geneid | 79694 |
---|---|
ensemblid | ENSG00000172469.17 |
hgncid | 21072 |
symbol | MANEA |
name | mannosidase endo-alpha |
refseq_nuc | NM_024641.4 |
refseq_prot | NP_078917.2 |
ensembl_nuc | ENST00000358812.9 |
ensembl_prot | ENSP00000351669.4 |
mane_status | MANE Select |
chr | chr6 |
start | 95577535 |
end | 95609452 |
strand | + |
ver | v1.2 |
region | chr6:95577535-95609452 |
region5000 | chr6:95572535-95614452 |
regionname0 | MANEA_chr6_95577535_95609452 |
regionname5000 | MANEA_chr6_95572535_95614452 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 462 | 354 | 71 | 64 | 181 | 8 | 28 | 145 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0002 | 0/0 | 462 | 25 | 0 | 8 | 15 | 1 | 1 | 11 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0003 | 0/0 | 462 | 14 | 9 | 3 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004 | 0/0 | 462 | 10 | 6 | 0 | 0 | 1 | 3 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0005 | 0/0 | 462 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0006 | 0/0 | 462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0007 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0008 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0009 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0010 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1389 | 354 | 71 | 64 | 181 | 8 | 28 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0002 | 0/0 | 1389 | 24 | 0 | 8 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0003 | 0/0 | 1389 | 14 | 9 | 3 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0004 | 0/0 | 1389 | 6 | 6 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0005 | 0/0 | 1389 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0006 | 0/0 | 1389 | 2 | 0 | 0 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0007 | 0/0 | 1389 | 2 | 0 | 0 | 0 | 1 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0008 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0009 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0010 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0011 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0012 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
c0013 | 0/0 | 1389 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3186 | 82 | 19 | 8 | 48 | 0 | 7 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0002 | 1/0 | 3190 | 69 | 3 | 30 | 28 | 2 | 5 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0003 | 0/0 | 3190 | 60 | 1 | 13 | 34 | 3 | 9 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0004 | 0/0 | 3190 | 57 | 15 | 4 | 31 | 2 | 5 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0005 | 0/1 | 3190 | 41 | 14 | 5 | 14 | 3 | 4 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0006 | 0/0 | 3190 | 32 | 6 | 9 | 15 | 1 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0007 | 0/0 | 3188 | 15 | 9 | 4 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0008 | 0/0 | 3190 | 14 | 6 | 0 | 7 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0009 | 0/0 | 3190 | 8 | 0 | 0 | 8 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0010 | 0/0 | 3190 | 5 | 5 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0011 | 0/0 | 3186 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0012 | 0/0 | 3190 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0013 | 0/0 | 3186 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0014 | 0/0 | 3190 | 2 | 1 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0015 | 0/0 | 3190 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0016 | 0/0 | 3190 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0017 | 0/0 | 3190 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0018 | 0/0 | 3190 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0019 | 0/0 | 3186 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0020 | 0/0 | 3186 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0021 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0022 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0023 | 0/0 | 3190 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0024 | 0/0 | 3190 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0025 | 0/0 | 3190 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0026 | 0/0 | 3190 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
t0027 | 0/0 | 3190 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 4 | 2 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0002 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0003 | 0/0 | 9 | 2 | 3 | 2 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0004 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0005 | 0/1 | 7 | 0 | 1 | 5 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0008 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0009 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0010 | 0/0 | 5 | 1 | 0 | 3 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0011 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0018 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0022 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0050 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1389 | 354 | 71 | 64 | 181 | 8 | 28 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0002c0002 | 0/0 | 1389 | 24 | 0 | 8 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0002c0011 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0003c0003 | 0/0 | 1389 | 14 | 9 | 3 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0004 | 0/0 | 1389 | 6 | 6 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0005 | 0/0 | 1389 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0007 | 0/0 | 1389 | 2 | 0 | 0 | 0 | 1 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0005c0006 | 0/0 | 1389 | 2 | 0 | 0 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0006c0013 | 0/0 | 1389 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0007c0012 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0008c0010 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0009c0009 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0010c0008 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4574 | 80 | 17 | 8 | 48 | 0 | 7 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0002 | 1/0 | 4578 | 69 | 3 | 30 | 28 | 2 | 5 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0003 | 0/0 | 4578 | 60 | 1 | 13 | 34 | 3 | 9 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0004 | 0/0 | 4578 | 56 | 14 | 4 | 31 | 2 | 5 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0005 | 0/1 | 4578 | 31 | 10 | 5 | 14 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0006 | 0/0 | 4578 | 7 | 6 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0008 | 0/0 | 4578 | 14 | 6 | 0 | 7 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0009 | 0/0 | 4578 | 8 | 0 | 0 | 8 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0010 | 0/0 | 4578 | 5 | 5 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0011 | 0/0 | 4574 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0012 | 0/0 | 4578 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0013 | 0/0 | 4574 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0014 | 0/0 | 4578 | 2 | 1 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0016 | 0/0 | 4578 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0017 | 0/0 | 4578 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0018 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0019 | 0/0 | 4574 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0020 | 0/0 | 4574 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0021 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0022 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0023 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0025 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0026 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0001c0001t0027 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0002c0002t0006 | 0/0 | 4578 | 24 | 0 | 8 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0002c0011t0006 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0003c0003t0007 | 0/0 | 4576 | 14 | 9 | 3 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0004t0005 | 0/0 | 4578 | 4 | 4 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0004t0015 | 0/0 | 4578 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0005t0005 | 0/0 | 4578 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0004c0007t0005 | 0/0 | 4578 | 2 | 0 | 0 | 0 | 1 | 1 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0005c0006t0005 | 0/0 | 4578 | 2 | 0 | 0 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0006c0013t0007 | 0/0 | 4576 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0007c0012t0024 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0008c0010t0004 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0009c0009t0001 | 0/0 | 4574 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
a0010c0008t0001 | 0/0 | 4574 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | copy fasta | chr6 | 95572535 | 95614452 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 4 | 2 | 15 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0002 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0008 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0005 | 0/1 | 7 | 0 | 1 | 5 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0006g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0010g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0010g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0012g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0013g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0013g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0014g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0017g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0018g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0020g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0021g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0023g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0025g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0026g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0001c0001t0027g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0002t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0002c0011t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0003c0003t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0004t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0004t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0004t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0004t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0004t0015g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0004t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0005t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0005t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0007t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0004c0007t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0005c0006t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0005c0006t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0006c0013t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0007c0012t0024g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0008c0010t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0009c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
