geneid | 9694 |
---|---|
ensemblid | ENSG00000104412.8 |
hgncid | 28963 |
symbol | EMC2 |
name | ER membrane protein complex subunit 2 |
refseq_nuc | NM_014673.5 |
refseq_prot | NP_055488.1 |
ensembl_nuc | ENST00000220853.8 |
ensembl_prot | ENSP00000220853.3 |
mane_status | MANE Select |
chr | chr8 |
start | 108443624 |
end | 108489196 |
strand | + |
ver | v1.2 |
region | chr8:108443624-108489196 |
region5000 | chr8:108438624-108494196 |
regionname0 | EMC2_chr8_108443624_108489196 |
regionname5000 | EMC2_chr8_108438624_108494196 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 297 | 362 | 89 | 64 | 143 | 18 | 46 | 109 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0002 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0003 | 0/0 | 297 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 894 | 359 | 86 | 64 | 143 | 18 | 46 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
c0002 | 0/0 | 894 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
c0003 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
c0004 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2634 | 123 | 16 | 28 | 64 | 6 | 8 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0002 | 0/1 | 2633 | 89 | 0 | 10 | 56 | 6 | 16 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0003 | 0/0 | 2633 | 55 | 14 | 10 | 17 | 5 | 9 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0004 | 0/0 | 2633 | 27 | 21 | 3 | 0 | 0 | 3 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0005 | 0/0 | 2634 | 10 | 9 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0006 | 0/0 | 2633 | 10 | 1 | 4 | 1 | 0 | 4 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0007 | 0/0 | 2633 | 5 | 5 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0008 | 0/0 | 2634 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0009 | 0/0 | 2633 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0010 | 0/0 | 2634 | 4 | 0 | 3 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0011 | 0/0 | 2634 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0012 | 0/0 | 2633 | 3 | 0 | 0 | 0 | 0 | 3 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0013 | 0/0 | 2633 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0014 | 0/0 | 2633 | 2 | 1 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0015 | 0/0 | 2633 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0016 | 0/0 | 2634 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0017 | 0/0 | 2633 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0018 | 0/0 | 2633 | 2 | 1 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0019 | 0/0 | 2634 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0020 | 0/0 | 2633 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0021 | 0/0 | 2633 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0022 | 0/0 | 2633 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0023 | 0/0 | 2634 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0024 | 0/0 | 2633 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0025 | 0/0 | 2634 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0026 | 0/0 | 2633 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0027 | 0/0 | 2634 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0028 | 0/0 | 2633 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0029 | 0/0 | 2633 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0030 | 0/0 | 2634 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
t0031 | 0/0 | 2633 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 1 | 3 | 10 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0002 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0003 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0005 | 0/1 | 5 | 0 | 2 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 894 | 359 | 86 | 64 | 143 | 18 | 46 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0002 | 0/0 | 894 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0002c0003 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0003c0004 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3527 | 123 | 16 | 28 | 64 | 6 | 8 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0002 | 0/1 | 3526 | 88 | 0 | 10 | 55 | 6 | 16 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0003 | 0/0 | 3526 | 52 | 11 | 10 | 17 | 5 | 9 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0004 | 0/0 | 3526 | 27 | 21 | 3 | 0 | 0 | 3 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0005 | 0/0 | 3527 | 10 | 9 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0006 | 0/0 | 3526 | 10 | 1 | 4 | 1 | 0 | 4 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0007 | 0/0 | 3526 | 5 | 5 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0008 | 0/0 | 3527 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0009 | 0/0 | 3526 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0010 | 0/0 | 3527 | 4 | 0 | 3 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0011 | 0/0 | 3527 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0012 | 0/0 | 3526 | 3 | 0 | 0 | 0 | 0 | 3 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0013 | 0/0 | 3526 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0014 | 0/0 | 3526 | 2 | 1 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0015 | 0/0 | 3526 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0016 | 0/0 | 3527 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0017 | 0/0 | 3526 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0018 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0019 | 0/0 | 3527 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0020 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0021 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0022 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0023 | 0/0 | 3527 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0024 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0025 | 0/0 | 3527 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0026 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0027 | 0/0 | 3527 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0028 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0029 | 0/0 | 3526 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0030 | 0/0 | 3527 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0001t0031 | 0/0 | 3526 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0001c0002t0003 | 0/0 | 3526 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0002c0003t0018 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
a0003c0004t0002 | 0/0 | 3526 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | copy fasta | chr8 | 108438624 | 108494196 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 1 | 3 | 10 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0005 | 0/1 | 5 | 0 | 2 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0002 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0009g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0010g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0011g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0012g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0013g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0014g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0015g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0018g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0019g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0020g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0021g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0022g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0023g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0025g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0026g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0027g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0028g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0029g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0030g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0001t0031g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0001c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0002c0003t0018g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
a0003c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0091 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0063 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0087 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0059 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00735 | hp2 | a0001 | c0001 | t0010 | g0221 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0177 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01070 | hp2 | a0001 | c0001 | t0021 | g0213 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0179 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01099 | hp1 | a0001 | c0001 | t0026 | g0079 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01099 | hp2 | a0001 | c0001 | t0010 | g0239 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01109 | hp2 | a0001 | c0001 | t0018 | g0055 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0184 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0187 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01261 | hp2 | a0001 | c0001 | t0027 | g0240 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0238 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0011 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0180 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02451 | hp2 | a0001 | c0001 | t0014 | g0185 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02630 | hp1 | a0001 | c0001 | t0024 | g0060 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02630 | hp2 | a0001 | c0001 | t0022 | g0045 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02735 | hp2 | a0001 | c0001 | t0006 | g0012 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02886 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02895 | hp2 | a0001 | c0001 | t0017 | g0027 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02896 | hp1 | a0001 | c0001 | t0015 | g0040 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02897 | hp2 | a0001 | c0001 | t0017 | g0155 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0243 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0244 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02970 | hp1 | a0001 | c0001 | t0025 | g0205 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0083 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02976 | hp1 | a0002 | c0003 | t0018 | g0056 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0085 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0097 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03239 | hp2 | a0001 | c0001 | t0029 | g0003 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0040 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03491 | hp2 | a0001 | c0001 | t0012 | g0017 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03492 | hp1 | a0001 | c0001 | t0012 | g0017 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0096 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03540 | hp1 | a0001 | c0001 | t0020 | g0164 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0241 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0181 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03688 | hp1 | a0001 | c0001 | t0019 | g0029 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03710 | hp2 | a0001 | c0001 | t0010 | g0222 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03831 | hp2 | a0001 | c0001 | t0012 | g0054 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0171 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0012 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0053 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18948 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18957 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18976 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18976 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18979 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18979 | hp2 | a0001 | c0001 | t0023 | g0237 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18985 | hp1 | a0003 | c0004 | t0002 | g0135 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19007 | hp1 | a0001 | c0001 | t0031 | g0118 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19062 | hp1 | a0001 | c0001 | t0030 | g0257 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0086 | AFR | ASW | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ASW | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20752 | hp2 | a0001 | c0001 | t0019 | g0029 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0019 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | GIH | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | GIH | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0049 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20300 | hp1 | a0001 | c0001 | t0028 | g0261 | AFR | USA | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0005 | REF | REF | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0229 | REF | REF | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:108469887
|
G | A | 1 | a0002 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.425G>A | p.Arg142Gln | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 6/11 | 460/3527 | 425/894 | 142/297 | chr8 | 108469887 | ||
chr8:108476797
|
G | A | 1 | a0003 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.607G>A | p.Gly203Ser | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/11 | 642/3527 | 607/894 | 203/297 | chr8 | 108476797 | ||
chr8:108476885
|
T | A | 1 | a0003 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.695T>A | p.Leu232His | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/11 | 730/3527 | 695/894 | 232/297 | chr8 | 108476885 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:108479008
|
G | A | 1 | a0001c0002 | 3 | HG02970.hp2 HG03041.hp2 NA20129.hp1 |
splice_region_variant&synonymous_variant | LOW | c.705G>A | p.Ser235Ser | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/11 | 740/3527 | 705/894 | 235/297 | chr8 | 108479008 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:108443634
|
C | T | 8 | a0001c0001t0002a0001c0001t0013a0001c0001t0027others(5): Show | 97 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/11 | 25 | chr8 | 108443634 | |||||
chr8:108443642
|
C | G | 1 | a0001c0001t0026 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/11 | 17 | chr8 | 108443642 | |||||
chr8:108486619
|
A | G | 1 | a0001c0001t0012 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 21 | chr8 | 108486619 | |||||
chr8:108486768
|
A | G | 1 | a0001c0001t0025 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*170A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 170 | chr8 | 108486768 | |||||
chr8:108486953
|
A | G | 6 | a0001c0001t0002a0001c0001t0013a0001c0001t0029others(3): Show | 95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 355 | chr8 | 108486953 | |||||
chr8:108487032
|
C | T | 1 | a0001c0001t0007 | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 434 | chr8 | 108487032 | |||||
