geneid | 4224 |
---|---|
ensemblid | ENSG00000112818.11 |
hgncid | 7015 |
symbol | MEP1A |
name | meprin A subunit alpha |
refseq_nuc | NM_005588.3 |
refseq_prot | NP_005579.2 |
ensembl_nuc | ENST00000230588.9 |
ensembl_prot | ENSP00000230588.4 |
mane_status | MANE Select |
chr | chr6 |
start | 46793389 |
end | 46839778 |
strand | + |
ver | v1.2 |
region | chr6:46793389-46839778 |
region5000 | chr6:46788389-46844778 |
regionname0 | MEP1A_chr6_46793389_46839778 |
regionname5000 | MEP1A_chr6_46788389_46844778 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 746 | 117 | 27 | 19 | 58 | 2 | 11 | 50 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002 | 1/0 | 746 | 94 | 5 | 20 | 55 | 3 | 10 | 46 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0003 | 0/1 | 746 | 62 | 10 | 12 | 20 | 6 | 13 | 18 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004 | 0/0 | 746 | 23 | 19 | 2 | 2 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0005 | 0/0 | 746 | 16 | 4 | 5 | 6 | 0 | 1 | 4 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0006 | 0/0 | 746 | 11 | 6 | 1 | 3 | 0 | 1 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007 | 0/0 | 746 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0008 | 0/0 | 746 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0009 | 0/0 | 746 | 4 | 0 | 0 | 0 | 2 | 2 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0010 | 0/0 | 746 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0011 | 0/0 | 746 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0012 | 0/0 | 746 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0013 | 0/0 | 746 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0014 | 0/0 | 746 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0015 | 0/0 | 746 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0016 | 0/0 | 746 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0017 | 0/0 | 746 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2241 | 115 | 27 | 19 | 58 | 2 | 9 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0002 | 1/0 | 2241 | 93 | 5 | 19 | 55 | 3 | 10 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0003 | 0/1 | 2241 | 62 | 10 | 12 | 20 | 6 | 13 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0004 | 0/0 | 2241 | 21 | 18 | 1 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0005 | 0/0 | 2241 | 11 | 6 | 1 | 3 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0006 | 0/0 | 2241 | 10 | 4 | 5 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0007 | 0/0 | 2241 | 9 | 8 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0008 | 0/0 | 2241 | 6 | 0 | 0 | 6 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0009 | 0/0 | 2241 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0010 | 0/0 | 2241 | 4 | 0 | 0 | 0 | 2 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0011 | 0/0 | 2241 | 3 | 0 | 0 | 0 | 0 | 3 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0012 | 0/0 | 2241 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0013 | 0/0 | 2241 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0014 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0015 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0016 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0017 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0018 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0019 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0020 | 0/0 | 2241 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0021 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0022 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
c0023 | 0/0 | 2241 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 665 | 128 | 29 | 19 | 62 | 4 | 14 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0002 | 1/0 | 653 | 110 | 21 | 21 | 54 | 3 | 10 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0003 | 0/1 | 665 | 96 | 24 | 18 | 29 | 7 | 17 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0004 | 0/0 | 653 | 7 | 6 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0005 | 0/0 | 653 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0006 | 0/0 | 653 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0007 | 0/0 | 665 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0008 | 0/0 | 665 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0009 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0010 | 0/0 | 653 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
t0011 | 0/0 | 665 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0286 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2241 | 115 | 27 | 19 | 58 | 2 | 9 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0001c0013 | 0/0 | 2241 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002c0002 | 1/0 | 2241 | 93 | 5 | 19 | 55 | 3 | 10 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002c0020 | 0/0 | 2241 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0003c0003 | 0/1 | 2241 | 62 | 10 | 12 | 20 | 6 | 13 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0004 | 0/0 | 2241 | 21 | 18 | 1 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0021 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0023 | 0/0 | 2241 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0005c0006 | 0/0 | 2241 | 10 | 4 | 5 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0005c0008 | 0/0 | 2241 | 6 | 0 | 0 | 6 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0006c0005 | 0/0 | 2241 | 11 | 6 | 1 | 3 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007c0007 | 0/0 | 2241 | 9 | 8 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007c0017 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0008c0009 | 0/0 | 2241 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0009c0010 | 0/0 | 2241 | 4 | 0 | 0 | 0 | 2 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0010c0011 | 0/0 | 2241 | 3 | 0 | 0 | 0 | 0 | 3 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0011c0012 | 0/0 | 2241 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0012c0015 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0013c0016 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0014c0019 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0015c0018 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0016c0022 | 0/0 | 2241 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0017c0014 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2905 | 108 | 21 | 19 | 57 | 2 | 9 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0001c0001t0005 | 0/0 | 2893 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0001c0001t0006 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0001c0001t0008 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0001c0013t0001 | 0/0 | 2905 | 2 | 0 | 0 | 0 | 0 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002c0002t0001 | 0/0 | 2905 | 4 | 0 | 0 | 4 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002c0002t0002 | 1/0 | 2893 | 88 | 5 | 18 | 51 | 3 | 10 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002c0002t0007 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0002c0020t0002 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0003c0003t0003 | 0/1 | 2905 | 61 | 10 | 12 | 20 | 6 | 12 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0003c0003t0011 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0004t0001 | 0/0 | 2905 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0004t0002 | 0/0 | 2893 | 15 | 12 | 1 | 2 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0004t0003 | 0/0 | 2905 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0021t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0004c0023t0002 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0005c0006t0003 | 0/0 | 2905 | 10 | 4 | 5 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0005c0008t0003 | 0/0 | 2905 | 6 | 0 | 0 | 6 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0006c0005t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0006c0005t0003 | 0/0 | 2905 | 10 | 5 | 1 | 3 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007c0007t0003 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007c0007t0004 | 0/0 | 2893 | 7 | 6 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007c0007t0010 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0007c0017t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0008c0009t0001 | 0/0 | 2905 | 4 | 4 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0009c0010t0001 | 0/0 | 2905 | 4 | 0 | 0 | 0 | 2 | 2 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0010c0011t0003 | 0/0 | 2905 | 3 | 0 | 0 | 0 | 0 | 3 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0011c0012t0002 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0012c0015t0009 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0013c0016t0003 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0014c0019t0002 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0015c0018t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0016c0022t0001 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
a0017c0014t0001 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | copy fasta | chr6 | 46788389 | 46844778 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0013t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0001c0013t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0286 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0002t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0002c0020t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0003c0003t0011g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0004t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0021t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0004c0023t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0006t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0008t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0008t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0008t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0008t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0008t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0005c0008t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0006c0005t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0007t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0007c0017t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0008c0009t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0008c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0008c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0008c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0009c0010t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0009c0010t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0009c0010t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0009c0010t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0010c0011t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0010c0011t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0010c0011t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0011c0012t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0011c0012t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0012c0015t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0013c0016t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0014c0019t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0015c0018t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0016c0022t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
a0017c0014t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0285 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00099 | hp2 | a0003 | c0003 | t0003 | g0051 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00140 | hp1 | a0013 | c0016 | t0003 | g0108 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0266 | EUR | GBR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00280 | hp2 | a0003 | c0003 | t0003 | g0015 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0057 | EUR | FIN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00408 | hp2 | a0014 | c0019 | t0002 | g0281 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00544 | hp1 | a0003 | c0003 | t0003 | g0043 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00544 | hp2 | a0016 | c0022 | t0001 | g0176 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00639 | hp1 | a0003 | c0003 | t0003 | g0347 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00639 | hp2 | a0005 | c0006 | t0003 | g0102 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0301 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0324 | EAS | CHS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00733 | hp1 | a0003 | c0003 | t0003 | g0106 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0320 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00738 | hp2 | a0003 | c0003 | t0003 | g0056 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG00741 | hp2 | a0004 | c0023 | t0002 | g0141 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01069 | hp1 | a0005 | c0006 | t0003 | g0060 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0276 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01071 | hp2 | a0005 | c0006 | t0003 | g0059 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0278 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0314 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0326 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01106 | hp2 | a0006 | c0005 | t0003 | g0124 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0275 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01167 | hp2 | a0005 | c0006 | t0003 | g0110 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0323 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01175 | hp1 | a0002 | c0002 | t0007 | g0262 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01175 | hp2 | a0005 | c0006 | t0003 | g0105 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01192 | hp1 | a0003 | c0003 | t0003 | g0104 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0315 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01243 | hp2 | a0007 | c0007 | t0004 | g0137 | AMR | PUR | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01255 | hp1 | a0004 | c0004 | t0002 | g0144 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0331 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0302 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01346 | hp1 | a0003 | c0003 | t0003 | g0048 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01346 | hp2 | a0002 | c0020 | t0002 | g0135 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01358 | hp1 | a0003 | c0003 | t0003 | g0050 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0308 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0045 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0265 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01496 | hp1 | a0003 | c0003 | t0003 | g0346 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0316 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01515 | hp2 | a0003 | c0003 | t0003 | g0053 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01516 | hp1 | a0003 | c0003 | t0003 | g0055 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01516 | hp2 | a0009 | c0010 | t0001 | g0213 | EUR | IBS | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01884 | hp1 | a0004 | c0004 | t0001 | g0114 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01884 | hp2 | a0007 | c0007 | t0004 | g0012 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01891 | hp1 | a0007 | c0007 | t0003 | g0037 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01928 | hp2 | a0003 | c0003 | t0003 | g0077 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0313 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01952 | hp2 | a0003 | c0003 | t0003 | g0052 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02055 | hp2 | a0003 | c0003 | t0003 | g0014 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02056 | hp2 | a0006 | c0005 | t0003 | g0023 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02129 | hp2 | a0005 | c0008 | t0003 | g0075 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0337 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02145 | hp1 | a0003 | c0003 | t0003 | g0116 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02145 | hp2 | a0011 | c0012 | t0002 | g0134 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02155 | hp1 | a0005 | c0008 | t0003 | g0078 | EAS | CDX | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0345 | EAS | CDX | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02257 | hp2 | a0006 | c0005 | t0003 | g0123 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02258 | hp1 | a0003 | c0003 | t0003 | g0111 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02273 | hp2 | a0003 | c0003 | t0003 | g0349 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02280 | hp1 | a0008 | c0009 | t0001 | g0026 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02280 | hp2 | a0004 | c0004 | t0002 | g0150 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02523 | hp1 | a0003 | c0003 | t0003 | g0074 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | KHV | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02602 | hp1 | a0003 | c0003 | t0003 | g0054 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02615 | hp2 | a0006 | c0005 | t0002 | g0018 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02622 | hp1 | a0004 | c0004 | t0002 | g0147 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02622 | hp2 | a0004 | c0004 | t0003 | g0004 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02630 | hp1 | a0003 | c0003 | t0003 | g0118 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0289 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0094 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02698 | hp2 | a0009 | c0010 | t0001 | g0214 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02723 | hp1 | a0007 | c0007 | t0004 | g0138 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02738 | hp1 | a0003 | c0003 | t0003 | g0082 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02818 | hp2 | a0003 | c0003 | t0003 | g0113 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02886 | hp2 | a0006 | c0005 | t0003 | g0122 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02896 | hp1 | a0004 | c0004 | t0002 | g0149 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02896 | hp2 | a0008 | c0009 | t0001 | g0027 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02897 | hp1 | a0003 | c0003 | t0003 | g0112 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02897 | hp2 | a0004 | c0004 | t0002 | g0148 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0130 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02965 | hp1 | a0004 | c0004 | t0003 | g0003 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0129 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02970 | hp1 | a0004 | c0004 | t0002 | g0142 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02976 | hp1 | a0007 | c0007 | t0004 | g0011 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02976 | hp2 | a0003 | c0003 | t0003 | g0117 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03041 | hp2 | a0005 | c0006 | t0003 | g0107 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03098 | hp1 | a0003 | c0003 | t0003 | g0085 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03098 | hp2 | a0004 | c0004 | t0002 | g0143 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03130 | hp1 | a0008 | c0009 | t0001 | g0025 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03130 | hp2 | a0003 | c0003 | t0003 | g0119 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03139 | hp1 | a0007 | c0007 | t0004 | g0010 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03139 | hp2 | a0008 | c0009 | t0001 | g0028 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03195 | hp1 | a0006 | c0005 | t0003 | g0030 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03209 | hp1 | a0005 | c0006 | t0003 | g0109 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03225 | hp1 | a0004 | c0004 | t0003 | g0121 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03225 | hp2 | a0007 | c0007 | t0004 | g0008 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0268 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03239 | hp2 | a0005 | c0006 | t0003 | g0049 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03453 | hp1 | a0006 | c0005 | t0003 | g0017 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03486 | hp1 | a0004 | c0004 | t0002 | g0001 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0267 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03491 | hp2 | a0001 | c0013 | t0001 | g0204 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03492 | hp1 | a0001 | c0013 | t0001 | g0206 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03492 | hp2 | a0010 | c0011 | t0003 | g0070 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03516 | hp1 | a0011 | c0012 | t0002 | g0132 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03516 | hp2 | a0004 | c0004 | t0002 | g0151 | AFR | ESN | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03540 | hp1 | a0004 | c0004 | t0003 | g0005 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03579 | hp1 | a0004 | c0004 | t0002 | g0145 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03579 | hp2 | a0005 | c0006 | t0003 | g0103 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03654 | hp1 | a0003 | c0003 | t0003 | g0093 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0264 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0072 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0269 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03688 | hp1 | a0003 | c0003 | t0003 | g0046 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0287 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0309 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0125 | SAS | PJL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03831 | hp1 | a0003 | c0003 | t0003 | g0061 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03831 | hp2 | a0003 | c0003 | t0003 | g0058 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03834 | hp1 | a0006 | c0005 | t0003 | g0022 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03927 | hp1 | a0003 | c0003 | t0003 | g0081 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03942 | hp1 | a0017 | c0014 | t0001 | g0232 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03942 | hp2 | a0003 | c0003 | t0003 | g0092 | SAS | BEB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04115 | hp1 | a0010 | c0011 | t0003 | g0068 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04115 | hp2 | a0009 | c0010 | t0001 | g0205 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04199 | hp1 | a0003 | c0003 | t0003 | g0067 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG04228 | hp2 | a0010 | c0011 | t0003 | g0076 | SAS | STU | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18522 | hp2 | a0003 | c0003 | t0003 | g0115 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18906 | hp2 | a0004 | c0004 | t0002 | g0152 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18941 | hp1 | a0003 | c0003 | t0003 | g0066 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0016 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18945 