a0010c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0010 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0117 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00140 | hp2 | a0001 | c0001 | t0014 | g0233 | EUR | GBR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0071 | EUR | FIN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00323 | hp2 | a0002 | c0011 | t0006 | g0022 | EUR | FIN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0210 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00597 | hp2 | a0001 | c0001 | t0022 | g0006 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00673 | hp2 | a0001 | c0001 | t0008 | g0010 | EAS | CHS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0118 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00738 | hp1 | a0002 | c0002 | t0006 | g0198 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01069 | hp1 | a0002 | c0002 | t0006 | g0185 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01070 | hp1 | a0003 | c0003 | t0007 | g0251 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01071 | hp2 | a0002 | c0002 | t0006 | g0188 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01099 | hp2 | a0003 | c0003 | t0007 | g0255 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01106 | hp1 | a0002 | c0002 | t0006 | g0184 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01109 | hp1 | a0002 | c0002 | t0006 | g0182 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01109 | hp2 | a0006 | c0013 | t0007 | g0199 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01175 | hp2 | a0003 | c0003 | t0007 | g0252 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01192 | hp1 | a0002 | c0002 | t0006 | g0189 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01243 | hp1 | a0001 | c0001 | t0025 | g0082 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01261 | hp1 | a0002 | c0002 | t0006 | g0197 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01346 | hp1 | a0001 | c0001 | t0026 | g0065 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01358 | hp2 | a0002 | c0002 | t0006 | g0196 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01361 | hp2 | a0001 | c0001 | t0023 | g0130 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01515 | hp1 | a0005 | c0006 | t0005 | g0204 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0119 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01516 | hp1 | a0003 | c0003 | t0007 | g0250 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01517 | hp2 | a0005 | c0006 | t0005 | g0208 | EUR | IBS | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0055 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0268 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01891 | hp1 | a0009 | c0009 | t0001 | g0035 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0205 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02055 | hp2 | a0003 | c0003 | t0007 | g0134 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02080 | hp2 | a0002 | c0002 | t0006 | g0045 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02132 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02132 | hp2 | a0002 | c0002 | t0006 | g0022 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0051 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02155 | hp2 | a0002 | c0002 | t0006 | g0022 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0106 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02258 | hp2 | a0007 | c0012 | t0024 | g0101 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02523 | hp1 | a0001 | c0001 | t0021 | g0030 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02523 | hp2 | a0002 | c0002 | t0006 | g0186 | EAS | KHV | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02602 | hp2 | a0004 | c0007 | t0005 | g0241 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0081 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02615 | hp2 | a0003 | c0003 | t0007 | g0034 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02630 | hp2 | a0003 | c0003 | t0007 | g0046 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02683 | hp2 | a0004 | c0005 | t0005 | g0243 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02818 | hp1 | a0004 | c0004 | t0005 | g0225 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0141 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02922 | hp2 | a0001 | c0001 | t0019 | g0139 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02965 | hp2 | a0004 | c0004 | t0005 | g0240 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02970 | hp2 | a0003 | c0003 | t0007 | g0046 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03098 | hp1 | a0001 | c0001 | t0011 | g0145 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03130 | hp2 | a0003 | c0003 | t0007 | g0133 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03139 | hp2 | a0003 | c0003 | t0007 | g0200 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03209 | hp1 | a0004 | c0004 | t0005 | g0050 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03225 | hp2 | a0008 | c0010 | t0004 | g0125 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03453 | hp1 | a0004 | c0004 | t0015 | g0254 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0264 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0270 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0140 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0206 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04115 | hp1 | a0001 | c0001 | t0008 | g0072 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | BEB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0116 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18522 | hp2 | a0004 | c0004 | t0005 | g0239 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18747 | hp2 | a0001 | c0001 | t0009 | g0150 | EAS | CHB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18906 | hp1 | a0010 | c0008 | t0001 | g0135 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18947 | hp1 | a0001 | c0001 | t0009 | g0155 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18948 | hp2 | a0001 | c0001 | t0013 | g0162 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18952 | hp1 | a0002 | c0002 | t0006 | g0179 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18960 | hp2 | a0001 | c0001 | t0016 | g0087 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0163 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18969 | hp1 | a0001 | c0001 | t0013 | g0037 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18970 | hp1 | a0002 | c0002 | t0006 | g0183 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18970 | hp2 | a0002 | c0002 | t0006 | g0044 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18971 | hp1 | a0002 | c0002 | t0006 | g0190 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18977 | hp2 | a0001 | c0001 | t0020 | g0037 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18978 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18978 | hp2 | a0001 | c0001 | t0013 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18980 | hp2 | a0001 | c0001 | t0009 | g0174 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18985 | hp2 | a0001 | c0001 | t0027 | g0026 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18986 | hp1 | a0002 | c0002 | t0006 | g0180 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18987 | hp2 | a0002 | c0002 | t0006 | g0193 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18999 | hp2 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19000 | hp2 | a0002 | c0002 | t0006 | g0045 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19002 | hp1 | a0001 | c0001 | t0017 | g0027 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19005 | hp1 | a0002 | c0002 | t0006 | g0191 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19009 | hp1 | a0001 | c0001 | t0009 | g0157 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19010 | hp1 | a0002 | c0002 | t0006 | g0192 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0269 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19043 | hp1 | a0003 | c0003 | t0007 | g0132 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19043 | hp2 | a0001 | c0001 | t0018 | g0253 | AFR | LWK | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19058 | hp1 | a0002 | c0002 | t0006 | g0044 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19064 | hp1 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19065 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19075 | hp1 | a0001 | c0001 | t0009 | g0137 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19081 | hp1 | a0002 | c0002 | t0006 | g0181 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19085 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19090 | hp1 | a0001 | c0001 | t0016 | g0088 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0154 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA19240 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | YRI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | ASW | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20129 | hp2 | a0003 | c0003 | t0007 | g0034 | AFR | ASW | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20805 | hp1 | a0004 | c0007 | t0005 | g0050 | EUR | TSI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20805 | hp2 | a0003 | c0003 | t0007 | g0249 | EUR | TSI | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20905 | hp1 | a0002 | c0002 | t0006 | g0187 | SAS | GIH | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20905 | hp2 | a0004 | c0005 | t0005 | g0242 | SAS | GIH | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02559 | hp1 | a0003 | c0003 | t0007 | g0201 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0259 | AFR | MSL | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18955 | hp1 | a0001 | c0001 | t0017 | g0027 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
NA20300 | hp2 | a0004 | c0004 | t0015 | g0226 | AFR | USA | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0005 | REF | REF | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0248 | REF | REF | MANEA_chr6_95572535_95614452 | MANEA | chr6 | 95572535 | 95614452 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:95586639
|
T | G | 1 | a0010 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.200T>G | p.Ile67Ser | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 342/4578 | 200/1389 | 67/462 | chr6 | 95586639 | ||
chr6:95586672
|
G | C | 1 | a0009 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.233G>C | p.Ser78Thr | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 375/4578 | 233/1389 | 78/462 | chr6 | 95586672 | ||
chr6:95586684
|
C | T | 1 | a0004 | 10 | HG02602.hp2 HG02683.hp2 HG02818.hp1 others(7): Show |
missense_variant | MODERATE | c.245C>T | p.Thr82Ile | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 387/4578 | 245/1389 | 82/462 | chr6 | 95586684 | ||
chr6:95586968
|
C | T | 2 | a0003a0006 | 15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
missense_variant | MODERATE | c.529C>T | p.Arg177Cys | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 671/4578 | 529/1389 | 177/462 | chr6 | 95586968 | ||
chr6:95586981
|
T | C | 1 | a0006 | 1 | HG01109.hp2 | missense_variant&splice_region_variant | MODERATE | c.542T>C | p.Ile181Thr | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 684/4578 | 542/1389 | 181/462 | chr6 | 95586981 | ||
chr6:95605787
|
G | C | 1 | a0008 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.771G>C | p.Lys257Asn | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 913/4578 | 771/1389 | 257/462 | chr6 | 95605787 | ||
chr6:95605879
|
G | T | 1 | a0005 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.863G>T | p.Arg288Leu | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1005/4578 | 863/1389 | 288/462 | chr6 | 95605879 | ||
chr6:95606046
|
T | A | 1 | a0002 | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