chr8:108487598
|
C | T | 2 | a0001c0001t0006a0001c0001t0019 | 12 | HG00738.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1000C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1000 | chr8 | 108487598 | |||||
chr8:108487812
|
C | G | 1 | a0001c0001t0031 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1214C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1214 | chr8 | 108487812 | |||||
chr8:108487825
|
T | A | 1 | a0001c0001t0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1227 | chr8 | 108487825 | |||||
chr8:108487856
|
C | A | 2 | a0001c0001t0008a0001c0001t0027 | 5 | HG01261.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1258C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1258 | chr8 | 108487856 | |||||
chr8:108487884
|
T | G | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1286T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1286 | chr8 | 108487884 | |||||
chr8:108487950
|
G | A | 1 | a0001c0001t0029 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1352 | chr8 | 108487950 | |||||
chr8:108487988
|
A | G | 4 | a0001c0001t0003a0001c0001t0024a0001c0001t0026others(1): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1390A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1390 | chr8 | 108487988 | |||||
chr8:108488011
|
A | G | 1 | a0001c0001t0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1413 | chr8 | 108488011 | |||||
chr8:108488040
|
G | T | 1 | a0001c0001t0020 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1442 | chr8 | 108488040 | |||||
chr8:108488114
|
A | T | 1 | a0001c0001t0017 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1516A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1516 | chr8 | 108488114 | |||||
chr8:108488144
|
A | G | 1 | a0001c0001t0016 | 2 | HG02486.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1546A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1546 | chr8 | 108488144 | |||||
chr8:108488166
|
CT | C | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1586delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1586 | INFO_REALIGN_3_PRIME | chr8 | 108488166 | ||||
chr8:108488225
|
C | T | 1 | a0001c0001t0010 | 4 | HG00735.hp2 HG01099.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1627C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1627 | chr8 | 108488225 | |||||
chr8:108488226
|
G | A | 1 | a0001c0001t0023 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1628G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1628 | chr8 | 108488226 | |||||
chr8:108488245
|
A | G | 3 | a0001c0001t0015a0001c0001t0018a0002c0003t0018 | 4 | HG01109.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1647A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1647 | chr8 | 108488245 | |||||
chr8:108488559
|
A | G | 1 | a0001c0001t0014 | 2 | HG01167.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1961A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1961 | chr8 | 108488559 | |||||
chr8:108488651
|
G | A | 3 | a0001c0001t0003a0001c0001t0026a0001c0002t0003 | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2053G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2053 | chr8 | 108488651 | |||||
chr8:108488802
|
A | G | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(14): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*2204A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2204 | chr8 | 108488802 | |||||
chr8:108488914
|
C | T | 1 | a0001c0001t0013 | 3 | NA18948.hp2 NA18957.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2316C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2316 | chr8 | 108488914 | |||||
chr8:108489135
|
G | A | 1 | a0001c0001t0022 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2537G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2537 | chr8 | 108489135 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:108443761
|
C | T | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.40+63C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108443761 | ||||||
chr8:108443792
|
G | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.40+94G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108443792 | ||||||
chr8:108444155
|
C | G | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+457C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444155 | ||||||
chr8:108444175
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+477C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444175 | ||||||
chr8:108444245
|
C | T | 1 | a0001c0001t0028g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.40+547C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444245 | ||||||
chr8:108444383
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+685A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444383 | ||||||
chr8:108444436
|
C | T | 2 | a0001c0001t0002g0256a0001c0001t0030g0257 | 2 | NA18978.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.40+738C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444436 | ||||||
chr8:108444817
|
C | G | 1 | a0001c0001t0002g0255 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.40+1119C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444817 | ||||||
chr8:108444849
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.40+1151A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444849 | ||||||
chr8:108444895
|
A | C | 1 | a0001c0001t0002g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.40+1197A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444895 | ||||||
chr8:108445147
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.40+1449T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445147 | ||||||
chr8:108445323
|
G | A | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.40+1625G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445323 | ||||||
chr8:108445503
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.40+1805T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445503 | ||||||
chr8:108445569
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.40+1871C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445569 | ||||||
chr8:108445589
|
C | A | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+1891C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445589 | ||||||
chr8:108446000
|
T | A | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.40+2302T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446000 | ||||||
chr8:108446035
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.40+2337C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446035 | ||||||
chr8:108446074
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.40+2376T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446074 | ||||||
chr8:108446121
|
A | G | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+2423A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446121 | ||||||
chr8:108446379
|
A | G | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+2681A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446379 | ||||||
chr8:108446469
|
A | C | 1 | a0001c0001t0004g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.40+2771A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446469 | ||||||
chr8:108446490
|
TCTTCGAA others(3): Show |
T | 1 | a0001c0001t0009g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40+2807_40+2816del others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108446490 | |||||
chr8:108446527
|
A | G | 1 | a0001c0001t0003g0026 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.40+2829A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446527 | ||||||
chr8:108446823
|
G | A | 1 | a0001c0001t0011g0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.41-3000G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446823 | ||||||
chr8:108446862
|
G | A | 1 | a0001c0001t0009g0007 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.41-2961G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446862 | ||||||
chr8:108446872
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.41-2951G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446872 | ||||||
chr8:108446923
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-2900T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446923 | ||||||
chr8:108447005
|
A | T | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-2818A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447005 | ||||||
chr8:108447103
|
A | G | 74 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.41-2720A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447103 | ||||||
chr8:108447109
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0249 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2714A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447109 | ||||||
chr8:108447211
|
C | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0095a0001c0001t0007g0096others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-2612C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447211 | ||||||
chr8:108447506
|
A | C | 1 | a0001c0001t0003g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.41-2317A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447506 | ||||||
chr8:108447625
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.41-2198C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447625 | ||||||
chr8:108447687
|
C | T | 1 | a0001c0001t0007g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.41-2136C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447687 | ||||||
chr8:108447778
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | NA18939.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.41-2045A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447778 | ||||||
chr8:108447930
|
T | A | 184 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(181): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.41-1893T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447930 | ||||||
chr8:108448075
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41-1748G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448075 | ||||||
chr8:108448193
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.41-1630C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448193 | ||||||
chr8:108448259
|
C | T | 1 | a0001c0001t0028g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.41-1564C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448259 | ||||||
chr8:108448339
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.41-1484C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448339 | ||||||
chr8:108448425
|
TGAG | T | 6 | a0001c0001t0004g0027a0001c0001t0004g0156a0001c0001t0004g0157others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-1391_41-1389del others(3): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108448425 | |||||
chr8:108448569
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0249 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-1254G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448569 | ||||||
chr8:108448670
|
T | C | 1 | a0001c0001t0006g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.41-1153T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448670 | ||||||
chr8:108448726
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.41-1097A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448726 | ||||||
chr8:108448937
|
T | G | 1 | a0001c0001t0004g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41-886T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448937 | ||||||
chr8:108449016
|
T | C | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.41-807T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449016 | ||||||
chr8:108449192
|
C | T | 2 | a0001c0001t0009g0007a0001c0001t0009g0053 | 4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-631C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449192 | ||||||
chr8:108449258
|
G | A | 2 | a0001c0001t0012g0017a0001c0001t0012g0054 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.41-565G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449258 | ||||||
chr8:108449275
|
CT | C | 180 | a0001c0001t0001g0188a0001c0001t0001g0268a0001c0001t0002g0003others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41-532delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108449275 | |||||
chr8:108449313
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41-510A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449313 | ||||||
chr8:108449432
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41-391T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449432 | ||||||
chr8:108449460
|
A | G | 1 | a0001c0001t0028g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.41-363A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449460 | ||||||
chr8:108449469
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41-354C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449469 | ||||||
chr8:108449495
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-328A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449495 | ||||||
chr8:108449497
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-326T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449497 | ||||||
chr8:108449500
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-323T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449500 | ||||||
chr8:108449501
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-322G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449501 | ||||||
chr8:108449502
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-321G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449502 | ||||||
chr8:108449504
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-319T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449504 | ||||||
chr8:108449516
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-307C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449516 | ||||||
chr8:108449519
|
ACCTTGGG others(4): Show |
A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-302_41-292delCT others(9): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108449519 | |||||
chr8:108449532
|
A | G | 4 | a0001c0001t0007g0020a0001c0001t0007g0095a0001c0001t0007g0096others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-291A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449532 | ||||||
chr8:108449533
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-290A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449533 | ||||||
chr8:108449535
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-288G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449535 | ||||||
chr8:108449538
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-285C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449538 | ||||||
chr8:108449539
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-284T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449539 | ||||||
chr8:108449540
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-283G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449540 | ||||||
chr8:108449544
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-279T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449544 | ||||||
chr8:108449546
