 | 3398 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0006c0008t0001 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0006c0008t0004 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0007c0007t0001 | 0/0 | 3397 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0007c0007t0003 | 0/0 | 3398 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0008c0006t0001 | 0/0 | 3397 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0009c0010t0005 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0010c0023t0003 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0011c0012t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0012c0021t0003 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0013c0022t0002 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0014c0019t0004 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0015c0014t0001 | 0/0 | 3382 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0016c0013t0001 | 0/0 | 3409 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
a0017c0011t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | copy fasta | chr7 | 74023173 | 74074907 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0009g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0016t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0017t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0018t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0020t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0015t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0005c0009t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0005c0009t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0006c0008t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0006c0008t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0007c0007t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0007c0007t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0008c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0008c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0009c0010t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0010c0023t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0011c0012t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0012c0021t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0013c0022t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0014c0019t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0015c0014t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0016c0013t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0017c0011t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0051 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00140 | hp1 | a0002 | c0002 | t0005 | g0068 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00140 | hp2 | a0004 | c0004 | t0003 | g0127 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0052 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00323 | hp2 | a0002 | c0002 | t0005 | g0088 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0319 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00738 | hp2 | a0004 | c0004 | t0003 | g0120 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01243 | hp1 | a0005 | c0009 | t0002 | g0105 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0058 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01256 | hp2 | a0007 | c0007 | t0003 | g0048 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01346 | hp1 | a0004 | c0004 | t0003 | g0125 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0082 | EUR | IBS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0333 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02083 | hp2 | a0001 | c0016 | t0001 | g0335 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02258 | hp1 | a0002 | c0005 | t0002 | g0066 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0327 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0096 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02622 | hp2 | a0013 | c0022 | t0002 | g0126 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02630 | hp2 | a0005 | c0009 | t0001 | g0119 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0348 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02698 | hp2 | a0004 | c0004 | t0003 | g0124 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02735 | hp2 | a0002 | c0015 | t0001 | g0069 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02738 | hp1 | a0004 | c0004 | t0001 | g0122 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02896 | hp2 | a0012 | c0021 | t0003 | g0135 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0336 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02965 | hp2 | a0014 | c0019 | t0004 | g0130 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03130 | hp1 | a0002 | c0002 | t0004 | g0116 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03239 | hp1 | a0001 | c0018 | t0001 | g0163 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03453 | hp1 | a0006 | c0008 | t0001 | g0140 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03453 | hp2 | a0006 | c0008 | t0004 | g0139 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03486 | hp1 | a0002 | c0005 | t0001 | g0064 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03516 | hp2 | a0002 | c0005 | t0001 | g0065 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03654 | hp1 | a0001 | c0020 | t0001 | g0104 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0061 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0176 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0289 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0343 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18939 | hp1 | a0009 | c0010 | t0005 | g0308 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18950 | hp2 | a0001 | c0017 | t0001 | g0008 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18954 | hp2 | a0001 | c0001 | t0009 | g0316 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18959 | hp1 | a0008 | c0006 | t0001 | g0279 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18960 | hp2 | a0003 | c0003 | t0002 | g0252 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18972 | hp2 | a0008 | c0006 | t0001 | g0282 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18983 | hp1 | a0017 | c0011 | t0001 | g0004 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18987 | hp2 | a0003 | c0003 | t0002 | g0241 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18991 | hp1 | a0011 | c0012 | t0001 | g0092 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18994 | hp2 | a0016 | c0013 | t0001 | g0276 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0238 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19012 | hp1 | a0015 | c0014 | t0001 | g0060 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19085 | hp2 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20129 | hp1 | a0004 | c0004 | t0003 | g0103 | AFR | ASW | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0353 | AFR | ASW | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0049 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0084 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01123 | hp1 | a0007 | c0007 | t0001 | g0045 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0295 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02486 | hp1 | a0002 | c0002 | t0008 | g0070 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA21309 | hp1 | a0010 | c0023 | t0003 | g0118 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74041231
|
C | T | 1 | a0003 | 7 | NA18944.hp2 NA18960.hp2 NA18987.hp2 others(4): Show |
missense_variant | MODERATE | c.212C>T | p.Ala71Val | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/33 | 227/3397 | 212/2175 | 71/724 | chr7 | 74041231 | ||
chr7:74043157
|
G | A | 1 | a0009 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.416G>A | p.Gly139Glu | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/33 | 431/3397 | 416/2175 | 139/724 | chr7 | 74043157 | ||
chr7:74045245
|
G | T | 2 | a0005a0010 | 3 | HG01243.hp1 HG02630.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.493G>T | p.Val165Leu | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/33 | 508/3397 | 493/2175 | 165/724 | chr7 | 74045245 | ||
chr7:74051755
|
G | A | 1 | a0017 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.805G>A | p.Gly269Arg | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 16/33 | 820/3397 | 805/2175 | 269/724 | chr7 | 74051755 | ||
chr7:74051803
|
G | A | 1 | a0011 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.853G>A | p.Val285Met | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 16/33 | 868/3397 | 853/2175 | 285/724 | chr7 | 74051803 | ||
chr7:74051926
|
G | A | 1 | a0010 | 1 | NA21309.hp1 | missense_variant&splice_region_variant | MODERATE | c.892G>A | p.Val298Ile | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/33 | 907/3397 | 892/2175 | 298/724 | chr7 | 74051926 | ||
chr7:74051965
|
G | A | 2 | a0008a0016 | 3 | NA18959.hp1 NA18972.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.931G>A | p.Ala311Thr | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/33 | 946/3397 | 931/2175 | 311/724 | chr7 | 74051965 | ||
chr7:74053290
|
CCCAGGTG others(8): Show |
C | 1 | a0015 | 1 | NA19012.hp1 | splice_donor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1085_1096+3delCTGC others(11): Show |
p.Ala362_Pro365del | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/33 | 1100/3397 | 1085/2175 | 362/724 | INFO_REALIGN_3_PRIME | chr7 | 74053290 | |
chr7:74056384
|
G | A | 7 | a0002a0005a0007others(4): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(61): Show |
missense_variant | MODERATE | c.1264G>A | p.Gly422Ser | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/33 | 1279/3397 | 1264/2175 | 422/724 | chr7 | 74056384 | ||
chr7:74056399
|
C | G | 1 | a0006 | 2 | HG03453.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1279C>G | p.Pro427Ala | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/33 | 1294/3397 | 1279/2175 | 427/724 | chr7 | 74056399 | ||
chr7:74057670
|
A | G | 1 | a0014 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1388A>G | p.Lys463Arg | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/33 | 1403/3397 | 1388/2175 | 463/724 | chr7 | 74057670 | ||
chr7:74060451
|
C | T | 1 | a0013 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1697C>T | p.Ala566Val | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/33 | 1712/3397 | 1697/2175 | 566/724 | chr7 | 74060451 | ||
chr7:74060495
|
G | C | 2 | a0004a0007 | 8 | HG00140.hp2 HG00738.hp2 HG01123.hp1 others(5): Show |
missense_variant | MODERATE | c.1741G>C | p.Gly581Arg | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/33 | 1756/3397 | 1741/2175 | 581/724 | chr7 | 74060495 | ||
chr7:74063194
|
G | A | 2 | a0012a0013 | 2 | HG02622.hp2 HG02896.hp2 |
missense_variant | MODERATE | c.1828G>A | p.Gly610Ser | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 27/33 | 1843/3397 | 1828/2175 | 610/724 | chr7 | 74063194 | ||
chr7:74065957
|
T | TGGAGGTG others(5): Show |
1 | a0016 | 1 | NA18994.hp2 | disruptive_inframe_insertion | MODERATE | c.2049_2060dupAGGTGT others(6): Show |
p.Gly687_Gly688insGl others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/33 | 2076/3397 | 2061/2175 | 687/724 | INFO_REALIGN_3_PRIME | chr7 | 74065957 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74051955
|
A | G | 2 | a0012c0021a0013c0022 | 2 | HG02622.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.921A>G | p.Ala307Ala | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/33 | 936/3397 | 921/2175 | 307/724 | chr7 | 74051955 | ||
chr7:74056389
|
C | T | 1 | a0002c0005 | 3 | HG02258.hp1 HG03486.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1269C>T | p.Val423Val | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/33 | 1284/3397 | 1269/2175 | 423/724 | chr7 | 74056389 | ||
