geneid | 4200 |
---|---|
ensemblid | ENSG00000082212.13 |
hgncid | 6984 |
symbol | ME2 |
name | malic enzyme 2 |
refseq_nuc | NM_002396.5 |
refseq_prot | NP_002387.1 |
ensembl_nuc | ENST00000321341.11 |
ensembl_prot | ENSP00000321070.5 |
mane_status | MANE Select |
chr | chr18 |
start | 50879118 |
end | 50954257 |
strand | + |
ver | v1.2 |
region | chr18:50879118-50954257 |
region5000 | chr18:50874118-50959257 |
regionname0 | ME2_chr18_50879118_50954257 |
regionname5000 | ME2_chr18_50874118_50959257 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 584 | 262 | 60 | 52 | 118 | 9 | 21 | 96 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002 | 0/0 | 584 | 74 | 29 | 9 | 30 | 1 | 5 | 24 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0003 | 0/0 | 584 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0004 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0005 | 0/0 | 224 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0006 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0007 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1755 | 248 | 60 | 51 | 106 | 9 | 20 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0002 | 0/0 | 1755 | 71 | 29 | 9 | 27 | 1 | 5 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0003 | 0/0 | 1755 | 10 | 0 | 1 | 9 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0004 | 0/0 | 1755 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0005 | 0/0 | 1755 | 2 | 0 | 0 | 1 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0006 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0007 | 0/0 | 1755 | 2 | 0 | 2 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0008 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0009 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0010 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
c0011 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7273 | 35 | 3 | 8 | 19 | 1 | 4 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0002 | 0/0 | 7274 | 13 | 1 | 6 | 5 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0003 | 0/0 | 7277 | 12 | 0 | 1 | 10 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0004 | 0/0 | 7274 | 10 | 9 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0005 | 0/0 | 7274 | 9 | 0 | 0 | 8 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0006 | 0/0 | 7276 | 8 | 0 | 2 | 6 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0007 | 0/0 | 7274 | 7 | 0 | 4 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0008 | 0/0 | 7277 | 6 | 0 | 0 | 6 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0009 | 0/0 | 7278 | 5 | 0 | 0 | 5 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0010 | 0/0 | 7277 | 5 | 2 | 0 | 1 | 1 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0011 | 0/0 | 7273 | 5 | 0 | 0 | 4 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0012 | 0/0 | 7258 | 5 | 4 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0013 | 0/0 | 7267 | 5 | 0 | 1 | 4 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0014 | 0/0 | 7278 | 4 | 0 | 4 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0015 | 0/0 | 7277 | 4 | 0 | 3 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0016 | 0/0 | 7279 | 4 | 1 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0017 | 0/0 | 7272 | 4 | 0 | 1 | 1 | 0 | 2 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0018 | 0/0 | 7275 | 4 | 0 | 2 | 1 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0019 | 0/0 | 7278 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0020 | 0/0 | 7270 | 3 | 0 | 2 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0021 | 0/0 | 7278 | 3 | 2 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0022 | 0/0 | 7276 | 3 | 1 | 0 | 0 | 0 | 2 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0023 | 0/0 | 7274 | 3 | 3 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0024 | 0/0 | 7275 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0025 | 0/0 | 7289 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0026 | 0/0 | 7290 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0027 | 0/0 | 7263 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0028 | 0/0 | 7276 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0029 | 0/0 | 7263 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0030 | 0/0 | 7278 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0031 | 0/0 | 7279 | 2 | 0 | 1 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0032 | 0/0 | 7276 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0033 | 0/0 | 7272 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0034 | 0/0 | 7275 | 2 | 1 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0035 | 0/0 | 7272 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0036 | 0/0 | 7280 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0037 | 0/0 | 7274 | 2 | 0 | 2 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0038 | 0/0 | 7259 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0039 | 0/0 | 7268 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0040 | 0/0 | 7275 | 2 | 0 | 0 | 1 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0041 | 0/0 | 7275 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0042 | 0/0 | 7273 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0043 | 0/0 | 7272 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0044 | 0/0 | 7290 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0045 | 0/0 | 7294 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0046 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0047 | 0/0 | 7277 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0048 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0049 | 0/0 | 7277 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0050 | 0/0 | 7274 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0051 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0052 | 0/0 | 7297 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0053 | 0/0 | 7277 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0054 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0055 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0056 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0057 | 0/0 | 7278 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0058 | 0/0 | 7278 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0059 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0060 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0061 | 0/0 | 7275 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0062 | 0/0 | 7276 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0063 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0064 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0065 | 0/0 | 7279 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0066 | 0/0 | 7268 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0067 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0068 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0069 | 0/0 | 7279 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0070 | 0/0 | 7276 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0071 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0072 | 0/0 | 7258 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0073 | 0/0 | 7278 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0074 | 0/0 | 7277 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0075 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0076 | 0/0 | 7278 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0077 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0078 | 0/0 | 7277 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0079 | 0/0 | 7279 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0080 | 0/0 | 7280 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0081 | 0/0 | 7278 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0082 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0083 | 0/0 | 7278 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0084 | 0/0 | 7272 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0085 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0086 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0087 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0088 | 0/0 | 7273 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0089 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0090 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0091 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0092 | 0/0 | 7278 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0093 | 0/0 | 7274 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0094 | 0/0 | 7270 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0095 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0096 | 0/0 | 7274 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0097 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0098 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0099 | 0/0 | 7277 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0100 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0101 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0102 | 0/0 | 7271 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0103 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0104 | 0/0 | 7271 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0105 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0106 | 0/0 | 7274 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0107 | 0/0 | 7279 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0108 | 0/0 | 7287 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0109 | 0/0 | 7279 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0110 | 0/0 | 7287 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0111 | 0/0 | 7287 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0112 | 0/0 | 7288 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0113 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0114 | 0/0 | 7278 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0115 | 0/0 | 7271 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0116 | 0/0 | 7274 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0117 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0118 | 0/0 | 7275 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0119 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0120 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0121 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0122 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0123 | 0/0 | 7296 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0124 | 0/0 | 7273 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0125 | 0/0 | 7274 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0126 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0127 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0128 | 0/0 | 7274 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0129 | 0/0 | 7273 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0130 | 0/0 | 7273 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0131 | 0/0 | 7284 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0132 | 0/0 | 7283 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0133 | 0/0 | 7282 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0134 | 0/0 | 7281 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0135 | 0/0 | 7272 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0136 | 0/0 | 7274 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0137 | 0/0 | 7284 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0138 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0139 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0140 | 0/0 | 7269 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0141 | 0/0 | 7266 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0142 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0143 | 0/0 | 7263 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0144 | 0/0 | 7270 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0145 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0146 | 0/0 | 7306 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0147 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0148 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0149 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0150 | 0/0 | 7276 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0151 | 0/0 | 7274 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0152 | 0/0 | 7284 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0153 | 0/0 | 7276 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0154 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0155 | 0/0 | 7290 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0156 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0157 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0158 | 0/0 | 7276 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0159 | 0/1 | 7274 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0160 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0161 | 0/0 | 7259 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0162 | 0/0 | 7274 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0163 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0164 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0165 | 0/0 | 7277 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0166 | 0/0 | 7276 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0167 | 0/0 | 7277 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0168 | 0/0 | 7281 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0169 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0170 | 0/0 | 7273 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0171 | 0/0 | 7276 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0172 | 0/0 | 7262 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0173 | 0/0 | 7272 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0174 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0175 | 0/0 | 7271 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0176 | 0/0 | 7270 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0177 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0178 | 1/0 | 7277 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0179 | 0/0 | 7274 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0180 | 0/0 | 7273 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0181 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0182 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0183 | 0/0 | 7275 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