missense_variant | MODERATE | c.1030T>A | p.Phe344Ile | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1172/4578 | 1030/1389 | 344/462 | chr6 | 95606046 | ||
chr6:95606299
|
G | A | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1283G>A | p.Arg428His | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1425/4578 | 1283/1389 | 428/462 | chr6 | 95606299 | ||
chr6:95606386
|
G | A | 2 | a0003a0006 | 15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
missense_variant | MODERATE | c.1370G>A | p.Arg457His | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1512/4578 | 1370/1389 | 457/462 | chr6 | 95606386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:95586454
|
G | A | 1 | a0004c0005 | 2 | HG02683.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.15G>A | p.Arg5Arg | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 157/4578 | 15/1389 | 5/462 | chr6 | 95586454 | ||
chr6:95586736
|
G | A | 2 | a0004c0005a0004c0007 | 4 | HG02602.hp2 HG02683.hp2 NA20805.hp1 others(1): Show |
synonymous_variant | LOW | c.297G>A | p.Leu99Leu | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/5 | 439/4578 | 297/1389 | 99/462 | chr6 | 95586736 | ||
chr6:95606378
|
A | G | 1 | a0002c0011 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1362A>G | p.Ala454Ala | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1504/4578 | 1362/1389 | 454/462 | chr6 | 95606378 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:95577570
|
A | G | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(11): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
5_prime_UTR_variant | MODIFIER | c.-107A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8870 | chr6 | 95577570 | |||||
chr6:95577573
|
T | A | 1 | a0001c0001t0011 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-104T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8867 | chr6 | 95577573 | |||||
chr6:95577574
|
C | A | 1 | a0001c0001t0011 | 3 | HG02896.hp2 HG03098.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8866 | chr6 | 95577574 | |||||
chr6:95577599
|
T | A | 1 | a0001c0001t0021 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8841 | chr6 | 95577599 | |||||
chr6:95577602
|
G | A | 1 | a0001c0001t0022 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/5 | 8838 | chr6 | 95577602 | |||||
chr6:95606533
|
A | T | 8 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(5): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 128 | chr6 | 95606533 | |||||
chr6:95606614
|
A | G | 1 | a0004c0004t0015 | 2 | HG03453.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*209A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 209 | chr6 | 95606614 | |||||
chr6:95606664
|
G | T | 7 | a0001c0001t0003a0001c0001t0016a0001c0001t0017others(4): Show | 68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*259G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 259 | chr6 | 95606664 | |||||
chr6:95606693
|
C | G | 1 | a0001c0001t0012 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*288C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 288 | chr6 | 95606693 | |||||
chr6:95606712
|
C | T | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*307C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 307 | chr6 | 95606712 | |||||
chr6:95606774
|
T | C | 1 | a0001c0001t0013 | 3 | NA18948.hp2 NA18969.hp1 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*369T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 369 | chr6 | 95606774 | |||||
chr6:95606825
|
G | A | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 420 | chr6 | 95606825 | |||||
chr6:95607059
|
C | A | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*654C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 654 | chr6 | 95607059 | |||||
chr6:95607117
|
C | G | 1 | a0001c0001t0017 | 2 | NA18955.hp1 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*712C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 712 | chr6 | 95607117 | |||||
chr6:95607140
|
G | A | 6 | a0001c0001t0005a0004c0004t0005a0004c0004t0015others(3): Show | 43 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 735 | chr6 | 95607140 | |||||
chr6:95607187
|
T | A | 2 | a0001c0001t0008a0001c0001t0010 | 19 | HG00423.hp1 HG00673.hp2 HG02055.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*782T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 782 | chr6 | 95607187 | |||||
chr6:95607500
|
T | C | 1 | a0001c0001t0026 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1095 | chr6 | 95607500 | |||||
chr6:95607668
|
G | A | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1263G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1263 | chr6 | 95607668 | |||||
chr6:95607801
|
T | A | 1 | a0001c0001t0023 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1396T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1396 | chr6 | 95607801 | |||||
chr6:95607900
|
G | A | 1 | a0001c0001t0019 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1495G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1495 | chr6 | 95607900 | |||||
chr6:95608039
|
G | C | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1634G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1634 | chr6 | 95608039 | |||||
chr6:95608130
|
C | T | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1725C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1725 | chr6 | 95608130 | |||||
chr6:95608240
|
C | G | 1 | a0007c0012t0024 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1835C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1835 | chr6 | 95608240 | |||||
chr6:95608325
|
G | A | 1 | a0001c0001t0020 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 1920 | chr6 | 95608325 | |||||
chr6:95608436
|
C | A | 1 | a0001c0001t0014 | 2 | HG00140.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2031C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2031 | chr6 | 95608436 | |||||
chr6:95608894
|
GAA | G | 2 | a0003c0003t0007a0006c0013t0007 | 15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2496_*2497delAA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2496 | INFO_REALIGN_3_PRIME | chr6 | 95608894 | ||||
chr6:95608930
|
C | T | 1 | a0001c0001t0010 | 5 | HG02615.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2525C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2525 | chr6 | 95608930 | |||||
chr6:95608972
|
G | A | 1 | a0001c0001t0016 | 2 | NA18960.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2567G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2567 | chr6 | 95608972 | |||||
chr6:95609017
|
TAGAG | T | 7 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(4): Show | 90 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2615_*2618delAGAG | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2615 | INFO_REALIGN_3_PRIME | chr6 | 95609017 | ||||
chr6:95609076
|
T | C | 1 | a0001c0001t0027 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2671T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2671 | chr6 | 95609076 | |||||
chr6:95609130
|
G | T | 35 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(32): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*2725G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 5/5 | 2725 | chr6 | 95609130 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:95577709
|
C | T | 4 | a0001c0001t0006g0024a0001c0001t0006g0268a0001c0001t0006g0269others(1): Show | 6 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+71C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95577709 | ||||||
chr6:95577767
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-39+129C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95577767 | ||||||
chr6:95577841
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(199): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-39+203G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95577841 | ||||||
chr6:95578033
|
G | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG00639.hp1 HG00642.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-39+395G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578033 | ||||||
chr6:95578121
|
C | T | 2 | a0001c0001t0005g0265a0001c0001t0005g0266 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-39+483C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578121 | ||||||
chr6:95578136
|
A | T | 2 | a0001c0001t0012g0055a0001c0001t0012g0264 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-39+498A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578136 | ||||||
chr6:95578268
|
TTTG | T | 4 | a0003c0003t0007g0046a0003c0003t0007g0200a0003c0003t0007g0201others(1): Show | 5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+636_-39+638del others(3): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95578268 | |||||
chr6:95578383
|
AAAC | A | 3 | a0002c0002t0006g0196a0002c0002t0006g0197a0002c0002t0006g0198 | 3 | HG00738.hp1 HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-39+754_-39+756del others(3): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95578383 | |||||
chr6:95578396
|
G | T | 1 | a0001c0001t0003g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-39+758G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578396 | ||||||
chr6:95578468
|
T | C | 3 | a0001c0001t0003g0060a0001c0001t0004g0059a0001c0001t0004g0061 | 3 | HG02015.hp1 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-39+830T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578468 | ||||||
chr6:95578510
|
A | G | 1 | a0001c0001t0008g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-39+872A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578510 | ||||||
chr6:95578512
|
A | C | 22 | a0002c0002t0006g0022a0002c0002t0006g0044a0002c0002t0006g0045others(19): Show | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-39+874A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578512 | ||||||
chr6:95578518
|
G | A | 111 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(108): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-39+880G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578518 | ||||||
chr6:95578549
|
T | G | 1 | a0002c0002t0006g0179 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-39+911T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578549 | ||||||
chr6:95578579
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-39+941A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95578579 | ||||||
chr6:95579096
|
C | T | 4 | a0001c0001t0005g0054a0001c0001t0005g0260a0001c0001t0005g0261others(1): Show | 5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+1458C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579096 | ||||||
chr6:95579098
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+1460C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579098 | ||||||
chr6:95579298
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(59): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+1660G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579298 | ||||||
chr6:95579369
|
C | G | 2 | a0001c0001t0005g0054a0001c0001t0005g0262 | 3 | HG02572.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-39+1731C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579369 | ||||||
chr6:95579890
|
A | G | 1 | a0001c0001t0003g0131 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-39+2252A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95579890 | ||||||
chr6:95580048
|
A | G | 1 | a0001c0001t0023g0130 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-39+2410A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580048 | ||||||
chr6:95580105
|
A | G | 2 | a0001c0001t0005g0257a0001c0001t0005g0258 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+2467A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580105 | ||||||