chr7:74056694
|
C | T | 1 | a0001c0020 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.1338C>T | p.Ala446Ala | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/33 | 1353/3397 | 1338/2175 | 446/724 | chr7 | 74056694 | ||
chr7:74059977
|
C | T | 1 | a0001c0018 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1506C>T | p.Gly502Gly | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 23/33 | 1521/3397 | 1506/2175 | 502/724 | chr7 | 74059977 | ||
chr7:74060037
|
T | A | 1 | a0002c0015 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1566T>A | p.Gly522Gly | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 23/33 | 1581/3397 | 1566/2175 | 522/724 | chr7 | 74060037 | ||
chr7:74060428
|
C | T | 1 | a0001c0017 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1674C>T | p.Gly558Gly | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/33 | 1689/3397 | 1674/2175 | 558/724 | chr7 | 74060428 | ||
chr7:74063320
|
C | T | 1 | a0001c0016 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1869C>T | p.Pro623Pro | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/33 | 1884/3397 | 1869/2175 | 623/724 | chr7 | 74063320 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74068872
|
G | A | 1 | a0001c0001t0006 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 172 | chr7 | 74068872 | |||||
chr7:74069083
|
T | G | 1 | a0001c0001t0007 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 383 | chr7 | 74069083 | |||||
chr7:74069201
|
C | CA | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 84 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*501_*502insA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 502 | chr7 | 74069201 | |||||
chr7:74069248
|
G | A | 1 | a0002c0002t0008 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*548G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 548 | chr7 | 74069248 | |||||
chr7:74069359
|
G | C | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(9): Show | 55 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 659 | chr7 | 74069359 | |||||
chr7:74069388
|
G | A | 1 | a0001c0001t0009 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*688G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 688 | chr7 | 74069388 | |||||
chr7:74069894
|
A | G | 9 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(6): Show | 42 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1194A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 1194 | chr7 | 74069894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74028653
|
G | A | 1 | a0002c0002t0001g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.82+384G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028653 | ||||||
chr7:74028682
|
C | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(25): Show | 30 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.82+413C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028682 | ||||||
chr7:74028685
|
G | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0075others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.82+416G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028685 | ||||||
chr7:74028802
|
G | T | 84 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0274others(81): Show | 87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+533G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028802 | ||||||
chr7:74028915
|
G | A | 87 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0274others(84): Show | 90 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.82+646G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028915 | ||||||
chr7:74028951
|
T | G | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(336): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.82+682T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028951 | ||||||
chr7:74028960
|
C | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG00733.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+691C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028960 | ||||||
chr7:74029005
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.82+736A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029005 | ||||||
chr7:74029121
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.82+852C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029121 | ||||||
chr7:74029138
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099 | 3 | HG02258.hp2 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.82+869G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029138 | ||||||
chr7:74029277
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0237a0001c0001t0001g0239others(15): Show | 18 | HG00738.hp1 HG01943.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.82+1008C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029277 | ||||||
chr7:74029340
|
A | C | 1 | a0002c0002t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.82+1071A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029340 | ||||||
chr7:74029438
|
G | A | 1 | a0001c0001t0004g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82+1169G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029438 | ||||||
chr7:74029815
|
G | A | 1 | a0004c0004t0003g0103 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82+1546G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029815 | ||||||
chr7:74029864
|
T | G | 1 | a0001c0020t0001g0104 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82+1595T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029864 | ||||||
chr7:74030346
|
C | T | 1 | a0001c0001t0001g0354 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82+2077C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030346 | ||||||
chr7:74030347
|
G | C | 1 | a0005c0009t0002g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82+2078G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030347 | ||||||
chr7:74030465
|
A | AT | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(75): Show | 80 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.82+2213dupT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | |||||
chr7:74030465
|
A | ATT | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0038others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.82+2212_82+2213dup others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | |||||
chr7:74030465
|
A | ATTT | 7 | a0001c0001t0001g0007a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 8 | HG00423.hp1 HG01257.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+2211_82+2213dup others(3): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | |||||
chr7:74030465
|
AT | A | 8 | a0001c0001t0001g0258a0001c0001t0001g0349a0001c0001t0001g0350others(5): Show | 8 | HG00408.hp2 HG00741.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2213delT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | |||||
chr7:74030465
|
ATT | A | 80 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(77): Show | 83 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.82+2212_82+2213del others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | |||||
chr7:74030723
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.82+2454C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030723 | ||||||
chr7:74030784
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0075others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.82+2515T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030784 | ||||||
chr7:74030858
|
G | T | 1 | a0005c0009t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.82+2589G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030858 | ||||||
chr7:74030976
|
G | GT | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(82): Show | 88 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.82+2712dupT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030976 | |||||
chr7:74031110
|
G | A | 1 | a0007c0007t0001g0045 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.82+2841G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031110 | ||||||
chr7:74031146
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.82+2877G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031146 | ||||||
chr7:74031160
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.82+2891G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031160 | ||||||
chr7:74031175
|
A | C | 1 | a0001c0001t0003g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.82+2906A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031175 | ||||||
chr7:74031308
|
T | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+3039T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031308 | ||||||
chr7:74031459
|
A | G | 152 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(149): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.82+3190A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031459 | ||||||
chr7:74031612
|
A | G | 86 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(83): Show | 89 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.82+3343A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031612 | ||||||
chr7:74031775
|
TAAAAAGA others(3): Show |
T | 2 | a0001c0001t0004g0143a0001c0001t0004g0229 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.82+3520_82+3529del others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031775 | |||||
chr7:74031847
|
A | C | 1 | a0010c0023t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83-3517A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031847 | ||||||
chr7:74031860
|
A | AGAAG | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.83-3452_83-3449dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
A | AGAAGGAA others(1): Show |
103 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(100): Show | 104 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.83-3456_83-3449dup others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
A | AGAAGGAA others(5): Show |
43 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0142others(40): Show | 44 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.83-3460_83-3449dup others(12): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
A | AGAAGGAA others(9): Show |
18 | a0001c0001t0001g0014a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 19 | HG00423.hp1 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-3464_83-3449dup others(16): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
A | AGAAGGAA others(13): Show |
4 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0352others(1): Show | 4 | HG00544.hp1 HG02647.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3468_83-3449dup others(20): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.83-3504A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031860 | ||||||
chr7:74031860
|
AGAAG | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0017others(25): Show | 30 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.83-3452_83-3449del others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
AGAAGGAA others(1): Show |
A | 7 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0149others(4): Show | 7 | HG00642.hp1 HG00738.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-3456_83-3449del others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74031860
|
AGAAGGAA others(5): Show |
A | 11 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0283others(8): Show | 11 | HG02165.hp1 HG03669.hp1 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-3460_83-3449del others(12): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | |||||
chr7:74032060
|
T | A | 1 | a0001c0001t0002g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.83-3304T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032060 | ||||||
chr7:74032067
|