t0184 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1755 | 248 | 60 | 51 | 106 | 9 | 20 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0003 | 0/0 | 1755 | 10 | 0 | 1 | 9 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0005 | 0/0 | 1755 | 2 | 0 | 0 | 1 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0006 | 0/0 | 1755 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002 | 0/0 | 1755 | 71 | 29 | 9 | 27 | 1 | 5 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0004 | 0/0 | 1755 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0003c0007 | 0/0 | 1755 | 2 | 0 | 2 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0004c0008 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0005c0011 | 0/0 | 1755 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0006c0009 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0007c0010 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9027 | 35 | 3 | 8 | 19 | 1 | 4 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0002 | 0/0 | 9028 | 12 | 1 | 5 | 5 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0003 | 0/0 | 9031 | 12 | 0 | 1 | 10 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0004 | 0/0 | 9028 | 9 | 8 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0006 | 0/0 | 9030 | 7 | 0 | 2 | 5 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0007 | 0/0 | 9028 | 7 | 0 | 4 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0008 | 0/0 | 9031 | 6 | 0 | 0 | 6 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0009 | 0/0 | 9032 | 5 | 0 | 0 | 5 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0010 | 0/0 | 9031 | 5 | 2 | 0 | 1 | 1 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0012 | 0/0 | 9012 | 4 | 4 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0014 | 0/0 | 9032 | 4 | 0 | 4 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0015 | 0/0 | 9031 | 4 | 0 | 3 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0016 | 0/0 | 9033 | 4 | 1 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0017 | 0/0 | 9026 | 4 | 0 | 1 | 1 | 0 | 2 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0018 | 0/0 | 9029 | 4 | 0 | 2 | 1 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0019 | 0/0 | 9032 | 3 | 0 | 0 | 3 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0022 | 0/0 | 9030 | 3 | 1 | 0 | 0 | 0 | 2 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0024 | 0/0 | 9029 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0025 | 0/0 | 9043 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0026 | 0/0 | 9044 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0027 | 0/0 | 9017 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0028 | 0/0 | 9030 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0029 | 0/0 | 9017 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0030 | 0/0 | 9032 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0031 | 0/0 | 9033 | 2 | 0 | 1 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0032 | 0/0 | 9030 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0033 | 0/0 | 9026 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0036 | 0/0 | 9034 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0037 | 0/0 | 9028 | 2 | 0 | 2 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0038 | 0/0 | 9013 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0040 | 0/0 | 9029 | 2 | 0 | 0 | 1 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0041 | 0/0 | 9029 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0043 | 0/0 | 9026 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0044 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0045 | 0/0 | 9048 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0046 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0047 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0048 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0049 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0050 | 0/0 | 9028 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0051 | 0/0 | 9051 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0052 | 0/0 | 9051 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0053 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0054 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0056 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0057 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0058 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0059 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0060 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0061 | 0/0 | 9029 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0062 | 0/0 | 9030 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0063 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0064 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0065 | 0/0 | 9033 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0066 | 0/0 | 9022 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0067 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0068 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0070 | 0/0 | 9030 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0071 | 0/0 | 9018 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0072 | 0/0 | 9012 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0073 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0074 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0075 | 0/0 | 9019 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0076 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0077 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0078 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0079 | 0/0 | 9033 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0080 | 0/0 | 9034 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0081 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0082 | 0/0 | 9033 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0083 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0084 | 0/0 | 9026 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0085 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0086 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0091 | 0/0 | 9026 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0092 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0093 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0107 | 0/0 | 9033 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0108 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0109 | 0/0 | 9033 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0110 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0111 | 0/0 | 9041 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0112 | 0/0 | 9042 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0123 | 0/0 | 9050 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0124 | 0/0 | 9027 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0125 | 0/0 | 9028 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0126 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0127 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0128 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0129 | 0/0 | 9027 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0135 | 0/0 | 9026 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0136 | 0/0 | 9028 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0138 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0139 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0142 | 0/0 | 9018 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0143 | 0/0 | 9017 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0145 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0146 | 0/0 | 9060 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0151 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0153 | 0/0 | 9030 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0154 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0155 | 0/0 | 9044 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0156 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0158 | 0/0 | 9030 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0159 | 0/1 | 9028 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0160 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0162 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0164 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0165 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0166 | 0/0 | 9030 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0167 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0168 | 0/0 | 9035 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0169 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0170 | 0/0 | 9027 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0171 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0172 | 0/0 | 9016 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0178 | 1/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0179 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0180 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0181 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0001t0184 | 0/0 | 9019 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0003t0013 | 0/0 | 9021 | 5 | 0 | 1 | 4 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0003t0039 | 0/0 | 9022 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0003t0140 | 0/0 | 9023 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0003t0141 | 0/0 | 9020 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0003t0144 | 0/0 | 9024 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0005t0024 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0005t0130 | 0/0 | 9027 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0006t0006 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0001c0006t0055 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0005 | 0/0 | 9028 | 8 | 0 | 0 | 7 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0011 | 0/0 | 9027 | 4 | 0 | 0 | 3 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0020 | 0/0 | 9024 | 3 | 0 | 2 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0021 | 0/0 | 9032 | 3 | 2 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0023 | 0/0 | 9028 | 3 | 3 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0034 | 0/0 | 9029 | 2 | 1 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0035 | 0/0 | 9026 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0042 | 0/0 | 9027 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0087 | 0/0 | 9069 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0089 | 0/0 | 9026 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0090 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0094 | 0/0 | 9024 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0095 | 0/0 | 9033 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0096 | 0/0 | 9028 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0097 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0098 | 0/0 | 9025 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0099 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0100 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0101 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0102 | 0/0 | 9025 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0103 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0104 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0105 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0106 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0113 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0114 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0115 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0116 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0117 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0118 | 0/0 | 9029 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0119 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0120 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0121 | 0/0 | 9033 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0122 | 0/0 | 9026 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0131 | 0/0 | 9038 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0132 | 0/0 | 9037 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0133 | 0/0 | 9036 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0134 | 0/0 | 9035 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0137 | 0/0 | 9038 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0148 | 0/0 | 9030 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0149 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0150 | 0/0 | 9030 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0152 | 0/0 | 9038 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0157 | 0/0 | 9025 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0163 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0173 | 0/0 | 9026 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0174 | 0/0 | 9025 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0175 | 0/0 | 9025 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0176 | 0/0 | 9024 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0177 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0182 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0002t0183 | 0/0 | 9029 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0004t0005 | 0/0 | 9028 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0004t0011 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0002c0004t0147 | 0/0 | 9027 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0003c0007t0012 | 0/0 | 9012 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0003c0007t0161 | 0/0 | 9013 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0004c0008t0004 | 0/0 | 9028 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0005c0011t0002 | 0/0 | 9028 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0006c0009t0069 | 0/0 | 9033 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
a0007c0010t0088 | 0/0 | 9027 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | copy fasta | chr18 | 50874118 | 50959257 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0014g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0014g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0014g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0015g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0015g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0015g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0015g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0016g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0016g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0017g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0017g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0017g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0018g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0018g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0018g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0022g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0022g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0022g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0024g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0024g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0026g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0026g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0027g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0027g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0028g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0029g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0029g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0030g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0030g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0031g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0031g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0032g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0033g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0033g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0036g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0036g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0037g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0037g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0038g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0038g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0040g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0040g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0041g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0041g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0043g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0043g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0044g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0045g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