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-277A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449546 | ||||||
chr8:108449548
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-275T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449548 | ||||||
chr8:108449549
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-274G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449549 | ||||||
chr8:108449552
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-271G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449552 | ||||||
chr8:108449553
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-270T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449553 | ||||||
chr8:108449556
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-267G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449556 | ||||||
chr8:108449560
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-263C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449560 | ||||||
chr8:108449561
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41-262C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449561 | ||||||
chr8:108449562
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-261G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449562 | ||||||
chr8:108449564
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-259G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449564 | ||||||
chr8:108449565
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-258C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449565 | ||||||
chr8:108449566
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-257C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449566 | ||||||
chr8:108449568
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-255G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449568 | ||||||
chr8:108449569
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-254G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449569 | ||||||
chr8:108449570
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-253C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449570 | ||||||
chr8:108449571
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-252C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449571 | ||||||
chr8:108449578
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-245T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449578 | ||||||
chr8:108449579
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-244C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449579 | ||||||
chr8:108449583
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-240T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449583 | ||||||
chr8:108449584
|
C | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-239C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449584 | ||||||
chr8:108449585
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-238T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449585 | ||||||
chr8:108449589
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-234G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449589 | ||||||
chr8:108449591
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-232T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449591 | ||||||
chr8:108449593
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-230G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449593 | ||||||
chr8:108449596
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-227A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449596 | ||||||
chr8:108449600
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-223T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449600 | ||||||
chr8:108449602
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-221C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449602 | ||||||
chr8:108449603
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-220C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449603 | ||||||
chr8:108449604
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-219A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449604 | ||||||
chr8:108449605
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-218G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449605 | ||||||
chr8:108449607
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-216T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449607 | ||||||
chr8:108449608
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-215G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449608 | ||||||
chr8:108449609
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-214T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449609 | ||||||
chr8:108449612
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-211T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449612 | ||||||
chr8:108449615
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-208T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449615 | ||||||
chr8:108449616
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-207G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449616 | ||||||
chr8:108449617
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-206T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449617 | ||||||
chr8:108449618
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-205T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449618 | ||||||
chr8:108449619
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-204T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449619 | ||||||
chr8:108449623
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-200T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449623 | ||||||
chr8:108449625
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-198T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449625 | ||||||
chr8:108449626
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-197T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449626 | ||||||
chr8:108449628
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-195T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449628 | ||||||
chr8:108449633
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-190G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449633 | ||||||
chr8:108449635
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-188T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449635 | ||||||
chr8:108449637
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-186T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449637 | ||||||
chr8:108449638
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-185G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449638 | ||||||
chr8:108449642
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-181C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449642 | ||||||
chr8:108449645
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-178T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449645 | ||||||
chr8:108449646
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-177T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449646 | ||||||
chr8:108449652
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.41-171A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449652 | ||||||
chr8:108449653
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-170T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449653 | ||||||
chr8:108449656
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-167A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449656 | ||||||
chr8:108449657
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-166T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449657 | ||||||
chr8:108449660
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-163T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449660 | ||||||
chr8:108449662
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-161T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449662 | ||||||
chr8:108449664
|
C | CCAACAGT others(5): Show |
1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-159_41-158insCA others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449664 | ||||||
chr8:108449669
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-154T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449669 | ||||||
chr8:108449670
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-153C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449670 | ||||||
chr8:108449703
|
G | T | 4 | a0001c0001t0008g0241a0001c0001t0008g0242a0001c0001t0008g0243others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-120G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449703 | ||||||
chr8:108449945
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.154+9T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108449945 | ||||||
chr8:108449986
|
C | CT | 6 | a0001c0001t0001g0016a0001c0001t0001g0249a0001c0001t0005g0031others(3): Show | 10 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+63dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 108449986 | |||||
chr8:108450045
|
C | G | 1 | a0001c0001t0027g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.154+109C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450045 | ||||||
chr8:108450135
|
A | C | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154+199A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450135 | ||||||
chr8:108450140
|
G | T | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154+204G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450140 | ||||||
chr8:108450400
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.155-28G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450400 | ||||||
chr8:108450516
|
A | G | 1 | a0001c0001t0003g0091 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.219+24A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450516 | ||||||
chr8:108450539
|
A | C | 1 | a0001c0001t0004g0158 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.219+47A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450539 | ||||||
chr8:108450562
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.219+70A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450562 | ||||||
chr8:108450606
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219+114T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450606 | ||||||
chr8:108450794
|
G | A | 2 | a0001c0001t0002g0098a0001c0001t0002g0150 | 2 | NA18959.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.219+302G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450794 | ||||||
chr8:108450837
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.219+345A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450837 | ||||||
chr8:108450922
|
C | T | 35 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(32): Show | 40 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.219+430C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450922 | ||||||
chr8:108451016
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.219+524A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451016 | ||||||
chr8:108451215
|
G | A | 1 | a0001c0001t0011g0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219+723G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451215 | ||||||
chr8:108451215
|
GA | G | 142 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(139): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.219+730delA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 108451215 | |||||
chr8:108451216
|
A | G | 3 | a0001c0001t0002g0148a0001c0001t0004g0052a0001c0001t0011g0011 | 5 | HG00733.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+724A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451216 | ||||||
chr8:108451219
|
AAAATC | A | 35 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(32): Show | 40 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.219+731_219+735del others(5): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 108451219 | |||||
chr8:108451243
|
T | C | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.219+751T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451243 | ||||||
chr8:108451308
|
TTACATCA others(359): Show |
T | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.219+817_219+1182de others(1): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451308 | ||||||
chr8:108451568
|
A | T | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219+1076A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451568 | ||||||
chr8:108451675
|
C | G | 6 | a0001c0001t0005g0031a0001c0001t0005g0160a0001c0001t0005g0161others(3): Show | 7 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+1183C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451675 | ||||||
chr8:108451676
|
G | GT | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.219+1188dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 108451676 | |||||
chr8:108451883
|
A | C | 2 | a0001c0001t0014g0184a0001c0001t0014g0185 | 2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.220-1179A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451883 | ||||||
chr8:108451990
|
T | G | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.220-1072T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451990 | ||||||
chr8:108452053
|
T | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-1009T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452053 | ||||||
chr8:108452073
|
G | T | 53 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(50): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.220-989G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452073 | ||||||
chr8:108452186
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.220-876A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452186 | ||||||
chr8:108452206
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.220-856G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452206 | ||||||
chr8:108452251
|
A | G | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220-811A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452251 | ||||||
chr8:108452342
|
G | A | 1 | a0001c0001t0007g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220-720G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452342 | ||||||
chr8:108452396
|
G | A | 2 | a0001c0001t0016g0048a0001c0001t0016g0049 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.220-666G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452396 | ||||||
chr8:108452425
|
G | T | 1 | a0001c0001t0001g0015 | 3 | NA18963.hp2 NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.220-637G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452425 | ||||||
chr8:108452914
|
A | G | 5 | a0001c0001t0003g0019a0001c0001t0003g0088a0001c0001t0003g0089others(2): Show | 6 | HG00099.hp1 HG00741.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-148A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452914 | ||||||
chr8:108453268
|
T | G | 1 | a0001c0001t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.305+121T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453268 | ||||||
chr8:108453318
|