A | G | 86 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(83): Show | 89 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.83-3297A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032067 | ||||||
chr7:74032106
|
T | C | 86 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(83): Show | 89 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.83-3258T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032106 | ||||||
chr7:74032107
|
G | A | 1 | a0001c0001t0002g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.83-3257G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032107 | ||||||
chr7:74032165
|
GATTCTAA others(12): Show |
G | 1 | a0001c0001t0005g0328 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.83-3197_83-3179del others(19): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74032165 | |||||
chr7:74032205
|
C | T | 1 | a0001c0001t0005g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.83-3159C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032205 | ||||||
chr7:74032226
|
C | T | 1 | a0001c0001t0004g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83-3138C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032226 | ||||||
chr7:74032313
|
A | C | 3 | a0002c0002t0001g0041a0002c0002t0001g0042a0002c0002t0003g0040 | 3 | HG02080.hp2 NA18970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.83-3051A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032313 | ||||||
chr7:74032425
|
T | TG | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(353): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.83-2939_83-2938ins others(1): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032425 | ||||||
chr7:74032427
|
G | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(353): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.83-2937G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032427 | ||||||
chr7:74032535
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0274others(7): Show | 11 | HG00609.hp1 HG00621.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.83-2829C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032535 | ||||||
chr7:74032546
|
A | C | 2 | a0001c0001t0002g0072a0002c0002t0002g0073 | 2 | HG02027.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.83-2818A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032546 | ||||||
chr7:74032603
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.83-2761G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032603 | ||||||
chr7:74032624
|
T | C | 1 | a0002c0002t0001g0093 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.83-2740T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032624 | ||||||
chr7:74032714
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83-2650C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032714 | ||||||
chr7:74032744
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83-2620A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032744 | ||||||
chr7:74032929
|
G | C | 1 | a0016c0013t0001g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.83-2435G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032929 | ||||||
chr7:74032965
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.83-2399C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032965 | ||||||
chr7:74033176
|
G | A | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.83-2188G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033176 | ||||||
chr7:74033328
|
T | C | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.83-2036T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033328 | ||||||
chr7:74033329
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.83-2035G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033329 | ||||||
chr7:74033372
|
A | G | 1 | a0010c0023t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83-1992A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033372 | ||||||
chr7:74033411
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0099 | 3 | HG02258.hp2 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.83-1953G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033411 | ||||||
chr7:74033441
|
C | T | 1 | a0003c0003t0002g0252 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.83-1923C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033441 | ||||||
chr7:74033798
|
G | A | 1 | a0001c0001t0003g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.83-1566G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033798 | ||||||
chr7:74033895
|
G | T | 1 | a0001c0001t0001g0337 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.83-1469G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033895 | ||||||
chr7:74033934
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0210 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.83-1430C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033934 | ||||||
chr7:74033986
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.83-1378C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033986 | ||||||
chr7:74034169
|
A | G | 3 | a0002c0002t0001g0013a0002c0002t0001g0052a0002c0002t0001g0053 | 3 | HG00280.hp2 HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.83-1195A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034169 | ||||||
chr7:74034443
|
C | T | 1 | a0002c0002t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.83-921C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034443 | ||||||
chr7:74034491
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.83-873C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034491 | ||||||
chr7:74034495
|
T | TGAGC | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.83-869_83-868insGA others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034495 | ||||||
chr7:74034664
|
T | C | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.83-700T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034664 | ||||||
chr7:74034807
|
T | C | 1 | a0001c0001t0004g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83-557T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034807 | ||||||
chr7:74034829
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.83-535G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034829 | ||||||
chr7:74034833
|
G | A | 1 | a0002c0002t0001g0076 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.83-531G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034833 | ||||||
chr7:74034916
|
C | A | 7 | a0001c0001t0001g0123a0004c0004t0001g0122a0004c0004t0003g0103others(4): Show | 7 | HG00140.hp2 HG00738.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-448C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034916 | ||||||
chr7:74035175
|
A | G | 1 | a0001c0001t0004g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83-189A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74035175 | ||||||
chr7:74035306
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.83-58T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74035306 | ||||||
chr7:74035516
|
G | A | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.133+102G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74035516 | ||||||
chr7:74035780
|
T | TA | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.133+375dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr7 | 74035780 | |||||
chr7:74035850
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.133+436G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74035850 | ||||||
chr7:74035866
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.133+452G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74035866 | ||||||
chr7:74036107
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.134-448G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036107 | ||||||
chr7:74036220
|
G | A | 1 | a0004c0004t0003g0103 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.134-335G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036220 | ||||||
chr7:74036383
|
C | T | 1 | a0005c0009t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-172C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036383 | ||||||
chr7:74036450
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.134-105G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036450 | ||||||
chr7:74036536
|
T | C | 1 | a0001c0001t0003g0287 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.134-19T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036536 | ||||||
chr7:74036750
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.163+166C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74036750 | ||||||
chr7:74037259
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.164-448T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037259 | ||||||
chr7:74037341
|
A | T | 1 | a0010c0023t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-366A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037341 | ||||||
chr7:74037350
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.164-357C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037350 | ||||||
chr7:74037383
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.164-324A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037383 | ||||||
chr7:74037436
|
C | G | 2 | a0001c0001t0001g0325a0001c0001t0005g0324 | 2 | HG00597.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.164-271C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037436 | ||||||
chr7:74037775
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18977.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.196+36G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037775 | ||||||
chr7:74037810
|
G | A | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+71G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037810 | ||||||
chr7:74037908
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+169C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037908 | ||||||
chr7:74037933
|
G | A | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+194G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037933 | ||||||
chr7:74038112
|
C | T | 1 | a0002c0002t0001g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196+373C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038112 | ||||||
chr7:74038113
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0196 | 2 | HG00408.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.196+374G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038113 | ||||||
chr7:74038348
|
C | A | 1 | a0001c0001t0001g0305 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.196+609C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038348 | ||||||
chr7:74038390
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.196+651C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038390 | ||||||
chr7:74038532
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.196+793C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038532 | ||||||
chr7:74038581
|
G | A | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+842G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038581 | ||||||
chr7:74038593
|
C | T | 1 | a0001c0001t0001g0351 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.196+854C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038593 | ||||||
chr7:74038765
|
T | C | 1 | a0002c0002t0001g0077 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196+1026T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038765 | ||||||
chr7:74038902
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+1163T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038902 | ||||||
chr7:74039191
|
G | A | 3 | a0001c0001t0005g0306a0001c0001t0005g0307a0001c0001t0005g0329 | 3 | HG02922.hp2 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.196+1452G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039191 | ||||||
chr7:74039332
|