0046g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0047g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0048g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0049g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0050g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0051g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0052g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0053g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0054g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0056g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0057g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0058g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0059g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0060g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0061g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0062g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0063g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0064g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0065g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0066g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0067g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0068g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0070g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0071g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0072g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0073g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0074g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0075g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0076g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0077g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0078g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0079g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0080g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0081g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0082g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0083g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0084g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0085g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0086g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0091g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0092g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0093g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0107g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0108g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0109g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0110g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0111g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0112g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0123g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0124g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0125g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0126g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0127g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0128g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0129g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0135g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0136g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0138g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0139g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0142g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0143g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0145g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0146g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0151g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0153g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0154g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0155g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0156g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0158g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0159g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0160g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0162g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0164g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0165g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0166g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0167g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0168g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0169g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0170g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0171g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0172g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0178g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0179g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0180g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0181g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0001t0184g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0013g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0013g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0013g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0039g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0039g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0140g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0141g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0003t0144g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0005t0024g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0005t0130g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0006t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0001c0006t0055g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0011g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0020g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0020g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0020g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0021g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0021g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0023g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0023g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0034g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0034g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0035g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0035g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0042g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0042g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0087g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0089g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0090g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0094g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0095g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0096g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0097g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0098g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0099g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0100g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0101g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0102g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0103g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0104g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0105g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0106g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0113g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0114g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0115g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0116g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0117g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0118g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0119g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0120g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0121g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0122g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0131g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0132g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0133g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0134g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0137g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0148g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0149g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0150g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0152g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0157g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0163g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0173g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0174g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0175g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0176g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0177g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0182g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0002t0183g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0004t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0004t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0002c0004t0147g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0003c0007t0012g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0003c0007t0161g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0004c0008t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0005c0011t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0006c0009t0069g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
a0007c0010t0088g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0010 | g0049 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00099 | hp2 | a0001 | c0001 | t0146 | g0302 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00140 | hp1 | a0001 | c0001 | t0136 | g0296 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00140 | hp2 | a0001 | c0001 | t0015 | g0085 | EUR | GBR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00280 | hp1 | a0001 | c0001 | t0040 | g0274 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00280 | hp2 | a0001 | c0001 | t0076 | g0088 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00323 | hp1 | a0001 | c0001 | t0124 | g0228 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00408 | hp1 | a0001 | c0001 | t0184 | g0247 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00408 | hp2 | a0001 | c0003 | t0013 | g0213 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00423 | hp1 | a0001 | c0001 | t0063 | g0022 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00423 | hp2 | a0002 | c0002 | t0005 | g0127 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00544 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00558 | hp2 | a0001 | c0001 | t0091 | g0270 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00597 | hp1 | a0001 | c0001 | t0085 | g0036 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00609 | hp1 | a0002 | c0002 | t0095 | g0156 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00609 | hp2 | a0001 | c0001 | t0040 | g0269 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00621 | hp2 | a0002 | c0002 | t0121 | g0150 | EAS | CHS | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00639 | hp1 | a0002 | c0002 | t0020 | g0323 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00639 | hp2 | a0001 | c0001 | t0074 | g0098 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00642 | hp1 | a0002 | c0002 | t0104 | g0324 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00642 | hp2 | a0001 | c0001 | t0031 | g0051 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00733 | hp1 | a0001 | c0001 | t0129 | g0001 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00735 | hp1 | a0001 | c0001 | t0030 | g0068 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0218 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00738 | hp2 | a0001 | c0001 | t0058 | g0031 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00741 | hp1 | a0001 | c0001 | t0053 | g0061 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG00741 | hp2 | a0001 | c0001 | t0158 | g0288 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01069 | hp2 | a0001 | c0001 | t0014 | g0115 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01070 | hp2 | a0001 | c0001 | t0015 | g0071 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01071 | hp1 | a0001 | c0001 | t0018 | g0255 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01071 | hp2 | a0001 | c0001 | t0015 | g0114 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01074 | hp1 | a0003 | c0007 | t0161 | g0311 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01074 | hp2 | a0001 | c0001 | t0017 | g0319 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01081 | hp1 | a0001 | c0001 | t0143 | g0224 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01081 | hp2 | a0002 | c0002 | t0115 | g0164 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01106 | hp1 | a0002 | c0002 | t0106 | g0133 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01106 | hp2 | a0003 | c0007 | t0012 | g0184 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01167 | hp1 | a0001 | c0001 | t0018 | g0320 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0067 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01168 | hp1 | a0001 | c0001 | t0037 | g0298 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01168 | hp2 | a0001 | c0001 | t0015 | g0074 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01169 | hp1 | a0001 | c0001 | t0061 | g0069 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01169 | hp2 | a0001 | c0001 | t0037 | g0297 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01175 | hp1 | a0002 | c0002 | t0175 | g0182 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01175 | hp2 | a0001 | c0001 | t0073 | g0097 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01192 | hp1 | a0001 | c0001 | t0123 | g0326 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01243 | hp1 | a0001 | c0001 | t0109 | g0157 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01261 | hp1 | a0005 | c0011 | t0002 | g0292 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01261 | hp2 | a0001 | c0001 | t0014 | g0090 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01346 | hp2 | a0002 | c0002 | t0035 | g0325 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01358 | hp2 | a0002 | c0002 | t0099 | g0158 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01361 | hp2 | a0001 | c0001 | t0084 | g0099 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01433 | hp1 | a0001 | c0001 | t0083 | g0063 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01433 | hp2 | a0001 | c0001 | t0093 | g0293 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01496 | hp1 | a0001 | c0001 | t0014 | g0032 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01496 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | CLM | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01884 | hp2 | a0002 | c0002 | t0132 | g0172 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01891 | hp1 | a0001 | c0001 | t0036 | g0191 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01891 | hp2 | a0001 | c0001 | t0026 | g0030 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01928 | hp1 | a0001 | c0001 | t0070 | g0034 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01934 | hp1 | a0001 | c0001 | t0162 | g0264 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01934 | hp2 | a0002 | c0002 | t0020 | g0322 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01943 | hp2 | a0001 | c0001 | t0082 | g0091 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01952 | hp1 | a0001 | c0001 | t0007 | g0222 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01952 | hp2 | a0001 | c0001 | t0007 | g0220 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01978 | hp1 | a0001 | c0003 | t0013 | g0210 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01993 | hp1 | a0001 | c0001 | t0014 | g0086 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG01993 | hp2 | a0002 | c0002 | t0021 | g0005 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02015 | hp1 | a0001 | c0003 | t0141 | g0214 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02040 | hp1 | a0001 | c0001 | t0029 | g0044 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02040 | hp2 | a0002 | c0002 | t0177 | g0148 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02056 | hp1 | a0001 | c0001 | t0027 | g0047 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02056 | hp2 | a0001 | c0001 | t0016 | g0062 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02071 | hp2 | a0001 | c0003 | t0144 | g0211 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02129 | hp1 | a0002 | c0002 | t0034 | g0147 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02145 | hp1 | a0002 | c0002 | t0150 | g0179 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02145 | hp2 | a0001 | c0001 | t0022 | g0261 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02155 | hp1 | a0001 | c0001 | t0064 | g0078 | EAS | CDX | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02155 | hp2 | a0001 | c0001 | t0180 | g0259 | EAS | CDX | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02257 | hp1 | a0001 | c0001 | t0012 | g0006 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02257 | hp2 | a0002 | c0002 | t0034 | g0159 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02258 | hp1 | a0002 | c0002 | t0105 | g0162 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02258 | hp2 | a0001 | c0001 | t0112 | g0204 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02280 | hp2 | a0002 | c0002 | t0098 | g0163 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02451 | hp1 | a0006 | c0009 | t0069 | g0053 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02572 | hp2 | a0002 | c0002 | t0042 | g0316 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02602 | hp1 | a0001 | c0005 | t0130 | g0312 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02622 | hp1 | a0002 | c0002 | t0163 | g0181 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02622 | hp2 | a0001 | c0001 | t0025 | g0027 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02630 | hp2 | a0001 | c0001 | t0036 | g0201 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02647 | hp1 | a0001 | c0001 | t0025 | g0029 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02647 | hp2 | a0001 | c0001 | t0068 | g0033 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02717 | hp1 | a0001 | c0001 | t0030 | g0060 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02717 | hp2 | a0002 | c0002 | t0120 | g0161 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02723 | hp2 | a0001 | c0001 | t0046 | g0087 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02735 | hp1 | a0001 | c0001 | t0062 | g0040 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0283 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02809 | hp1 | a0002 | c0002 | t0134 | g0173 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02818 | hp1 | a0002 | c0002 | t0182 | g0015 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02818 | hp2 | a0004 | c0008 | t0004 | g0303 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02895 | hp1 | a0001 | c0001 | t0032 | g0004 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02895 | hp2 | a0002 | c0002 | t0152 | g0169 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02896 | hp2 | a0002 | c0002 | t0174 | g0318 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02897 | hp1 | a0001 | c0001 | t0032 | g0004 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02922 | hp1 | a0001 | c0001 | t0059 | g0017 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02922 | hp2 | a0001 | c0001 | t0041 | g0198 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02965 | hp1 | a0001 | c0001 | t0092 | g0189 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02965 | hp2 | a0001 | c0001 | t0125 | g0196 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02970 | hp1 | a0002 | c0002 | t0149 | g0160 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02970 | hp2 | a0001 | c0001 | t0045 | g0002 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02976 | hp1 | a0001 | c0001 | t0041 | g0200 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02976 | hp2 | a0001 | c0001 | t0110 | g0007 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03041 | hp1 | a0002 | c0002 | t0183 | g0015 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03041 | hp2 | a0002 | c0002 | t0094 | g0177 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03098 | hp1 | a0002 | c0002 | t0023 | g0180 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03098 | hp2 | a0001 | c0001 | t0169 | g0192 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03130 | hp1 | a0002 | c0002 | t0021 | g0126 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0186 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03195 | hp1 | a0001 | c0001 | t0108 | g0203 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03195 | hp2 | a0002 | c0002 | t0131 | g0171 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03225 | hp1 | a0001 | c0001 | t0028 | g0057 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03225 | hp2 | a0001 | c0001 | t0107 | g0202 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03453 | hp1 | a0001 | c0001 | t0170 | g0193 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03453 | hp2 | a0001 | c0001 | t0047 | g0055 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03486 | hp1 | a0001 | c0001 | t0111 | g0007 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03516 | hp1 | a0001 | c0001 | t0051 | g0118 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03516 | hp2 | a0001 | c0001 | t0038 | g0006 | AFR | ESN | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03540 | hp1 | a0001 | c0001 | t0160 | g0307 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03540 | hp2 | a0002 | c0002 | t0023 | g0174 | AFR | GWD | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03579 | hp1 | a0002 | c0002 | t0042 | g0315 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03579 | hp2 | a0001 | c0001 | t0026 | g0002 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03654 | hp1 | a0001 | c0001 | t0018 | g0278 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0052 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03688 | hp1 | a0001 | c0001 | t0153 | g0242 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03688 | hp2 | a0002 | c0002 | t0020 | g0120 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03704 | hp1 | a0002 | c0002 | t0102 | g0122 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03710 | hp2 | a0001 | c0001 | t0078 | g0050 | SAS | PJL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03831 | hp1 | a0001 | c0001 | t0022 | g0225 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03831 | hp2 | a0001 | c0001 | t0022 | g0237 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03834 | hp1 | a0002 | c0002 | t0005 | g0134 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03834 | hp2 | a0001 | c0001 | t0017 | g0250 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03927 | hp2 | a0001 | c0001 | t0166 | g0223 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG04184 | hp1 | a0001 | c0001 | t0050 | g0105 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG04184 | hp2 | a0001 | c0001 | t0079 | g0037 | SAS | BEB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG04204 | hp1 | a0002 | c0002 | t0011 | g0165 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG04204 | hp2 | a0001 | c0001 | t0049 | g0016 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG04228 | hp1 | a0001 | c0001 | t0167 | g0263 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG04228 | hp2 | a0002 | c0002 | t0114 | g0125 | SAS | STU | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18522 | hp1 | a0001 | c0001 | t0181 | g0197 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18522 | hp2 | a0002 | c0002 | t0096 | g0175 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18612 | hp1 | a0002 | c0002 | t0005 | g0149 | EAS | CHB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18906 | hp1 | a0001 | c0001 | t0048 | g0056 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18906 | hp2 | a0002 | c0002 | t0173 | g0317 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18940 | hp1 | a0001 | c0001 | t0128 | g0246 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18940 | hp2 | a0001 | c0001 | t0009 | g0106 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18945 | hp1 | a0002 | c0002 | t0148 | g0141 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18948 | hp2 | a0002 | c0002 | t0005 | g0140 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18949 | hp1 | a0001 | c0001 | t0172 | g0251 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18949 | hp2 | a0001 | c0001 | t0019 | g0003 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18953 | hp2 | a0002 | c0002 | t0097 | g0135 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18957 | hp1 | a0001 | c0006 | t0006 | g0103 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18957 | hp2 | a0001 | c0001 | t0027 | g0042 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18960 | hp2 | a0001 | c0003 | t0013 | g0206 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18964 | hp1 | a0002 | c0002 | t0103 | g0155 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18964 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18965 | hp1 | a0001 | c0005 | t0024 | g0313 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18965 | hp2 | a0001 | c0001 | t0019 | g0070 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18966 | hp1 | a0001 | c0003 | t0140 | g0009 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18966 | hp2 | a0001 | c0001 | t0145 | g0012 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18967 | hp1 | a0001 | c0001 | t0080 | g0064 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18967 | hp2 | a0001 | c0001 | t0168 | g0282 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18968 | hp2 | a0002 | c0004 | t0005 | g0138 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18969 | hp1 | a0002 | c0002 | t0089 | g0151 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18969 | hp2 | a0001 | c0001 | t0033 | g0248 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18970 | hp1 | a0002 | c0002 | t0011 | g0139 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18971 | hp1 | a0001 | c0001 | t0171 | g0212 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18974 | hp2 | a0001 | c0001 | t0043 | g0300 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18978 | hp1 | a0001 | c0001 | t0077 | g0093 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18982 | hp1 | a0001 | c0001 | t0033 | g0231 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18982 | hp2 | a0001 | c0001 | t0054 | g0119 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18984 | hp1 | a0001 | c0001 | t0126 | g0275 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0072 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18985 | hp2 | a0002 | c0002 | t0118 | g0124 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18990 | hp1 | a0001 | c0003 | t0039 | g0208 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18990 | hp2 | a0002 | c0002 | t0011 | g0154 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18992 | hp2 | a0001 | c0001 | t0066 | g0075 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18994 | hp1 | a0001 | c0001 | t0060 | g0024 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18995 | hp1 | a0001 | c0001 | t0179 | g0260 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18998 | hp1 | a0002 | c0002 | t0090 | g0146 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18998 | hp2 | a0001 | c0001 | t0017 | g0280 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18999 | hp1 | a0002 | c0002 | t0119 | g0131 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18999 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19000 | hp1 | a0001 | c0001 | t0075 | g0039 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19000 | hp2 | a0001 | c0001 | t0165 | g0301 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19001 | hp1 | a0001 | c0001 | t0156 | g0267 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19001 | hp2 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19002 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19004 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19005 | hp1 | a0002 | c0002 | t0011 | g0132 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19005 | hp2 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19006 | hp1 | a0001 | c0001 | t0024 | g0286 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19006 | hp2 | a0001 | c0001 | t0056 | g0082 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19007 | hp1 | a0001 | c0001 | t0072 | g0041 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19007 | hp2 | a0002 | c0002 | t0117 | g0152 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19009 | hp2 | a0002 | c0002 | t0113 | g0145 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19010 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19011 | hp2 | a0001 | c0001 | t0127 | g0249 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19030 | hp1 | a0002 | c0002 | t0122 | g0123 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19030 | hp2 | a0001 | c0001 | t0086 | g0116 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19043 | hp1 | a0001 | c0001 | t0028 | g0059 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19043 | hp2 | a0001 | c0001 | t0164 | g0194 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19054 | hp2 | a0001 | c0001 | t0151 | g0013 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19056 | hp1 | a0002 | c0002 | t0005 | g0142 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19056 | hp2 | a0001 | c0006 | t0055 | g0104 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19057 | hp1 | a0002 | c0002 | t0005 | g0137 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19057 | hp2 | a0001 | c0001 | t0081 | g0018 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19058 | hp1 | a0002 | c0004 | t0011 | g0143 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19058 | hp2 | a0001 | c0001 | t0154 | g0268 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19065 | hp1 | a0002 | c0002 | t0100 | g0166 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19065 | hp2 | a0001 | c0001 | t0016 | g0089 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19066 | hp2 | a0002 | c0002 | t0116 | g0128 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19067 | hp1 | a0001 | c0001 | t0031 | g0094 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19067 | hp2 | a0001 | c0001 | t0067 | g0038 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19068 | hp1 | a0002 | c0002 | t0005 | g0129 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19068 | hp2 | a0001 | c0001 | t0016 | g0073 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19070 | hp1 | a0001 | c0001 | t0019 | g0101 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19070 | hp2 | a0001 | c0001 | t0043 | g0299 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19072 | hp1 | a0001 | c0001 | t0135 | g0277 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19072 | hp2 | a0002 | c0004 | t0147 | g0130 