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18946 | hp2 | a0006 | c0005 | t0003 | g0024 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18951 | hp1 | a0006 | c0005 | t0003 | g0021 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18954 | hp2 | a0005 | c0008 | t0003 | g0083 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0306 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18960 | hp2 | a0003 | c0003 | t0003 | g0047 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18961 | hp1 | a0005 | c0008 | t0003 | g0084 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18962 | hp1 | a0003 | c0003 | t0003 | g0073 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18967 | hp2 | a0004 | c0004 | t0002 | g0098 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18972 | hp1 | a0003 | c0003 | t0003 | g0088 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18973 | hp1 | a0003 | c0003 | t0003 | g0080 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0344 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18980 | hp1 | a0003 | c0003 | t0003 | g0044 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18989 | hp2 | a0003 | c0003 | t0003 | g0089 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18990 | hp1 | a0005 | c0008 | t0003 | g0090 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18998 | hp1 | a0004 | c0004 | t0002 | g0071 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18999 | hp1 | a0005 | c0008 | t0003 | g0086 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19007 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0321 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19010 | hp1 | a0003 | c0003 | t0003 | g0079 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19030 | hp1 | a0007 | c0007 | t0010 | g0136 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19043 | hp1 | a0007 | c0017 | t0001 | g0019 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0329 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19054 | hp2 | a0003 | c0003 | t0003 | g0065 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19059 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19060 | hp1 | a0003 | c0003 | t0003 | g0097 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19062 | hp2 | a0003 | c0003 | t0003 | g0096 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19064 | hp2 | a0003 | c0003 | t0003 | g0087 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0327 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19072 | hp2 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19079 | hp1 | a0003 | c0003 | t0003 | g0064 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0343 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19086 | hp1 | a0003 | c0003 | t0003 | g0091 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0325 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA19240 | hp2 | a0005 | c0006 | t0003 | g0100 | AFR | YRI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20129 | hp2 | a0004 | c0004 | t0002 | g0001 | AFR | ASW | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20752 | hp1 | a0009 | c0010 | t0001 | g0209 | EUR | TSI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20752 | hp2 | a0003 | c0003 | t0003 | g0101 | EUR | TSI | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20905 | hp1 | a0003 | c0003 | t0011 | g0095 | SAS | GIH | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0312 | SAS | GIH | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0332 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG01123 | hp2 | a0003 | c0003 | t0003 | g0013 | AMR | CLM | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02109 | hp1 | a0006 | c0005 | t0003 | g0020 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02109 | hp2 | a0004 | c0021 | t0002 | g0038 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02486 | hp1 | a0015 | c0018 | t0001 | g0029 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG02559 | hp2 | a0004 | c0004 | t0002 | g0146 | AFR | ACB | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
HG03471 | hp2 | a0007 | c0007 | t0004 | g0009 | AFR | MSL | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0099 | EAS | JPT | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0128 | AFR | USA | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0348 | AFR | USA | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
NA21309 | hp2 | a0012 | c0015 | t0009 | g0002 | AFR | LWK | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0003 | g0139 | REF | REF | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0286 | REF | REF | MEP1A_chr6_46788389_46844778 | MEP1A | chr6 | 46788389 | 46844778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46793456
|
G | A | 1 | a0017 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.58G>A | p.Ala20Thr | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 1/14 | 68/2893 | 58/2241 | 20/746 | chr6 | 46793456 | ||
chr6:46799146
|
C | A | 1 | a0012 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.227C>A | p.Thr76Lys | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/14 | 237/2893 | 227/2241 | 76/746 | chr6 | 46799146 | ||
chr6:46829452
|
A | G | 1 | a0016 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.1025A>G | p.Gln342Arg | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/14 | 1035/2893 | 1025/2241 | 342/746 | chr6 | 46829452 | ||
chr6:46833086
|
A | G | 1 | a0015 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1157A>G | p.His386Arg | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1167/2893 | 1157/2241 | 386/746 | chr6 | 46833086 | ||
chr6:46833116
|
A | G | 1 | a0011 | 2 | HG02145.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1187A>G | p.Lys396Arg | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1197/2893 | 1187/2241 | 396/746 | chr6 | 46833116 | ||
chr6:46833334
|
G | T | 9 | a0003a0004a0005others(6): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
missense_variant | MODERATE | c.1405G>T | p.Val469Leu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1415/2893 | 1405/2241 | 469/746 | chr6 | 46833334 | ||
chr6:46833355
|
A | G | 1 | a0006 | 11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
missense_variant | MODERATE | c.1426A>G | p.Arg476Gly | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1436/2893 | 1426/2241 | 476/746 | chr6 | 46833355 | ||
chr6:46833377
|
G | C | 1 | a0011 | 2 | HG02145.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1448G>C | p.Arg483Thr | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1458/2893 | 1448/2241 | 483/746 | chr6 | 46833377 | ||
chr6:46833421
|
G | A | 1 | a0014 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1492G>A | p.Glu498Lys | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1502/2893 | 1492/2241 | 498/746 | chr6 | 46833421 | ||
chr6:46833477
|
T | A | 1 | a0013 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1548T>A | p.Asp516Glu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1558/2893 | 1548/2241 | 516/746 | chr6 | 46833477 | ||
chr6:46833482
|
G | A | 1 | a0005 | 16 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
missense_variant | MODERATE | c.1553G>A | p.Arg518Gln | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1563/2893 | 1553/2241 | 518/746 | chr6 | 46833482 | ||
chr6:46835281
|
A | T | 6 | a0001a0008a0009others(3): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
missense_variant | MODERATE | c.1816A>T | p.Thr606Ser | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/14 | 1826/2893 | 1816/2241 | 606/746 | chr6 | 46835281 | ||
chr6:46835365
|
A | G | 7 | a0001a0007a0008others(4): Show | 138 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
missense_variant | MODERATE | c.1900A>G | p.Met634Val | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/14 | 1910/2893 | 1900/2241 | 634/746 | chr6 | 46835365 | ||
chr6:46835426
|
C | T | 1 | a0010 | 3 | HG03492.hp2 HG04115.hp1 HG04228.hp2 |
missense_variant | MODERATE | c.1961C>T | p.Ser654Leu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/14 | 1971/2893 | 1961/2241 | 654/746 | chr6 | 46835426 | ||
chr6:46839029
|
G | A | 1 | a0009 | 4 | HG01516.hp2 HG02698.hp2 HG04115.hp2 others(1): Show |
missense_variant | MODERATE | c.2134G>A | p.Val712Met | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 2144/2893 | 2134/2241 | 712/746 | chr6 | 46839029 | ||
chr6:46839072
|
C | T | 4 | a0003a0005a0010others(1): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
missense_variant | MODERATE | c.2177C>T | p.Thr726Met | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 2187/2893 | 2177/2241 | 726/746 | chr6 | 46839072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46809469
|
C | T | 1 | a0001c0013 | 2 | HG03491.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.312C>T | p.Leu104Leu | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/14 | 322/2893 | 312/2241 | 104/746 | chr6 | 46809469 | ||
chr6:46825405
|
C | T | 1 | a0004c0023 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.690C>T | p.Ala230Ala | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/14 | 700/2893 | 690/2241 | 230/746 | chr6 | 46825405 | ||
chr6:46825438
|
G | A | 12 | a0003c0003a0004c0004a0004c0023others(9): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
synonymous_variant | LOW | c.723G>A | p.Gln241Gln | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/14 | 733/2893 | 723/2241 | 241/746 | chr6 | 46825438 | ||
chr6:46833183
|
A | G | 1 | a0005c0008 | 6 | HG02129.hp2 HG02155.hp1 NA18954.hp2 others(3): Show |
synonymous_variant | LOW | c.1254A>G | p.Gly418Gly | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/14 | 1264/2893 | 1254/2241 | 418/746 | chr6 | 46833183 | ||
chr6:46834633
|
G | A | 19 | a0001c0001a0001c0013a0003c0003others(16): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
synonymous_variant | LOW | c.1665G>A | p.Thr555Thr | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/14 | 1675/2893 | 1665/2241 | 555/746 | chr6 | 46834633 | ||
chr6:46834726
|
C | T | 1 | a0002c0020 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1758C>T | p.Asp586Asp | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/14 | 1768/2893 | 1758/2241 | 586/746 | chr6 | 46834726 | ||
chr6:46839079
|
C | T | 1 | a0007c0017 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2184C>T | p.Gly728Gly | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 2194/2893 | 2184/2241 | 728/746 | chr6 | 46839079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46839172
|
C | A | 1 | a0001c0001t0005 | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 36 | chr6 | 46839172 | |||||
chr6:46839202
|
G | T | 9 | a0003c0003t0003a0003c0003t0011a0004c0004t0003others(6): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*66G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 66 | chr6 | 46839202 | |||||
chr6:46839211
|
G | GTTTGGGG others(5): Show |
22 | a0001c0001t0001a0001c0001t0008a0001c0013t0001others(19): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*78_*79insGGGGCAGC others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 79 | INFO_REALIGN_3_PRIME | chr6 | 46839211 | ||||
chr6:46839239
|
C | A | 1 | a0002c0002t0007 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 103 | chr6 | 46839239 | |||||
chr6:46839265
|
C | T | 1 | a0012c0015t0009 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 129 | chr6 | 46839265 | |||||
chr6:46839274
|
C | A | 1 | a0001c0001t0008 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 138 | chr6 | 46839274 | |||||
chr6:46839303
|
C | A | 22 | a0001c0001t0001a0001c0001t0008a0001c0013t0001others(19): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*167C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 167 | chr6 | 46839303 | |||||
chr6:46839349
|
C | A | 1 | a0003c0003t0011 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*213C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 213 | chr6 | 46839349 | |||||
chr6:46839387
|
T | C | 2 | a0001c0001t0005a0001c0001t0006 | 6 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 251 | chr6 | 46839387 | |||||
chr6:46839502
|
A | G | 2 | a0007c0007t0004a0007c0007t0010 | 8 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*366A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 366 | chr6 | 46839502 | |||||
chr6:46839655
|
T | G | 1 | a0007c0007t0010 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 519 | chr6 | 46839655 | |||||
chr6:46839768
|
T | C | 2 | a0001c0001t0005a0001c0001t0006 | 6 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*632T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 14/14 | 632 | chr6 | 46839768 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46793758
|
G | A | 152 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.145+42G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793758 | ||||||
chr6:46793786
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+70T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793786 | ||||||
chr6:46793795
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+79T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793795 | ||||||
chr6:46793797
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+81A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793797 | ||||||
chr6:46793803
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+87T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793803 | ||||||
chr6:46793814
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+98T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793814 | ||||||
chr6:46793836
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+120G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793836 | ||||||
chr6:46793838
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+122G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793838 | ||||||
chr6:46793843
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+127G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793843 | ||||||
chr6:46793849
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+133A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793849 | ||||||
chr6:46793851
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+135T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793851 | ||||||
chr6:46793867
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+151A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793867 | ||||||
chr6:46793869
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+153A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793869 | ||||||
chr6:46793870
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+154A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793870 | ||||||
chr6:46793871
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+155A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793871 | ||||||
chr6:46793877
|
G | A | 6 | a0001c0001t0006g0006a0001c0001t0006g0007a0004c0004t0003g0003others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+161G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793877 | ||||||
chr6:46793914
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+198G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793914 | ||||||
chr6:46793915
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+199C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793915 | ||||||
chr6:46793924
|
C | T | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.145+208C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793924 | ||||||
chr6:46793953
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+237T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793953 | ||||||
chr6:46793961
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+245T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793961 | ||||||
chr6:46793963
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+247T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793963 | ||||||
chr6:46793964
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+248A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793964 | ||||||
chr6:46793975
|
T | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+259T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793975 | ||||||
chr6:46793998
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+282A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46793998 | ||||||
chr6:46794001
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+285G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794001 | ||||||
chr6:46794013
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+297G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794013 | ||||||
chr6:46794030
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+314T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794030 | ||||||
chr6:46794032
|
A | AAGAAACA others(95): Show |
1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.145+317_145+318ins others(102): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46794032 | |||||
chr6:46794129
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.145+413T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794129 | ||||||
chr6:46794142
|
T | C | 5 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(2): Show | 5 | HG01884.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+426T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794142 | ||||||
chr6:46794146
|
T | C | 3 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015 | 3 | HG00280.hp2 HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.145+430T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794146 | ||||||
chr6:46794316
|
G | A | 1 | a0002c0002t0002g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.145+600G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794316 | ||||||
chr6:46794400
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.145+684T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794400 | ||||||
chr6:46794757
|
C | G | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.145+1041C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46794757 | ||||||
chr6:46794830
|
TAG | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0350a0001c0001t0001g0351 | 3 | HG02602.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.145+1117_145+1118d others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46794830 | |||||
chr6:46795020
|
C | A | 1 | a0003c0003t0003g0016 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.145+1304C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795020 | ||||||
chr6:46795020
|
C | T | 1 | a0003c0003t0003g0139 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.145+1304C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795020 | ||||||
chr6:46795100
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.145+1384G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795100 | ||||||
chr6:46795425
|
C | T | 8 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.145+1709C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795425 | ||||||
chr6:46795509
|
T | C | 8 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(5): Show | 8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.145+1793T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795509 | ||||||
chr6:46795695
|
C | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+1979C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795695 | ||||||
chr6:46795783
|
A | G | 7 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+2067A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795783 | ||||||
chr6:46795998
|
A | T | 6 | a0001c0001t0006g0006a0001c0001t0006g0007a0004c0004t0003g0003others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+2282A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46795998 | ||||||
chr6:46796005
|
G | C | 1 | a0002c0002t0002g0158 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.145+2289G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796005 | ||||||
chr6:46796124
|
C | T | 10 | a0002c0002t0002g0126a0002c0002t0002g0127a0002c0002t0002g0128others(7): Show | 10 | HG01261.hp2 HG01346.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.145+2408C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796124 | ||||||
chr6:46796174
|
A | G | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146-2432A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796174 | ||||||
chr6:46796195
|
C | T | 1 | a0003c0003t0003g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146-2411C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796195 | ||||||
chr6:46796199
|
G | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.146-2407G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796199 | ||||||
chr6:46796213
|
A | G | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.146-2393A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796213 | ||||||
chr6:46796226
|
C | T | 97 | a0001c0001t0001g0120a0002c0002t0002g0063a0003c0003t0003g0013others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.146-2380C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796226 | ||||||
chr6:46796252
|
CAAGT | C | 5 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-2353_146-2350d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796252 | ||||||
chr6:46796520
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.146-2086T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796520 | ||||||
chr6:46796807
|
C | G | 3 | a0002c0002t0002g0343a0002c0002t0002g0344a0002c0002t0002g0345 | 3 | HG02155.hp2 NA18975.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.146-1799C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796807 | ||||||
chr6:46796881
|
T | G | 6 | a0001c0001t0006g0006a0001c0001t0006g0007a0004c0004t0003g0003others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1725T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796881 | ||||||
chr6:46796978
|
C | T | 7 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-1628C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46796978 | ||||||
chr6:46797445
|
G | A | 87 | a0002c0002t0002g0063a0003c0003t0003g0013a0003c0003t0003g0014others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.146-1161G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797445 | ||||||
chr6:46797596
|
A | C | 1 | a0001c0001t0001g0342 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.146-1010A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797596 | ||||||
chr6:46797637
|
G | A | 2 | a0003c0003t0003g0043a0003c0003t0003g0044 | 2 | HG00544.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.146-969G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797637 | ||||||
chr6:46797697
|
T | C | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-909T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797697 | ||||||
chr6:46797716
|
C | T | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-890C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797716 | ||||||
chr6:46797772
|
TTTTCTTT others(23): Show |
T | 1 | a0006c0005t0003g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.146-812_146-783del others(30): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797772 | |||||
chr6:46797772
|
TTTTCTTT others(27): Show |
T | 2 | a0006c0005t0003g0122a0006c0005t0003g0123 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.146-812_146-779del others(34): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797772 | |||||
chr6:46797778
|