chr6:95580117
|
A | G | 1 | a0001c0001t0002g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-39+2479A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580117 | ||||||
chr6:95580174
|
G | A | 15 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(12): Show | 25 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-39+2536G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580174 | ||||||
chr6:95580183
|
G | C | 1 | a0001c0001t0003g0062 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-39+2545G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580183 | ||||||
chr6:95580231
|
T | C | 1 | a0010c0008t0001g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-39+2593T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580231 | ||||||
chr6:95580455
|
G | A | 4 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0066others(1): Show | 4 | HG01243.hp2 HG01346.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+2817G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580455 | ||||||
chr6:95580497
|
G | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+2859G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580497 | ||||||
chr6:95580542
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+2904G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580542 | ||||||
chr6:95580586
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-39+2948G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580586 | ||||||
chr6:95580686
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+3048C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580686 | ||||||
chr6:95580716
|
C | T | 1 | a0001c0001t0005g0211 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-39+3078C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580716 | ||||||
chr6:95580724
|
C | CA | 21 | a0001c0001t0001g0136a0001c0001t0002g0007a0001c0001t0002g0212others(18): Show | 29 | HG01952.hp1 HG01978.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39+3104dupA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95580724 | |||||
chr6:95580724
|
CA | C | 27 | a0001c0001t0001g0178a0001c0001t0003g0062a0001c0001t0018g0253others(24): Show | 30 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.-39+3104delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95580724 | |||||
chr6:95580786
|
A | T | 9 | a0003c0003t0007g0034a0003c0003t0007g0132a0003c0003t0007g0133others(6): Show | 10 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+3148A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580786 | ||||||
chr6:95580903
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(284): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.-39+3265T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95580903 | ||||||
chr6:95581078
|
T | C | 4 | a0002c0002t0006g0044a0002c0002t0006g0045a0002c0002t0006g0180others(1): Show | 6 | HG02080.hp2 NA18970.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+3440T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581078 | ||||||
chr6:95581122
|
G | C | 5 | a0003c0003t0007g0249a0003c0003t0007g0250a0003c0003t0007g0251others(2): Show | 5 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+3484G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581122 | ||||||
chr6:95581268
|
G | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0138a0001c0001t0001g0142others(9): Show | 12 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-39+3630G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581268 | ||||||
chr6:95581299
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0148a0001c0001t0001g0149 | 4 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3661T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581299 | ||||||
chr6:95581318
|
C | G | 4 | a0003c0003t0007g0034a0003c0003t0007g0132a0003c0003t0007g0133others(1): Show | 5 | HG02055.hp2 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+3680C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581318 | ||||||
chr6:95581354
|
T | G | 1 | a0001c0001t0002g0212 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-39+3716T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581354 | ||||||
chr6:95581510
|
CTTTTCAT others(4): Show |
C | 15 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(12): Show | 25 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-39+3875_-39+3885d others(13): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95581510 | |||||
chr6:95581683
|
T | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0213a0001c0001t0002g0219others(2): Show | 8 | HG00738.hp2 HG01081.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+4045T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581683 | ||||||
chr6:95581770
|
C | T | 27 | a0001c0001t0003g0060a0001c0001t0004g0006a0001c0001t0004g0013others(24): Show | 42 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-39+4132C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581770 | ||||||
chr6:95581795
|
T | A | 1 | a0001c0001t0002g0221 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-39+4157T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581795 | ||||||
chr6:95581950
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-39+4312A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95581950 | ||||||
chr6:95582076
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-38-4326C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582076 | ||||||
chr6:95582106
|
GTGATGTC others(2): Show |
G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-4291_-38-4283d others(11): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582106 | |||||
chr6:95582122
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-4280G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582122 | ||||||
chr6:95582173
|
C | CT | 50 | a0001c0001t0001g0043a0001c0001t0001g0146a0001c0001t0001g0147others(47): Show | 55 | HG00423.hp2 HG01123.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.-38-4201dupT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582173 | |||||
chr6:95582173
|
CT | C | 37 | a0001c0001t0001g0021a0001c0001t0001g0151a0001c0001t0002g0215others(34): Show | 44 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-38-4201delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582173 | |||||
chr6:95582173
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0003g0070a0001c0001t0003g0195 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-38-4214_-38-4201d others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95582173 | |||||
chr6:95582180
|
T | G | 3 | a0001c0001t0005g0214a0001c0001t0005g0257a0001c0001t0005g0258 | 3 | HG02809.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-4222T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582180 | ||||||
chr6:95582223
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-38-4179G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582223 | ||||||
chr6:95582711
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-3691T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582711 | ||||||
chr6:95582958
|
C | T | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38-3444C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95582958 | ||||||
chr6:95583045
|
T | G | 22 | a0002c0002t0006g0022a0002c0002t0006g0044a0002c0002t0006g0045others(19): Show | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38-3357T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583045 | ||||||
chr6:95583107
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-3295T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583107 | ||||||
chr6:95583112
|
A | G | 4 | a0001c0001t0002g0007a0001c0001t0002g0215a0001c0001t0002g0217others(1): Show | 9 | NA18950.hp1 NA18952.hp2 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38-3290A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583112 | ||||||
chr6:95583113
|
T | C | 1 | a0001c0001t0018g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38-3289T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583113 | ||||||
chr6:95583233
|
T | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(245): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-38-3169T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583233 | ||||||
chr6:95583235
|
A | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-3167A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583235 | ||||||
chr6:95583268
|
A | G | 1 | a0001c0001t0003g0105 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-38-3134A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583268 | ||||||
chr6:95583413
|
A | T | 35 | a0001c0001t0003g0060a0001c0001t0004g0006a0001c0001t0004g0013others(32): Show | 50 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-38-2989A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583413 | ||||||
chr6:95583447
|
G | A | 33 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(30): Show | 44 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-38-2955G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583447 | ||||||
chr6:95583548
|
ATTTAC | A | 4 | a0001c0001t0005g0054a0001c0001t0005g0260a0001c0001t0005g0261others(1): Show | 5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-2851_-38-2847d others(7): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95583548 | |||||
chr6:95583595
|
A | G | 9 | a0003c0003t0007g0034a0003c0003t0007g0132a0003c0003t0007g0133others(6): Show | 10 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-2807A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583595 | ||||||
chr6:95583731
|
T | C | 1 | a0004c0004t0005g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38-2671T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583731 | ||||||
chr6:95583759
|
GT | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-2640delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95583759 | |||||
chr6:95583766
|
T | C | 1 | a0001c0001t0023g0130 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-38-2636T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583766 | ||||||
chr6:95583834
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-38-2568T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583834 | ||||||
chr6:95583879
|
A | G | 1 | a0001c0001t0005g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38-2523A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95583879 | ||||||
chr6:95584057
|
T | C | 1 | a0001c0001t0004g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38-2345T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584057 | ||||||
chr6:95584084
|
C | T | 10 | a0004c0004t0005g0050a0004c0004t0005g0225a0004c0004t0005g0239others(7): Show | 10 | HG02602.hp2 HG02683.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-2318C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584084 | ||||||
chr6:95584144
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-38-2258G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584144 | ||||||
chr6:95584227
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-2175G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584227 | ||||||
chr6:95584323
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-2079G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584323 | ||||||
chr6:95584480
|
C | T | 3 | a0001c0001t0003g0060a0001c0001t0004g0059a0001c0001t0004g0061 | 3 | HG02015.hp1 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-38-1922C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584480 | ||||||
chr6:95584800
|
C | G | 17 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0015others(14): Show | 38 | HG01074.hp2 HG01167.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38-1602C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584800 | ||||||