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19074 | hp2 | a0001 | c0001 | t0029 | g0046 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19077 | hp1 | a0001 | c0001 | t0139 | g0215 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19077 | hp2 | a0002 | c0002 | t0005 | g0136 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19080 | hp1 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19082 | hp1 | a0001 | c0003 | t0013 | g0207 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19082 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19084 | hp1 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19084 | hp2 | a0001 | c0001 | t0071 | g0045 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19086 | hp2 | a0002 | c0002 | t0101 | g0144 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19088 | hp1 | a0001 | c0003 | t0039 | g0209 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19088 | hp2 | a0001 | c0001 | t0024 | g0271 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19089 | hp1 | a0002 | c0002 | t0087 | g0153 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19091 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19091 | hp2 | a0001 | c0001 | t0142 | g0294 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19240 | hp1 | a0002 | c0002 | t0133 | g0168 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA19240 | hp2 | a0002 | c0002 | t0021 | g0005 | AFR | YRI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20129 | hp2 | a0007 | c0010 | t0088 | g0321 | AFR | ASW | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20805 | hp1 | a0001 | c0001 | t0065 | g0095 | EUR | TSI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20805 | hp2 | a0002 | c0002 | t0176 | g0183 | EUR | TSI | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | GIH | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02109 | hp1 | a0002 | c0002 | t0023 | g0176 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02109 | hp2 | a0001 | c0001 | t0038 | g0185 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02486 | hp1 | a0001 | c0001 | t0155 | g0190 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02486 | hp2 | a0001 | c0001 | t0052 | g0117 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0048 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG02559 | hp2 | a0002 | c0002 | t0157 | g0178 | AFR | ACB | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03471 | hp1 | a0001 | c0001 | t0138 | g0306 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG03471 | hp2 | a0002 | c0002 | t0137 | g0170 | AFR | MSL | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG06807 | hp1 | a0001 | c0001 | t0057 | g0058 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
HG06807 | hp2 | a0002 | c0002 | t0035 | g0314 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18955 | hp1 | a0001 | c0003 | t0013 | g0009 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA20300 | hp2 | a0001 | c0001 | t0016 | g0096 | AFR | USA | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA21309 | hp1 | a0001 | c0001 | t0044 | g0028 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
NA21309 | hp2 | a0001 | c0001 | t0010 | g0100 | AFR | LWK | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0159 | g0221 | REF | REF | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0178 | g0167 | REF | REF | ME2_chr18_50874118_50959257 | ME2 | chr18 | 50874118 | 50959257 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:50917459
|
G | A | 1 | a0004 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.581G>A | p.Arg194Gln | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/16 | 784/9031 | 581/1755 | 194/584 | chr18 | 50917459 | ||
chr18:50918152
|
C | T | 1 | a0005 | 1 | HG01261.hp1 | stop_gained | HIGH | c.673C>T | p.Arg225* | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/16 | 876/9031 | 673/1755 | 225/584 | chr18 | 50918152 | ||
chr18:50921092
|
A | C | 1 | a0003 | 2 | HG01074.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.961A>C | p.Asn321His | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/16 | 1164/9031 | 961/1755 | 321/584 | chr18 | 50921092 | ||
chr18:50924113
|
A | G | 1 | a0007 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1072A>G | p.Ile358Val | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/16 | 1275/9031 | 1072/1755 | 358/584 | chr18 | 50924113 | ||
chr18:50924131
|
C | G | 2 | a0006a0007 | 2 | HG02451.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1090C>G | p.Pro364Ala | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/16 | 1293/9031 | 1090/1755 | 364/584 | chr18 | 50924131 | ||
chr18:50932292
|
G | A | 2 | a0002a0007 | 75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
missense_variant | MODERATE | c.1349G>A | p.Gly450Glu | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/16 | 1552/9031 | 1349/1755 | 450/584 | chr18 | 50932292 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:50912900
|
G | A | 1 | a0001c0005 | 2 | HG02602.hp1 NA18965.hp1 |
synonymous_variant | LOW | c.342G>A | p.Pro114Pro | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/16 | 545/9031 | 342/1755 | 114/584 | chr18 | 50912900 | ||
chr18:50932347
|
T | A | 1 | a0001c0003 | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
synonymous_variant | LOW | c.1404T>A | p.Val468Val | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/16 | 1607/9031 | 1404/1755 | 468/584 | chr18 | 50932347 | ||
chr18:50947031
|
A | G | 1 | a0001c0006 | 2 | NA18957.hp1 NA19056.hp2 |
synonymous_variant | LOW | c.1602A>G | p.Leu534Leu | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1805/9031 | 1602/1755 | 534/584 | chr18 | 50947031 | ||
chr18:50947127
|
G | T | 1 | a0002c0004 | 3 | NA18968.hp2 NA19058.hp1 NA19072.hp2 |
synonymous_variant | LOW | c.1698G>T | p.Leu566Leu | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1901/9031 | 1698/1755 | 566/584 | chr18 | 50947127 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:50879119
|
T | A | 61 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(58): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-202T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16702 | chr18 | 50879119 | |||||
chr18:50879160
|
C | A | 4 | a0001c0001t0025a0001c0001t0026a0001c0001t0044others(1): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-161C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16661 | chr18 | 50879160 | |||||
chr18:50879168
|
T | C | 1 | a0001c0001t0046 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16653 | chr18 | 50879168 | |||||
chr18:50879294
|
G | A | 2 | a0001c0001t0047a0001c0001t0048 | 2 | HG03453.hp2 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-27G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/16 | 16527 | chr18 | 50879294 | |||||
chr18:50947383
|
G | A | 122 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(119): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*199G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 199 | chr18 | 50947383 | |||||
chr18:50947416
|
C | T | 2 | a0001c0001t0041a0001c0001t0170 | 3 | HG02922.hp2 HG02976.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*232C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 232 | chr18 | 50947416 | |||||
chr18:50947492
|
A | G | 2 | a0001c0001t0032a0001c0001t0086 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*308A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 308 | chr18 | 50947492 | |||||
chr18:50947629
|
G | A | 1 | a0002c0002t0087 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 445 | chr18 | 50947629 | |||||
chr18:50947706
|
G | C | 1 | a0001c0001t0053 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 522 | chr18 | 50947706 | |||||
chr18:50948167
|
T | C | 1 | a0002c0002t0087 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 983 | chr18 | 50948167 | |||||
chr18:50948263
|
T | A | 2 | a0001c0001t0032a0001c0001t0086 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1079T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1079 | chr18 | 50948263 | |||||
chr18:50948378
|
A | G | 4 | a0001c0001t0025a0001c0001t0026a0001c0001t0044others(1): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1194A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1194 | chr18 | 50948378 | |||||
chr18:50948449
|
G | A | 4 | a0001c0001t0025a0001c0001t0026a0001c0001t0044others(1): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1265G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1265 | chr18 | 50948449 | |||||
chr18:50948470
|
A | G | 1 | a0001c0001t0169 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1286 | chr18 | 50948470 | |||||
chr18:50948541
|
C | CT | 20 | a0001c0001t0040a0001c0001t0041a0001c0001t0081others(17): Show | 22 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1378dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1379 | INFO_REALIGN_3_PRIME | chr18 | 50948541 | ||||
chr18:50948541
|
CT | C | 60 | a0001c0001t0027a0001c0001t0028a0001c0001t0033others(57): Show | 81 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1378delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1378 | INFO_REALIGN_3_PRIME | chr18 | 50948541 | ||||
chr18:50948581
|
G | C | 4 | a0001c0001t0025a0001c0001t0026a0001c0001t0044others(1): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1397G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1397 | chr18 | 50948581 | |||||
chr18:50948743
|
C | A | 1 | a0002c0002t0087 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1559C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1559 | chr18 | 50948743 | |||||
chr18:50948785
|
G | A | 1 | a0001c0001t0059 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1601G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1601 | chr18 | 50948785 | |||||
chr18:50948814
|
T | A | 1 | a0002c0002t0087 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1630T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1630 | chr18 | 50948814 | |||||
chr18:50948830
|
C | A | 1 | a0007c0010t0088 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1646C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1646 | chr18 | 50948830 | |||||
chr18:50948834
|
A | G | 136 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(133): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1650A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1650 | chr18 | 50948834 | |||||
chr18:50948838
|
A | T | 1 | a0001c0001t0080 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1654A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1654 | chr18 | 50948838 | |||||
chr18:50948843
|
A | AT | 9 | a0001c0001t0031a0001c0001t0077a0001c0001t0078others(6): Show | 10 | HG00621.hp2 HG00642.hp2 HG02717.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1679dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1680 | INFO_REALIGN_3_PRIME | chr18 | 50948843 | ||||
chr18:50948843
|
AT | A | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(74): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1679delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1679 | INFO_REALIGN_3_PRIME | chr18 | 50948843 | ||||
chr18:50949032
|
G | A | 1 | a0001c0001t0123 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1848G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1848 | chr18 | 50949032 | |||||
chr18:50949070
|
C | CTTCAGGT others(26): Show |
1 | a0001c0001t0146 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1888_*1920dupTCAG others(29): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1921 | INFO_REALIGN_3_PRIME | chr18 | 50949070 | ||||
chr18:50949123
|
A | G | 1 | a0001c0001t0076 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1939A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 1939 | chr18 | 50949123 | |||||
chr18:50949286
|
T | C | 1 | a0002c0002t0087 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2102 | chr18 | 50949286 | |||||
chr18:50949318
|
G | A | 1 | a0001c0001t0037 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2134G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2134 | chr18 | 50949318 | |||||
chr18:50949384
|
G | C | 1 | a0002c0002t0095 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2200G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2200 | chr18 | 50949384 | |||||
chr18:50949387
|
C | G | 3 | a0002c0002t0116a0002c0002t0117a0002c0002t0118 | 3 | NA18985.hp2 NA19007.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2203C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2203 | chr18 | 50949387 | |||||
chr18:50949425
|
C | A | 1 | a0001c0001t0124 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2241C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2241 | chr18 | 50949425 | |||||
chr18:50949446
|
G | A | 1 | a0001c0001t0125 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2262G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2262 | chr18 | 50949446 | |||||
chr18:50949544
|
G | A | 1 | a0001c0001t0126 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2360 | chr18 | 50949544 | |||||
chr18:50949827
|
A | G | 1 | a0002c0002t0115 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2643 | chr18 | 50949827 | |||||
chr18:50949870
|
A | AT | 3 | a0002c0002t0042a0002c0002t0173a0002c0002t0174 | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2688dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2689 | INFO_REALIGN_3_PRIME | chr18 | 50949870 | ||||
chr18:50949962
|
T | TAAAACAT others(31): Show |
1 | a0002c0002t0087 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2779_*2816dupAAAA others(34): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2817 | INFO_REALIGN_3_PRIME | chr18 | 50949962 | ||||
chr18:50950030
|
A | G | 2 | a0001c0001t0051a0001c0001t0052 | 2 | HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2846A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2846 | chr18 | 50950030 | |||||
chr18:50950058
|
C | T | 1 | a0002c0002t0095 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2874C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2874 | chr18 | 50950058 | |||||
chr18:50950080
|
G | A | 28 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(25): Show | 65 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2896G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 2896 | chr18 | 50950080 | |||||
chr18:50950232
|
C | G | 1 | a0002c0002t0114 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3048C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3048 | chr18 | 50950232 | |||||
chr18:50950305
|
C | T | 1 | a0001c0001t0046 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3121C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3121 | chr18 | 50950305 | |||||
chr18:50950309
|
C | T | 1 | a0001c0001t0162 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3125 | chr18 | 50950309 | |||||
chr18:50950350
|
T | A | 2 | a0001c0001t0170a0002c0002t0182 | 2 | HG02818.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3166T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3166 | chr18 | 50950350 | |||||
chr18:50950417
|
C | T | 1 | a0001c0001t0145 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3233C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3233 | chr18 | 50950417 | |||||
chr18:50950466
|
G | GC | 33 | a0002c0002t0005a0002c0002t0011a0002c0002t0020others(30): Show | 51 | HG00423.hp2 HG00639.hp1 HG01175.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3283dupC | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | INFO_REALIGN_3_PRIME | chr18 | 50950466 | ||||
chr18:50950466
|
G | GCTTTTTT others(3): Show |
36 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(33): Show | 86 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3292dupCTTT others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950466 | ||||
chr18:50950467
|