A | C | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.305+171A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453318 | ||||||
chr8:108453407
|
T | C | 1 | a0001c0001t0020g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.305+260T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453407 | ||||||
chr8:108453469
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+322C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453469 | ||||||
chr8:108453503
|
A | G | 1 | a0001c0001t0005g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305+356A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453503 | ||||||
chr8:108453582
|
T | C | 1 | a0001c0001t0018g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.305+435T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453582 | ||||||
chr8:108453700
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.305+553T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453700 | ||||||
chr8:108453864
|
C | T | 1 | a0001c0001t0020g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.305+717C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453864 | ||||||
chr8:108453866
|
A | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 8 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+719A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453866 | ||||||
chr8:108453949
|
C | T | 4 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0146others(1): Show | 4 | NA18939.hp2 NA19001.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+802C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453949 | ||||||
chr8:108454033
|
T | A | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.305+886T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454033 | ||||||
chr8:108454355
|
C | T | 127 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(124): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.305+1208C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454355 | ||||||
chr8:108454428
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0249 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+1281A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454428 | ||||||
chr8:108454466
|
A | G | 2 | a0001c0001t0010g0238a0001c0001t0010g0239 | 2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.305+1319A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454466 | ||||||
chr8:108454932
|
C | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 8 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.306-941C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454932 | ||||||
chr8:108454983
|
T | C | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.306-890T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454983 | ||||||
chr8:108455040
|
G | C | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.306-833G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455040 | ||||||
chr8:108455215
|
C | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.306-658C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455215 | ||||||
chr8:108455266
|
A | G | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.306-607A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455266 | ||||||
chr8:108455285
|
A | C | 1 | a0001c0001t0023g0237 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.306-588A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455285 | ||||||
chr8:108455400
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.306-473T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455400 | ||||||
chr8:108455639
|
T | G | 1 | a0001c0001t0002g0099 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.306-234T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455639 | ||||||
chr8:108455718
|
G | A | 1 | a0001c0001t0004g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.306-155G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455718 | ||||||
chr8:108455733
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(39): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.306-140C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455733 | ||||||
chr8:108455825
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306-48A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455825 | ||||||
chr8:108456001
|
T | TAGAA | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+74_363+75insAA others(2): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456001 | |||||
chr8:108456078
|
A | G | 2 | a0001c0001t0009g0007a0001c0001t0009g0053 | 4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+148A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456078 | ||||||
chr8:108456088
|
A | G | 1 | a0001c0001t0003g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.363+158A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456088 | ||||||
chr8:108456097
|
T | G | 1 | a0001c0001t0002g0100 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.363+167T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456097 | ||||||
chr8:108456139
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.363+209C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456139 | ||||||
chr8:108456193
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+263T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456193 | ||||||
chr8:108456194
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.363+264G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456194 | ||||||
chr8:108456228
|
G | T | 1 | a0001c0001t0003g0090 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.363+298G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456228 | ||||||
chr8:108456332
|
C | CA | 9 | a0001c0001t0004g0028a0001c0001t0004g0165a0001c0001t0004g0166others(6): Show | 10 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+417dupA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456332 | |||||
chr8:108456332
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0004g0051 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.363+417_363+418ins others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456332 | |||||
chr8:108456332
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0004g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.363+417_363+418ins others(27): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456332 | |||||
chr8:108456344
|
AAAAG | A | 106 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(103): Show | 143 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.363+418_363+421del others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456344 | |||||
chr8:108456345
|
AAAG | A | 22 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0100others(19): Show | 25 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.363+418_363+420del others(3): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456345 | |||||
chr8:108456347
|
AG | A | 6 | a0001c0001t0004g0030a0001c0001t0005g0031a0001c0001t0005g0161others(3): Show | 10 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+418delG | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456347 | ||||||
chr8:108456348
|
G | A | 43 | a0001c0001t0001g0192a0001c0001t0004g0027a0001c0001t0004g0028others(40): Show | 48 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.363+418G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456348 | ||||||
chr8:108456349
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.363+419A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456349 | ||||||
chr8:108456359
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0016g0048 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.363+431_363+432ins others(13): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456359 | |||||
chr8:108456359
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0016g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+431_363+432ins others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456359 | |||||
chr8:108456362
|
C | A | 1 | a0001c0001t0002g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.363+432C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456362 | ||||||
chr8:108456463
|
A | G | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.363+533A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456463 | ||||||
chr8:108456646
|
G | A | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.363+716G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456646 | ||||||
chr8:108456682
|
G | A | 4 | a0001c0001t0003g0008a0001c0001t0003g0062a0001c0001t0003g0069others(1): Show | 6 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+752G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456682 | ||||||
chr8:108456843
|
C | T | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+913C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456843 | ||||||
chr8:108456846
|
C | T | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+916C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456846 | ||||||
chr8:108456924
|
A | G | 1 | a0001c0001t0006g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.363+994A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456924 | ||||||
chr8:108457130
|
A | G | 1 | a0001c0001t0004g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+1200A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457130 | ||||||
chr8:108457267
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.363+1337A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457267 | ||||||
chr8:108457303
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.363+1373G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457303 | ||||||
chr8:108457321
|
CGTGTGTG others(13): Show |
C | 1 | a0001c0001t0002g0025 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.363+1401_363+1420d others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457321 | |||||
chr8:108457321
|
CGTGTGTG others(15): Show |
C | 8 | a0001c0001t0002g0005a0001c0001t0002g0138a0001c0001t0002g0139others(5): Show | 12 | HG00738.hp2 HG01081.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.363+1401_363+1422d others(24): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457321 | |||||
chr8:108457331
|
C | CGT | 55 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0044others(52): Show | 78 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.363+1442_363+1443d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
C | CGTGT | 12 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0189others(9): Show | 15 | HG00140.hp1 HG00323.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.363+1440_363+1443d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
C | CGTGTGT | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0002g0253others(2): Show | 5 | HG02004.hp1 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1438_363+1443d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
CGT | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0196others(31): Show | 42 | HG00438.hp1 HG00639.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+1442_363+1443d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
CGTGT | C | 20 | a0001c0001t0001g0195a0001c0001t0001g0249a0001c0001t0001g0268others(17): Show | 22 | HG00733.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.363+1440_363+1443d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
CGTGTGT | C | 12 | a0001c0001t0001g0194a0001c0001t0001g0262a0001c0001t0003g0087others(9): Show | 15 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.363+1438_363+1443d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
CGTGTGTG others(1): Show |
C | 44 | a0001c0001t0001g0193a0001c0001t0001g0258a0001c0001t0003g0002others(41): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.363+1436_363+1443d others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.363+1432_363+1443d others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457331
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0002g0107a0001c0001t0019g0029 | 3 | HG03688.hp1 NA19058.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.363+1428_363+1443d others(18): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | |||||
chr8:108457364
|
GTGTGTGT others(26): Show |
G | 1 | a0001c0001t0003g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.363+1438_363+1470d others(35): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457364 | |||||
chr8:108457403
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.363+1473A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457403 | ||||||
chr8:108457426
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+1496A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457426 | ||||||
chr8:108457654
|
G | A | 1 | a0001c0001t0001g0015 | 3 | NA18963.hp2 NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.363+1724G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457654 | ||||||
chr8:108457703
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 5 | HG00735.hp1 NA18939.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1773C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457703 | ||||||
chr8:108457715
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.363+1785T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457715 | ||||||
chr8:108457804
|
T | C | 184 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(181): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.363+1874T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457804 | ||||||
chr8:108457923
|
T | C | 2 | a0001c0001t0004g0167a0001c0001t0004g0168 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.363+1993T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457923 | ||||||
chr8:108458026
|
G | A | 1 | a0001c0001t0014g0184 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.363+2096G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458026 | ||||||
chr8:108458300
|
C | T | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+2370C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458300 | ||||||
chr8:108458318
|
A | G | 1 | a0001c0001t0005g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.363+2388A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458318 | ||||||
chr8:108458370
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.363+2440C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458370 | ||||||
chr8:108458419
|
G | A | 26 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(23): Show | 28 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.363+2489G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458419 | ||||||
chr8:108458660
|
T | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+2730T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458660 | ||||||
chr8:108458664
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.363+2734C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458664 | ||||||
chr8:108458665
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+2735G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458665 | ||||||
chr8:108458752
|
A | G | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.363+2822A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458752 | ||||||
chr8:108458832
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+2902T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458832 | ||||||