chr6:95584819
|
G | T | 1 | a0001c0001t0003g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-38-1583G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584819 | ||||||
chr6:95584828
|
C | G | 33 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(30): Show | 44 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-38-1574C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584828 | ||||||
chr6:95584874
|
C | T | 5 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(2): Show | 7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-1528C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584874 | ||||||
chr6:95584904
|
C | A | 1 | a0004c0004t0005g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-1498C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584904 | ||||||
chr6:95584905
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-38-1497G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584905 | ||||||
chr6:95584975
|
T | C | 3 | a0001c0001t0005g0214a0001c0001t0005g0257a0001c0001t0005g0258 | 3 | HG02809.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-1427T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95584975 | ||||||
chr6:95585002
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-1400C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585002 | ||||||
chr6:95585003
|
G | A | 13 | a0003c0003t0007g0034a0003c0003t0007g0046a0003c0003t0007g0132others(10): Show | 15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-38-1399G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585003 | ||||||
chr6:95585135
|
C | CAT | 16 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(13): Show | 26 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-1251_-38-1250d others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585135 | |||||
chr6:95585135
|
C | CATAT | 6 | a0001c0001t0005g0054a0001c0001t0005g0260a0001c0001t0005g0261others(3): Show | 7 | HG01515.hp1 HG01517.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-1253_-38-1250d others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585135 | |||||
chr6:95585135
|
CAT | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-1251_-38-1250d others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585135 | |||||
chr6:95585248
|
A | G | 5 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(2): Show | 7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-1154A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585248 | ||||||
chr6:95585342
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-38-1060C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585342 | ||||||
chr6:95585377
|
A | G | 15 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(12): Show | 25 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38-1025A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585377 | ||||||
chr6:95585379
|
G | A | 1 | a0001c0001t0006g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-38-1023G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585379 | ||||||
chr6:95585414
|
A | G | 1 | a0004c0004t0005g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-988A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585414 | ||||||
chr6:95585514
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-38-888G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585514 | ||||||
chr6:95585557
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-845T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585557 | ||||||
chr6:95585647
|
T | TA | 3 | a0001c0001t0003g0060a0001c0001t0004g0059a0001c0001t0004g0061 | 3 | HG02015.hp1 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-38-754dupA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95585647 | |||||
chr6:95585767
|
A | T | 2 | a0001c0001t0005g0257a0001c0001t0005g0258 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-635A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585767 | ||||||
chr6:95585886
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-38-516T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585886 | ||||||
chr6:95585908
|
A | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(59): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-494A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585908 | ||||||
chr6:95585917
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(59): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-485A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95585917 | ||||||
chr6:95586027
|
G | T | 1 | a0001c0001t0004g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-38-375G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586027 | ||||||
chr6:95586103
|
A | G | 1 | a0001c0001t0005g0207 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-38-299A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586103 | ||||||
chr6:95586103
|
A | T | 1 | a0004c0005t0005g0243 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-299A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586103 | ||||||
chr6:95586104
|
T | G | 1 | a0004c0005t0005g0243 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-298T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586104 | ||||||
chr6:95586174
|
T | C | 22 | a0002c0002t0006g0022a0002c0002t0006g0044a0002c0002t0006g0045others(19): Show | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38-228T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586174 | ||||||
chr6:95586213
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-38-189C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586213 | ||||||
chr6:95586252
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-38-150G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586252 | ||||||
chr6:95586293
|
TATTA | T | 27 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(24): Show | 32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-104_-38-101del others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 95586293 | |||||
chr6:95586336
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-38-66G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 1/4 | chr6 | 95586336 | ||||||
chr6:95586993
|
G | GTATA | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(58): Show | 97 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.544+20_544+23dupAT others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95586993 | |||||
chr6:95587005
|
A | ATATATG | 23 | a0001c0001t0004g0019a0001c0001t0004g0116a0001c0001t0004g0117others(20): Show | 28 | HG00099.hp2 HG00323.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.544+23_544+24insAT others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587005 | |||||
chr6:95587005
|
A | ATATATGT others(1): Show |
3 | a0002c0002t0006g0196a0002c0002t0006g0197a0002c0002t0006g0198 | 3 | HG00738.hp1 HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.544+23_544+24insAT others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587005 | |||||
chr6:95587005
|
A | ATATG | 110 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(107): Show | 146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.544+23_544+24insAT others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587005 | |||||
chr6:95587013
|
T | G | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+30T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587013 | ||||||
chr6:95587019
|
C | G | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+36C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587019 | ||||||
chr6:95587021
|
G | C | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+38G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587021 | ||||||
chr6:95587299
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(210): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.544+316T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587299 | ||||||
chr6:95587426
|
G | A | 1 | a0001c0001t0018g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.544+443G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587426 | ||||||
chr6:95587442
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544+459A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587442 | ||||||
chr6:95587451
|
GGATCTGA others(9): Show |
G | 2 | a0001c0001t0004g0075a0002c0002t0006g0182 | 2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544+485_544+500del others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95587451 | |||||
chr6:95587534
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(59): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.544+551A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587534 | ||||||
chr6:95587722
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+739A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587722 | ||||||
chr6:95587851
|
C | T | 2 | a0001c0001t0005g0257a0001c0001t0005g0258 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.544+868C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587851 | ||||||
chr6:95587979
|
C | T | 1 | a0001c0001t0002g0049 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.544+996C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95587979 | ||||||
chr6:95588040
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+1057C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588040 | ||||||
chr6:95588119
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.544+1136T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588119 | ||||||
chr6:95588347
|
A | G | 1 | a0001c0001t0003g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.544+1364A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588347 | ||||||
chr6:95588398
|
T | G | 110 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(107): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.544+1415T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588398 | ||||||
chr6:95588619
|
T | G | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+1636T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588619 | ||||||
chr6:95588858
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+1875T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588858 | ||||||
chr6:95588867
|
A | G | 11 | a0001c0001t0003g0012a0001c0001t0003g0070a0001c0001t0003g0089others(8): Show | 14 | HG00438.hp2 HG00558.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.544+1884A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588867 | ||||||
chr6:95588952
|
A | T | 9 | a0003c0003t0007g0034a0003c0003t0007g0132a0003c0003t0007g0133others(6): Show | 10 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.544+1969A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95588952 | ||||||
chr6:95589076
|
C | A | 33 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(30): Show | 44 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.544+2093C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589076 | ||||||
chr6:95589094
|
A | T | 111 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(108): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.544+2111A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589094 | ||||||
chr6:95589133
|
TAAAG | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+2154_544+2157d others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95589133 | |||||
chr6:95589242
|
G | T | 5 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(2): Show | 7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+2259G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589242 | ||||||
chr6:95589423
|
T | C | 2 | a0001c0001t0003g0012a0001c0001t0003g0089 | 5 | NA18964.hp1 NA18971.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.544+2440T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589423 | ||||||