T | TTC | 4 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0137others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-826_146-825dup others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797778 | |||||
chr6:46797778
|
TTCTTTCT others(7): Show |
T | 2 | a0003c0003t0003g0111a0003c0003t0003g0112 | 2 | HG02258.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.146-812_146-799del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797778 | |||||
chr6:46797782
|
TTCTTTCT others(3): Show |
T | 1 | a0003c0003t0003g0119 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146-812_146-803del others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797782 | |||||
chr6:46797786
|
TTCTTTC | T | 3 | a0003c0003t0003g0113a0003c0003t0003g0115a0004c0004t0001g0114 | 3 | HG01884.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-812_146-807del others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797786 | |||||
chr6:46797790
|
TTC | T | 8 | a0003c0003t0003g0116a0003c0003t0003g0117a0003c0003t0003g0118others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-812_146-811del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797790 | |||||
chr6:46797792
|
C | CTCTT | 18 | a0002c0002t0002g0308a0002c0002t0002g0309a0002c0002t0002g0310others(15): Show | 18 | HG00738.hp1 HG01081.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.146-770_146-767dup others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
C | CTCTTTCT others(1): Show |
15 | a0002c0002t0001g0334a0002c0002t0002g0158a0002c0002t0002g0323others(12): Show | 15 | HG00673.hp2 HG01099.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.146-774_146-767dup others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
C | CTCTTTCT others(5): Show |
3 | a0002c0002t0001g0336a0002c0002t0002g0337a0002c0002t0002g0338 | 3 | HG00438.hp1 HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.146-778_146-767dup others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
C | CTCTTTCT others(9): Show |
1 | a0002c0002t0001g0340 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.146-782_146-767dup others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
C | CTT | 3 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0138 | 3 | HG02723.hp1 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.146-813_146-812ins others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
C | T | 6 | a0002c0002t0002g0341a0006c0005t0003g0020a0006c0005t0003g0021others(3): Show | 6 | HG02056.hp2 HG02109.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-814C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797792 | ||||||
chr6:46797792
|
CTCTT | C | 25 | a0002c0002t0002g0131a0002c0002t0002g0133a0002c0002t0002g0263others(22): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.146-770_146-767del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
CTCTTTCT others(1): Show |
C | 23 | a0001c0001t0005g0042a0002c0002t0002g0128a0002c0002t0002g0129others(20): Show | 23 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.146-774_146-767del others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
CTCTTTCT others(5): Show |
C | 54 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(51): Show | 54 | HG00544.hp1 HG00639.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.146-778_146-767del others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
CTCTTTCT others(9): Show |
C | 23 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.146-782_146-767del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
CTCTTTCT others(13): Show |
C | 118 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(115): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.146-786_146-767del others(20): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797792
|
CTCTTTCT others(17): Show |
C | 2 | a0001c0001t0001g0160a0003c0003t0003g0045 | 2 | HG01361.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.146-790_146-767del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797792 | |||||
chr6:46797798
|
CTT | C | 3 | a0003c0003t0003g0116a0003c0003t0003g0117a0003c0003t0003g0118 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.146-806_146-805del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797798 | |||||
chr6:46797802
|
CTT | C | 3 | a0003c0003t0003g0113a0003c0003t0003g0115a0004c0004t0001g0114 | 3 | HG01884.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146-802_146-801del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797802 | |||||
chr6:46797808
|
T | TTC | 3 | a0006c0005t0003g0021a0006c0005t0003g0022a0006c0005t0003g0023 | 3 | HG02056.hp2 HG03834.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.146-796_146-795dup others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797808 | |||||
chr6:46797810
|
CTT | C | 3 | a0003c0003t0003g0111a0003c0003t0003g0112a0006c0005t0003g0020 | 3 | HG02109.hp1 HG02258.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.146-794_146-793del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797810 | |||||
chr6:46797836
|
T | C | 1 | a0005c0006t0003g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.146-770T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797836 | ||||||
chr6:46797840
|
C | T | 2 | a0002c0002t0002g0322a0002c0002t0002g0339 | 2 | NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.146-766C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797840 | ||||||
chr6:46797844
|
C | T | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-762C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797844 | ||||||
chr6:46797848
|
T | C | 2 | a0002c0002t0002g0322a0007c0007t0003g0037 | 2 | HG01891.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.146-758T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797848 | ||||||
chr6:46797856
|
T | C | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-750T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797856 | ||||||
chr6:46797860
|
T | C | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-746T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797860 | ||||||
chr6:46797861
|
A | T | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-745A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797861 | ||||||
chr6:46797868
|
A | T | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-738A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797868 | ||||||
chr6:46797869
|
C | T | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-737C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797869 | ||||||
chr6:46797871
|
T | TTTCC | 8 | a0002c0002t0002g0265a0002c0002t0002g0274a0002c0002t0002g0275others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-679_146-676dup others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797871 | |||||
chr6:46797878
|
C | T | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-728C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797878 | ||||||
chr6:46797881
|
T | A | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.146-725T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797881 | ||||||
chr6:46797899
|
CTTCCTTC others(25): Show |
C | 2 | a0001c0001t0001g0254a0003c0003t0003g0094 | 2 | HG02698.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.146-676_146-645del others(32): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797899 | |||||
chr6:46797903
|
CTTCCTTC others(21): Show |
C | 26 | a0001c0001t0001g0160a0001c0001t0001g0233a0001c0001t0001g0234others(23): Show | 26 | HG00408.hp1 HG00673.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.146-675_146-648del others(28): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797903 | |||||
chr6:46797907
|
CTTCCTTC others(17): Show |
C | 48 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0001t0001g0156others(45): Show | 48 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.146-675_146-652del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797907 | |||||
chr6:46797911
|
C | A | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-695C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797911 | ||||||
chr6:46797911
|
CTTCCTTC others(13): Show |
C | 67 | a0001c0001t0001g0036a0001c0001t0001g0157a0001c0001t0001g0159others(64): Show | 67 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.146-675_146-656del others(20): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797911 | |||||
chr6:46797915
|
CTTCCTTC others(9): Show |
C | 25 | a0001c0001t0001g0140a0001c0001t0001g0186a0001c0001t0001g0187others(22): Show | 25 | HG00323.hp1 HG00544.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.146-675_146-660del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797915 | |||||
chr6:46797919
|
CTTCCTTC others(5): Show |
C | 25 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(22): Show | 25 | HG01070.hp1 HG01106.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.146-675_146-664del others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797919 | |||||
chr6:46797923
|
CTTCCTTC others(1): Show |
C | 17 | a0002c0002t0001g0300a0002c0002t0001g0334a0002c0002t0002g0268others(14): Show | 17 | HG00609.hp1 HG00642.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.146-675_146-668del others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797923 | |||||
chr6:46797927
|
C | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.146-679C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797927 | ||||||
chr6:46797927
|
CTTCT | C | 14 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(11): Show | 14 | HG00280.hp1 HG00438.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.146-675_146-672del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797927 | |||||
chr6:46797931
|
T | C | 56 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(53): Show | 57 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.146-675T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797931 | ||||||
chr6:46797931
|
TTTCC | T | 29 | a0002c0002t0001g0336a0002c0002t0001g0340a0002c0002t0002g0129others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.146-648_146-645del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797931 | |||||
chr6:46797931
|
TTTCCTTC others(1): Show |
T | 22 | a0001c0001t0001g0153a0001c0001t0001g0166a0001c0001t0001g0167others(19): Show | 22 | HG00544.hp2 HG00741.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.146-652_146-645del others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797931 | |||||
chr6:46797931
|
TTTCCTTC others(5): Show |
T | 7 | a0002c0002t0002g0063a0003c0003t0003g0046a0003c0003t0003g0061others(4): Show | 7 | HG02523.hp2 HG03688.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-656_146-645del others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797931 | |||||
chr6:46797935
|
C | CTTCCTTC others(5): Show |
1 | a0002c0002t0002g0158 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.146-660_146-659ins others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797935 | |||||
chr6:46797935
|
C | CTTCT | 7 | a0002c0002t0002g0131a0002c0002t0002g0261a0002c0002t0002g0263others(4): Show | 7 | HG00609.hp2 HG02145.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-668_146-667ins others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797935 | |||||
chr6:46797935
|
C | T | 50 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(47): Show | 50 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.146-671C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797935 | ||||||
chr6:46797939
|
C | CTTCT | 10 | a0004c0004t0002g0001a0004c0004t0002g0143a0004c0004t0002g0144others(7): Show | 11 | HG01255.hp1 HG02559.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.146-664_146-663ins others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr6 | 46797939 | |||||
chr6:46797939
|
C | T | 128 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.146-667C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797939 | ||||||
chr6:46797943
|
C | T | 79 | a0001c0001t0001g0254a0003c0003t0003g0013a0003c0003t0003g0014others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.146-663C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46797943 | ||||||
chr6:46798000
|
C | T | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.146-606C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798000 | ||||||
chr6:46798103
|
G | T | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.146-503G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798103 | ||||||
chr6:46798292
|
C | T | 7 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(4): Show | 7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-314C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798292 | ||||||
chr6:46798333
|
T | G | 1 | a0006c0005t0003g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.146-273T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798333 | ||||||
chr6:46798356
|
T | C | 2 | a0003c0003t0003g0096a0003c0003t0003g0097 | 2 | NA19060.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.146-250T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798356 | ||||||
chr6:46798378
|
G | A | 5 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-228G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 3/13 | chr6 | 46798378 | ||||||
chr6:46798730
|
G | C | 124 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.186+84G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 4/13 | chr6 | 46798730 | ||||||
chr6:46798731
|
G | C | 124 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.186+85G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 4/13 | chr6 | 46798731 | ||||||
chr6:46799437
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.262+256C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46799437 | ||||||
chr6:46799908
|
A | G | 123 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.262+727A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46799908 | ||||||
chr6:46799951
|
G | A | 36 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0001t0001g0162others(33): Show | 36 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.262+770G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46799951 | ||||||
chr6:46800068
|
T | C | 255 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.262+887T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800068 | ||||||
chr6:46800250
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.262+1069A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800250 | ||||||
chr6:46800284
|
C | T | 1 | a0003c0003t0003g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.262+1103C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800284 | ||||||
chr6:46800312
|
T | C | 255 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.262+1131T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800312 | ||||||
chr6:46800746
|
C | T | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262+1565C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800746 | ||||||
chr6:46800926
|
C | T | 1 | a0001c0001t0008g0193 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.262+1745C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46800926 | ||||||
chr6:46801089
|
T | C | 98 | a0001c0001t0001g0179a0002c0002t0002g0063a0003c0003t0003g0013others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.262+1908T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801089 | ||||||
chr6:46801173
|
G | T | 1 | a0008c0009t0001g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.262+1992G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801173 | ||||||
chr6:46801192
|
G | A | 12 | a0002c0002t0002g0063a0003c0003t0003g0046a0003c0003t0003g0061others(9): Show | 12 | HG02523.hp2 HG03669.hp1 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.262+2011G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801192 | ||||||
chr6:46801273
|
G | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262+2092G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801273 | ||||||
chr6:46801393
|
A | G | 31 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(28): Show | 31 | HG00438.hp2 HG00544.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.262+2212A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801393 | ||||||
chr6:46801582
|
T | A | 2 | a0005c0006t0003g0059a0005c0006t0003g0060 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.262+2401T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801582 | ||||||
chr6:46801815
|
T | C | 111 | a0001c0001t0001g0179a0002c0002t0002g0063a0003c0003t0003g0013others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.262+2634T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801815 | ||||||
chr6:46801880
|
C | T | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262+2699C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801880 | ||||||
chr6:46801891
|
C | T | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.262+2710C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46801891 | ||||||
chr6:46802126
|
G | A | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.262+2945G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802126 | ||||||
chr6:46802222
|
C | A | 1 | a0006c0005t0003g0024 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.262+3041C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802222 | ||||||
chr6:46802287
|
C | A | 1 | a0001c0001t0001g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.262+3106C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802287 | ||||||
chr6:46802361
|
T | G | 3 | a0001c0001t0001g0153a0001c0001t0001g0350a0001c0001t0001g0351 | 3 | HG02602.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.262+3180T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802361 | ||||||
chr6:46802461
|
A | G | 1 | a0003c0003t0003g0087 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262+3280A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802461 | ||||||
chr6:46802564
|
G | T | 1 | a0006c0005t0003g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.262+3383G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802564 | ||||||
chr6:46802643
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.262+3462T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802643 | ||||||
chr6:46802692
|
C | CTGTA | 3 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110 | 3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.262+3512_262+3515d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46802692 | |||||
chr6:46802711
|
G | A | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.262+3530G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802711 | ||||||
chr6:46802757
|
G | A | 10 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(7): Show | 10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.262+3576G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802757 | ||||||
chr6:46802862
|
G | A | 1 | a0002c0002t0002g0299 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.262+3681G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802862 | ||||||
chr6:46802874
|
T | A | 1 | a0012c0015t0009g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.262+3693T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46802874 | ||||||
chr6:46803159
|
C | G | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.262+3978C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803159 | ||||||
chr6:46803162
|
C | T | 5 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(2): Show | 5 | HG01074.hp2 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+3981C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803162 | ||||||
chr6:46803183
|
T | C | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.262+4002T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803183 | ||||||
chr6:46803414
|
G | GTAGAATC others(339): Show |
1 | a0005c0008t0003g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.262+4243_262+4244i others(348): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46803414 | |||||
chr6:46803458
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.262+4277A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803458 | ||||||
chr6:46803501
|
A | G | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.262+4320A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803501 | ||||||
chr6:46803685
|
A | C | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.262+4504A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803685 | ||||||
chr6:46803738
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.262+4557T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803738 | ||||||
chr6:46803738
|
TA | T | 125 | a0002c0002t0002g0063a0003c0003t0003g0013a0003c0003t0003g0014others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.262+4560delA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46803738 | |||||
chr6:46803828
|
A | G | 2 | a0011c0012t0002g0132a0011c0012t0002g0134 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.262+4647A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46803828 | ||||||
chr6:46804044
|
T | A | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.262+4863T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804044 | ||||||
chr6:46804292
|
C | T | 2 | a0002c0002t0002g0297a0002c0002t0002g0298 | 2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.262+5111C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804292 | ||||||
chr6:46804415
|
A | G | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263-5005A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804415 | ||||||
chr6:46804417
|
C | T | 10 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(7): Show | 10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.263-5003C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804417 | ||||||
chr6:46804505
|
C | CT | 88 | a0001c0001t0001g0179a0002c0002t0002g0063a0003c0003t0003g0013others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.263-4914dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46804505 | |||||
chr6:46804630
|
C | T | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4790C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804630 | ||||||
chr6:46804632
|
T | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4788T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804632 | ||||||
chr6:46804690
|
A | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4730A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804690 | ||||||
chr6:46804700
|
C | A | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4720C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804700 | ||||||
chr6:46804701
|
A | T | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4719A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804701 | ||||||
chr6:46804703
|
C | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4717C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804703 | ||||||
chr6:46804704
|
T | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4716T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804704 | ||||||
chr6:46804705
|
A | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4715A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804705 | ||||||
chr6:46804716
|
A | T | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-4704A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804716 | ||||||
chr6:46804797
|
T | G | 123 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.263-4623T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804797 | ||||||
chr6:46804888
|