chr8:108458927
|
G | A | 32 | a0001c0001t0003g0002a0001c0001t0003g0018a0001c0001t0003g0019others(29): Show | 44 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.363+2997G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458927 | ||||||
chr8:108458973
|
A | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+3043A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458973 | ||||||
chr8:108459109
|
C | G | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.363+3179C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459109 | ||||||
chr8:108459265
|
T | G | 1 | a0001c0001t0001g0232 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.363+3335T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459265 | ||||||
chr8:108459286
|
C | T | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+3356C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459286 | ||||||
chr8:108459345
|
G | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+3415G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459345 | ||||||
chr8:108459545
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+3615A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459545 | ||||||
chr8:108459680
|
G | A | 75 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(72): Show | 96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.363+3750G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459680 | ||||||
chr8:108459703
|
T | TGA | 10 | a0001c0001t0001g0233a0001c0001t0005g0275a0001c0001t0006g0012others(7): Show | 13 | HG00738.hp1 HG01074.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+3791_363+3792d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | |||||
chr8:108459703
|
T | TGAGA | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(73): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.363+3789_363+3792d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | |||||
chr8:108459703
|
T | TGAGAGA | 13 | a0001c0001t0002g0010a0001c0001t0002g0103a0001c0001t0002g0112others(10): Show | 16 | HG00558.hp1 HG00609.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+3787_363+3792d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | |||||
chr8:108459703
|
T | TGAGAGAG others(1): Show |
53 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(50): Show | 71 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.363+3785_363+3792d others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | |||||
chr8:108459703
|
T | TGAGAGAG others(3): Show |
17 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(14): Show | 19 | HG00733.hp2 HG01192.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.363+3783_363+3792d others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | |||||
chr8:108459703
|
T | TGAGAGAG others(5): Show |
1 | a0001c0001t0002g0104 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.363+3781_363+3792d others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | |||||
chr8:108459721
|
A | AGAGAGAG others(9): Show |
1 | a0001c0001t0004g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+3792_363+3793i others(18): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(11): Show |
1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.363+3792_363+3793i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(5): Show |
4 | a0001c0001t0004g0157a0001c0001t0005g0031a0001c0001t0005g0163others(1): Show | 5 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(3): Show |
2 | a0001c0001t0011g0011a0001c0001t0020g0164 | 4 | HG01884.hp2 HG02486.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(5): Show |
9 | a0001c0001t0004g0027a0001c0001t0004g0030a0001c0001t0004g0158others(6): Show | 10 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(7): Show |
9 | a0001c0001t0004g0028a0001c0001t0004g0165a0001c0001t0004g0167others(6): Show | 10 | HG01167.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(16): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(9): Show |
1 | a0001c0001t0009g0007 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363+3792_363+3793i others(18): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(1): Show |
32 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(29): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(3): Show |
9 | a0001c0001t0003g0058a0001c0001t0003g0065a0001c0001t0003g0066others(6): Show | 10 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(5): Show |
3 | a0001c0001t0012g0017a0001c0001t0014g0185a0001c0001t0028g0261 | 4 | HG02451.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(7): Show |
2 | a0001c0001t0009g0053a0001c0001t0024g0060 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+3792_363+3793i others(16): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGAG others(11): Show |
1 | a0001c0001t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+3792_363+3793i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGT | 15 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0191others(12): Show | 15 | HG01106.hp1 HG01256.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGAGTG others(1): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0225a0001c0001t0012g0054 | 4 | HG03831.hp2 NA18981.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | AGAGT | 4 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0003g0067others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459721
|
A | T | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.363+3791A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459721 | ||||||
chr8:108459721
|
AGT | A | 3 | a0001c0001t0004g0169a0001c0001t0018g0055a0002c0003t0018g0056 | 3 | HG01109.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.363+3823_363+3824d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | |||||
chr8:108459723
|
T | A | 92 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0233others(89): Show | 116 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.363+3793T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459723 | ||||||
chr8:108459725
|
T | A | 77 | a0001c0001t0001g0210a0001c0001t0002g0003a0001c0001t0002g0005others(74): Show | 99 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.363+3795T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459725 | ||||||
chr8:108459727
|
T | A | 5 | a0001c0001t0002g0109a0001c0001t0002g0112a0001c0001t0002g0123others(2): Show | 5 | HG00544.hp1 HG02129.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+3797T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459727 | ||||||
chr8:108459729
|
T | A | 1 | a0001c0001t0004g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+3799T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459729 | ||||||
chr8:108459731
|
T | A | 1 | a0001c0001t0004g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+3801T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459731 | ||||||
chr8:108459753
|
T | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | NA18947.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.363+3823T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459753 | ||||||
chr8:108459769
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363+3839G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459769 | ||||||
chr8:108459850
|
A | G | 3 | a0001c0001t0002g0100a0001c0001t0002g0129a0001c0001t0002g0130 | 3 | NA18962.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.363+3920A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459850 | ||||||
chr8:108459852
|
CTG | C | 42 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(39): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.363+3924_363+3925d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459852 | |||||
chr8:108459893
|
A | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+3963A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459893 | ||||||
chr8:108459956
|
A | T | 1 | a0001c0001t0003g0080 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.363+4026A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459956 | ||||||
chr8:108460181
|
G | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+4251G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460181 | ||||||
chr8:108460280
|
A | T | 6 | a0001c0001t0002g0006a0001c0001t0002g0104a0001c0001t0002g0128others(3): Show | 9 | HG01934.hp1 HG02056.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+4350A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460280 | ||||||
chr8:108460389
|
T | C | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.363+4459T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460389 | ||||||
chr8:108460415
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.363+4485T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460415 | ||||||
chr8:108460531
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.363+4601C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460531 | ||||||
chr8:108460560
|
C | T | 1 | a0001c0001t0004g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.363+4630C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460560 | ||||||
chr8:108460665
|
A | G | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+4735A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460665 | ||||||
chr8:108460696
|
T | C | 2 | a0001c0001t0009g0007a0001c0001t0009g0053 | 4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+4766T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460696 | ||||||
chr8:108460814
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.363+4884G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460814 | ||||||
chr8:108460927
|
T | C | 1 | a0001c0001t0004g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+4997T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460927 | ||||||
chr8:108461104
|
G | A | 3 | a0001c0001t0008g0241a0001c0001t0008g0243a0001c0001t0008g0244 | 3 | HG02922.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.363+5174G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461104 | ||||||
chr8:108461163
|
T | C | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.363+5233T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461163 | ||||||
chr8:108461182
|
T | G | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.363+5252T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461182 | ||||||
chr8:108461203
|
A | G | 1 | a0001c0001t0026g0079 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.363+5273A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461203 | ||||||
chr8:108461319
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+5389A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461319 | ||||||
chr8:108461420
|
A | G | 1 | a0001c0001t0004g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.363+5490A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461420 | ||||||
chr8:108461714
|
C | G | 2 | a0001c0001t0003g0067a0001c0001t0003g0082 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.363+5784C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461714 | ||||||
chr8:108461797
|
C | T | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.363+5867C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461797 | ||||||
chr8:108461819
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.363+5889T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461819 | ||||||
chr8:108461901
|
C | T | 1 | a0001c0001t0004g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.363+5971C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461901 | ||||||
chr8:108461933
|
C | G | 75 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(72): Show | 96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.363+6003C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461933 | ||||||
chr8:108461936
|
G | T | 1 | a0001c0001t0002g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.363+6006G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461936 | ||||||
chr8:108461969
|
C | T | 1 | a0001c0002t0003g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.363+6039C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461969 | ||||||
chr8:108461974
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.363+6044A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461974 | ||||||
chr8:108462082
|
T | C | 184 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(181): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.363+6152T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462082 | ||||||
chr8:108462121
|
A | C | 1 | a0001c0001t0002g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.363+6191A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462121 | ||||||
chr8:108462177
|
CGT | C | 2 | a0001c0001t0009g0007a0001c0001t0015g0040 | 5 | HG02896.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+6260_363+6261d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462177 | |||||
chr8:108462213
|
T | TTGTGTGC others(13): Show |
1 | a0001c0001t0009g0007 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363+6290_363+6291i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | |||||
chr8:108462213
|
T | TTGTGTGC others(11): Show |
1 | a0001c0001t0009g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+6300_363+6301i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | |||||
chr8:108462213
|
T | TTGTGTGC others(13): Show |
101 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(98): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.363+6300_363+6301i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | |||||
chr8:108462213
|
T | TTGTGTGC others(15): Show |
2 | a0001c0001t0012g0017a0001c0001t0012g0054 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.363+6300_363+6301i others(24): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | |||||
chr8:108462222
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0002g0124 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.363+6300_363+6301i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462222 | |||||
chr8:108462222
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0002g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.363+6300_363+6301i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462222 | |||||
chr8:108462222
|
T | TGTGTGTG others(13): Show |
73 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(70): Show | 94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.363+6300_363+6301i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462222 | |||||
chr8:108462299
|
G | T | 1 | a0001c0001t0024g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+6369G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462299 | ||||||
chr8:108462308
|
A | G | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+6378A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462308 | ||||||
chr8:108462355
|
G | A | 1 | a0001c0001t0028g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.363+6425G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462355 | ||||||
chr8:108462470
|
G | A | 1 | a0001c0001t0025g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.363+6540G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462470 | ||||||
chr8:108462476
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.363+6546G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462476 | ||||||