G | A | 1 | a0012c0021t0003g0135 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.196+1593G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039332 | ||||||
chr7:74039406
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.196+1667C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039406 | ||||||
chr7:74039491
|
G | A | 1 | a0010c0023t0003g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.197-1725G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039491 | ||||||
chr7:74039735
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.197-1481G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039735 | ||||||
chr7:74039869
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0039others(71): Show | 75 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.197-1347G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039869 | ||||||
chr7:74040009
|
C | T | 1 | a0001c0001t0004g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.197-1207C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040009 | ||||||
chr7:74040079
|
T | G | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-1137T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040079 | ||||||
chr7:74040084
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.197-1132G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040084 | ||||||
chr7:74040144
|
C | T | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-1072C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040144 | ||||||
chr7:74040166
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.197-1050T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040166 | ||||||
chr7:74040225
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0183 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.197-991G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040225 | ||||||
chr7:74040299
|
T | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(324): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.197-917T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040299 | ||||||
chr7:74040352
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.197-864C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040352 | ||||||
chr7:74040443
|
T | A | 3 | a0002c0002t0001g0041a0002c0002t0001g0042a0002c0002t0003g0040 | 3 | HG02080.hp2 NA18970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.197-773T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040443 | ||||||
chr7:74040446
|
C | T | 1 | a0002c0002t0001g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.197-770C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040446 | ||||||
chr7:74040461
|
G | A | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-755G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040461 | ||||||
chr7:74040569
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.197-647C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040569 | ||||||
chr7:74040681
|
C | G | 2 | a0005c0009t0001g0119a0005c0009t0002g0105 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.197-535C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040681 | ||||||
chr7:74040693
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02257.hp1 HG02615.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-523G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040693 | ||||||
chr7:74040721
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.197-495C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040721 | ||||||
chr7:74040722
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.197-494G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040722 | ||||||
chr7:74040872
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0004g0116 | 2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.197-344C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040872 | ||||||
chr7:74040895
|
C | T | 1 | a0001c0001t0004g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.197-321C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040895 | ||||||
chr7:74040900
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.197-316A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040900 | ||||||
chr7:74040946
|
T | C | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-270T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040946 | ||||||
chr7:74041054
|
G | A | 82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(79): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-162G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74041054 | ||||||
chr7:74041330
|
G | A | 1 | a0009c0010t0005g0308 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.232+79G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041330 | ||||||
chr7:74041378
|
G | A | 1 | a0002c0002t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.232+127G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041378 | ||||||
chr7:74041834
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.232+583G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041834 | ||||||
chr7:74041928
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.232+677C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041928 | ||||||
chr7:74041932
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+681G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041932 | ||||||
chr7:74042061
|
G | GA | 6 | a0001c0001t0001g0198a0001c0001t0001g0232a0001c0001t0001g0283others(3): Show | 6 | HG01952.hp2 NA18939.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-540dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042061 | |||||
chr7:74042062
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.233-552A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042062 | ||||||
chr7:74042117
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-497G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042117 | ||||||
chr7:74042118
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-496G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042118 | ||||||
chr7:74042119
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-495C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042119 | ||||||
chr7:74042121
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-493C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042121 | ||||||
chr7:74042123
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-491C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042123 | ||||||
chr7:74042125
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-489A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042125 | ||||||
chr7:74042129
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-485A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042129 | ||||||
chr7:74042132
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-482T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042132 | ||||||
chr7:74042137
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-477T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042137 | ||||||
chr7:74042146
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-468G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042146 | ||||||
chr7:74042156
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-458A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042156 | ||||||
chr7:74042195
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-419A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042195 | ||||||
chr7:74042197
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-417A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042197 | ||||||
chr7:74042198
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-416T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042198 | ||||||
chr7:74042199
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-415G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042199 | ||||||
chr7:74042214
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.233-400G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042214 | ||||||
chr7:74042260
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-354A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042260 | ||||||
chr7:74042265
|
C | CA | 72 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0063others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.233-336dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042265 | |||||
chr7:74042265
|
C | CAA | 81 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(78): Show | 84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.233-337_233-336dup others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042265 | |||||
chr7:74042274
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-340A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042274 | ||||||
chr7:74042318
|
C | G | 3 | a0002c0002t0005g0088a0002c0002t0008g0070a0002c0015t0001g0069 | 3 | HG00323.hp2 HG02486.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.233-296C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042318 | ||||||
chr7:74042333
|
C | T | 1 | a0002c0002t0001g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.233-281C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042333 | ||||||
chr7:74042427
|
C | CA | 89 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(86): Show | 92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-174dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042427 | |||||
chr7:74042520
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0039others(71): Show | 75 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.233-94G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042520 | ||||||
chr7:74042793
|
C | G | 1 | a0001c0001t0005g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.325+87C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 6/32 | chr7 | 74042793 | ||||||
chr7:74042892
|
G | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG00544.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.326-92G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 6/32 | chr7 | 74042892 | ||||||
chr7:74042925
|
G | A | 4 | a0001c0001t0001g0123a0004c0004t0003g0103a0004c0004t0003g0120others(1): Show | 4 | HG00140.hp2 HG00738.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-59G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 6/32 | chr7 | 74042925 | ||||||
chr7:74043083
|
T | A | 1 | a0006c0008t0004g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.377-35T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 7/32 | chr7 | 74043083 | ||||||
chr7:74043176
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0210 | 2 | HG01358.hp2 HG01361.hp1 |
splice_region_variant&intron_variant | LOW | c.427+8C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043176 | ||||||
chr7:74043260
|
G | C | 3 | a0002c0002t0005g0088a0002c0002t0008g0070a0002c0015t0001g0069 | 3 | HG00323.hp2 HG02486.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.427+92G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043260 | ||||||
chr7:74043371
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0184others(2): Show | 5 | HG00280.hp1 HG02602.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+203G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043371 | ||||||
chr7:74043593
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.428-286G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043593 | ||||||
chr7:74043647
|
T | C | 1 | a0002c0002t0001g0003 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.428-232T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043647 | ||||||
chr7:74043934
|
G | A | 1 | a0001c0001t0004g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.469+14G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74043934 | ||||||
chr7:74044221
|
A | AATCGTAG others(27): Show |