AG | A | 10 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(7): Show | 10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.263-4530delG | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46804888 | |||||
chr6:46804980
|
T | G | 7 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(4): Show | 7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.263-4440T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46804980 | ||||||
chr6:46805143
|
A | T | 1 | a0004c0004t0003g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.263-4277A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805143 | ||||||
chr6:46805187
|
A | T | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.263-4233A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805187 | ||||||
chr6:46805283
|
G | C | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4137G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805283 | ||||||
chr6:46805284
|
T | A | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4136T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805284 | ||||||
chr6:46805285
|
T | C | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4135T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805285 | ||||||
chr6:46805287
|
C | A | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4133C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805287 | ||||||
chr6:46805288
|
G | GATCGCGT others(3): Show |
1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-4132_263-4131i others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805288 | ||||||
chr6:46805326
|
T | C | 1 | a0002c0002t0002g0321 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.263-4094T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805326 | ||||||
chr6:46805480
|
C | T | 7 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-3940C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805480 | ||||||
chr6:46805666
|
T | A | 2 | a0002c0002t0002g0297a0002c0002t0002g0298 | 2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.263-3754T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805666 | ||||||
chr6:46805670
|
T | A | 2 | a0003c0003t0003g0116a0003c0003t0003g0117 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.263-3750T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46805670 | ||||||
chr6:46806109
|
A | T | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.263-3311A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806109 | ||||||
chr6:46806311
|
G | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.263-3109G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806311 | ||||||
chr6:46806312
|
C | T | 1 | a0003c0003t0003g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.263-3108C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806312 | ||||||
chr6:46806639
|
T | A | 1 | a0007c0007t0004g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.263-2781T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806639 | ||||||
chr6:46806887
|
A | G | 1 | a0003c0003t0003g0015 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.263-2533A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46806887 | ||||||
chr6:46807145
|
G | A | 1 | a0003c0003t0003g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.263-2275G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807145 | ||||||
chr6:46807157
|
A | T | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.263-2263A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807157 | ||||||
chr6:46807159
|
C | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-2261C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807159 | ||||||
chr6:46807315
|
T | C | 3 | a0001c0001t0006g0006a0001c0001t0006g0007a0004c0021t0002g0038 | 3 | HG02109.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.263-2105T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807315 | ||||||
chr6:46807320
|
A | C | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-2100A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807320 | ||||||
chr6:46807439
|
C | T | 1 | a0002c0002t0002g0320 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.263-1981C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807439 | ||||||
chr6:46807512
|
T | G | 3 | a0002c0002t0002g0126a0002c0002t0002g0127a0002c0002t0002g0266 | 3 | HG00140.hp2 HG01261.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.263-1908T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807512 | ||||||
chr6:46807512
|
T | TAAAG | 15 | a0001c0001t0001g0120a0001c0001t0001g0160a0001c0001t0001g0170others(12): Show | 15 | HG00733.hp2 HG01074.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.263-1855_263-1852d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAAGAAA others(1): Show |
7 | a0001c0001t0001g0167a0001c0013t0001g0206a0002c0002t0002g0290others(4): Show | 7 | HG00099.hp2 HG01516.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-1859_263-1852d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAAGAAA others(5): Show |
14 | a0001c0001t0001g0178a0001c0001t0001g0195a0001c0013t0001g0204others(11): Show | 14 | HG00438.hp1 HG00642.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-1863_263-1852d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAAGAAA others(9): Show |
8 | a0001c0001t0001g0166a0001c0001t0005g0039a0002c0002t0002g0268others(5): Show | 8 | HG02155.hp2 HG02486.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-1867_263-1852d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAAGAAA others(13): Show |
4 | a0002c0002t0001g0300a0002c0002t0002g0128a0002c0002t0002g0297others(1): Show | 4 | NA18955.hp1 NA18968.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1871_263-1852d others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAAGAAA others(17): Show |
1 | a0002c0002t0002g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.263-1875_263-1852d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAATAAA others(13): Show |
1 | a0001c0001t0006g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-1905_263-1904i others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
T | TAAATAAA others(9): Show |
1 | a0001c0001t0006g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263-1905_263-1904i others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
TAAAG | T | 4 | a0002c0002t0002g0276a0002c0002t0002g0277a0002c0002t0002g0293others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1855_263-1852d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807512
|
TAAAGAAA others(5): Show |
T | 1 | a0002c0002t0002g0306 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.263-1863_263-1852d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807512 | |||||
chr6:46807516
|
G | T | 21 | a0001c0001t0001g0192a0001c0001t0001g0202a0001c0001t0008g0193others(18): Show | 21 | HG01069.hp2 HG01106.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.263-1904G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807516 | ||||||
chr6:46807520
|
G | T | 15 | a0001c0001t0001g0192a0001c0001t0008g0193a0003c0003t0003g0096others(12): Show | 15 | HG01069.hp2 HG01106.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.263-1900G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807520 | ||||||
chr6:46807524
|
G | T | 9 | a0001c0001t0001g0192a0006c0005t0002g0018a0006c0005t0003g0017others(6): Show | 9 | HG01069.hp2 HG01106.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-1896G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807524 | ||||||
chr6:46807525
|
A | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.263-1895A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807525 | ||||||
chr6:46807528
|
G | T | 5 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0122others(2): Show | 5 | HG01106.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1892G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807528 | ||||||
chr6:46807529
|
A | G | 1 | a0002c0002t0002g0284 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.263-1891A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807529 | ||||||
chr6:46807541
|
A | G | 1 | a0005c0008t0003g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.263-1879A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807541 | ||||||
chr6:46807553
|
AAAGAAAG others(9): Show |
A | 1 | a0002c0002t0002g0339 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.263-1863_263-1848d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807553 | |||||
chr6:46807553
|
AAAGAAAG others(17): Show |
A | 1 | a0002c0002t0002g0299 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.263-1863_263-1840d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807553 | |||||
chr6:46807557
|
AAAGAAAG others(5): Show |
A | 5 | a0002c0002t0002g0264a0002c0002t0002g0283a0002c0002t0002g0296others(2): Show | 5 | HG03654.hp2 NA18948.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1859_263-1848d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | |||||
chr6:46807557
|
AAAGAAAG others(9): Show |
A | 6 | a0002c0002t0002g0282a0002c0002t0002g0294a0002c0002t0002g0295others(3): Show | 6 | NA18939.hp2 NA18943.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-1859_263-1844d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | |||||
chr6:46807557
|
AAAGAAAG others(33): Show |
A | 2 | a0003c0003t0003g0111a0007c0007t0004g0138 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.263-1859_263-1820d others(42): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | |||||
chr6:46807557
|
AAAGAAAG others(41): Show |
A | 1 | a0007c0007t0004g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.263-1859_263-1812d others(50): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807557 | |||||
chr6:46807561
|
A | AAAGAAAG others(6): Show |
1 | a0011c0012t0002g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.263-1852_263-1851i others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | |||||
chr6:46807561
|
AAAGAAAG others(5): Show |
A | 2 | a0001c0001t0001g0253a0002c0002t0002g0269 | 2 | HG03669.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.263-1855_263-1844d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | |||||
chr6:46807561
|
AAAGAAAG others(9): Show |
A | 3 | a0001c0001t0001g0185a0001c0001t0001g0252a0002c0002t0002g0320 | 3 | HG00738.hp1 HG03209.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.263-1855_263-1840d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | |||||
chr6:46807561
|
AAAGAAAG others(21): Show |
A | 5 | a0001c0001t0001g0180a0001c0001t0001g0190a0003c0003t0003g0064others(2): Show | 5 | HG01070.hp1 HG01081.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-1855_263-1828d others(30): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | |||||
chr6:46807561
|
AAAGAAAG others(25): Show |
A | 1 | a0003c0003t0003g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.263-1855_263-1824d others(34): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807561 | |||||
chr6:46807562
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.263-1858A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807562 | ||||||
chr6:46807563
|
A | G | 1 | a0001c0001t0006g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-1857A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807563 | ||||||
chr6:46807565
|
A | AAAGAAAG others(13): Show |
2 | a0002c0002t0002g0324a0002c0020t0002g0135 | 2 | HG00673.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807565
|
A | AAAGAAAG others(5): Show |
3 | a0002c0002t0002g0278a0002c0002t0002g0285a0014c0019t0002g0281 | 3 | HG00099.hp1 HG00408.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807565
|
A | AAAGAAAG others(9): Show |
1 | a0002c0002t0002g0298 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.263-1852_263-1851i others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807565
|
A | AAAGAAAG others(1): Show |
3 | a0002c0002t0002g0261a0002c0002t0002g0272a0002c0002t0002g0325 | 3 | HG00609.hp2 NA19064.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807565
|
A | AAAGAAAG others(5): Show |
2 | a0002c0002t0002g0309a0002c0002t0002g0317 | 2 | HG03710.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.263-1852_263-1851i others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807565
|
A | G | 2 | a0002c0002t0002g0314a0002c0002t0002g0327 | 2 | HG01081.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.263-1855A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807565 | ||||||
chr6:46807565
|
AAAGG | A | 3 | a0002c0002t0002g0308a0002c0002t0002g0316a0002c0002t0002g0331 | 3 | HG01255.hp2 HG01358.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.263-1800_263-1797d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807565
|
AAAGGAAG others(1): Show |
A | 8 | a0001c0001t0005g0041a0002c0002t0002g0155a0002c0002t0002g0263others(5): Show | 8 | HG01175.hp1 HG01361.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.263-1804_263-1797d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807565 | |||||
chr6:46807566
|
AAGGAAGG others(7): Show |
A | 1 | a0001c0001t0001g0251 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.263-1853_263-1840d others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807566 | ||||||
chr6:46807567
|
A | G | 1 | a0001c0001t0006g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263-1853A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807567 | ||||||
chr6:46807567
|
AGGAAGGA others(6): Show |
A | 1 | a0003c0003t0003g0091 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.263-1851_263-1839d others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807567 | |||||
chr6:46807569
|
G | A | 261 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(258): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.263-1851G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807569 | ||||||
chr6:46807572
|
GGAAGGAA others(45): Show |
G | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.263-1836_263-1785d others(54): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807572 | |||||
chr6:46807573
|
G | A | 207 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(204): Show | 208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.263-1847G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807573 | ||||||
chr6:46807576
|
GGAAGGAA others(7): Show |
G | 1 | a0003c0003t0003g0055 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.263-1843_263-1830d others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807576 | ||||||
chr6:46807577
|
G | A | 156 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(153): Show | 157 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.263-1843G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807577 | ||||||
chr6:46807580
|
GGAAGGAA others(37): Show |
G | 1 | a0004c0004t0003g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.263-1828_263-1785d others(46): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807580 | |||||
chr6:46807581
|
G | A | 97 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(94): Show | 98 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.263-1839G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807581 | ||||||
chr6:46807584
|
G | A | 4 | a0003c0003t0003g0091a0007c0007t0004g0008a0007c0007t0004g0011others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1836G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807584 | ||||||
chr6:46807585
|
G | A | 38 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0162others(35): Show | 38 | HG00099.hp2 HG00544.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.263-1835G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807585 | ||||||
chr6:46807588
|
G | A | 1 | a0003c0003t0003g0091 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.263-1832G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807588 | ||||||
chr6:46807588
|
GGAAGGAA others(29): Show |
G | 5 | a0004c0004t0002g0152a0006c0005t0002g0018a0006c0005t0003g0017others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-1820_263-1785d others(38): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807588 | |||||
chr6:46807589
|
G | A | 16 | a0001c0001t0001g0031a0001c0001t0001g0162a0001c0001t0001g0194others(13): Show | 16 | HG00544.hp1 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1831G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807589 | ||||||
chr6:46807592
|
G | A | 2 | a0003c0003t0003g0055a0003c0003t0003g0091 | 2 | HG01516.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.263-1828G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807592 | ||||||
chr6:46807592
|
GGAAGGAA others(25): Show |
G | 9 | a0004c0004t0002g0146a0004c0004t0002g0148a0004c0004t0002g0149others(6): Show | 9 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.263-1816_263-1785d others(34): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807592 | |||||
chr6:46807593
|
G | A | 3 | a0004c0004t0002g0150a0004c0004t0003g0003a0008c0009t0001g0027 | 3 | HG02280.hp2 HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.263-1827G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807593 | ||||||
chr6:46807596
|
G | A | 3 | a0003c0003t0003g0091a0007c0007t0004g0009a0007c0007t0004g0010 | 3 | HG03139.hp1 HG03471.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.263-1824G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807596 | ||||||
chr6:46807596
|
GGAAGGAA others(21): Show |
G | 11 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0144others(8): Show | 12 | HG00140.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-1812_263-1785d others(30): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807596 | |||||
chr6:46807597
|
G | A | 2 | a0004c0004t0002g0150a0008c0009t0001g0027 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.263-1823G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807597 | ||||||
chr6:46807600
|
GGAAGGAA others(17): Show |
G | 6 | a0001c0001t0001g0189a0003c0003t0003g0119a0004c0004t0002g0143others(3): Show | 6 | HG00323.hp1 HG01167.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-1808_263-1785d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807600 | |||||
chr6:46807601
|
G | A | 1 | a0004c0004t0002g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263-1819G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807601 | ||||||
chr6:46807604
|
GGAAGGAA others(13): Show |
G | 11 | a0001c0001t0001g0161a0001c0001t0001g0191a0003c0003t0003g0058others(8): Show | 11 | HG00280.hp1 HG02965.hp1 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.263-1804_263-1785d others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807604 | |||||
chr6:46807605
|
G | A | 1 | a0004c0004t0002g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263-1815G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807605 | ||||||
chr6:46807608
|
GGAAGGAA others(9): Show |
G | 19 | a0001c0001t0001g0200a0001c0001t0001g0201a0002c0002t0002g0063others(16): Show | 19 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.263-1800_263-1785d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807608 | |||||
chr6:46807612
|
GGAAGGAA others(5): Show |
G | 34 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0001g0164others(31): Show | 34 | HG00738.hp2 HG01069.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.263-1794_263-1783d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807612 | |||||
chr6:46807616
|
GGAAGGAA others(1): Show |
G | 51 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0159others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1796_263-1789d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807616 | |||||
chr6:46807620
|
GGAAA | G | 36 | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0001g0154others(33): Show | 36 | HG00280.hp2 HG00323.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.263-1796_263-1793d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807620 | |||||
chr6:46807624
|
A | G | 64 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0036others(61): Show | 64 | HG00099.hp2 HG00423.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.263-1796A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807624 | ||||||
chr6:46807702
|
G | GA | 4 | a0001c0001t0001g0228a0002c0002t0002g0126a0002c0002t0002g0303others(1): Show | 4 | HG04204.hp2 NA18959.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-1712dupA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807702 | |||||
chr6:46807747
|
A | AAAGG | 96 | a0001c0001t0001g0035a0001c0001t0001g0120a0001c0001t0001g0153others(93): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.263-1660_263-1657d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807747 | |||||
chr6:46807763
|
GGAGA | G | 83 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.263-1656_263-1653d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807763 | ||||||
chr6:46807763
|
GGAGAAAG others(2): Show |
G | 16 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0184others(13): Show | 16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1656_263-1648d others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807763 | ||||||
chr6:46807763
|
GGAGAAAG others(6): Show |
G | 2 | a0008c0009t0001g0026a0013c0016t0003g0108 | 2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.263-1656_263-1644d others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807763 | ||||||
chr6:46807764
|
G | A | 51 | a0001c0001t0001g0036a0001c0001t0001g0140a0001c0001t0001g0159others(48): Show | 51 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1656G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807764 | ||||||
chr6:46807767
|
A | G | 51 | a0001c0001t0001g0036a0001c0001t0001g0140a0001c0001t0001g0159others(48): Show | 51 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1653A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807767 | ||||||
chr6:46807768
|
A | G | 51 | a0001c0001t0001g0036a0001c0001t0001g0140a0001c0001t0001g0159others(48): Show | 51 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.263-1652A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807768 | ||||||
chr6:46807770
|
G | GGAAA | 26 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0237others(23): Show | 27 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.263-1584_263-1581d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
G | GGAAAGAA others(1): Show |
5 | a0001c0001t0001g0240a0002c0002t0002g0318a0002c0002t0002g0320others(2): Show | 5 | HG00408.hp1 HG00738.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1588_263-1581d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
G | GGAAAGAA others(5): Show |
4 | a0001c0001t0001g0219a0003c0003t0003g0058a0003c0003t0003g0104others(1): Show | 4 | HG01192.hp1 HG03831.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.263-1592_263-1581d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
GGAAA | G | 25 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0155others(22): Show | 25 | HG00609.hp1 HG00609.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.263-1584_263-1581d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
GGAAAGAA others(1): Show |
G | 24 | a0001c0001t0006g0007a0002c0002t0001g0300a0002c0002t0002g0127others(21): Show | 24 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.263-1588_263-1581d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
GGAAAGAA others(5): Show |
G | 21 | a0002c0002t0001g0334a0002c0002t0001g0336a0002c0002t0001g0340others(18): Show | 21 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.263-1592_263-1581d others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