chr8:108462548
|
C | A | 1 | a0001c0001t0001g0197 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.363+6618C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462548 | ||||||
chr8:108462742
|
GT | G | 14 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(11): Show | 16 | HG00733.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+6824delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462742 | |||||
chr8:108462742
|
GTT | G | 170 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(167): Show | 218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.363+6823_363+6824d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462742 | |||||
chr8:108462776
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.363+6846T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462776 | ||||||
chr8:108462976
|
A | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-6850A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462976 | ||||||
chr8:108463026
|
C | T | 1 | a0001c0001t0025g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364-6800C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463026 | ||||||
chr8:108463240
|
A | G | 1 | a0001c0001t0016g0048 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.364-6586A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463240 | ||||||
chr8:108463287
|
G | A | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-6539G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463287 | ||||||
chr8:108463320
|
G | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0095a0001c0001t0007g0096others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-6506G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463320 | ||||||
chr8:108463372
|
A | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-6454A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463372 | ||||||
chr8:108463409
|
T | A | 2 | a0001c0001t0003g0072a0001c0001t0026g0079 | 2 | HG01099.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.364-6417T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463409 | ||||||
chr8:108463423
|
A | T | 4 | a0001c0001t0007g0020a0001c0001t0007g0095a0001c0001t0007g0096others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-6403A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463423 | ||||||
chr8:108463459
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.364-6367A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463459 | ||||||
chr8:108463596
|
T | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 4 | HG01123.hp1 HG02738.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-6230T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463596 | ||||||
chr8:108463596
|
T | G | 1 | a0001c0001t0003g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.364-6230T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463596 | ||||||
chr8:108463914
|
T | A | 2 | a0001c0001t0009g0007a0001c0001t0009g0053 | 4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-5912T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463914 | ||||||
chr8:108463946
|
C | T | 2 | a0001c0001t0010g0221a0001c0001t0010g0222 | 2 | HG00735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.364-5880C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463946 | ||||||
chr8:108464253
|
T | A | 2 | a0001c0001t0009g0007a0001c0001t0009g0053 | 4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-5573T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464253 | ||||||
chr8:108464338
|
G | A | 44 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(41): Show | 53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.364-5488G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464338 | ||||||
chr8:108464504
|
C | G | 1 | a0001c0001t0004g0158 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-5322C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464504 | ||||||
chr8:108464598
|
C | T | 1 | a0001c0001t0009g0007 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.364-5228C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464598 | ||||||
chr8:108464628
|
A | G | 2 | a0001c0001t0012g0017a0001c0001t0012g0054 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.364-5198A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464628 | ||||||
chr8:108464699
|
G | C | 53 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(50): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.364-5127G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464699 | ||||||
chr8:108464808
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.364-5018C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464808 | ||||||
chr8:108465021
|
C | T | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.364-4805C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465021 | ||||||
chr8:108465204
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-4622G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465204 | ||||||
chr8:108465220
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(262): Show | 349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.364-4606G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465220 | ||||||
chr8:108465294
|
A | G | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.364-4532A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465294 | ||||||
chr8:108465574
|
T | G | 1 | a0001c0001t0003g0026 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.364-4252T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465574 | ||||||
chr8:108465614
|
A | G | 3 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0273 | 3 | HG01192.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.364-4212A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465614 | ||||||
chr8:108465638
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0271 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.364-4188A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465638 | ||||||
chr8:108465685
|
T | C | 1 | a0001c0001t0003g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.364-4141T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465685 | ||||||
chr8:108465804
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-4022G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465804 | ||||||
chr8:108465826
|
A | G | 2 | a0001c0001t0003g0078a0001c0001t0003g0094 | 2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.364-4000A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465826 | ||||||
chr8:108465828
|
CATTT | C | 6 | a0001c0001t0005g0031a0001c0001t0005g0160a0001c0001t0005g0161others(3): Show | 7 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-3996_364-3993d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108465828 | |||||
chr8:108466029
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-3797A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466029 | ||||||
chr8:108466051
|
T | C | 1 | a0001c0001t0009g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-3775T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466051 | ||||||
chr8:108466125
|
T | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-3701T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466125 | ||||||
chr8:108466176
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.364-3650G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466176 | ||||||
chr8:108466268
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(273): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.364-3558G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466268 | ||||||
chr8:108466307
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-3519T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466307 | ||||||
chr8:108466369
|
CTTG | C | 6 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0114others(3): Show | 6 | HG01192.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-3454_364-3452d others(5): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466369 | |||||
chr8:108466442
|
A | AT | 20 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0189others(17): Show | 22 | HG01099.hp2 HG01361.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-3356dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
A | ATTATTTT others(3): Show |
1 | a0001c0001t0025g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364-3382_364-3381i others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0008g0241a0001c0001t0008g0242a0001c0001t0027g0240 | 3 | HG01261.hp2 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.364-3365_364-3356d others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0008g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-3366_364-3356d others(13): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
AT | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0154others(7): Show | 13 | HG00558.hp2 HG01256.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-3356delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
ATTT | A | 10 | a0001c0001t0003g0008a0001c0001t0003g0057a0001c0001t0003g0061others(7): Show | 12 | HG00733.hp1 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-3358_364-3356d others(5): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
ATTTT | A | 38 | a0001c0001t0002g0102a0001c0001t0002g0128a0001c0001t0003g0002others(35): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.364-3359_364-3356d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
ATTTTT | A | 87 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(84): Show | 113 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.364-3360_364-3356d others(7): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
ATTTTTT | A | 40 | a0001c0001t0002g0125a0001c0001t0002g0139a0001c0001t0002g0140others(37): Show | 45 | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.364-3361_364-3356d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466442
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0016g0048a0001c0001t0016g0049 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.364-3367_364-3356d others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | |||||
chr8:108466518
|
T | TTA | 4 | a0001c0001t0006g0012a0001c0001t0006g0171a0001c0001t0006g0180others(1): Show | 6 | HG01255.hp2 HG02004.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-3305_364-3304d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466518 | |||||
chr8:108466852
|
A | G | 1 | a0001c0001t0014g0184 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.364-2974A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466852 | ||||||
chr8:108466993
|
A | G | 1 | a0001c0001t0024g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.364-2833A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466993 | ||||||
chr8:108467019
|
T | G | 2 | a0001c0001t0004g0170a0001c0001t0004g0172 | 2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.364-2807T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467019 | ||||||
chr8:108467024
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-2802A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467024 | ||||||
chr8:108467171
|
A | G | 1 | a0001c0001t0031g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.364-2655A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467171 | ||||||
chr8:108467216
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(2): Show | 7 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2610C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467216 | ||||||
chr8:108467217
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.364-2609G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467217 | ||||||
chr8:108467255
|
T | G | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-2571T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467255 | ||||||
chr8:108467477
|
T | G | 1 | a0001c0001t0024g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.364-2349T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467477 | ||||||
chr8:108467507
|
CTCAGCTA others(6): Show |
C | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.364-2317_364-2305d others(15): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108467507 | |||||
chr8:108467570
|
C | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.364-2256C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467570 | ||||||
chr8:108467759
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.364-2067T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467759 | ||||||
chr8:108468055
|
A | G | 4 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(1): Show | 4 | HG00733.hp2 HG02683.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1771A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468055 | ||||||
chr8:108468074
|
T | C | 53 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(50): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.364-1752T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468074 | ||||||
chr8:108468202
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.364-1624G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468202 | ||||||
chr8:108468223
|
T | C | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.364-1603T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468223 | ||||||
chr8:108468248
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.364-1578T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468248 | ||||||
chr8:108468382
|
C | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0044 | 3 | HG02040.hp1 NA18962.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.364-1444C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468382 | ||||||
chr8:108468494
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0216 | 3 | NA18960.hp2 NA19070.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.364-1332A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468494 | ||||||
chr8:108468541
|
A | G | 44 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(41): Show | 53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.364-1285A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468541 | ||||||
chr8:108468549
|
G | A | 13 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0023others(10): Show | 18 | HG00438.hp2 NA18612.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.364-1277G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468549 | ||||||
chr8:108468589
|
CTTTCA | C | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1232_364-1228d others(7): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108468589 | |||||
chr8:108468809
|
G | C | 2 | a0001c0001t0004g0030a0001c0001t0004g0178 | 3 | HG01884.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.364-1017G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468809 | ||||||
chr8:108468858
|
C | T | 26 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(23): Show | 28 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-968C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468858 | ||||||
chr8:108468897
|
T | G | 1 | a0001c0001t0001g0042 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.364-929T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468897 | ||||||
chr8:108468931
|