C | CCT | 12 | a0002c0002t0035a0002c0002t0087a0002c0002t0095others(9): Show | 13 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | |||||
chr18:50950467
|
C | CCTTTTTT others(11): Show |
1 | a0001c0001t0123 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCTTT others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | |||||
chr18:50950467
|
C | CCTTTTTT others(12): Show |
1 | a0001c0001t0051 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCTTT others(15): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | |||||
chr18:50950467
|
C | CCTTTTTT others(13): Show |
1 | a0001c0001t0052 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3283_*3284insCTTT others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950467 | |||||
chr18:50950467
|
C | CT | 9 | a0001c0001t0008a0001c0001t0009a0001c0001t0016others(6): Show | 22 | HG00544.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3311dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(4): Show |
18 | a0001c0001t0002a0001c0001t0018a0001c0001t0022others(15): Show | 37 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0154a0001c0001t0155a0001c0001t0168 | 3 | HG02486.hp1 NA18967.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0139 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0156 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3293_*3294insCTTT others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3294 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0025 | 2 | HG02622.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3300_*3311dupTTTT others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0026a0001c0001t0044 | 3 | HG01891.hp2 HG03579.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3299_*3311dupTTTT others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0045 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3294_*3311dupTTTT others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3312 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
CTT | C | 5 | a0001c0001t0068a0001c0003t0013a0001c0003t0039others(2): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3310_*3311delTT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3310 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950467
|
CTTTTTTT | C | 5 | a0001c0001t0012a0001c0001t0038a0001c0001t0084others(2): Show | 9 | HG01074.hp1 HG01106.hp2 HG01361.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3305_*3311delTTTT others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3305 | INFO_REALIGN_3_PRIME | chr18 | 50950467 | ||||
chr18:50950468
|
T | C | 1 | a0002c0004t0147 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3284T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3284 | chr18 | 50950468 | |||||
chr18:50950468
|
T | TTTTTTTT others(2): Show |
7 | a0001c0001t0017a0001c0001t0033a0001c0001t0043others(4): Show | 12 | HG01074.hp2 HG02735.hp2 HG03453.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3292_*3293insCTTT others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3293 | INFO_REALIGN_3_PRIME | chr18 | 50950468 | ||||
chr18:50950479
|
T | C | 1 | a0001c0001t0107 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3295T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3295 | chr18 | 50950479 | |||||
chr18:50950497
|
A | G | 189 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(186): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*3313A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3313 | chr18 | 50950497 | |||||
chr18:50950573
|
T | C | 140 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(137): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3389T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3389 | chr18 | 50950573 | |||||
chr18:50950597
|
G | A | 1 | a0001c0001t0068 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3413G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3413 | chr18 | 50950597 | |||||
chr18:50950764
|
C | T | 1 | a0002c0002t0103 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3580C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3580 | chr18 | 50950764 | |||||
chr18:50951034
|
A | C | 5 | a0001c0003t0013a0001c0003t0039a0001c0003t0140others(2): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3850A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3850 | chr18 | 50951034 | |||||
chr18:50951064
|
G | A | 187 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(184): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*3880G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3880 | chr18 | 50951064 | |||||
chr18:50951168
|
A | G | 2 | a0002c0002t0182a0002c0002t0183 | 2 | HG02818.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3984A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 3984 | chr18 | 50951168 | |||||
chr18:50951443
|
G | A | 3 | a0001c0001t0027a0001c0001t0029a0001c0001t0085 | 5 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4259G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4259 | chr18 | 50951443 | |||||
chr18:50951456
|
A | G | 1 | a0001c0001t0079 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4272A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4272 | chr18 | 50951456 | |||||
chr18:50951547
|
C | CT | 6 | a0001c0001t0014a0001c0001t0015a0001c0001t0076others(3): Show | 12 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4380dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4381 | INFO_REALIGN_3_PRIME | chr18 | 50951547 | ||||
chr18:50951547
|
CT | C | 70 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(67): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*4380delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4380 | INFO_REALIGN_3_PRIME | chr18 | 50951547 | ||||
chr18:50951565
|
A | T | 1 | a0001c0001t0067 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4381A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4381 | chr18 | 50951565 | |||||
chr18:50951567
|
C | A | 1 | a0001c0001t0067 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4383C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4383 | chr18 | 50951567 | |||||
chr18:50951568
|
T | C | 1 | a0001c0001t0067 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4384T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4384 | chr18 | 50951568 | |||||
chr18:50951634
|
T | G | 1 | a0001c0003t0144 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4450T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4450 | chr18 | 50951634 | |||||
chr18:50951705
|
T | C | 138 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(135): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*4521T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4521 | chr18 | 50951705 | |||||
chr18:50951839
|
C | T | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(56): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*4655C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4655 | chr18 | 50951839 | |||||
chr18:50951853
|
T | C | 132 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(129): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*4669T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4669 | chr18 | 50951853 | |||||
chr18:50951866
|
C | CA | 9 | a0001c0001t0016a0001c0001t0019a0001c0001t0030others(6): Show | 15 | HG00735.hp1 HG00738.hp2 HG01175.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4719dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4720 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
C | CAA | 8 | a0001c0001t0025a0001c0001t0026a0001c0001t0051others(5): Show | 10 | HG01192.hp1 HG01891.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4718_*4719dupAA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4720 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CA | C | 16 | a0001c0001t0006a0001c0001t0008a0001c0001t0015others(13): Show | 30 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4719delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4719 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAA | C | 9 | a0001c0003t0039a0001c0003t0144a0002c0002t0034others(6): Show | 11 | HG02071.hp2 HG02129.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4717_*4719delAAA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4717 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAA | C | 23 | a0001c0003t0013a0001c0003t0140a0002c0002t0005others(20): Show | 37 | HG00408.hp2 HG00423.hp2 HG01884.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4716_*4719delAAAA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4716 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAA | C | 15 | a0001c0003t0141a0002c0002t0011a0002c0002t0094others(12): Show | 18 | HG01106.hp1 HG02015.hp1 HG02040.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4715_*4719delAAAA others(1): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4715 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAA | C | 5 | a0002c0002t0035a0002c0002t0098a0002c0002t0102others(2): Show | 6 | HG01175.hp1 HG01346.hp2 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4714_*4719delAAAA others(2): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4714 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA | C | 4 | a0002c0002t0020a0002c0002t0104a0002c0002t0115others(1): Show | 6 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4713_*4719delAAAA others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4713 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0036a0001c0001t0049a0001c0001t0092others(2): Show | 6 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4712_*4719delAAAA others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4712 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0066a0001c0001t0158a0001c0001t0168 | 3 | HG00741.hp2 NA18967.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4710_*4719delAAAA others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4710 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(4): Show |
C | 16 | a0001c0001t0007a0001c0001t0018a0001c0001t0022others(13): Show | 30 | HG00408.hp1 HG00735.hp2 HG01071.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4709_*4719delAAAA others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4709 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(5): Show |
C | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*4708_*4719delAAAA others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4708 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0027a0001c0001t0071a0001c0001t0075 | 4 | HG02056.hp1 NA18957.hp2 NA19000.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4707_*4719delAAAA others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4707 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0029 | 2 | HG02040.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4706_*4719delAAAA others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4706 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951866
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0072 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4701_*4719delAAAA others(15): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4701 | INFO_REALIGN_3_PRIME | chr18 | 50951866 | ||||
chr18:50951977
|
T | G | 5 | a0001c0003t0013a0001c0003t0039a0001c0003t0140others(2): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4793T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4793 | chr18 | 50951977 | |||||
chr18:50952076
|
G | A | 3 | a0001c0001t0051a0001c0001t0052a0001c0001t0123 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4892G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4892 | chr18 | 50952076 | |||||
chr18:50952163
|
G | T | 55 | a0001c0001t0036a0001c0001t0092a0001c0001t0107others(52): Show | 75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*4979G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4979 | chr18 | 50952163 | |||||
chr18:50952456
|
G | A | 1 | a0001c0001t0156 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5272G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5272 | chr18 | 50952456 | |||||
chr18:50952887
|
C | T | 1 | a0001c0001t0136 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5703C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5703 | chr18 | 50952887 | |||||
chr18:50952893
|
T | C | 3 | a0002c0002t0042a0002c0002t0173a0002c0002t0174 | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5709T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5709 | chr18 | 50952893 | |||||
chr18:50953074
|
T | C | 58 | a0001c0001t0036a0001c0001t0092a0001c0001t0107others(55): Show | 78 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5890T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5890 | chr18 | 50953074 | |||||
chr18:50953092
|
C | CT | 65 | a0001c0001t0012a0001c0001t0022a0001c0001t0036others(62): Show | 91 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*5926dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5927 | INFO_REALIGN_3_PRIME | chr18 | 50953092 | ||||
chr18:50953092
|
CTT | C | 5 | a0001c0001t0135a0001c0003t0013a0001c0003t0039others(2): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5925_*5926delTT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5925 | INFO_REALIGN_3_PRIME | chr18 | 50953092 | ||||
chr18:50953148
|
G | C | 1 | a0001c0001t0129 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5964G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 5964 | chr18 | 50953148 | |||||
chr18:50953199
|
T | C | 2 | a0001c0001t0051a0001c0001t0052 | 2 | HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6015T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6015 | chr18 | 50953199 | |||||
chr18:50953648
|
C | G | 1 | a0002c0002t0105 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6464C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6464 | chr18 | 50953648 | |||||
chr18:50953702
|
T | C | 1 | a0001c0001t0032 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6518T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6518 | chr18 | 50953702 | |||||
chr18:50953795
|
A | T | 1 | a0001c0001t0051 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6611A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6611 | chr18 | 50953795 | |||||
chr18:50953847
|
T | A | 4 | a0001c0001t0025a0001c0001t0026a0001c0001t0044others(1): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6663T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6663 | chr18 | 50953847 | |||||
chr18:50953867
|
T | C | 5 | a0001c0001t0012a0001c0001t0038a0003c0007t0012others(2): Show | 9 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6683T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6683 | chr18 | 50953867 | |||||
chr18:50953868
|
T | G | 117 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(114): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*6684T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6684 | chr18 | 50953868 | |||||
chr18:50954124
|
G | A | 4 | a0001c0001t0012a0001c0001t0038a0003c0007t0012others(1): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6940G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 6940 | chr18 | 50954124 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:50879366
|
C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+58C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879366 | ||||||
chr18:50879476
|
T | C | 109 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-13+168T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879476 | ||||||
chr18:50879529
|
C | G | 4 | a0002c0002t0020g0322a0002c0002t0020g0323a0002c0002t0035g0325others(1): Show | 4 | HG00639.hp1 HG00642.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+221C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879529 | ||||||
chr18:50879653
|