GGAAAGAA others(9): Show |
G | 3 | a0002c0002t0002g0295a0002c0002t0002g0314a0002c0002t0002g0323 | 3 | HG01081.hp2 HG01168.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.263-1596_263-1581d others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
GGAAAGAA others(13): Show |
G | 2 | a0002c0002t0002g0269a0002c0002t0002g0308 | 2 | HG01358.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.263-1600_263-1581d others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807770
|
GGAAAGAA others(17): Show |
G | 2 | a0002c0002t0002g0288a0002c0002t0002g0345 | 2 | HG02155.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.263-1604_263-1581d others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807770 | |||||
chr6:46807771
|
G | A | 52 | a0001c0001t0001g0036a0001c0001t0001g0140a0001c0001t0001g0159others(49): Show | 52 | HG00733.hp1 HG00733.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.263-1649G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807771 | ||||||
chr6:46807771
|
GA | G | 47 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(44): Show | 47 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.263-1646delA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807771 | |||||
chr6:46807772
|
A | G | 36 | a0001c0001t0001g0033a0001c0001t0001g0157a0001c0001t0001g0164others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.263-1648A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807772 | ||||||
chr6:46807773
|
A | G | 47 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(44): Show | 47 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.263-1647A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807773 | ||||||
chr6:46807774
|
A | G | 88 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0140others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.263-1646A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807774 | ||||||
chr6:46807775
|
G | A | 37 | a0001c0001t0001g0033a0001c0001t0001g0157a0001c0001t0001g0164others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.263-1645G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807775 | ||||||
chr6:46807776
|
A | AAAGAAAG others(9): Show |
1 | a0001c0001t0005g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.263-1629_263-1628i others(18): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807776 | |||||
chr6:46807776
|
A | G | 16 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0184others(13): Show | 16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1644A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807776 | ||||||
chr6:46807777
|
A | G | 16 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0184others(13): Show | 16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1643A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807777 | ||||||
chr6:46807778
|
A | G | 36 | a0001c0001t0001g0033a0001c0001t0001g0157a0001c0001t0001g0164others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.263-1642A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807778 | ||||||
chr6:46807779
|
GAAA | G | 47 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(44): Show | 47 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.263-1640_263-1638d others(5): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807779 | ||||||
chr6:46807780
|
A | AAAGAAAG others(5): Show |
1 | a0001c0001t0005g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.263-1629_263-1628i others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807780 | |||||
chr6:46807780
|
A | G | 2 | a0008c0009t0001g0026a0013c0016t0003g0108 | 2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.263-1640A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807780 | ||||||
chr6:46807781
|
A | AAGAAAGA others(4): Show |
1 | a0001c0001t0005g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.263-1629_263-1628i others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807781 | |||||
chr6:46807781
|
A | G | 2 | a0008c0009t0001g0026a0013c0016t0003g0108 | 2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.263-1639A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807781 | ||||||
chr6:46807783
|
GAAA | G | 16 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0184others(13): Show | 16 | HG01070.hp1 HG01346.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.263-1636_263-1634d others(5): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807783 | ||||||
chr6:46807788
|
A | G | 1 | a0001c0001t0006g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-1632A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807788 | ||||||
chr6:46807792
|
A | G | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.263-1628A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807792 | ||||||
chr6:46807796
|
A | G | 1 | a0001c0001t0006g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.263-1624A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807796 | ||||||
chr6:46807800
|
A | G | 1 | a0001c0001t0005g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.263-1620A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807800 | ||||||
chr6:46807822
|
A | AGAAAGAA others(17): Show |
1 | a0004c0004t0003g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.263-1581_263-1580i others(26): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807822 | |||||
chr6:46807822
|
A | AGAAAGAA others(13): Show |
2 | a0004c0004t0003g0003a0004c0004t0003g0005 | 2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.263-1581_263-1580i others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807822 | |||||
chr6:46807829
|
AAGAAAGA others(3): Show |
A | 1 | a0002c0002t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.263-1590_263-1581d others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807829 | ||||||
chr6:46807836
|
A | G | 5 | a0003c0003t0003g0116a0003c0003t0003g0117a0005c0008t0003g0078others(2): Show | 5 | HG02145.hp1 HG02155.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-1584A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807836 | ||||||
chr6:46807840
|
G | A | 65 | a0002c0002t0002g0063a0003c0003t0003g0013a0003c0003t0003g0014others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.263-1580G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46807840 | ||||||
chr6:46807840
|
G | GAAGA | 20 | a0003c0003t0003g0111a0003c0003t0003g0112a0003c0003t0003g0113others(17): Show | 20 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.263-1576_263-1573d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46807840 | |||||
chr6:46808143
|
C | CT | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-1268dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46808143 | |||||
chr6:46808293
|
C | T | 1 | a0006c0005t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.263-1127C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808293 | ||||||
chr6:46808473
|
C | A | 1 | a0006c0005t0003g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.263-947C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808473 | ||||||
chr6:46808600
|
G | T | 122 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.263-820G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808600 | ||||||
chr6:46808602
|
G | A | 2 | a0007c0007t0003g0037a0015c0018t0001g0029 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.263-818G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808602 | ||||||
chr6:46808685
|
G | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-735G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46808685 | ||||||
chr6:46809136
|
ATTATT | A | 13 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005others(10): Show | 13 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.263-277_263-273del others(5): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 46809136 | |||||
chr6:46809261
|
T | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0218 | 2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.263-159T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46809261 | ||||||
chr6:46809266
|
A | G | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.263-154A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46809266 | ||||||
chr6:46809407
|
C | T | 2 | a0003c0003t0003g0111a0003c0003t0003g0113 | 2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.263-13C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 5/13 | chr6 | 46809407 | ||||||
chr6:46809640
|
T | C | 339 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(336): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.380+103T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809640 | ||||||
chr6:46809653
|
CTT | C | 3 | a0003c0003t0003g0045a0003c0003t0003g0051a0003c0003t0003g0054 | 3 | HG00099.hp2 HG01361.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.380+117_380+118del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809653 | ||||||
chr6:46809690
|
G | GT | 8 | a0002c0002t0002g0272a0002c0002t0002g0273a0002c0002t0002g0288others(5): Show | 8 | HG01261.hp1 HG04115.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.380+159dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46809690 | |||||
chr6:46809772
|
C | G | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.380+235C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809772 | ||||||
chr6:46809801
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.380+264T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809801 | ||||||
chr6:46809812
|
G | A | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+275G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809812 | ||||||
chr6:46809813
|
T | A | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+276T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809813 | ||||||
chr6:46809814
|
A | G | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+277A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809814 | ||||||
chr6:46809828
|
T | A | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+291T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809828 | ||||||
chr6:46809831
|
A | T | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+294A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809831 | ||||||
chr6:46809832
|
C | T | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+295C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809832 | ||||||
chr6:46809832
|
CAT | C | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.380+300_380+301del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46809832 | |||||
chr6:46809834
|
T | C | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380+297T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809834 | ||||||
chr6:46809836
|
TA | T | 111 | a0002c0002t0002g0063a0003c0003t0003g0013a0003c0003t0003g0014others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.380+300delA | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809836 | ||||||
chr6:46809867
|
A | G | 1 | a0014c0019t0002g0281 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.380+330A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809867 | ||||||
chr6:46809966
|
G | C | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.380+429G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46809966 | ||||||
chr6:46810002
|
A | T | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+465A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810002 | ||||||
chr6:46810134
|
T | A | 3 | a0001c0001t0006g0006a0001c0001t0006g0007a0004c0021t0002g0038 | 3 | HG02109.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.380+597T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810134 | ||||||
chr6:46810141
|
T | G | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+604T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810141 | ||||||
chr6:46810152
|
G | T | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+615G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810152 | ||||||
chr6:46810219
|
A | T | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+682A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810219 | ||||||
chr6:46810287
|
A | T | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.380+750A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810287 | ||||||
chr6:46810343
|
G | C | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+806G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810343 | ||||||
chr6:46810453
|
C | A | 2 | a0003c0003t0003g0116a0003c0003t0003g0117 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.380+916C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810453 | ||||||
chr6:46810766
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380+1229C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810766 | ||||||
chr6:46810876
|
C | T | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.380+1339C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810876 | ||||||
chr6:46810952
|
T | C | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+1415T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810952 | ||||||
chr6:46810978
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0140 | 2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.380+1441A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810978 | ||||||
chr6:46810986
|
T | C | 126 | a0001c0001t0001g0179a0002c0002t0002g0063a0003c0003t0003g0013others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.380+1449T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46810986 | ||||||
chr6:46811173
|
T | C | 339 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(336): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.380+1636T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811173 | ||||||
chr6:46811217
|
T | G | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.380+1680T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811217 | ||||||
chr6:46811245
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.380+1708T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811245 | ||||||
chr6:46811267
|
A | T | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+1730A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811267 | ||||||
chr6:46811273
|
G | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG01106.hp1 HG02615.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+1736G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811273 | ||||||
chr6:46811432
|
C | T | 1 | a0003c0003t0003g0077 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.380+1895C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811432 | ||||||
chr6:46811496
|
T | C | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+1959T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811496 | ||||||
chr6:46811497
|
T | A | 1 | a0004c0004t0002g0098 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.380+1960T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811497 | ||||||
chr6:46811687
|
G | T | 1 | a0007c0017t0001g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380+2150G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811687 | ||||||
chr6:46811841
|
A | G | 9 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.380+2304A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811841 | ||||||
chr6:46811897
|
C | A | 255 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.380+2360C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46811897 | ||||||
chr6:46812081
|
T | G | 245 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(242): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.380+2544T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812081 | ||||||
chr6:46812092
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.380+2555A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812092 | ||||||
chr6:46812387
|
A | G | 1 | a0003c0003t0003g0048 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.380+2850A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812387 | ||||||
chr6:46812395
|
A | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2858A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812395 | ||||||
chr6:46812397
|
T | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2860T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812397 | ||||||
chr6:46812399
|
T | A | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2862T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812399 | ||||||
chr6:46812400
|
T | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2863T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812400 | ||||||
chr6:46812403
|
T | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2866T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812403 | ||||||
chr6:46812404
|
T | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2867T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812404 | ||||||
chr6:46812405
|
A | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2868A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812405 | ||||||
chr6:46812406
|
T | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2869T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812406 | ||||||
chr6:46812408
|
T | G | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+2871T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812408 | ||||||
chr6:46812454
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380+2917T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812454 | ||||||
chr6:46812515
|
A | G | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.380+2978A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812515 | ||||||
chr6:46812608
|
T | C | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.380+3071T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812608 | ||||||
chr6:46812718
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.380+3181G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46812718 | ||||||
chr6:46813124
|
C | T | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+3587C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813124 | ||||||
chr6:46813410
|
A | T | 1 | a0003c0003t0003g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.380+3873A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813410 | ||||||
chr6:46813445
|
A | G | 123 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.380+3908A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813445 | ||||||
chr6:46813648
|
G | A | 1 | a0006c0005t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.380+4111G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813648 | ||||||
chr6:46813723
|
C | A | 10 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(7): Show | 10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.380+4186C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813723 | ||||||
chr6:46813764
|
G | A | 1 | a0003c0003t0003g0077 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.380+4227G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813764 | ||||||
chr6:46813824
|
G | A | 2 | a0001c0001t0001g0036a0006c0005t0003g0030 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.380+4287G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813824 | ||||||
chr6:46813869
|
A | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+4332A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813869 | ||||||
chr6:46813871
|
A | C | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+4334A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813871 | ||||||
chr6:46813875
|
G | T | 1 | a0002c0002t0002g0307 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380+4338G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813875 | ||||||
chr6:46813930
|
G | T | 2 | a0003c0003t0003g0115a0003c0003t0003g0119 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.380+4393G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46813930 | ||||||
chr6:46814021
|
G | A | 255 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.380+4484G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814021 | ||||||
chr6:46814032
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0175 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.380+4495C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814032 | ||||||
chr6:46814239
|
A | C | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.380+4702A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814239 | ||||||
chr6:46814270
|
G | A | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+4733G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814270 | ||||||
chr6:46814395
|
T | C | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.380+4858T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814395 | ||||||
chr6:46814522
|
C | T | 255 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.380+4985C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814522 | ||||||
chr6:46814556
|
G | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | NA18945.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.381-4973G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814556 | ||||||
chr6:46814664
|
A | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-4865A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814664 | ||||||
chr6:46814704
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381-4825G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814704 | ||||||
chr6:46814868
|
GGAGTACA others(2): Show |
G | 97 | a0002c0002t0002g0063a0003c0003t0003g0013a0003c0003t0003g0014others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.381-4656_381-4648d others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46814868 | |||||
chr6:46814913
|
G | C | 3 | a0002c0002t0002g0328a0002c0002t0002g0329a0002c0002t0002g0330 | 3 | NA18941.hp2 NA18999.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.381-4616G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814913 | ||||||
chr6:46814945
|
T | C | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.381-4584T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46814945 | ||||||
chr6:46815113
|
T | C | 123 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(120): Show | 123 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.381-4416T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815113 | ||||||
chr6:46815202
|
C | A | 10 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(7): Show | 10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.381-4327C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815202 | ||||||
chr6:46815359
|
A | G | 1 | a0002c0002t0002g0287 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.381-4170A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815359 | ||||||
chr6:46815414
|
G | A | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.381-4115G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815414 | ||||||
chr6:46815491
|
A | G | 255 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.381-4038A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815491 | ||||||
chr6:46815509
|
G | A | 249 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(246): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.381-4020G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815509 | ||||||
chr6:46815515
|
C | T | 122 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.381-4014C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815515 | ||||||
chr6:46815540
|