1 | a0003c0003t0002g0241 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+301_469+302ins others(34): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044221 | ||||||
chr7:74044230
|
G | T | 1 | a0003c0003t0002g0241 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+310G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044230 | ||||||
chr7:74044237
|
T | C | 1 | a0003c0003t0002g0241 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+317T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044237 | ||||||
chr7:74044239
|
T | A | 1 | a0003c0003t0002g0241 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+319T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044239 | ||||||
chr7:74044242
|
A | T | 1 | a0003c0003t0002g0241 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+322A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044242 | ||||||
chr7:74044243
|
AACAAAGA others(25): Show |
A | 1 | a0003c0003t0002g0241 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+324_469+355del others(32): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044243 | ||||||
chr7:74044487
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.469+567G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044487 | ||||||
chr7:74044852
|
C | A | 1 | a0002c0002t0001g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.470-370C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044852 | ||||||
chr7:74044894
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.470-328G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044894 | ||||||
chr7:74045094
|
C | T | 1 | a0001c0001t0001g0346 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.470-128C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74045094 | ||||||
chr7:74045197
|
C | T | 8 | a0001c0001t0001g0222a0001c0001t0001g0350a0001c0001t0002g0336others(5): Show | 9 | HG01884.hp1 HG02109.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-25C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74045197 | ||||||
chr7:74045407
|
T | A | 1 | a0001c0001t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.541+114T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045407 | ||||||
chr7:74045412
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.541+119A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045412 | ||||||
chr7:74045519
|
G | A | 3 | a0001c0001t0001g0100a0002c0002t0001g0117a0002c0002t0004g0116 | 3 | HG02723.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.541+226G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045519 | ||||||
chr7:74045735
|
T | C | 1 | a0013c0022t0002g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541+442T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045735 | ||||||
chr7:74045930
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542-258G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045930 | ||||||
chr7:74046067
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.542-121G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74046067 | ||||||
chr7:74046116
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.542-72C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74046116 | ||||||
chr7:74046499
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.572-197C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 11/32 | chr7 | 74046499 | ||||||
chr7:74046806
|
G | A | 1 | a0005c0009t0002g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.643+39G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | chr7 | 74046806 | ||||||
chr7:74046884
|
G | T | 2 | a0001c0001t0001g0325a0001c0001t0005g0324 | 2 | HG00597.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.643+117G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | chr7 | 74046884 | ||||||
chr7:74046937
|
A | G | 1 | a0002c0002t0008g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.643+170A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | chr7 | 74046937 | ||||||
chr7:74047100
|
G | GA | 80 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0106others(77): Show | 83 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.643+343dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr7 | 74047100 | |||||
chr7:74047888
|
G | T | 1 | a0002c0002t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.685+172G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 13/32 | chr7 | 74047888 | ||||||
chr7:74048125
|
G | A | 1 | a0016c0013t0001g0276 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.686-17G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 13/32 | chr7 | 74048125 | ||||||
chr7:74048389
|
T | G | 1 | a0001c0001t0005g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.746-114T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 14/32 | chr7 | 74048389 | ||||||
chr7:74048475
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0173 | 2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.746-28G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 14/32 | chr7 | 74048475 | ||||||
chr7:74048865
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.799+309G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74048865 | ||||||
chr7:74049068
|
T | TATCC | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(329): Show | 341 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.799+543_799+546dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049068 | |||||
chr7:74049068
|
T | TATCCATC others(1): Show |
10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0156others(7): Show | 10 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.799+539_799+546dup others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049068 | |||||
chr7:74049129
|
A | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0007g0110 | 3 | HG02896.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.799+573A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049129 | ||||||
chr7:74049248
|
A | G | 1 | a0001c0001t0001g0354 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.799+692A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049248 | ||||||
chr7:74049399
|
T | C | 152 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(149): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.799+843T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049399 | ||||||
chr7:74049516
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.799+960T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049516 | ||||||
chr7:74049593
|
GCATCCAT others(5): Show |
G | 1 | a0001c0001t0001g0291 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.799+1059_799+1070d others(14): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049593 | |||||
chr7:74049665
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0006g0132 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.799+1109C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049665 | ||||||
chr7:74049703
|
T | C | 1 | a0001c0001t0003g0199 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.799+1147T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049703 | ||||||
chr7:74049719
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.799+1163T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049719 | ||||||
chr7:74049906
|
CATCCATA others(5): Show |
C | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(353): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.799+1368_799+1379d others(14): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049906 | |||||
chr7:74050068
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(23): Show | 28 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+1512T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050068 | ||||||
chr7:74050139
|
TTCCA | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.800-1578_800-1575d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050139 | |||||
chr7:74050139
|
TTCCATCC others(1): Show |
T | 5 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0001t0001g0213others(2): Show | 5 | HG01346.hp2 HG01943.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-1582_800-1575d others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050139 | |||||
chr7:74050506
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.800-1244C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050506 | ||||||
chr7:74050559
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800-1191A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050559 | ||||||
chr7:74050605
|
G | GCATT | 58 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0158others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.800-1111_800-1108d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | |||||
chr7:74050605
|
G | GCATTCAT others(1): Show |
4 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(1): Show | 4 | HG01175.hp2 NA18995.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-1115_800-1108d others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | |||||
chr7:74050605
|
GCATT | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0100others(10): Show | 14 | HG02273.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.800-1111_800-1108d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | |||||
chr7:74050605
|
GCATTCAT others(5): Show |
G | 1 | a0001c0001t0004g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800-1119_800-1108d others(14): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | |||||
chr7:74050644
|
T | C | 1 | a0002c0002t0001g0085 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.800-1106T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050644 | ||||||
chr7:74051251
|
TCCCAGTG others(4): Show |
T | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.800-495_800-485del others(11): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74051251 | |||||
chr7:74051307
|
C | T | 3 | a0001c0001t0002g0072a0001c0001t0003g0303a0002c0002t0002g0073 | 3 | HG02027.hp1 HG02132.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.800-443C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74051307 | ||||||
chr7:74051443
|
C | T | 3 | a0001c0020t0001g0104a0002c0002t0001g0051a0002c0002t0005g0068 | 3 | HG00099.hp1 HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.800-307C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74051443 | ||||||
chr7:74051987
|
AGTGCCTC others(5): Show |
A | 1 | a0001c0001t0001g0345 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.949+8_949+19delCCT others(9): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74051987 | |||||
chr7:74052052
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.949+69A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052052 | ||||||
chr7:74052275
|
A | G | 1 | a0001c0001t0005g0263 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.949+292A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052275 | ||||||
chr7:74052321
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.949+338C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052321 | ||||||
chr7:74052479
|
C | T | 2 | a0002c0002t0001g0047a0002c0002t0001g0062 | 2 | HG03831.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.949+496C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052479 | ||||||
chr7:74052480
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(330): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.949+497A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052480 | ||||||
chr7:74052523
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.949+540T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052523 | ||||||
chr7:74052615
|
C | CAGGA | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(22): Show | 27 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.950-526_950-523dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052615 | |||||
chr7:74052664
|