chr6:95589525
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.544+2542A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589525 | ||||||
chr6:95589625
|
T | C | 7 | a0001c0001t0001g0156a0001c0001t0009g0137a0001c0001t0009g0150others(4): Show | 7 | NA18747.hp2 NA18947.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.544+2642T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589625 | ||||||
chr6:95589641
|
G | A | 22 | a0002c0002t0006g0022a0002c0002t0006g0044a0002c0002t0006g0045others(19): Show | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.544+2658G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589641 | ||||||
chr6:95589701
|
G | A | 13 | a0003c0003t0007g0034a0003c0003t0007g0046a0003c0003t0007g0132others(10): Show | 15 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.544+2718G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589701 | ||||||
chr6:95589870
|
G | C | 1 | a0001c0001t0003g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.544+2887G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589870 | ||||||
chr6:95589966
|
C | T | 111 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(108): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.544+2983C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95589966 | ||||||
chr6:95590022
|
C | T | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+3039C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590022 | ||||||
chr6:95590023
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+3040A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590023 | ||||||
chr6:95590323
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+3340T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590323 | ||||||
chr6:95590629
|
A | G | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544+3646A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590629 | ||||||
chr6:95590771
|
T | C | 15 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(12): Show | 25 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.544+3788T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590771 | ||||||
chr6:95590849
|
G | A | 2 | a0001c0001t0012g0055a0001c0001t0012g0264 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.544+3866G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95590849 | ||||||
chr6:95591027
|
T | C | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.544+4044T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591027 | ||||||
chr6:95591080
|
T | A | 2 | a0001c0001t0012g0055a0001c0001t0012g0264 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.544+4097T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591080 | ||||||
chr6:95591088
|
T | C | 111 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(108): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.544+4105T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591088 | ||||||
chr6:95591125
|
A | G | 22 | a0002c0002t0006g0022a0002c0002t0006g0044a0002c0002t0006g0045others(19): Show | 25 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.544+4142A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591125 | ||||||
chr6:95591390
|
C | G | 1 | a0001c0001t0002g0245 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.544+4407C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591390 | ||||||
chr6:95591488
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544+4505A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591488 | ||||||
chr6:95591675
|
T | C | 1 | a0001c0001t0004g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.544+4692T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591675 | ||||||
chr6:95591690
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+4707C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591690 | ||||||
chr6:95591737
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.544+4754G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591737 | ||||||
chr6:95591747
|
G | T | 1 | a0001c0001t0004g0019 | 3 | HG02735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.544+4764G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591747 | ||||||
chr6:95591779
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.544+4796C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591779 | ||||||
chr6:95591862
|
C | T | 2 | a0002c0002t0006g0191a0002c0002t0006g0193 | 2 | NA18987.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.545-4875C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591862 | ||||||
chr6:95591923
|
C | T | 1 | a0001c0001t0005g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.545-4814C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591923 | ||||||
chr6:95591982
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.545-4755G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591982 | ||||||
chr6:95591999
|
G | C | 1 | a0001c0001t0004g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.545-4738G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95591999 | ||||||
chr6:95592092
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.545-4645A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592092 | ||||||
chr6:95592367
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.545-4370T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592367 | ||||||
chr6:95592391
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-4346G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592391 | ||||||
chr6:95592528
|
C | T | 1 | a0001c0001t0009g0157 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.545-4209C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592528 | ||||||
chr6:95592611
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.545-4126T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592611 | ||||||
chr6:95592937
|
A | G | 1 | a0001c0001t0005g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.545-3800A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592937 | ||||||
chr6:95592948
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.545-3789A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95592948 | ||||||
chr6:95593023
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-3714T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593023 | ||||||
chr6:95593209
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-3528C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593209 | ||||||
chr6:95593210
|
G | A | 33 | a0001c0001t0005g0005a0001c0001t0005g0023a0001c0001t0005g0047others(30): Show | 44 | HG00423.hp2 HG00558.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.545-3527G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593210 | ||||||
chr6:95593239
|
T | C | 3 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0244 | 3 | HG02293.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.545-3498T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593239 | ||||||
chr6:95593370
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.545-3367T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593370 | ||||||
chr6:95593601
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-3136C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593601 | ||||||
chr6:95593672
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.545-3065T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593672 | ||||||
chr6:95593986
|
T | G | 1 | a0001c0001t0003g0078 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.545-2751T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95593986 | ||||||
chr6:95594018
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(244): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.545-2719T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594018 | ||||||
chr6:95594032
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.545-2705A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594032 | ||||||
chr6:95594060
|
CA | C | 6 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(3): Show | 8 | HG00741.hp1 HG01517.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.545-2666delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 95594060 | |||||
chr6:95594181
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.545-2556A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594181 | ||||||
chr6:95594374
|
A | G | 2 | a0001c0001t0016g0087a0001c0001t0016g0088 | 2 | NA18960.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.545-2363A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594374 | ||||||
chr6:95594448
|
T | C | 1 | a0001c0001t0004g0119 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.545-2289T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594448 | ||||||
chr6:95594462
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(245): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.545-2275A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594462 | ||||||
chr6:95594642
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.545-2095G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594642 | ||||||
chr6:95594804
|
T | G | 12 | a0001c0001t0005g0214a0001c0001t0005g0257a0001c0001t0005g0258others(9): Show | 12 | HG02602.hp2 HG02683.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.545-1933T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594804 | ||||||
chr6:95594817
|
T | C | 2 | a0001c0001t0002g0222a0001c0001t0002g0231 | 2 | HG01496.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.545-1920T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594817 | ||||||
chr6:95594958
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.545-1779G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95594958 | ||||||
chr6:95595030
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.545-1707G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595030 | ||||||
chr6:95595191
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-1546C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595191 | ||||||
chr6:95595213
|
C | G | 1 | a0001c0001t0004g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.545-1524C>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595213 | ||||||
chr6:95595419
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-1318C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595419 | ||||||
chr6:95595598
|
A | T | 1 | a0001c0001t0006g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.545-1139A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595598 | ||||||
chr6:95595659
|
A | C | 1 | a0002c0002t0006g0190 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.545-1078A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595659 | ||||||
chr6:95595797
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.545-940C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595797 | ||||||
chr6:95595948
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0143a0001c0001t0001g0146others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.545-789C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95595948 | ||||||
chr6:95596063
|
A | G | 1 | a0001c0001t0018g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.545-674A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95596063 | ||||||
chr6:95596218
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.545-519G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 2/4 | chr6 | 95596218 | ||||||
chr6:95596885
|
CT | C | 3 | a0001c0001t0003g0012a0001c0001t0003g0089a0001c0001t0008g0194 | 6 | NA18964.hp1 NA18971.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+43delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95596885 | |||||
chr6:95596895