C | T | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13+345C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879653 | ||||||
chr18:50879693
|
AC | A | 3 | a0002c0002t0182g0015a0002c0002t0183g0015a0007c0010t0088g0321 | 3 | HG02818.hp1 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13+388delC | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50879693 | |||||
chr18:50879926
|
T | A | 1 | a0001c0001t0049g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13+618T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879926 | ||||||
chr18:50879996
|
A | T | 2 | a0001c0001t0017g0319a0001c0001t0018g0320 | 2 | HG01074.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-13+688A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50879996 | ||||||
chr18:50880138
|
A | G | 1 | a0001c0001t0054g0119 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-13+830A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880138 | ||||||
chr18:50880141
|
G | A | 1 | a0002c0002t0020g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13+833G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880141 | ||||||
chr18:50880168
|
G | A | 1 | a0001c0001t0004g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-13+860G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880168 | ||||||
chr18:50880179
|
G | A | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+871G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880179 | ||||||
chr18:50880378
|
A | G | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-13+1070A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880378 | ||||||
chr18:50880527
|
A | C | 4 | a0002c0002t0042g0315a0002c0002t0042g0316a0002c0002t0173g0317others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1219A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880527 | ||||||
chr18:50880539
|
C | T | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-13+1231C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880539 | ||||||
chr18:50880645
|
T | A | 1 | a0002c0002t0102g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-13+1337T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880645 | ||||||
chr18:50880703
|
C | G | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+1395C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880703 | ||||||
chr18:50880728
|
C | T | 2 | a0001c0001t0014g0115a0001c0001t0015g0114 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+1420C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880728 | ||||||
chr18:50880956
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-13+1648C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50880956 | ||||||
chr18:50881026
|
A | G | 2 | a0002c0002t0175g0182a0002c0002t0176g0183 | 2 | HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-13+1718A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881026 | ||||||
chr18:50881084
|
A | C | 2 | a0001c0005t0024g0313a0001c0005t0130g0312 | 2 | HG02602.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-13+1776A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881084 | ||||||
chr18:50881182
|
C | T | 1 | a0003c0007t0161g0311 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-13+1874C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881182 | ||||||
chr18:50881252
|
G | A | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13+1944G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881252 | ||||||
chr18:50881282
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-13+1974C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881282 | ||||||
chr18:50881303
|
C | G | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+1995C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881303 | ||||||
chr18:50881332
|
C | T | 10 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0111others(7): Show | 10 | HG00544.hp1 NA18940.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2024C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881332 | ||||||
chr18:50881423
|
A | G | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+2115A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881423 | ||||||
chr18:50881470
|
A | G | 4 | a0002c0002t0042g0315a0002c0002t0042g0316a0002c0002t0173g0317others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+2162A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881470 | ||||||
chr18:50881793
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-13+2485A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881793 | ||||||
chr18:50881915
|
T | A | 107 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-13+2607T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881915 | ||||||
chr18:50881946
|
G | A | 10 | a0001c0001t0003g0019a0001c0001t0006g0025a0001c0001t0008g0020others(7): Show | 10 | HG00423.hp1 NA18971.hp2 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2638G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881946 | ||||||
chr18:50881990
|
A | G | 1 | a0002c0002t0134g0173 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+2682A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50881990 | ||||||
chr18:50882026
|
G | A | 1 | a0001c0001t0139g0215 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-13+2718G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882026 | ||||||
chr18:50882029
|
C | A | 105 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+2721C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882029 | ||||||
chr18:50882049
|
A | G | 1 | a0001c0001t0004g0205 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-13+2741A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882049 | ||||||
chr18:50882201
|
G | A | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+2893G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882201 | ||||||
chr18:50882239
|
C | T | 1 | a0002c0002t0163g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-13+2931C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882239 | ||||||
chr18:50882241
|
C | T | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+2933C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882241 | ||||||
chr18:50882451
|
T | C | 1 | a0001c0001t0007g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+3143T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882451 | ||||||
chr18:50882746
|
C | G | 2 | a0001c0006t0006g0103a0001c0006t0055g0104 | 2 | NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-13+3438C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882746 | ||||||
chr18:50882778
|
G | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0007g0218 | 3 | HG00735.hp2 HG01361.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-13+3470G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882778 | ||||||
chr18:50882810
|
A | G | 1 | a0001c0001t0003g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-13+3502A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882810 | ||||||
chr18:50882813
|
G | A | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3505G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882813 | ||||||
chr18:50882864
|
G | A | 1 | a0002c0002t0023g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-13+3556G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50882864 | ||||||
chr18:50883005
|
A | T | 7 | a0001c0001t0001g0308a0001c0001t0004g0304a0001c0001t0004g0305others(4): Show | 7 | HG01109.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+3697A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883005 | ||||||
chr18:50883233
|
G | C | 1 | a0001c0001t0007g0220 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-13+3925G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883233 | ||||||
chr18:50883245
|
A | G | 4 | a0001c0001t0036g0201a0001c0001t0107g0202a0001c0001t0108g0203others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3937A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883245 | ||||||
chr18:50883325
|
C | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-13+4017C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883325 | ||||||
chr18:50883373
|
T | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+4065T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883373 | ||||||
chr18:50883587
|
G | A | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+4279G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883587 | ||||||
chr18:50883637
|
C | T | 105 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+4329C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883637 | ||||||
chr18:50883650
|
A | T | 3 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200 | 3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-13+4342A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883650 | ||||||
chr18:50883755
|
T | G | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+4447T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883755 | ||||||
chr18:50883984
|
T | A | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13+4676T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50883984 | ||||||
chr18:50884047
|
A | T | 1 | a0001c0001t0019g0101 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-13+4739A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884047 | ||||||
chr18:50884082
|
G | A | 1 | a0001c0001t0159g0221 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-13+4774G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884082 | ||||||
chr18:50884381
|
A | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-13+5073A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884381 | ||||||
chr18:50884494
|
C | T | 1 | a0002c0002t0132g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-13+5186C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884494 | ||||||
chr18:50884697
|
A | G | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-13+5389A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884697 | ||||||
chr18:50884704
|
G | A | 1 | a0001c0001t0007g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-13+5396G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884704 | ||||||
chr18:50884842
|
TTG | T | 74 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(71): Show | 75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.-13+5560_-13+5561d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50884842 | |||||
chr18:50884842
|
TTGTG | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-13+5558_-13+5561d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50884842 | |||||
chr18:50884858
|
G | A | 1 | a0001c0001t0058g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-13+5550G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884858 | ||||||
chr18:50884876
|
C | T | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-13+5568C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884876 | ||||||
chr18:50884884
|
C | T | 1 | a0001c0001t0004g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13+5576C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884884 | ||||||
chr18:50884958
|
A | G | 107 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-13+5650A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50884958 | ||||||
chr18:50885117
|
A | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+5809A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885117 | ||||||
chr18:50885184
|
A | G | 5 | a0001c0001t0010g0100a0001c0001t0059g0017a0001c0001t0073g0097others(2): Show | 5 | HG00639.hp2 HG01175.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+5876A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885184 | ||||||
chr18:50885259
|
T | C | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-13+5951T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885259 | ||||||
chr18:50885345
|
C | T | 1 | a0001c0001t0016g0096 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-13+6037C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885345 | ||||||
chr18:50885373
|
C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+6065C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885373 | ||||||
chr18:50885528
|
A | T | 7 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(4): Show | 7 | HG00099.hp2 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+6220A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885528 | ||||||
chr18:50885552
|
A | G | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+6244A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885552 | ||||||
chr18:50885821
|
G | C | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+6513G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885821 | ||||||
chr18:50885945
|
G | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+6637G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50885945 | ||||||
chr18:50886031
|
T | C | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+6723T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886031 | ||||||
chr18:50886108
|
CTA | C | 105 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+6808_-13+6809d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50886108 | |||||
chr18:50886166
|
T | TAAA | 9 | a0001c0001t0036g0191a0001c0001t0036g0201a0001c0001t0092g0189others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+6858_-13+6859i others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886166 | ||||||
chr18:50886167
|
T | A | 9 | a0001c0001t0036g0191a0001c0001t0036g0201a0001c0001t0092g0189others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+6859T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886167 | ||||||
chr18:50886167
|
T | TAAA | 135 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-13+6866_-13+6868d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50886167 | |||||
chr18:50886246
|
A | AT | 115 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(112): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-13+6953dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50886246 | |||||
chr18:50886263
|
A | G | 1 | a0001c0001t0043g0299 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-13+6955A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886263 | ||||||
chr18:50886444
|
A | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+7136A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886444 | ||||||
chr18:50886445
|
T | C | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+7137T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886445 | ||||||
chr18:50886524
|
G | A | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13+7216G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886524 | ||||||
chr18:50886750
|
C | T | 1 | a0002c0002t0023g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-13+7442C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886750 | ||||||
chr18:50886782
|
A | G | 4 | a0002c0002t0042g0315a0002c0002t0042g0316a0002c0002t0173g0317others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7474A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886782 | ||||||
chr18:50886949
|
T | C | 105 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13+7641T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50886949 | ||||||
chr18:50887204
|
T | C | 2 | a0001c0003t0013g0009a0001c0003t0140g0009 | 2 | NA18955.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-13+7896T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887204 | ||||||
chr18:50887546
|
C | T | 1 | a0002c0002t0011g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13+8238C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887546 | ||||||
chr18:50887865
|
A | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-12-7944A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887865 | ||||||
chr18:50887961
|
A | G | 105 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12-7848A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50887961 | ||||||