C | CGGAA | 8 | a0001c0001t0001g0153a0001c0001t0001g0255a0001c0001t0004g0288others(5): Show | 8 | HG00609.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.950-476_950-473dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052664 | |||||
chr7:74052664
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.950-499C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052664 | ||||||
chr7:74052664
|
CGGAA | C | 3 | a0001c0001t0004g0129a0002c0002t0001g0046a0002c0015t0001g0069 | 3 | HG00642.hp1 HG02735.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.950-476_950-473del others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052664 | |||||
chr7:74052687
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0213 | 2 | HG00673.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.950-476A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052687 | ||||||
chr7:74052835
|
G | C | 1 | a0001c0001t0001g0224 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.950-328G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052835 | ||||||
chr7:74052871
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.950-292A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052871 | ||||||
chr7:74052871
|
AAG | A | 3 | a0002c0002t0004g0116a0005c0009t0001g0119a0010c0023t0003g0118 | 3 | HG02630.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.950-274_950-273del others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052871 | |||||
chr7:74052886
|
A | G | 3 | a0001c0001t0001g0259a0001c0001t0001g0262a0001c0001t0005g0263 | 3 | HG02165.hp2 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.950-277A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052886 | ||||||
chr7:74052927
|
AAAG | A | 6 | a0001c0001t0001g0291a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG01952.hp1 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.950-233_950-231del others(3): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052927 | |||||
chr7:74053105
|
C | G | 1 | a0001c0001t0001g0344 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.950-58C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74053105 | ||||||
chr7:74053320
|
C | CTG | 46 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0115others(43): Show | 49 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1096+49_1096+50dup others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | |||||
chr7:74053320
|
C | CTGTG | 11 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0267others(8): Show | 11 | HG00673.hp1 HG01123.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096+47_1096+50dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | |||||
chr7:74053320
|
CTG | C | 21 | a0001c0001t0001g0108a0001c0001t0001g0154a0001c0001t0001g0159others(18): Show | 21 | HG00438.hp1 HG02015.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.1096+49_1096+50del others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | |||||
chr7:74053320
|
CTGTG | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1096+47_1096+50del others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | |||||
chr7:74053320
|
CTGTGTG | C | 3 | a0006c0008t0001g0140a0006c0008t0004g0139a0011c0012t0001g0092 | 3 | HG03453.hp1 HG03453.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1096+45_1096+50del others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | |||||
chr7:74053636
|
G | A | 1 | a0002c0002t0002g0055 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1096+327G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74053636 | ||||||
chr7:74053830
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1096+521G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74053830 | ||||||
chr7:74054000
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1096+691G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054000 | ||||||
chr7:74054255
|
G | A | 2 | a0004c0004t0001g0122a0004c0004t0003g0124 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1097-461G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054255 | ||||||
chr7:74054347
|
G | A | 3 | a0005c0009t0001g0119a0005c0009t0002g0105a0010c0023t0003g0118 | 3 | HG01243.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1097-369G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054347 | ||||||
chr7:74054393
|
C | G | 1 | a0002c0002t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1097-323C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054393 | ||||||
chr7:74054470
|
C | CA | 9 | a0001c0001t0001g0184a0001c0001t0001g0294a0001c0001t0003g0338others(6): Show | 9 | HG00642.hp1 HG01123.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097-231dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74054470 | |||||
chr7:74054583
|
T | C | 3 | a0001c0001t0001g0332a0001c0001t0001g0337a0001c0001t0001g0342 | 3 | HG01884.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1097-133T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054583 | ||||||
chr7:74054839
|
C | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0098others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1150+70C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74054839 | ||||||
chr7:74054957
|
C | T | 2 | a0002c0002t0001g0081a0002c0002t0001g0091 | 2 | HG01257.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1150+188C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74054957 | ||||||
chr7:74055001
|
G | C | 1 | a0001c0001t0003g0322 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1150+232G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055001 | ||||||
chr7:74055168
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1150+399A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055168 | ||||||
chr7:74055519
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0106a0001c0001t0001g0274others(14): Show | 18 | HG00609.hp1 HG00621.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1150+750G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055519 | ||||||
chr7:74055654
|
A | G | 1 | a0002c0002t0004g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1151-617A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055654 | ||||||
chr7:74055868
|
G | C | 3 | a0002c0002t0001g0013a0002c0002t0001g0052a0002c0002t0001g0053 | 3 | HG00280.hp2 HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1151-403G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055868 | ||||||
chr7:74055948
|
G | A | 1 | a0004c0004t0003g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1151-323G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055948 | ||||||
chr7:74056452
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1315+17C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/32 | chr7 | 74056452 | ||||||
chr7:74056509
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1315+74G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/32 | chr7 | 74056509 | ||||||
chr7:74056869
|
C | G | 1 | a0002c0002t0002g0067 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1357+156C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/32 | chr7 | 74056869 | ||||||
chr7:74057304
|
C | T | 2 | a0001c0001t0004g0143a0001c0001t0004g0229 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1358-336C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/32 | chr7 | 74057304 | ||||||
chr7:74057402
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1358-238C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/32 | chr7 | 74057402 | ||||||
chr7:74057716
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1414+20G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74057716 | ||||||
chr7:74057720
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1414+24C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74057720 | ||||||
chr7:74057876
|
A | G | 35 | a0001c0001t0001g0115a0001c0001t0001g0145a0001c0001t0001g0146others(32): Show | 35 | HG02074.hp2 HG02132.hp2 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1414+180A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74057876 | ||||||
chr7:74058007
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1414+311C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058007 | ||||||
chr7:74058179
|
C | CCTCCTCC others(8): Show |
1 | a0001c0001t0004g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1414+494_1414+495i others(17): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058179 | |||||
chr7:74058207
|
CCTTCTTC others(9): Show |
C | 2 | a0001c0001t0001g0188a0002c0002t0001g0117 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1414+522_1414+537d others(18): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058207 | |||||
chr7:74058218
|
TTTC | T | 6 | a0001c0001t0001g0115a0001c0001t0001g0149a0001c0001t0001g0151others(3): Show | 6 | HG02257.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414+535_1414+537d others(5): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058218 | |||||
chr7:74058249
|
T | TTTC | 72 | a0001c0001t0001g0010a0001c0001t0001g0098a0001c0001t0001g0100others(69): Show | 74 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1414+562_1414+564d others(5): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058249 | |||||
chr7:74058249
|
T | TTTCTTCT others(27): Show |
1 | a0002c0002t0005g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1414+564_1414+565i others(36): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058249 | |||||
chr7:74058249
|
T | TTTCTTCT others(12): Show |
1 | a0001c0001t0005g0333 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1414+564_1414+565i others(21): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058249 | |||||
chr7:74058261
|
T | C | 1 | a0001c0001t0005g0333 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1414+565T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058261 | ||||||
chr7:74058278
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414+582T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058278 | ||||||
chr7:74058285
|
G | GCTCCTT | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(339): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1414+591_1414+592i others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058285 | |||||
chr7:74058285
|
G | T | 1 | a0001c0001t0001g0246 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414+589G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058285 | ||||||
chr7:74058467
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1414+771G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058467 | ||||||
chr7:74058491
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1414+795C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058491 | ||||||
chr7:74058699
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1414+1003A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058699 | ||||||
chr7:74058871
|
G | A | 1 | a0015c0014t0001g0060 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1415-1015G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058871 | ||||||
chr7:74058995
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0183 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1415-891G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058995 | ||||||
chr7:74059086
|
TA | T | 8 | a0001c0001t0002g0353a0001c0001t0003g0287a0001c0001t0003g0300others(5): Show | 8 | HG01169.hp1 HG02056.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415-786delA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74059086 | |||||
chr7:74059158
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1415-728A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059158 | ||||||
chr7:74059164
|
T | C | 71 | a0001c0001t0001g0010a0001c0001t0001g0100a0001c0001t0001g0108others(68): Show | 74 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1415-722T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059164 | ||||||
chr7:74059258
|