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.654+49A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95596895 | ||||||
chr6:95597236
|
A | G | 4 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0244others(1): Show | 4 | HG02293.hp1 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+390A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597236 | ||||||
chr6:95597344
|
A | C | 3 | a0004c0005t0005g0242a0004c0005t0005g0243a0004c0007t0005g0241 | 3 | HG02602.hp2 HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.654+498A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597344 | ||||||
chr6:95597487
|
C | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+641C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597487 | ||||||
chr6:95597853
|
C | T | 1 | a0001c0001t0002g0049 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.654+1007C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95597853 | ||||||
chr6:95598046
|
A | AT | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(170): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.654+1208dupT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95598046 | |||||
chr6:95598218
|
T | C | 1 | a0001c0001t0004g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.654+1372T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598218 | ||||||
chr6:95598324
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+1478T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598324 | ||||||
chr6:95598427
|
G | A | 1 | a0002c0002t0006g0183 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.654+1581G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598427 | ||||||
chr6:95598487
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.654+1641A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598487 | ||||||
chr6:95598998
|
A | G | 5 | a0003c0003t0007g0249a0003c0003t0007g0250a0003c0003t0007g0251others(2): Show | 5 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+2152A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95598998 | ||||||
chr6:95599093
|
A | G | 1 | a0001c0001t0014g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.654+2247A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599093 | ||||||
chr6:95599137
|
G | T | 5 | a0003c0003t0007g0249a0003c0003t0007g0250a0003c0003t0007g0251others(2): Show | 5 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.654+2291G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599137 | ||||||
chr6:95599157
|
G | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+2311G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599157 | ||||||
chr6:95599288
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+2442C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599288 | ||||||
chr6:95599330
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+2484T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599330 | ||||||
chr6:95599408
|
G | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0056others(20): Show | 30 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.654+2562G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599408 | ||||||
chr6:95599412
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.654+2566A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599412 | ||||||
chr6:95599416
|
CA | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(189): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.654+2586delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95599416 | |||||
chr6:95599435
|
G | A | 1 | a0004c0004t0005g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.654+2589G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599435 | ||||||
chr6:95599436
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.654+2590A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599436 | ||||||
chr6:95599660
|
T | C | 110 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(107): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.654+2814T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95599660 | ||||||
chr6:95600085
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0173 | 2 | HG00673.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.654+3239T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600085 | ||||||
chr6:95600411
|
T | A | 1 | a0001c0001t0003g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.654+3565T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600411 | ||||||
chr6:95600507
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.654+3661C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600507 | ||||||
chr6:95600593
|
A | ATGAATAT others(7): Show |
1 | a0001c0001t0002g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.654+3747_654+3748i others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600593 | ||||||
chr6:95600835
|
T | C | 1 | a0001c0001t0012g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.654+3989T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600835 | ||||||
chr6:95600859
|
A | C | 27 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(24): Show | 32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-3968A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95600859 | ||||||
chr6:95601175
|
T | G | 5 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(2): Show | 7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3652T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601175 | ||||||
chr6:95601263
|
C | T | 1 | a0001c0001t0005g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.655-3564C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601263 | ||||||
chr6:95601334
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.655-3493G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601334 | ||||||
chr6:95601380
|
T | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-3447T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601380 | ||||||
chr6:95601433
|
G | C | 5 | a0001c0001t0004g0019a0001c0001t0004g0116a0001c0001t0004g0117others(2): Show | 7 | HG00099.hp2 HG00735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3394G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601433 | ||||||
chr6:95601556
|
A | G | 10 | a0004c0004t0005g0050a0004c0004t0005g0225a0004c0004t0005g0239others(7): Show | 10 | HG02602.hp2 HG02683.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.655-3271A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601556 | ||||||
chr6:95601652
|
C | T | 1 | a0001c0001t0005g0265 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655-3175C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601652 | ||||||
chr6:95601689
|
G | A | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | HG01069.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.655-3138G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601689 | ||||||
chr6:95601716
|
A | ATTT | 5 | a0001c0001t0005g0258a0003c0003t0007g0034a0003c0003t0007g0132others(2): Show | 6 | HG02055.hp2 HG02615.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-3085_655-3083d others(5): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(4): Show |
5 | a0003c0003t0007g0249a0003c0003t0007g0250a0003c0003t0007g0251others(2): Show | 5 | HG01070.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3093_655-3083d others(13): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(5): Show |
4 | a0003c0003t0007g0046a0003c0003t0007g0201a0003c0003t0007g0252others(1): Show | 5 | HG01175.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-3094_655-3083d others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(6): Show |
1 | a0003c0003t0007g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.655-3095_655-3083d others(15): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(14): Show |
2 | a0004c0005t0005g0242a0004c0005t0005g0243 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.655-3103_655-3083d others(23): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(15): Show |
1 | a0004c0004t0005g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.655-3104_655-3083d others(24): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0018g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-3106_655-3083d others(26): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
A | ATTTTTTT others(20): Show |
1 | a0004c0007t0005g0241 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.655-3087_655-3086i others(29): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
AT | A | 6 | a0001c0001t0001g0169a0001c0001t0003g0068a0001c0001t0003g0111others(3): Show | 6 | HG00735.hp1 HG02818.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-3083delT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
ATT | A | 52 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(49): Show | 64 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.655-3084_655-3083d others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
ATTT | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(169): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.655-3085_655-3083d others(5): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
ATTTT | A | 18 | a0001c0001t0002g0238a0001c0001t0004g0121a0001c0001t0009g0163others(15): Show | 20 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.655-3086_655-3083d others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
ATTTTT | A | 5 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(2): Show | 7 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-3087_655-3083d others(7): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.655-3092_655-3083d others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601716
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0004g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.655-3094_655-3083d others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95601716 | |||||
chr6:95601816
|
T | G | 1 | a0002c0002t0006g0196 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.655-3011T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601816 | ||||||
chr6:95601946
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.655-2881A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95601946 | ||||||
chr6:95602218
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(37): Show | 69 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.655-2609G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602218 | ||||||
chr6:95602298
|
C | A | 1 | a0001c0001t0004g0115 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.655-2529C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602298 | ||||||
chr6:95602525
|
G | A | 2 | a0001c0001t0012g0055a0001c0001t0012g0264 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.655-2302G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602525 | ||||||
chr6:95602585
|
T | G | 1 | a0001c0001t0018g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-2242T>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602585 | ||||||
chr6:95602674
|
A | G | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | HG01069.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.655-2153A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602674 | ||||||
chr6:95602743
|
G | A | 1 | a0001c0001t0019g0139 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.655-2084G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602743 | ||||||
chr6:95602877
|
G | A | 1 | a0001c0001t0005g0207 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.655-1950G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602877 | ||||||
chr6:95602933
|
T | A | 1 | a0001c0001t0003g0025 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.655-1894T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602933 | ||||||
chr6:95602962