C | A | 1 | a0002c0002t0002g0284 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.381-3989C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815540 | ||||||
chr6:46815657
|
A | C | 1 | a0002c0002t0002g0280 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.381-3872A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815657 | ||||||
chr6:46815661
|
C | A | 16 | a0005c0006t0003g0049a0005c0006t0003g0059a0005c0006t0003g0060others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.381-3868C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815661 | ||||||
chr6:46815842
|
A | G | 1 | a0002c0002t0002g0275 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381-3687A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815842 | ||||||
chr6:46815863
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.381-3666T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815863 | ||||||
chr6:46815965
|
C | A | 122 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.381-3564C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46815965 | ||||||
chr6:46816081
|
C | T | 2 | a0003c0003t0003g0101a0003c0003t0003g0104 | 2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.381-3448C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816081 | ||||||
chr6:46816159
|
A | T | 111 | a0001c0001t0001g0179a0002c0002t0002g0063a0003c0003t0003g0013others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.381-3370A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816159 | ||||||
chr6:46816204
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.381-3325C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816204 | ||||||
chr6:46816252
|
C | T | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.381-3277C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816252 | ||||||
chr6:46816273
|
A | T | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.381-3256A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816273 | ||||||
chr6:46816446
|
A | G | 248 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(245): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.381-3083A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816446 | ||||||
chr6:46816773
|
G | A | 11 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(8): Show | 11 | HG01106.hp2 HG01891.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-2756G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816773 | ||||||
chr6:46816873
|
G | A | 10 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(7): Show | 10 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.381-2656G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816873 | ||||||
chr6:46816928
|
A | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0218 | 2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.381-2601A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816928 | ||||||
chr6:46816932
|
A | G | 2 | a0002c0002t0002g0264a0002c0002t0002g0269 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.381-2597A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46816932 | ||||||
chr6:46817110
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.381-2419T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817110 | ||||||
chr6:46817185
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381-2344G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817185 | ||||||
chr6:46817219
|
A | C | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.381-2310A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817219 | ||||||
chr6:46817236
|
G | T | 129 | a0002c0002t0002g0063a0003c0003t0003g0013a0003c0003t0003g0014others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.381-2293G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817236 | ||||||
chr6:46817296
|
A | C | 1 | a0003c0003t0003g0054 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381-2233A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817296 | ||||||
chr6:46817313
|
G | A | 119 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(116): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.381-2216G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817313 | ||||||
chr6:46817339
|
A | G | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-2190A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817339 | ||||||
chr6:46817391
|
T | C | 1 | a0004c0004t0003g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381-2138T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817391 | ||||||
chr6:46817603
|
T | A | 1 | a0002c0002t0002g0326 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.381-1926T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817603 | ||||||
chr6:46817741
|
G | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381-1788G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817741 | ||||||
chr6:46817875
|
G | A | 1 | a0003c0003t0003g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.381-1654G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817875 | ||||||
chr6:46817946
|
G | C | 1 | a0016c0022t0001g0176 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.381-1583G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46817946 | ||||||
chr6:46818205
|
T | A | 1 | a0002c0002t0002g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.381-1324T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818205 | ||||||
chr6:46818400
|
T | G | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.381-1129T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818400 | ||||||
chr6:46818446
|
G | T | 128 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.381-1083G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818446 | ||||||
chr6:46818490
|
C | T | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381-1039C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818490 | ||||||
chr6:46818594
|
T | C | 128 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.381-935T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818594 | ||||||
chr6:46818626
|
G | A | 1 | a0002c0002t0002g0311 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.381-903G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818626 | ||||||
chr6:46818652
|
A | G | 86 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.381-877A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818652 | ||||||
chr6:46818665
|
G | A | 1 | a0002c0002t0002g0308 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.381-864G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818665 | ||||||
chr6:46818725
|
T | A | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-804T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818725 | ||||||
chr6:46818736
|
C | T | 1 | a0004c0004t0003g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381-793C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818736 | ||||||
chr6:46818854
|
G | A | 1 | a0013c0016t0003g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.381-675G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818854 | ||||||
chr6:46818971
|
A | G | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381-558A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46818971 | ||||||
chr6:46818982
|
C | CTGGGTGT others(9): Show |
128 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.381-545_381-544ins others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 46818982 | |||||
chr6:46819034
|
C | A | 11 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(8): Show | 11 | HG01106.hp2 HG01891.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-495C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819034 | ||||||
chr6:46819228
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.381-301G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819228 | ||||||
chr6:46819229
|
C | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381-300C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819229 | ||||||
chr6:46819438
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0239 | 2 | NA18946.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.381-91A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 6/13 | chr6 | 46819438 | ||||||
chr6:46820195
|
A | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.556+491A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820195 | ||||||
chr6:46820262
|
A | G | 1 | a0002c0002t0002g0296 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.556+558A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820262 | ||||||
chr6:46820327
|
T | G | 254 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.556+623T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820327 | ||||||
chr6:46820346
|
G | T | 1 | a0001c0001t0001g0254 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.556+642G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820346 | ||||||
chr6:46820429
|
G | T | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.556+725G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820429 | ||||||
chr6:46820454
|
G | A | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.556+750G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820454 | ||||||
chr6:46820480
|
T | C | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.556+776T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820480 | ||||||
chr6:46820588
|
A | G | 2 | a0002c0002t0002g0128a0002c0002t0002g0131 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.556+884A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820588 | ||||||
chr6:46820778
|
A | G | 2 | a0002c0002t0002g0288a0002c0002t0002g0291 | 2 | NA18947.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.556+1074A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820778 | ||||||
chr6:46820855
|
T | C | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.556+1151T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820855 | ||||||
chr6:46820906
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0140 | 2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.556+1202T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46820906 | ||||||
chr6:46821057
|
T | C | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556+1353T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821057 | ||||||
chr6:46821270
|
A | T | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.556+1566A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821270 | ||||||
chr6:46821304
|
C | G | 5 | a0003c0003t0003g0112a0003c0003t0003g0116a0003c0003t0003g0117others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+1600C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821304 | ||||||
chr6:46821330
|
C | A | 1 | a0001c0001t0001g0246 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.556+1626C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821330 | ||||||
chr6:46821668
|
A | C | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.556+1964A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821668 | ||||||
chr6:46821840
|
G | A | 13 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(10): Show | 13 | HG01106.hp2 HG01891.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.556+2136G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821840 | ||||||
chr6:46821864
|
C | T | 2 | a0011c0012t0002g0132a0011c0012t0002g0134 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.556+2160C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821864 | ||||||
chr6:46821990
|
C | T | 1 | a0002c0002t0002g0331 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.556+2286C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46821990 | ||||||
chr6:46822120
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0244 | 2 | HG01167.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.556+2416G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822120 | ||||||
chr6:46822334
|
T | C | 6 | a0005c0006t0003g0100a0005c0006t0003g0102a0005c0006t0003g0103others(3): Show | 6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+2630T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822334 | ||||||
chr6:46822375
|
A | G | 1 | a0010c0011t0003g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.556+2671A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822375 | ||||||
chr6:46822387
|
G | A | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.556+2683G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822387 | ||||||
chr6:46822391
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.556+2687A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822391 | ||||||
chr6:46822474
|
A | T | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.556+2770A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822474 | ||||||
chr6:46822732
|
A | T | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-2540A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822732 | ||||||
chr6:46822989
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.557-2283A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46822989 | ||||||
chr6:46823364
|
C | T | 11 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(8): Show | 11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.557-1908C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823364 | ||||||
chr6:46823417
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.557-1855G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823417 | ||||||
chr6:46823472
|
C | T | 1 | a0002c0002t0002g0331 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.557-1800C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823472 | ||||||
chr6:46823486
|
C | T | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557-1786C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823486 | ||||||
chr6:46823551
|
G | A | 1 | a0003c0003t0003g0047 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.557-1721G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823551 | ||||||
chr6:46823731
|
C | T | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.557-1541C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823731 | ||||||
chr6:46823798
|
C | T | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-1474C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823798 | ||||||
chr6:46823824
|
C | A | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.557-1448C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46823824 | ||||||
chr6:46824003
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.557-1269G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824003 | ||||||
chr6:46824048
|
C | T | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.557-1224C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824048 | ||||||
chr6:46824113
|
T | G | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.557-1159T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824113 | ||||||
chr6:46824122
|
C | T | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-1150C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824122 | ||||||
chr6:46824151
|
A | G | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.557-1121A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824151 | ||||||
chr6:46824261
|
C | T | 125 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(122): Show | 125 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.557-1011C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824261 | ||||||
chr6:46824365
|
A | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557-907A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824365 | ||||||
chr6:46824408
|
G | A | 9 | a0003c0003t0003g0111a0003c0003t0003g0112a0003c0003t0003g0113others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.557-864G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824408 | ||||||
chr6:46824483
|
A | C | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-789A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824483 | ||||||
chr6:46824483
|
ATATTTAA others(7): Show |
A | 3 | a0001c0001t0001g0199a0002c0002t0002g0287a0002c0002t0002g0317 | 3 | HG03688.hp2 NA19090.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.557-764_557-751del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824483 | |||||
chr6:46824553
|
TTATATAT others(29): Show |
T | 1 | a0002c0002t0002g0333 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.557-687_557-652del others(36): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824553 | |||||
chr6:46824567
|
G | GATGTATT others(66): Show |
1 | a0002c0002t0002g0306 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.557-692_557-620dup others(73): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824567 | |||||
chr6:46824586
|
A | T | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.557-686A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824586 | ||||||
chr6:46824595
|
ATTAAATA others(63): Show |
A | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-643_557-574del others(70): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824595 | |||||
chr6:46824605
|
T | A | 1 | a0007c0007t0004g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.557-667T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824605 | ||||||
chr6:46824606
|
G | A | 1 | a0001c0001t0006g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.557-666G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824606 | ||||||
chr6:46824613
|
AAT | A | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-651_557-650del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824613 | |||||
chr6:46824632
|
T | TA | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-640_557-639ins others(1): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824632 | ||||||
chr6:46824640
|
A | G | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-632A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824640 | ||||||
chr6:46824653
|
T | A | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-619T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824653 | ||||||
chr6:46824659
|
A | AAATT | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-612_557-611ins others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824659 | |||||
chr6:46824659
|
AATGTATT others(67): Show |
A | 6 | a0001c0001t0001g0182a0001c0001t0001g0220a0001c0001t0001g0230others(3): Show | 6 | HG00544.hp2 HG01243.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.557-539_557-466del others(74): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824659 | |||||
chr6:46824662
|
G | A | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-610G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824662 | ||||||
chr6:46824673
|
G | A | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-599G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824673 | ||||||
chr6:46824686
|
A | T | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-586A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824686 | ||||||
chr6:46824692
|
AAATT | A | 4 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0131others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-578_557-575del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824692 | |||||
chr6:46824699
|
G | A | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-573G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824699 | ||||||
chr6:46824710
|
G | A | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-562G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824710 | ||||||
chr6:46824723
|
A | T | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-549A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824723 | ||||||
chr6:46824733
|
T | G | 124 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.557-539T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824733 | ||||||
chr6:46824733
|
TATGTATT others(7): Show |
T | 7 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-525_557-512del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824733 | |||||
chr6:46824736
|
G | A | 120 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(117): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.557-536G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824736 | ||||||
chr6:46824743
|
AATAGATG others(9): Show |
A | 5 | a0003c0003t0003g0053a0003c0003t0003g0055a0003c0003t0003g0056others(2): Show | 5 | HG00738.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-525_557-510del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824743 | |||||
chr6:46824744
|
A | T | 120 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(117): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.557-528A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824744 | ||||||
chr6:46824750
|
G | A | 1 | a0007c0017t0001g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557-522G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824750 | ||||||
chr6:46824757
|
A | AATATATA others(6): Show |
115 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(112): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.557-512_557-500dup others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824757 | |||||
chr6:46824759
|
T | TATATATA others(41): Show |
1 | a0001c0001t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.557-500_557-499ins others(48): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824759 | |||||
chr6:46824769
|
T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.557-500_557-499ins others(50): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824769 | |||||
chr6:46824770
|
T | G | 17 | a0002c0002t0002g0278a0003c0003t0003g0053a0003c0003t0003g0055others(14): Show | 17 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.557-502T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824770 | ||||||
chr6:46824770
|
TATGTATT others(17): Show |
T | 2 | a0001c0001t0001g0036a0001c0001t0006g0007 | 2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.557-499_557-476del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824770 | |||||
chr6:46824770
|
TATGTATT others(265): Show |
T | 1 | a0001c0001t0001g0243 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.557-499_557-228del | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824770 | |||||
chr6:46824773
|
G | A | 133 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(130): Show | 133 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.557-499G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824773 | ||||||
chr6:46824780
|
AATAGATG others(9): Show |
A | 82 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.557-488_557-473del others(16): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824780 | |||||
chr6:46824781
|
A | ATAGATGT others(104): Show |
13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-463_557-462ins others(111): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824781 | |||||
chr6:46824781
|
A | T | 17 | a0002c0002t0002g0278a0003c0003t0003g0053a0003c0003t0003g0055others(14): Show | 17 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.557-491A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824781 | ||||||
chr6:46824787
|
G | C | 117 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(114): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.557-485G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824787 | ||||||
chr6:46824787
|
GTATTTAA others(80): Show |
G | 1 | a0002c0002t0002g0278 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.557-465_557-379del others(87): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824787 | |||||
chr6:46824794
|
A | AATATATA others(6): Show |