T | C | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.364-895T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468931 | ||||||
chr8:108468965
|
G | A | 3 | a0001c0002t0003g0083a0001c0002t0003g0085a0001c0002t0003g0086 | 3 | HG02970.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.364-861G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468965 | ||||||
chr8:108468983
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.364-843T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468983 | ||||||
chr8:108468994
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.364-832G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468994 | ||||||
chr8:108469007
|
G | A | 74 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.364-819G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108469007 | ||||||
chr8:108469704
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.364-122G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108469704 | ||||||
chr8:108470298
|
A | G | 1 | a0001c0001t0024g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.509+177A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470298 | ||||||
chr8:108470445
|
A | G | 129 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.509+324A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470445 | ||||||
chr8:108470477
|
T | C | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.509+356T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470477 | ||||||
chr8:108470608
|
A | G | 2 | a0001c0001t0012g0017a0001c0001t0012g0054 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.509+487A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470608 | ||||||
chr8:108470808
|
T | G | 21 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0156others(18): Show | 22 | HG01243.hp1 HG01261.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.509+687T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470808 | ||||||
chr8:108470936
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+815A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470936 | ||||||
chr8:108471096
|
A | G | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.509+975A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471096 | ||||||
chr8:108471107
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.509+986A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471107 | ||||||
chr8:108471299
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+1178A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471299 | ||||||
chr8:108471400
|
A | G | 1 | a0001c0001t0005g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.509+1279A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471400 | ||||||
chr8:108471480
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.509+1359A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471480 | ||||||
chr8:108471544
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0234 | 3 | HG00140.hp1 HG00323.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.509+1423T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471544 | ||||||
chr8:108471704
|
G | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.509+1583G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471704 | ||||||
chr8:108471855
|
C | G | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.509+1734C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471855 | ||||||
chr8:108471883
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.509+1762A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471883 | ||||||
chr8:108472005
|
C | T | 1 | a0001c0001t0028g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.509+1884C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472005 | ||||||
chr8:108472290
|
T | A | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.509+2169T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472290 | ||||||
chr8:108472338
|
T | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0126 | 2 | HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.509+2217T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472338 | ||||||
chr8:108472514
|
A | G | 53 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(50): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.509+2393A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472514 | ||||||
chr8:108472743
|
G | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.509+2622G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472743 | ||||||
chr8:108472761
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509+2640C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472761 | ||||||
chr8:108472772
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.509+2651C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472772 | ||||||
chr8:108472773
|
G | A | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.509+2652G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472773 | ||||||
chr8:108472773
|
G | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+2652G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472773 | ||||||
chr8:108473056
|
A | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0142 | 2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.510-2826A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473056 | ||||||
chr8:108473138
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0271 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.510-2744T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473138 | ||||||
chr8:108473263
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.510-2619G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473263 | ||||||
chr8:108473272
|
A | G | 74 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.510-2610A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473272 | ||||||
chr8:108473302
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0271 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.510-2580T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473302 | ||||||
chr8:108473672
|
C | CA | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.510-2208dupA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108473672 | |||||
chr8:108473675
|
C | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.510-2207C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473675 | ||||||
chr8:108473710
|
T | G | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.510-2172T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473710 | ||||||
chr8:108473717
|
A | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.510-2165A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473717 | ||||||
chr8:108473765
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.510-2117T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473765 | ||||||
chr8:108473832
|
A | G | 1 | a0001c0001t0006g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.510-2050A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473832 | ||||||
chr8:108474292
|
G | T | 50 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(47): Show | 60 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.510-1590G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474292 | ||||||
chr8:108474388
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(66): Show | 101 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.510-1494G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474388 | ||||||
chr8:108474447
|
A | C | 2 | a0001c0001t0012g0017a0001c0001t0012g0054 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.510-1435A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474447 | ||||||
chr8:108474479
|
T | C | 1 | a0001c0001t0003g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.510-1403T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474479 | ||||||
chr8:108474554
|
TAC | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(80): Show | 120 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.510-1306_510-1305d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108474554 | |||||
chr8:108474554
|
TACAC | T | 181 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(178): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.510-1308_510-1305d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108474554 | |||||
chr8:108474584
|
T | C | 1 | a0001c0001t0003g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.510-1298T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474584 | ||||||
chr8:108474782
|
T | C | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.510-1100T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474782 | ||||||
chr8:108474846
|
A | G | 1 | a0001c0001t0006g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.510-1036A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474846 | ||||||
chr8:108474892
|
TACATGTA others(2): Show |
T | 43 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(40): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.510-985_510-977del others(9): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108474892 | |||||
chr8:108474948
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-934A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474948 | ||||||
chr8:108475234
|
G | A | 4 | a0001c0001t0007g0020a0001c0001t0007g0095a0001c0001t0007g0096others(1): Show | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-648G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475234 | ||||||
chr8:108475236
|
C | T | 35 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(32): Show | 40 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-646C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475236 | ||||||
chr8:108475487
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.510-395C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475487 | ||||||
chr8:108475737
|
A | G | 74 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.510-145A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475737 | ||||||
chr8:108476208
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.591+245T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476208 | ||||||
chr8:108476309
|
A | G | 6 | a0001c0001t0005g0031a0001c0001t0005g0160a0001c0001t0005g0161others(3): Show | 7 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+346A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476309 | ||||||
chr8:108476321
|
G | A | 1 | a0001c0001t0004g0158 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.591+358G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476321 | ||||||
chr8:108476358
|
A | G | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.591+395A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476358 | ||||||
chr8:108476361
|
A | G | 74 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(71): Show | 95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.591+398A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476361 | ||||||
chr8:108476418
|
A | C | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-364A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476418 | ||||||
chr8:108476436
|
T | G | 1 | a0001c0001t0002g0132 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.592-346T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476436 | ||||||
chr8:108476450
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.592-332A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476450 | ||||||
chr8:108476625
|
T | C | 1 | a0001c0001t0008g0243 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.592-157T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476625 | ||||||
chr8:108476708
|
A | G | 181 | a0001c0001t0001g0154a0001c0001t0002g0003a0001c0001t0002g0005others(178): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.592-74A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476708 | ||||||
chr8:108477007
|
T | C | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.702+115T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477007 | ||||||
chr8:108477041
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.702+149G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477041 | ||||||
chr8:108477162
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.702+270G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477162 | ||||||
chr8:108477281
|
C | A | 64 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(61): Show | 85 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.702+389C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477281 | ||||||
chr8:108477290
|
A | G | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.702+398A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477290 | ||||||
chr8:108477470
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.702+578C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477470 | ||||||
chr8:108477745
|
G | A | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.702+853G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477745 | ||||||
chr8:108477947
|
A | G | 44 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(41): Show | 53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.702+1055A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477947 | ||||||
chr8:108477950
|
A | G | 1 | a0001c0001t0003g0077 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.703-1056A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477950 | ||||||
chr8:108478456
|
G | A | 2 | a0001c0001t0003g0072a0001c0001t0026g0079 | 2 | HG01099.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.703-550G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478456 | ||||||
chr8:108478513
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.703-493T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478513 | ||||||
chr8:108478702
|
G | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.703-304G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478702 | ||||||
chr8:108478737
|
T | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200 | 3 | NA18947.hp1 NA18956.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.703-269T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478737 | ||||||
chr8:108478743
|
G | C | 1 | a0001c0001t0002g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-263G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478743 | ||||||
chr8:108478796
|
C | T | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.703-210C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478796 | ||||||
chr8:108478847
|
T | G | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.703-159T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478847 | ||||||
chr8:108478880
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-126A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478880 | ||||||
chr8:108478905
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.703-101A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478905 | ||||||
chr8:108479170
|
A | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.807+60A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479170 | ||||||
chr8:108479320
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.807+210T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479320 | ||||||
chr8:108479367
|