G | T | 1 | a0001c0001t0002g0336 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1415-628G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059258 | ||||||
chr7:74059366
|
G | A | 1 | a0001c0001t0006g0132 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1415-520G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059366 | ||||||
chr7:74059387
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1415-499G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059387 | ||||||
chr7:74059421
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1415-465A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059421 | ||||||
chr7:74059504
|
A | G | 9 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0004g0102others(6): Show | 9 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415-382A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059504 | ||||||
chr7:74059692
|
CAA | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0023others(5): Show | 9 | HG00621.hp2 NA18940.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415-192_1415-191d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74059692 | |||||
chr7:74060103
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1577-37C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 23/32 | chr7 | 74060103 | ||||||
chr7:74060219
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1621+35A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 24/32 | chr7 | 74060219 | ||||||
chr7:74060363
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0223 | 2 | HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1622-13C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 24/32 | chr7 | 74060363 | ||||||
chr7:74060550
|
G | C | 1 | a0002c0002t0001g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1747+49G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060550 | ||||||
chr7:74060583
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1747+82C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060583 | ||||||
chr7:74060606
|
T | G | 1 | a0001c0001t0003g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1747+105T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060606 | ||||||
chr7:74060655
|
C | T | 6 | a0001c0001t0001g0136a0001c0001t0001g0228a0001c0001t0001g0254others(3): Show | 6 | HG00733.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747+154C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060655 | ||||||
chr7:74060728
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1747+227G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060728 | ||||||
chr7:74061081
|
C | T | 3 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214 | 3 | NA18995.hp2 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1748-20C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74061081 | ||||||
chr7:74061180
|
A | G | 1 | a0007c0007t0001g0045 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1786+41A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061180 | ||||||
chr7:74061445
|
G | A | 31 | a0001c0001t0001g0159a0001c0001t0001g0323a0001c0001t0002g0099others(28): Show | 32 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1786+306G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061445 | ||||||
chr7:74061622
|
G | A | 1 | a0001c0001t0001g0346 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1786+483G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061622 | ||||||
chr7:74061630
|
C | T | 4 | a0001c0001t0001g0224a0003c0003t0001g0248a0003c0003t0001g0249others(1): Show | 4 | NA18944.hp2 NA19004.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786+491C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061630 | ||||||
chr7:74061748
|
C | A | 1 | a0002c0002t0002g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1786+609C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061748 | ||||||
chr7:74061766
|
A | C | 2 | a0002c0002t0001g0081a0002c0002t0001g0091 | 2 | HG01257.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1786+627A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061766 | ||||||
chr7:74061906
|
T | C | 16 | a0001c0001t0001g0193a0001c0001t0001g0267a0001c0001t0001g0268others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1786+767T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061906 | ||||||
chr7:74061919
|
C | T | 19 | a0001c0001t0001g0193a0001c0001t0001g0267a0001c0001t0001g0268others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1786+780C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061919 | ||||||
chr7:74062019
|
G | A | 1 | a0005c0009t0002g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1786+880G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062019 | ||||||
chr7:74062047
|
A | G | 1 | a0001c0001t0004g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1786+908A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062047 | ||||||
chr7:74062368
|
A | G | 9 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(6): Show | 9 | HG02074.hp2 NA18970.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.1787-785A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062368 | ||||||
chr7:74062543
|
G | GTTGT | 10 | a0001c0001t0001g0010a0001c0001t0001g0315a0001c0001t0005g0180others(7): Show | 11 | HG00558.hp1 HG00597.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1787-587_1787-584d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr7 | 74062543 | |||||
chr7:74062614
|
G | A | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1787-539G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062614 | ||||||
chr7:74062644
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1787-509G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062644 | ||||||
chr7:74062804
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1787-349G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062804 | ||||||
chr7:74062893
|
C | T | 4 | a0001c0001t0004g0137a0001c0001t0004g0143a0010c0023t0003g0118others(1): Show | 4 | HG02280.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1787-260C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062893 | ||||||
chr7:74063398
|
C | T | 1 | a0001c0001t0005g0324 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1918+29C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063398 | ||||||
chr7:74063413
|
C | T | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1918+44C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063413 | ||||||
chr7:74063421
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1918+52G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063421 | ||||||
chr7:74063490
|
T | C | 1 | a0002c0002t0001g0057 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1918+121T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063490 | ||||||
chr7:74063593
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1919-28G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063593 | ||||||
chr7:74063753
|
G | GGAGACA | 3 | a0001c0001t0002g0128a0001c0001t0002g0134a0005c0009t0002g0105 | 3 | HG01074.hp2 HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1993+76_1993+81dup others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74063753 | |||||
chr7:74063878
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1993+183G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74063878 | ||||||
chr7:74064146
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG01123.hp2 HG02895.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1993+451T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064146 | ||||||
chr7:74064189
|
T | C | 2 | a0001c0001t0001g0224a0002c0002t0001g0047 | 2 | HG03831.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1993+494T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064189 | ||||||
chr7:74064194
|
A | G | 9 | a0001c0001t0001g0210a0001c0001t0001g0254a0001c0001t0003g0144others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1993+499A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064194 | ||||||
chr7:74064215
|
A | G | 2 | a0001c0001t0001g0297a0002c0002t0001g0047 | 2 | HG03831.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1993+520A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064215 | ||||||
chr7:74064219
|
T | C | 1 | a0014c0019t0004g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1993+524T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064219 | ||||||
chr7:74064232
|
A | G | 15 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0210others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.1993+537A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064232 | ||||||
chr7:74064244
|
T | C | 2 | a0002c0002t0001g0046a0002c0002t0001g0093 | 2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1993+549T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064244 | ||||||
chr7:74064251
|
T | TA | 49 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0157others(46): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1993+561dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064251 | |||||
chr7:74064276
|
G | A | 1 | a0006c0008t0004g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1993+581G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064276 | ||||||
chr7:74064284
|
A | G | 4 | a0001c0001t0001g0310a0001c0001t0004g0129a0001c0001t0004g0141others(1): Show | 4 | HG02148.hp1 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1993+589A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064284 | ||||||
chr7:74064286
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1993+591A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064286 | ||||||
chr7:74064294
|
A | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0235 | 3 | HG00639.hp2 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1993+599A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064294 | ||||||
chr7:74064330
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0017others(25): Show | 29 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1993+635G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064330 | ||||||
chr7:74064339
|
T | C | 4 | a0001c0001t0003g0322a0001c0001t0005g0306a0001c0001t0005g0329others(1): Show | 4 | HG02922.hp2 HG03017.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1993+644T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064339 | ||||||
chr7:74064364
|
G | A | 1 | a0001c0001t0003g0278 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1993+669G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064364 | ||||||
chr7:74064414
|
C | CA | 19 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0108others(16): Show | 21 | HG00642.hp2 HG01106.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1993+729dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064414 | |||||
chr7:74064414
|
C | CAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0185a0001c0001t0001g0189others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1993+728_1993+729d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064414 | |||||
chr7:74064421
|
A | AAT | 27 | a0001c0001t0001g0021a0001c0001t0001g0100a0001c0001t0001g0101others(24): Show | 27 | HG00735.hp2 HG01109.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1993+727_1993+728i others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064421 | |||||
chr7:74064421
|
A | T | 6 | a0001c0001t0001g0142a0001c0001t0001g0188a0001c0001t0001g0243others(3): Show | 6 | HG00738.hp1 HG02155.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1993+726A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064421 | ||||||
chr7:74064423
|
A | AAT | 19 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0111others(16): Show | 19 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1993+749_1993+750d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064423 | |||||
chr7:74064423
|