3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0225 | 3 | NA18982.hp1 NA19059.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.557-466_557-465ins others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824794 | |||||
chr6:46824794
|
AAT | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(2): Show | 5 | HG01106.hp1 HG02615.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-470_557-469del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824794 | |||||
chr6:46824794
|
AATAT | A | 12 | a0003c0003t0003g0053a0003c0003t0003g0055a0003c0003t0003g0056others(9): Show | 12 | HG00738.hp2 HG01243.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.557-472_557-469del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824794 | |||||
chr6:46824798
|
T | TATATAAA others(115): Show |
1 | a0007c0017t0001g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557-466_557-465ins others(122): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824798 | |||||
chr6:46824807
|
G | T | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(134): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.557-465G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824807 | ||||||
chr6:46824810
|
G | A | 244 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(241): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.557-462G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824810 | ||||||
chr6:46824818
|
T | A | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(134): Show | 137 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.557-454T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824818 | ||||||
chr6:46824824
|
G | C | 119 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(116): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.557-448G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824824 | ||||||
chr6:46824824
|
GTATTTAA others(43): Show |
G | 4 | a0002c0002t0002g0130a0002c0020t0002g0135a0011c0012t0002g0132others(1): Show | 4 | HG01346.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.557-371_557-322del others(50): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824824 | |||||
chr6:46824831
|
AATATATA others(6): Show |
A | 84 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(81): Show | 84 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.557-421_557-409del others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824831 | |||||
chr6:46824831
|
AATATATA others(8): Show |
A | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.557-433_557-419del others(15): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824831 | |||||
chr6:46824831
|
AATATATA others(10): Show |
A | 82 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.557-435_557-419del others(17): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824831 | |||||
chr6:46824843
|
T | TGATATAT others(17): Show |
3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-429_557-428ins others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824843 | ||||||
chr6:46824844
|
T | A | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-428T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824844 | ||||||
chr6:46824844
|
T | TATATATT others(17): Show |
51 | a0001c0001t0001g0033a0001c0001t0001g0153a0001c0001t0001g0154others(48): Show | 51 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.557-422_557-421ins others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824844 | |||||
chr6:46824844
|
T | TATATATT others(54): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0175 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.557-422_557-421ins others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824844 | |||||
chr6:46824846
|
T | TATATTTA others(15): Show |
1 | a0001c0001t0005g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.557-422_557-421ins others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824846 | |||||
chr6:46824851
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-421A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824851 | ||||||
chr6:46824857
|
T | G | 105 | a0001c0001t0001g0190a0002c0002t0002g0126a0002c0002t0002g0127others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.557-415T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824857 | ||||||
chr6:46824860
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-412A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824860 | ||||||
chr6:46824860
|
A | G | 8 | a0002c0002t0002g0126a0002c0002t0002g0127a0002c0002t0002g0128others(5): Show | 8 | HG01261.hp2 HG02647.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-412A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824860 | ||||||
chr6:46824868
|
A | T | 104 | a0002c0002t0002g0126a0002c0002t0002g0127a0002c0002t0002g0128others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.557-404A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824868 | ||||||
chr6:46824871
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-401G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824871 | ||||||
chr6:46824874
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-398C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824874 | ||||||
chr6:46824874
|
C | G | 106 | a0002c0002t0002g0126a0002c0002t0002g0127a0002c0002t0002g0128others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.557-398C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824874 | ||||||
chr6:46824878
|
T | C | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-394T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824878 | ||||||
chr6:46824881
|
AAT | A | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-383_557-382del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824881 | |||||
chr6:46824881
|
AATATATA others(6): Show |
A | 106 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(103): Show | 106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.557-371_557-359del others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824881 | |||||
chr6:46824881
|
AATATATA others(10): Show |
A | 3 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110 | 3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.557-385_557-369del others(17): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824881 | |||||
chr6:46824885
|
T | G | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-387T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824885 | ||||||
chr6:46824888
|
A | AAATTATA others(4): Show |
1 | a0001c0001t0005g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.557-384_557-383ins others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824888 | ||||||
chr6:46824888
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-384A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824888 | ||||||
chr6:46824891
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-381A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824891 | ||||||
chr6:46824892
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.557-380A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824892 | ||||||
chr6:46824893
|
T | TAGATCTA others(4): Show |
1 | a0001c0001t0005g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.557-379_557-378ins others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824893 | ||||||
chr6:46824893
|
TTA | T | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-370_557-369del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824893 | |||||
chr6:46824894
|
T | A | 2 | a0001c0001t0001g0190a0001c0001t0005g0042 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.557-378T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824894 | ||||||
chr6:46824894
|
T | TATATATA others(30): Show |
1 | a0002c0002t0002g0333 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.557-303_557-267dup others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATATATT others(17): Show |
25 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(22): Show | 25 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATATATT others(54): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0179a0007c0017t0001g0019 | 3 | HG03927.hp2 NA18943.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.557-372_557-371ins others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATATATT others(91): Show |
12 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0177others(9): Show | 12 | HG00280.hp1 HG00438.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(98): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATATATT others(126): Show |
3 | a0004c0004t0002g0001a0004c0004t0002g0143a0004c0004t0002g0144 | 4 | HG01255.hp1 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(133): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATATATT others(128): Show |
6 | a0001c0001t0001g0153a0001c0001t0001g0165a0001c0001t0001g0171others(3): Show | 6 | HG01928.hp1 HG02004.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.557-372_557-371ins others(135): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATGTATT others(3): Show |
1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-376_557-375ins others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
T | TATGTATT others(91): Show |
1 | a0001c0001t0001g0170 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.557-376_557-375ins others(98): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824894
|
TATATATA others(30): Show |
T | 1 | a0002c0002t0002g0266 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.557-303_557-267del others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824894 | |||||
chr6:46824896
|
T | TATATTTA others(15): Show |
2 | a0001c0001t0005g0040a0001c0001t0005g0041 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.557-372_557-371ins others(22): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824896 | |||||
chr6:46824901
|
A | T | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-371A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824901 | ||||||
chr6:46824904
|
AATTATAT others(22): Show |
A | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.557-365_557-337del others(29): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824904 | |||||
chr6:46824907
|
T | G | 14 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-365T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824907 | ||||||
chr6:46824918
|
A | T | 14 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-354A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824918 | ||||||
chr6:46824924
|
C | G | 14 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-348C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824924 | ||||||
chr6:46824928
|
T | C | 1 | a0006c0005t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.557-344T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824928 | ||||||
chr6:46824944
|
T | G | 8 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(5): Show | 8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-328T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824944 | ||||||
chr6:46824944
|
TATATATT others(17): Show |
T | 5 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-321_557-298del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824944 | |||||
chr6:46824945
|
ATATATTT others(54): Show |
A | 1 | a0006c0005t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.557-321_557-261del others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824945 | |||||
chr6:46824955
|
A | T | 8 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(5): Show | 8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-317A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824955 | ||||||
chr6:46824958
|
GATCTATT others(104): Show |
G | 4 | a0003c0003t0003g0053a0003c0003t0003g0055a0003c0003t0003g0056others(1): Show | 4 | HG00738.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-299_557-189del | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824958 | |||||
chr6:46824961
|
C | G | 8 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(5): Show | 8 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-311C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824961 | ||||||
chr6:46824965
|
T | C | 7 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(4): Show | 7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-307T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824965 | ||||||
chr6:46824969
|
ATATATAT others(30): Show |
A | 1 | a0003c0003t0003g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.557-266_557-230del others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824969 | |||||
chr6:46824973
|
A | T | 11 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.557-299A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46824973 | ||||||
chr6:46824982
|
ATATATTT others(17): Show |
A | 7 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(4): Show | 7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-284_557-261del others(24): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824982 | |||||
chr6:46824986
|
ATTTAAAT others(54): Show |
A | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.557-284_557-224del others(61): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824986 | |||||
chr6:46824992
|
ATAGATCT others(7): Show |
A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG00323.hp1 HG01081.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.557-277_557-264del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824992 | |||||
chr6:46824995
|
GATCTATT others(67): Show |
G | 89 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.557-266_557-193del others(74): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46824995 | |||||
chr6:46825002
|
TTA | T | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-269_557-268del others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825002 | ||||||
chr6:46825006
|
G | A | 146 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(143): Show | 147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.557-266G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825006 | ||||||
chr6:46825007
|
T | TATATATA others(26): Show |
1 | a0006c0005t0003g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.557-258_557-257ins others(33): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825007 | |||||
chr6:46825010
|
A | T | 1 | a0003c0003t0003g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.557-262A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825010 | ||||||
chr6:46825015
|
A | T | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.557-257A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825015 | ||||||
chr6:46825016
|
A | T | 1 | a0003c0003t0003g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.557-256A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825016 | ||||||
chr6:46825021
|
A | ATATTTAA others(30): Show |
4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-240_557-204dup others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825021 | |||||
chr6:46825023
|
ATTTAAAT others(65): Show |
A | 1 | a0003c0003t0003g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.557-247_557-176del others(72): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825023 | |||||
chr6:46825032
|
GATCTATT others(30): Show |
G | 22 | a0001c0001t0001g0120a0001c0001t0001g0159a0001c0001t0001g0182others(19): Show | 22 | HG01243.hp1 HG02273.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.557-155_557-119del others(37): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 46825032 | |||||
chr6:46825043
|
A | G | 1 | a0002c0002t0002g0295 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.557-229A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825043 | ||||||
chr6:46825047
|
T | A | 138 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(135): Show | 139 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.557-225T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825047 | ||||||
chr6:46825058
|
G | A | 139 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(136): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.557-214G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825058 | ||||||
chr6:46825069
|
A | G | 144 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(141): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.557-203A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825069 | ||||||
chr6:46825069
|
A | T | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.557-203A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825069 | ||||||
chr6:46825084
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.557-188T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825084 | ||||||
chr6:46825095
|
G | A | 128 | a0001c0001t0001g0174a0003c0003t0003g0013a0003c0003t0003g0014others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.557-177G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825095 | ||||||
chr6:46825106
|
A | G | 140 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(137): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.557-166A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 7/13 | chr6 | 46825106 | ||||||
chr6:46825623
|
G | A | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.778+130G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825623 | ||||||
chr6:46825677
|
G | GT | 96 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.778+189dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr6 | 46825677 | |||||
chr6:46825789
|
A | G | 1 | a0003c0003t0003g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.778+296A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825789 | ||||||
chr6:46825810
|
G | A | 1 | a0007c0017t0001g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.778+317G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825810 | ||||||
chr6:46825929
|
G | A | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-425G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46825929 | ||||||
chr6:46826053
|
A | G | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.779-301A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46826053 | ||||||
chr6:46826171
|
G | A | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.779-183G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46826171 | ||||||
chr6:46826311
|
C | G | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.779-43C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 8/13 | chr6 | 46826311 | ||||||
chr6:46826555
|
AG | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG02615.hp1 HG03540.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.928+54delG | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46826555 | |||||
chr6:46826911
|
G | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+408G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46826911 | ||||||
chr6:46827074
|
C | A | 1 | a0001c0001t0006g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928+571C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827074 | ||||||
chr6:46827153
|
A | G | 2 | a0002c0002t0002g0289a0002c0002t0002g0312 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.928+650A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827153 | ||||||
chr6:46827264
|
C | T | 11 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(8): Show | 11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.928+761C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827264 | ||||||
chr6:46827547
|
G | A | 7 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005others(4): Show | 7 | HG02280.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+1044G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827547 | ||||||
chr6:46827561
|
G | A | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.928+1058G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827561 | ||||||
chr6:46827614
|
C | T | 1 | a0003c0003t0003g0055 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.928+1111C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827614 | ||||||
chr6:46827745
|
T | G | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+1242T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827745 | ||||||
chr6:46827815
|
G | A | 96 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.928+1312G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827815 | ||||||
chr6:46827883
|
T | C | 1 | a0007c0017t0001g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.928+1380T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46827883 | ||||||
chr6:46828123
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.929-1233G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828123 | ||||||
chr6:46828236
|
G | GT | 13 | a0001c0001t0001g0185a0001c0001t0001g0222a0001c0001t0001g0224others(10): Show | 13 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.929-1106dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828236 | |||||
chr6:46828236
|
G | GTT | 113 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.929-1107_929-1106d others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828236 | |||||
chr6:46828236
|
GT | G | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-1106delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828236 | |||||
chr6:46828503
|
A | T | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-853A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828503 | ||||||
chr6:46828529
|
T | A | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-827T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828529 | ||||||
chr6:46828616
|
T | A | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.929-740T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828616 | ||||||
chr6:46828631
|
G | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-725G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828631 | ||||||
chr6:46828757
|
T | C | 7 | a0001c0001t0001g0159a0001c0001t0001g0196a0001c0001t0001g0197others(4): Show | 7 | HG00642.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.929-599T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828757 | ||||||
chr6:46828829
|
T | C | 11 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(8): Show | 11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-527T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828829 | ||||||
chr6:46828841
|
G | T | 96 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.929-515G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828841 | ||||||
chr6:46828847
|
A | T | 11 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(8): Show | 11 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-509A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828847 | ||||||
chr6:46828862
|
C | G | 2 | a0002c0002t0002g0289a0002c0002t0002g0312 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.929-494C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46828862 | ||||||
chr6:46828911
|
T | TATC | 127 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(124): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.929-443_929-442ins others(3): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46828911 | |||||
chr6:46829103
|
A | G | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.929-253A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | chr6 | 46829103 | ||||||
chr6:46829285
|
CTTTG | C | 13 | a0004c0004t0002g0001a0004c0004t0002g0142a0004c0004t0002g0143others(10): Show | 14 | HG00741.hp2 HG01255.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-66_929-63delTT others(2): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 46829285 | |||||