A | G | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.807+257A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479367 | ||||||
chr8:108479447
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0271 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.807+337T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479447 | ||||||
chr8:108479576
|
G | A | 43 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0018others(40): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.807+466G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479576 | ||||||
chr8:108479680
|
A | G | 1 | a0001c0001t0023g0237 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.807+570A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479680 | ||||||
chr8:108479699
|
GA | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0178 | 3 | HG01884.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.807+590delA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479699 | ||||||
chr8:108479871
|
T | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(263): Show | 350 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.807+761T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479871 | ||||||
chr8:108479941
|
T | C | 2 | a0001c0001t0014g0184a0001c0001t0014g0185 | 2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.807+831T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479941 | ||||||
chr8:108479990
|
C | T | 2 | a0001c0001t0002g0024a0003c0004t0002g0135 | 3 | NA18976.hp2 NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.807+880C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479990 | ||||||
chr8:108480185
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.807+1075G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480185 | ||||||
chr8:108480192
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.807+1082G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480192 | ||||||
chr8:108480237
|
A | T | 1 | a0001c0001t0022g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.807+1127A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480237 | ||||||
chr8:108480335
|
G | A | 1 | a0001c0001t0014g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.807+1225G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480335 | ||||||
chr8:108480336
|
G | T | 1 | a0001c0001t0014g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.807+1226G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480336 | ||||||
chr8:108480341
|
A | G | 184 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(181): Show | 234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.807+1231A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480341 | ||||||
chr8:108480841
|
T | C | 1 | a0001c0001t0002g0106 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.807+1731T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480841 | ||||||
chr8:108481009
|
G | C | 3 | a0001c0001t0002g0144a0001c0001t0002g0146a0001c0001t0002g0147 | 3 | NA19001.hp2 NA19005.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.807+1899G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481009 | ||||||
chr8:108481149
|
C | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.807+2039C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481149 | ||||||
chr8:108481266
|
A | G | 2 | a0001c0001t0005g0043a0001c0001t0005g0275 | 3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.807+2156A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481266 | ||||||
chr8:108481269
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.807+2159A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481269 | ||||||
chr8:108481421
|
CAG | C | 2 | a0001c0001t0005g0031a0001c0001t0005g0187 | 3 | HG01243.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.807+2314_807+2315d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108481421 | |||||
chr8:108481599
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.807+2489A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481599 | ||||||
chr8:108481663
|
A | C | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.807+2553A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481663 | ||||||
chr8:108481830
|
T | C | 75 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(72): Show | 96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.807+2720T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481830 | ||||||
chr8:108481833
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.807+2723A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481833 | ||||||
chr8:108481905
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.807+2795T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481905 | ||||||
chr8:108481934
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.807+2824G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481934 | ||||||
chr8:108482273
|
G | T | 26 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(23): Show | 28 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.807+3163G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482273 | ||||||
chr8:108482360
|
G | A | 1 | a0001c0001t0011g0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.807+3250G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482360 | ||||||
chr8:108482383
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.807+3273C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482383 | ||||||
chr8:108482426
|
G | A | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.807+3316G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482426 | ||||||
chr8:108482609
|
CTGGT | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.807+3505_807+3508d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108482609 | |||||
chr8:108482728
|
C | T | 2 | a0001c0001t0016g0048a0001c0001t0016g0049 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.807+3618C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482728 | ||||||
chr8:108482738
|
C | T | 50 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(47): Show | 60 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+3628C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482738 | ||||||
chr8:108482828
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.808-3684C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482828 | ||||||
chr8:108483204
|
C | T | 1 | a0001c0001t0021g0213 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.808-3308C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483204 | ||||||
chr8:108483389
|
A | G | 44 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(41): Show | 53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.808-3123A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483389 | ||||||
chr8:108483421
|
T | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0178 | 3 | HG01884.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.808-3091T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483421 | ||||||
chr8:108483650
|
A | G | 51 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0030others(48): Show | 61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.808-2862A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483650 | ||||||
chr8:108483918
|
G | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0076 | 3 | HG01168.hp2 HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.808-2594G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483918 | ||||||
chr8:108483945
|
G | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.808-2567G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483945 | ||||||
chr8:108484051
|
G | T | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.808-2461G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484051 | ||||||
chr8:108484167
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.808-2345T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484167 | ||||||
chr8:108484261
|
A | G | 7 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(4): Show | 8 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.808-2251A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484261 | ||||||
chr8:108484312
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.808-2200A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484312 | ||||||
chr8:108484460
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.808-2052C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484460 | ||||||
chr8:108484463
|
T | C | 134 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(131): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.808-2049T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484463 | ||||||
chr8:108484705
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.808-1807C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484705 | ||||||
chr8:108485042
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.808-1470T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485042 | ||||||
chr8:108485048
|
A | C | 1 | a0001c0001t0002g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.808-1464A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485048 | ||||||
chr8:108485093
|
A | G | 1 | a0001c0001t0002g0025 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.808-1419A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485093 | ||||||
chr8:108485117
|
G | T | 1 | a0001c0001t0001g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.808-1395G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485117 | ||||||
chr8:108485274
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.808-1238A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485274 | ||||||
chr8:108485321
|
T | A | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1191T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485321 | ||||||
chr8:108485325
|
T | A | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1187T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485325 | ||||||
chr8:108485327
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1185G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485327 | ||||||
chr8:108485329
|
T | A | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1183T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485329 | ||||||
chr8:108485330
|
T | G | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1182T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485330 | ||||||
chr8:108485331
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1181G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485331 | ||||||
chr8:108485332
|
A | C | 179 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(176): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-1180A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485332 | ||||||
chr8:108485334
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1178G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485334 | ||||||
chr8:108485362
|
A | G | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-1150A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485362 | ||||||
chr8:108485452
|
T | TACATATA others(17): Show |
9 | a0001c0001t0006g0012a0001c0001t0006g0159a0001c0001t0006g0171others(6): Show | 12 | HG00738.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.808-1048_808-1025d others(26): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108485452 | |||||
chr8:108485533
|
A | T | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-979A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485533 | ||||||
chr8:108485549
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-963A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485549 | ||||||
chr8:108485552
|
TATAC | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-958_808-955del others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108485552 | |||||
chr8:108485552
|
TATACAC | T | 179 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(176): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-958_808-953del others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108485552 | |||||
chr8:108485556
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-956C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485556 | ||||||
chr8:108485558
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-954C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485558 | ||||||
chr8:108485703
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.808-809G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485703 | ||||||
chr8:108486060
|
T | C | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.808-452T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486060 | ||||||
chr8:108486150
|
C | T | 2 | a0001c0001t0018g0055a0002c0003t0018g0056 | 2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.808-362C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486150 | ||||||
chr8:108486173
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.808-339C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486173 | ||||||
chr8:108486206
|
C | CAT | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.808-305_808-304dup others(2): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486206 | |||||
chr8:108486291
|
G | A | 1 | a0001c0001t0015g0040 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.808-221G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486291 | ||||||
chr8:108486328
|
C | T | 6 | a0001c0001t0008g0241a0001c0001t0008g0242a0001c0001t0008g0243others(3): Show | 6 | HG01261.hp2 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-184C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486328 | ||||||
chr8:108486352
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.808-160C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486352 | ||||||
chr8:108486427
|
T | G | 180 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(177): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.808-85T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486427 | ||||||
chr8:108486430
|
C | T | 1 | a0001c0001t0011g0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.808-82C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486430 | ||||||
chr8:108486452
|
A | G | 6 | a0001c0001t0004g0047a0001c0001t0004g0050a0001c0001t0004g0051others(3): Show | 6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-60A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486452 | ||||||
chr8:108486488
|
C | CT | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(92): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
splice_region_variant&intron_variant | LOW | c.808-7dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486488 | |||||
chr8:108486488
|
C | CTT | 45 | a0001c0001t0002g0129a0001c0001t0002g0143a0001c0001t0003g0074others(42): Show | 53 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(50): Show |
splice_region_variant&intron_variant | LOW | c.808-8_808-7dupTT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486488 | |||||
chr8:108486488
|
C | CTTT | 127 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(124): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
splice_region_variant&intron_variant | LOW | c.808-9_808-7dupTTT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486488 |