A | AATAT | 7 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0275others(4): Show | 7 | HG01255.hp1 HG01255.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1993+747_1993+750d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064423 | |||||
chr7:74064423
|
A | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(157): Show | 163 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1993+728A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064423 | ||||||
chr7:74064425
|
T | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0024others(47): Show | 53 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1993+730T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064425 | ||||||
chr7:74064427
|
T | A | 26 | a0001c0001t0004g0012a0001c0001t0004g0102a0001c0001t0004g0113others(23): Show | 27 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.1993+732T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064427 | ||||||
chr7:74064429
|
T | A | 9 | a0001c0001t0004g0102a0001c0001t0004g0129a0001c0001t0004g0141others(6): Show | 9 | HG02647.hp2 HG02723.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993+734T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064429 | ||||||
chr7:74064431
|
T | A | 1 | a0001c0001t0004g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1993+736T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064431 | ||||||
chr7:74064433
|
T | A | 1 | a0001c0001t0004g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1993+738T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064433 | ||||||
chr7:74064442
|
A | ATATG | 3 | a0001c0001t0002g0181a0003c0003t0002g0241a0003c0003t0002g0252 | 3 | NA18960.hp2 NA18987.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1993+763_1993+766d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064442 | |||||
chr7:74064508
|
C | T | 3 | a0001c0001t0002g0290a0001c0001t0002g0301a0001c0001t0002g0304 | 3 | NA18979.hp2 NA19062.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1993+813C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064508 | ||||||
chr7:74064555
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1993+860G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064555 | ||||||
chr7:74064827
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1994-867G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064827 | ||||||
chr7:74064962
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1994-732C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064962 | ||||||
chr7:74065065
|
A | AC | 29 | a0001c0001t0001g0142a0001c0001t0001g0164a0001c0001t0001g0188others(26): Show | 29 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1994-620dupC | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74065065 | |||||
chr7:74065072
|
C | A | 28 | a0001c0001t0001g0217a0001c0001t0001g0254a0001c0001t0002g0128others(25): Show | 29 | HG00733.hp1 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1994-622C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065072 | ||||||
chr7:74065414
|
C | A | 4 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0007g0110others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994-280C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065414 | ||||||
chr7:74065475
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1994-219G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065475 | ||||||
chr7:74065517
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1994-177G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065517 | ||||||
chr7:74065562
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1994-132C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065562 | ||||||
chr7:74065571
|
G | A | 1 | a0002c0002t0008g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1994-123G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065571 | ||||||
chr7:74065592
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1994-102C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065592 | ||||||
chr7:74065616
|
G | GA | 11 | a0001c0001t0001g0146a0001c0001t0001g0194a0001c0001t0001g0226others(8): Show | 11 | HG00544.hp1 HG01981.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1994-60dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74065616 | |||||
chr7:74065675
|
A | G | 1 | a0001c0001t0004g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1994-19A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065675 | ||||||
chr7:74065831
|
C | T | 7 | a0001c0001t0001g0280a0001c0001t0001g0320a0001c0001t0001g0325others(4): Show | 7 | HG00558.hp2 HG02056.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.2032+99C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 30/32 | chr7 | 74065831 | ||||||
chr7:74065928
|
A | G | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2033-16A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 30/32 | chr7 | 74065928 | ||||||
chr7:74066002
|
G | C | 4 | a0001c0001t0004g0012a0001c0001t0004g0131a0001c0001t0004g0137others(1): Show | 5 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2086+5G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066002 | ||||||
chr7:74066239
|
G | A | 29 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(26): Show | 29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2086+242G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066239 | ||||||
chr7:74066475
|
G | A | 27 | a0001c0001t0003g0056a0001c0001t0003g0144a0001c0001t0003g0155others(24): Show | 27 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.2087-257G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066475 | ||||||
chr7:74066698
|
C | T | 29 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(26): Show | 29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2087-34C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066698 | ||||||
chr7:74066901
|
G | A | 1 | a0002c0002t0001g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2131+125G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74066901 | ||||||
chr7:74066976
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2131+200A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74066976 | ||||||
chr7:74067142
|
C | T | 1 | a0001c0001t0002g0353 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2131+366C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067142 | ||||||
chr7:74067159
|
G | A | 1 | a0002c0002t0001g0085 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2131+383G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067159 | ||||||
chr7:74067219
|
A | G | 54 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(51): Show | 55 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.2131+443A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067219 | ||||||
chr7:74067262
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2131+486T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067262 | ||||||
chr7:74067274
|
CT | C | 55 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(52): Show | 56 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.2131+509delT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067274 | |||||
chr7:74067330
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2131+554C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067330 | ||||||
chr7:74067371
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2131+595G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067371 | ||||||
chr7:74067508
|
C | T | 1 | a0002c0005t0001g0064 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2131+732C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067508 | ||||||
chr7:74067559
|
T | A | 29 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(26): Show | 29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2131+783T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067559 | ||||||
chr7:74067594
|
C | T | 29 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(26): Show | 29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2131+818C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067594 | ||||||
chr7:74067721
|
C | T | 16 | a0001c0001t0001g0106a0001c0001t0001g0192a0001c0001t0001g0274others(13): Show | 16 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.2132-936C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067721 | ||||||
chr7:74067748
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2132-909G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067748 | ||||||
chr7:74067762
|
C | CA | 28 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(25): Show | 28 | HG00099.hp2 HG00639.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.2132-879dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067762 | |||||
chr7:74067762
|
CA | C | 9 | a0001c0001t0001g0206a0001c0001t0001g0268a0001c0001t0003g0338others(6): Show | 9 | HG00558.hp1 HG01256.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.2132-879delA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067762 | |||||
chr7:74067794
|
G | A | 21 | a0001c0001t0004g0012a0001c0001t0004g0102a0001c0001t0004g0107others(18): Show | 22 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2132-863G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067794 | ||||||
chr7:74067805
|
G | C | 1 | a0002c0002t0005g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2132-852G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067805 | ||||||
chr7:74067933
|
C | CA | 84 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(81): Show | 87 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2132-697dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | |||||
chr7:74067933
|
C | CAA | 23 | a0001c0001t0001g0026a0001c0001t0001g0150a0001c0001t0001g0169others(20): Show | 23 | HG00408.hp1 HG01928.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2132-698_2132-697d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | |||||
chr7:74067933
|
C | CAAA | 8 | a0001c0001t0004g0113a0001c0001t0004g0131a0001c0001t0004g0143others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2132-699_2132-697d others(5): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | |||||
chr7:74067933
|
CA | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0121a0001c0001t0001g0153others(9): Show | 12 | HG00609.hp2 HG01074.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.2132-697delA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | |||||
chr7:74068015
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2132-642G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068015 | ||||||
chr7:74068044
|
A | C | 1 | a0002c0002t0005g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2132-613A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068044 | ||||||
chr7:74068062
|
G | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0289 | 2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2132-595G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068062 | ||||||
chr7:74068192
|
A | G | 21 | a0001c0001t0004g0012a0001c0001t0004g0102a0001c0001t0004g0107others(18): Show | 22 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2132-465A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068192 | ||||||
chr7:74068291
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2132-366G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068291 | ||||||
chr7:74068371
|
A | G | 29 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0035others(26): Show | 29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2132-286A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068371 | ||||||
chr7:74068441
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2132-216G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068441 | ||||||
chr7:74068593
|
C | T | 1 | a0001c0001t0007g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2132-64C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068593 |