chr6:46829592
|
G | A | 84 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1144+21G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829592 | ||||||
chr6:46829654
|
A | C | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+83A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829654 | ||||||
chr6:46829778
|
G | A | 129 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1144+207G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829778 | ||||||
chr6:46829783
|
A | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1144+212A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829783 | ||||||
chr6:46829875
|
A | T | 1 | a0001c0001t0001g0244 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1144+304A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829875 | ||||||
chr6:46829983
|
C | T | 2 | a0001c0001t0006g0006a0001c0001t0006g0007 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1144+412C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46829983 | ||||||
chr6:46830100
|
T | C | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+529T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830100 | ||||||
chr6:46830230
|
C | G | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1144+659C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830230 | ||||||
chr6:46830235
|
C | G | 9 | a0003c0003t0003g0111a0003c0003t0003g0112a0003c0003t0003g0113others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144+664C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830235 | ||||||
chr6:46830247
|
TAAAA | T | 44 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0169others(41): Show | 44 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1144+707_1144+710d others(6): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830247
|
TAAAAA | T | 171 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(168): Show | 171 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1144+706_1144+710d others(7): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830247
|
TAAAAAA | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0211a0001c0001t0001g0225others(9): Show | 12 | HG01070.hp2 HG01106.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1144+705_1144+710d others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830247
|
TAAAAAAA others(1): Show |
T | 14 | a0003c0003t0003g0014a0003c0003t0003g0077a0003c0003t0003g0088others(11): Show | 14 | HG00639.hp1 HG01175.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1144+703_1144+710d others(10): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830247
|
TAAAAAAA others(2): Show |
T | 86 | a0003c0003t0003g0013a0003c0003t0003g0015a0003c0003t0003g0016others(83): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1144+702_1144+710d others(11): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830247
|
TAAAAAAA others(3): Show |
T | 13 | a0003c0003t0003g0096a0003c0003t0003g0097a0004c0004t0002g0144others(10): Show | 13 | HG01069.hp1 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+701_1144+710d others(12): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830247
|
TAAAAAAA others(4): Show |
T | 1 | a0007c0007t0004g0011 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1144+700_1144+710d others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46830247 | |||||
chr6:46830363
|
G | T | 1 | a0002c0002t0002g0289 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1144+792G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830363 | ||||||
chr6:46830450
|
T | C | 1 | a0006c0005t0003g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144+879T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830450 | ||||||
chr6:46830464
|
T | A | 1 | a0002c0002t0002g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1144+893T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830464 | ||||||
chr6:46830681
|
T | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1110T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830681 | ||||||
chr6:46830721
|
G | A | 1 | a0004c0021t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1144+1150G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830721 | ||||||
chr6:46830873
|
T | A | 4 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1302T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830873 | ||||||
chr6:46830959
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1144+1388C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830959 | ||||||
chr6:46830998
|
T | C | 4 | a0003c0003t0003g0346a0003c0003t0003g0347a0003c0003t0003g0349others(1): Show | 4 | HG00639.hp1 HG01496.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+1427T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46830998 | ||||||
chr6:46831006
|
A | C | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1144+1435A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831006 | ||||||
chr6:46831068
|
T | G | 4 | a0003c0003t0003g0116a0003c0003t0003g0117a0003c0003t0003g0118others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+1497T>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831068 | ||||||
chr6:46831171
|
C | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1144+1600C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831171 | ||||||
chr6:46831205
|
T | C | 2 | a0003c0003t0003g0016a0003c0003t0003g0074 | 2 | HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1144+1634T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831205 | ||||||
chr6:46831206
|
A | G | 1 | a0015c0018t0001g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+1635A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831206 | ||||||
chr6:46831325
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1145-1749A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831325 | ||||||
chr6:46831382
|
A | G | 2 | a0007c0017t0001g0019a0012c0015t0009g0002 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1145-1692A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831382 | ||||||
chr6:46831431
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1145-1643C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831431 | ||||||
chr6:46831461
|
A | G | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1613A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831461 | ||||||
chr6:46831547
|
G | A | 7 | a0006c0005t0002g0018a0006c0005t0003g0017a0006c0005t0003g0020others(4): Show | 7 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1145-1527G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831547 | ||||||
chr6:46831584
|
T | C | 6 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG00642.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145-1490T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831584 | ||||||
chr6:46831596
|
C | A | 1 | a0001c0001t0001g0246 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1145-1478C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831596 | ||||||
chr6:46831793
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1145-1281C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831793 | ||||||
chr6:46831871
|
A | G | 1 | a0001c0001t0008g0193 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1145-1203A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46831871 | ||||||
chr6:46832029
|
TAGAG | T | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1041_1145-103 others(8): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 46832029 | |||||
chr6:46832124
|
A | C | 1 | a0004c0004t0003g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1145-950A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832124 | ||||||
chr6:46832272
|
T | C | 86 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1145-802T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832272 | ||||||
chr6:46832322
|
G | C | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-752G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832322 | ||||||
chr6:46832338
|
T | C | 3 | a0003c0003t0003g0061a0004c0004t0002g0071a0004c0004t0002g0098 | 3 | HG03831.hp1 NA18967.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1145-736T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832338 | ||||||
chr6:46832591
|
T | C | 1 | a0007c0007t0010g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1145-483T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832591 | ||||||
chr6:46832720
|
T | C | 130 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(127): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1145-354T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832720 | ||||||
chr6:46832831
|
C | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1145-243C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 10/13 | chr6 | 46832831 | ||||||
chr6:46833926
|
A | G | 12 | a0002c0002t0002g0280a0006c0005t0002g0018a0006c0005t0003g0017others(9): Show | 12 | HG01106.hp2 HG02056.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609+388A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46833926 | ||||||
chr6:46833978
|
AT | A | 98 | a0001c0001t0001g0159a0001c0001t0001g0226a0001c0001t0001g0229others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1609+456delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46833978 | |||||
chr6:46834101
|
C | T | 1 | a0007c0007t0004g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1610-477C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834101 | ||||||
chr6:46834128
|
G | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1610-450G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834128 | ||||||
chr6:46834226
|
AT | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0007a0005c0006t0003g0100others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1610-339delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834226 | |||||
chr6:46834227
|
T | A | 60 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1610-351T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834227 | ||||||
chr6:46834275
|
C | T | 1 | a0006c0005t0003g0021 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1610-303C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834275 | ||||||
chr6:46834308
|
G | A | 254 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1610-270G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834308 | ||||||
chr6:46834385
|
C | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-193C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834385 | ||||||
chr6:46834426
|
TTTATTTT others(12): Show |
T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-149_1610-131d others(21): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834426 | |||||
chr6:46834431
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1610-147T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834431 | ||||||
chr6:46834435
|
ATATT | A | 77 | a0001c0001t0001g0120a0001c0001t0001g0159a0001c0001t0001g0160others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1610-97_1610-94del others(4): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | |||||
chr6:46834435
|
ATATTTAT others(1): Show |
A | 67 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0161others(64): Show | 67 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1610-101_1610-94de others(9): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | |||||
chr6:46834435
|
ATATTTAT others(5): Show |
A | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG00544.hp2 HG01106.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1610-105_1610-94de others(13): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | |||||
chr6:46834435
|
ATATTTAT others(9): Show |
A | 3 | a0001c0001t0001g0157a0001c0001t0001g0228a0001c0001t0001g0230 | 3 | HG01891.hp2 NA18948.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1610-109_1610-94de others(17): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | |||||
chr6:46834435
|
ATATTTAT others(13): Show |
A | 113 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(110): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1610-113_1610-94de others(21): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 46834435 | |||||
chr6:46834443
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1610-135T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834443 | ||||||
chr6:46834453
|
A | T | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-125A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834453 | ||||||
chr6:46834455
|
T | A | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1610-123T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834455 | ||||||
chr6:46834520
|
A | C | 1 | a0007c0007t0004g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1610-58A>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 11/13 | chr6 | 46834520 | ||||||
chr6:46834767
|
TTCCTGAG others(7): Show |
T | 3 | a0005c0006t0003g0059a0005c0006t0003g0060a0005c0006t0003g0110 | 3 | HG01069.hp1 HG01071.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1783+21_1783+34del others(14): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 46834767 | |||||
chr6:46834833
|
C | T | 29 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005others(26): Show | 29 | HG01106.hp2 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1783+82C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834833 | ||||||
chr6:46834850
|
G | T | 1 | a0002c0002t0002g0303 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1783+99G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834850 | ||||||
chr6:46834867
|
T | C | 3 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005 | 3 | HG02622.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1783+116T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834867 | ||||||
chr6:46834901
|
C | T | 1 | a0002c0020t0002g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1783+150C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46834901 | ||||||
chr6:46835041
|
G | A | 6 | a0006c0005t0002g0018a0006c0005t0003g0020a0006c0005t0003g0021others(3): Show | 6 | HG02056.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1784-208G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46835041 | ||||||
chr6:46835164
|
G | C | 152 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(149): Show | 153 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1784-85G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 12/13 | chr6 | 46835164 | ||||||
chr6:46835603
|
T | A | 1 | a0002c0002t0002g0285 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2084+54T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835603 | ||||||
chr6:46835608
|
G | A | 91 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.2084+59G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835608 | ||||||
chr6:46835673
|
G | A | 1 | a0007c0007t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2084+124G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835673 | ||||||
chr6:46835748
|
C | T | 1 | a0003c0003t0003g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2084+199C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835748 | ||||||
chr6:46835778
|
C | T | 2 | a0002c0002t0002g0126a0002c0002t0002g0127 | 2 | HG01261.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2084+229C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835778 | ||||||
chr6:46835872
|
T | C | 87 | a0001c0001t0001g0035a0001c0001t0001g0211a0001c0001t0001g0215others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2084+323T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835872 | ||||||
chr6:46835877
|
G | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2084+328G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46835877 | ||||||
chr6:46835976
|
AT | A | 3 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027 | 3 | HG02280.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2084+429delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46835976 | |||||
chr6:46836487
|
C | T | 1 | a0002c0002t0002g0316 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2084+938C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836487 | ||||||
chr6:46836591
|
T | C | 1 | a0002c0002t0002g0328 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2084+1042T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836591 | ||||||
chr6:46836690
|
G | T | 6 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2084+1141G>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836690 | ||||||
chr6:46836739
|
C | G | 1 | a0002c0002t0002g0302 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2084+1190C>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836739 | ||||||
chr6:46836775
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0239 | 2 | NA18946.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2084+1226G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836775 | ||||||
chr6:46836793
|
A | AT | 83 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2084+1260dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46836793 | |||||
chr6:46836793
|
AT | A | 139 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(136): Show | 139 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2084+1260delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46836793 | |||||
chr6:46836873
|
G | C | 1 | a0003c0003t0011g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2084+1324G>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836873 | ||||||
chr6:46836896
|
G | A | 6 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | NA18950.hp2 NA18990.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.2084+1347G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836896 | ||||||
chr6:46836968
|
T | A | 4 | a0004c0004t0003g0003a0004c0004t0003g0004a0004c0004t0003g0005others(1): Show | 4 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2084+1419T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46836968 | ||||||
chr6:46837071
|
T | C | 1 | a0007c0017t0001g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2084+1522T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837071 | ||||||
chr6:46837229
|
T | A | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2084+1680T>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837229 | ||||||
chr6:46837249
|
G | A | 93 | a0003c0003t0003g0013a0003c0003t0003g0014a0003c0003t0003g0015others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2084+1700G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837249 | ||||||
chr6:46837265
|
T | C | 5 | a0001c0001t0001g0187a0008c0009t0001g0025a0008c0009t0001g0026others(2): Show | 5 | HG02056.hp1 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2085-1715T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837265 | ||||||
chr6:46837267
|
A | T | 242 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2085-1713A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837267 | ||||||
chr6:46837503
|
C | T | 228 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(225): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2085-1477C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837503 | ||||||
chr6:46837666
|
C | A | 228 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(225): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2085-1314C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837666 | ||||||
chr6:46837723
|
A | G | 5 | a0002c0002t0002g0274a0002c0002t0002g0276a0002c0002t0002g0277others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2085-1257A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837723 | ||||||
chr6:46837762
|
A | G | 242 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2085-1218A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837762 | ||||||
chr6:46837791
|
C | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0350a0001c0001t0001g0351 | 3 | HG02602.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2085-1189C>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837791 | ||||||
chr6:46837803
|
C | T | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085-1177C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837803 | ||||||
chr6:46837832
|
A | T | 1 | a0001c0001t0001g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2085-1148A>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837832 | ||||||
chr6:46837842
|
G | A | 4 | a0008c0009t0001g0025a0008c0009t0001g0026a0008c0009t0001g0027others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085-1138G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46837842 | ||||||
chr6:46837895
|
A | AT | 9 | a0001c0001t0001g0162a0001c0001t0001g0252a0002c0002t0002g0273others(6): Show | 9 | HG02056.hp2 HG02280.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2085-1071dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46837895 | |||||
chr6:46837895
|
AT | A | 11 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0041others(8): Show | 11 | HG02486.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2085-1071delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46837895 | |||||
chr6:46838017
|
G | A | 3 | a0006c0005t0003g0122a0006c0005t0003g0123a0006c0005t0003g0124 | 3 | HG01106.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2085-963G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838017 | ||||||
chr6:46838057
|
A | AT | 6 | a0001c0001t0001g0197a0001c0001t0001g0242a0002c0002t0002g0297others(3): Show | 6 | HG02970.hp2 NA18955.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.2085-907dupT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46838057 | |||||
chr6:46838057
|
AT | A | 30 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0005g0039others(27): Show | 31 | HG01099.hp2 HG01255.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.2085-907delT | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46838057 | |||||
chr6:46838131
|
C | T | 1 | a0002c0002t0002g0341 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2085-849C>T | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838131 | ||||||
chr6:46838331
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A | G | 227 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2085-649A>G | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838331 | ||||||
chr6:46838473
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2085-507T>C | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838473 | ||||||
chr6:46838555
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G | GGTCTATA others(33): Show |
1 | a0002c0002t0002g0292 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2085-423_2085-384d others(42): Show |
MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 46838555 | |||||
chr6:46838646
|
G | A | 145 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(142): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2085-334G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838646 | ||||||
chr6:46838884
|
G | A | 7 | a0007c0007t0004g0008a0007c0007t0004g0009a0007c0007t0004g0010others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2085-96G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838884 | ||||||
chr6:46838886
|
G | A | 2 | a0002c0002t0002g0326a0007c0017t0001g0019 | 2 | HG01099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2085-94G>A | MEP1A | ENSG00000112818.11 | transcript | ENST00000230588.9 | protein_coding | 13/13 | chr6 | 46838886 |