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.655-1865G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95602962 | ||||||
chr6:95603026
|
C | CA | 22 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0213others(19): Show | 25 | HG00741.hp1 HG01109.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.655-1775dupA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95603026 | |||||
chr6:95603026
|
CA | C | 108 | a0001c0001t0002g0221a0001c0001t0002g0232a0001c0001t0002g0236others(105): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.655-1775delA | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95603026 | |||||
chr6:95603052
|
A | AAAAAAC | 7 | a0001c0001t0001g0156a0001c0001t0009g0137a0001c0001t0009g0150others(4): Show | 7 | HG02132.hp1 NA18747.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.655-1775_655-1774i others(8): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603052 | ||||||
chr6:95603052
|
A | AC | 16 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0041others(13): Show | 24 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.655-1775_655-1774i others(3): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603052 | ||||||
chr6:95603052
|
A | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(31): Show | 61 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.655-1775A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603052 | ||||||
chr6:95603102
|
A | C | 1 | a0001c0001t0002g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655-1725A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603102 | ||||||
chr6:95603182
|
T | C | 1 | a0008c0010t0004g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.655-1645T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603182 | ||||||
chr6:95603300
|
A | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-1527A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603300 | ||||||
chr6:95603388
|
A | C | 27 | a0001c0001t0006g0024a0001c0001t0006g0259a0001c0001t0006g0268others(24): Show | 32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.655-1439A>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603388 | ||||||
chr6:95603397
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.655-1430C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603397 | ||||||
chr6:95603507
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-1320A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603507 | ||||||
chr6:95603545
|
A | AT | 4 | a0001c0001t0005g0054a0001c0001t0005g0260a0001c0001t0005g0261others(1): Show | 5 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-1274dupT | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95603545 | |||||
chr6:95603553
|
T | A | 111 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(108): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.655-1274T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603553 | ||||||
chr6:95603636
|
A | G | 1 | a0001c0001t0004g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655-1191A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603636 | ||||||
chr6:95603769
|
G | C | 1 | a0001c0001t0017g0027 | 2 | NA18955.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.655-1058G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603769 | ||||||
chr6:95603945
|
C | A | 3 | a0001c0001t0003g0080a0001c0001t0003g0083a0001c0001t0025g0082 | 3 | HG01243.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.655-882C>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603945 | ||||||
chr6:95603992
|
T | A | 2 | a0001c0001t0012g0055a0001c0001t0012g0264 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.655-835T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95603992 | ||||||
chr6:95604016
|
C | CAT | 5 | a0001c0001t0004g0126a0003c0003t0007g0034a0003c0003t0007g0132others(2): Show | 6 | HG01346.hp2 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-799_655-798dup others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604016 | |||||
chr6:95604042
|
G | A | 1 | a0001c0001t0003g0195 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.655-785G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604042 | ||||||
chr6:95604045
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.655-782C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604045 | ||||||
chr6:95604056
|
A | AGGTGTGT others(5): Show |
4 | a0001c0001t0004g0073a0001c0001t0004g0102a0001c0001t0004g0103others(1): Show | 4 | HG02258.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-771_655-770ins others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604056 | ||||||
chr6:95604060
|
A | G | 5 | a0001c0001t0004g0073a0001c0001t0004g0102a0001c0001t0004g0103others(2): Show | 5 | HG01433.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.655-767A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604060 | ||||||
chr6:95604061
|
G | GGGGTGT | 4 | a0003c0003t0007g0046a0003c0003t0007g0200a0003c0003t0007g0201others(1): Show | 5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-765_655-764ins others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGGGTGTG others(5): Show |
2 | a0003c0003t0007g0132a0003c0003t0007g0249 | 2 | NA19043.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.655-765_655-764ins others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGGGTGTG others(7): Show |
4 | a0003c0003t0007g0250a0003c0003t0007g0251a0003c0003t0007g0252others(1): Show | 4 | HG01070.hp1 HG01099.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.655-765_655-764ins others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGGGTGTG others(9): Show |
1 | a0003c0003t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.655-765_655-764ins others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
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G | GGGGTGTG others(11): Show |
2 | a0003c0003t0007g0034a0003c0003t0007g0134 | 3 | HG02055.hp2 HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.655-765_655-764ins others(18): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGT | 33 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0166others(30): Show | 41 | HG00558.hp1 HG00673.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.655-733_655-732dup others(2): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGT | 38 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0035others(35): Show | 69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.655-735_655-732dup others(4): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGT | 6 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0160others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-737_655-732dup others(6): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(1): Show |
29 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0057others(26): Show | 38 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.655-739_655-732dup others(8): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(3): Show |
18 | a0001c0001t0001g0056a0001c0001t0001g0164a0001c0001t0003g0011others(15): Show | 23 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-741_655-732dup others(10): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(5): Show |
25 | a0001c0001t0003g0003a0001c0001t0003g0010a0001c0001t0003g0031others(22): Show | 36 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.655-743_655-732dup others(12): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(7): Show |
26 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0063others(23): Show | 33 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.655-745_655-732dup others(14): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(9): Show |
30 | a0001c0001t0003g0018a0001c0001t0003g0025a0001c0001t0003g0026others(27): Show | 34 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.655-747_655-732dup others(16): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(11): Show |
8 | a0001c0001t0003g0066a0001c0001t0004g0013a0001c0001t0004g0016others(5): Show | 14 | HG00621.hp2 HG01346.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.655-749_655-732dup others(18): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(13): Show |
13 | a0001c0001t0003g0060a0001c0001t0003g0067a0001c0001t0004g0006others(10): Show | 19 | HG00597.hp2 HG01069.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.655-751_655-732dup others(20): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(15): Show |
2 | a0001c0001t0003g0084a0001c0001t0004g0121 | 2 | HG01257.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.655-753_655-732dup others(22): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(17): Show |
1 | a0001c0001t0004g0128 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.655-755_655-732dup others(24): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | GGTGTGTG others(19): Show |
2 | a0001c0001t0003g0085a0001c0001t0004g0061 | 2 | HG01175.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.655-757_655-732dup others(26): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 95604061 | |||||
chr6:95604061
|
G | T | 5 | a0001c0001t0004g0073a0001c0001t0004g0102a0001c0001t0004g0103others(2): Show | 5 | HG01433.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.655-766G>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604061 | ||||||
chr6:95604273
|
G | C | 4 | a0003c0003t0007g0046a0003c0003t0007g0200a0003c0003t0007g0201others(1): Show | 5 | HG01109.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.655-554G>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604273 | ||||||
chr6:95604466
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.655-361C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604466 | ||||||
chr6:95604611
|
T | C | 1 | a0001c0001t0023g0130 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.655-216T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604611 | ||||||
chr6:95604718
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-109T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | chr6 | 95604718 | ||||||
chr6:95604937
|
A | G | 5 | a0001c0001t0004g0073a0001c0001t0004g0102a0001c0001t0004g0103others(2): Show | 5 | HG01433.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+34A>G | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95604937 | ||||||
chr6:95605111
|
T | C | 3 | a0002c0002t0006g0182a0002c0002t0006g0184a0002c0002t0006g0187 | 3 | HG01106.hp1 HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.731+208T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605111 | ||||||
chr6:95605193
|
A | T | 2 | a0005c0006t0005g0204a0005c0006t0005g0208 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.731+290A>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605193 | ||||||
chr6:95605303
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.731+400C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605303 | ||||||
chr6:95605454
|
T | C | 120 | a0001c0001t0001g0156a0001c0001t0003g0003a0001c0001t0003g0009others(117): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.732-294T>C | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605454 | ||||||
chr6:95605474
|
G | A | 12 | a0001c0001t0001g0035a0001c0001t0001g0138a0001c0001t0001g0142others(9): Show | 12 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.732-274G>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605474 | ||||||
chr6:95605565
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.732-183C>T | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605565 | ||||||
chr6:95605602
|
T | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0021others(197): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.732-146T>A | MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 4/4 | chr6 | 95605602 |