chr18:50888034
|
G | A | 97 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-12-7775G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888034 | ||||||
chr18:50888244
|
C | T | 2 | a0001c0001t0037g0297a0001c0001t0037g0298 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-12-7565C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888244 | ||||||
chr18:50888310
|
A | C | 2 | a0001c0001t0049g0016a0001c0001t0050g0105 | 2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-12-7499A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888310 | ||||||
chr18:50888344
|
CA | C | 11 | a0001c0001t0081g0018a0001c0001t0166g0223a0001c0001t0169g0192others(8): Show | 12 | HG01358.hp2 HG01993.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-7448delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888344 | |||||
chr18:50888344
|
CAA | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-12-7449_-12-7448d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888344 | |||||
chr18:50888344
|
CAAA | C | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-7450_-12-7448d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888344 | |||||
chr18:50888452
|
C | G | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-12-7357C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888452 | ||||||
chr18:50888520
|
G | A | 328 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(325): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-12-7289G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888520 | ||||||
chr18:50888556
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-12-7253T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888556 | ||||||
chr18:50888567
|
A | AT | 8 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(5): Show | 9 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-7233dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50888567 | |||||
chr18:50888876
|
A | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-12-6933A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888876 | ||||||
chr18:50888885
|
A | T | 97 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-12-6924A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50888885 | ||||||
chr18:50889024
|
GTTC | G | 6 | a0002c0002t0023g0176a0002c0002t0023g0180a0002c0002t0094g0177others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6780_-12-6778d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50889024 | |||||
chr18:50889067
|
T | C | 1 | a0001c0001t0143g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-12-6742T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889067 | ||||||
chr18:50889075
|
A | G | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-6734A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889075 | ||||||
chr18:50889283
|
G | C | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-12-6526G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889283 | ||||||
chr18:50889381
|
T | C | 1 | a0001c0001t0068g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-6428T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889381 | ||||||
chr18:50889764
|
G | A | 3 | a0001c0001t0070g0034a0001c0006t0006g0103a0001c0006t0055g0104 | 3 | HG01928.hp1 NA18957.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-12-6045G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889764 | ||||||
chr18:50889914
|
T | G | 1 | a0001c0001t0022g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12-5895T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50889914 | ||||||
chr18:50890273
|
ATT | A | 4 | a0002c0002t0042g0315a0002c0002t0042g0316a0002c0002t0173g0317others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-5533_-12-5532d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50890273 | |||||
chr18:50890411
|
G | A | 1 | a0001c0001t0006g0035 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-12-5398G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890411 | ||||||
chr18:50890502
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-12-5307C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890502 | ||||||
chr18:50890547
|
C | T | 1 | a0002c0002t0023g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-12-5262C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890547 | ||||||
chr18:50890578
|
A | C | 105 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12-5231A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890578 | ||||||
chr18:50890583
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12-5226T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890583 | ||||||
chr18:50890842
|
G | A | 17 | a0001c0001t0010g0043a0001c0001t0010g0048a0001c0001t0010g0049others(14): Show | 17 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-4967G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890842 | ||||||
chr18:50890914
|
G | C | 1 | a0001c0001t0002g0227 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-12-4895G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50890914 | ||||||
chr18:50891016
|
A | G | 1 | a0002c0002t0163g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12-4793A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891016 | ||||||
chr18:50891194
|
A | G | 6 | a0002c0002t0023g0176a0002c0002t0023g0180a0002c0002t0094g0177others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-4615A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891194 | ||||||
chr18:50891294
|
C | T | 1 | a0001c0001t0136g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-12-4515C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891294 | ||||||
chr18:50891326
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-12-4483A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891326 | ||||||
chr18:50891600
|
A | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-12-4209A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891600 | ||||||
chr18:50891715
|
A | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-4094A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891715 | ||||||
chr18:50891791
|
G | A | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-4018G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891791 | ||||||
chr18:50891812
|
T | C | 1 | a0001c0001t0124g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-12-3997T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891812 | ||||||
chr18:50891903
|
C | T | 8 | a0001c0001t0001g0308a0001c0001t0004g0121a0001c0001t0004g0304others(5): Show | 8 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-3906C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50891903 | ||||||
chr18:50891988
|
G | GT | 90 | a0001c0001t0001g0295a0001c0001t0025g0027a0001c0001t0025g0029others(87): Show | 91 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-12-3809dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50891988 | |||||
chr18:50892041
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-12-3768G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892041 | ||||||
chr18:50892169
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-12-3640T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892169 | ||||||
chr18:50892207
|
G | A | 70 | a0001c0001t0109g0157a0002c0002t0005g0127a0002c0002t0005g0129others(67): Show | 71 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12-3602G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892207 | ||||||
chr18:50892221
|
C | A | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-3588C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892221 | ||||||
chr18:50892398
|
G | C | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3411G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892398 | ||||||
chr18:50892528
|
T | C | 2 | a0001c0001t0047g0055a0001c0001t0048g0056 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-12-3281T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892528 | ||||||
chr18:50892727
|
T | C | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-3082T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50892727 | ||||||
chr18:50893026
|
G | A | 4 | a0001c0001t0028g0057a0001c0001t0028g0059a0001c0001t0057g0058others(1): Show | 4 | HG00738.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-2783G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893026 | ||||||
chr18:50893124
|
C | CA | 40 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0102others(37): Show | 40 | HG00423.hp1 HG00423.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12-2657dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
C | CAA | 5 | a0001c0001t0030g0060a0001c0001t0085g0036a0002c0002t0021g0005others(2): Show | 6 | HG00597.hp1 HG01358.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-2658_-12-2657d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0181g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-12-2667_-12-2657d others(13): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0032g0004a0001c0001t0170g0193 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-12-2674_-12-2657d others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0038g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-12-2683_-12-2657d others(29): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-12-2657_-12-2656i others(31): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0041g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-12-2657_-12-2656i others(35): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
CA | C | 17 | a0001c0001t0003g0092a0001c0001t0010g0100a0001c0001t0014g0090others(14): Show | 17 | HG00609.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-2657delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
CAAAAAAA others(2): Show |
C | 118 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-2665_-12-2657d others(11): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893124
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0308a0001c0001t0004g0304a0001c0001t0004g0305others(6): Show | 9 | HG01109.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12-2666_-12-2657d others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893124 | |||||
chr18:50893148
|
A | C | 2 | a0001c0001t0068g0033a0006c0009t0069g0053 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-12-2661A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893148 | ||||||
chr18:50893151
|
A | AAAAAAAA others(10): Show |
1 | a0003c0007t0012g0184 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12-2657_-12-2656i others(19): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50893151 | |||||
chr18:50893153
|
C | A | 4 | a0001c0001t0028g0057a0001c0001t0028g0059a0001c0001t0057g0058others(1): Show | 4 | HG00738.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-2656C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893153 | ||||||
chr18:50893264
|
A | T | 6 | a0002c0002t0023g0176a0002c0002t0023g0180a0002c0002t0094g0177others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2545A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893264 | ||||||
chr18:50893710
|
A | T | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-2099A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893710 | ||||||
chr18:50893858
|
A | G | 1 | a0001c0001t0164g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-12-1951A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893858 | ||||||
chr18:50893898
|
C | T | 7 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG01069.hp1 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-1911C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50893898 | ||||||
chr18:50894002
|
A | C | 3 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200 | 3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-12-1807A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894002 | ||||||
chr18:50894057
|
C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-12-1752C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894057 | ||||||
chr18:50894137
|
C | T | 1 | a0001c0001t0007g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-12-1672C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894137 | ||||||
chr18:50894166
|
A | G | 1 | a0001c0001t0010g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-12-1643A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894166 | ||||||
chr18:50894289
|
C | T | 11 | a0001c0001t0003g0019a0001c0001t0006g0025a0001c0001t0008g0020others(8): Show | 11 | HG00423.hp1 NA18965.hp2 NA18971.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-1520C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894289 | ||||||
chr18:50894291
|
C | T | 1 | a0001c0003t0144g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-12-1518C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894291 | ||||||
chr18:50894366
|
C | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-12-1443C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894366 | ||||||
chr18:50894517
|
G | A | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-1292G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894517 | ||||||
chr18:50894528
|
G | A | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-1281G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894528 | ||||||
chr18:50894567
|
CA | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-12-1231delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50894567 | |||||
chr18:50894653
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(234): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-12-1156A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894653 | ||||||
chr18:50894746
|
G | A | 7 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG01069.hp1 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-1063G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894746 | ||||||
chr18:50894750
|
G | T | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-1059G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894750 | ||||||
chr18:50894856
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12-953A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894856 | ||||||
chr18:50894860
|
G | C | 1 | a0001c0001t0079g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-12-949G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894860 | ||||||
chr18:50894876
|
CA | C | 15 | a0001c0001t0001g0287a0001c0001t0014g0115a0001c0001t0061g0069others(12): Show | 15 | HG00408.hp2 HG01069.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12-917delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50894876 | |||||
chr18:50894892
|
A | T | 14 | a0001c0001t0123g0326a0001c0001t0158g0288a0001c0001t0171g0212others(11): Show | 14 | HG00408.hp2 HG00741.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-917A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894892 | ||||||
chr18:50894955
|
CA | C | 13 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(10): Show | 13 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-840delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50894955 | |||||
chr18:50894966
|
A | C | 1 | a0001c0001t0010g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12-843A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50894966 | ||||||
chr18:50895002
|
A | G | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-807A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895002 | ||||||
chr18:50895115
|
T | C | 1 | a0002c0002t0042g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-694T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895115 | ||||||
chr18:50895185
|
T | C | 1 | a0001c0001t0032g0004 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-12-624T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895185 | ||||||
chr18:50895252
|
ATTAC | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-12-554_-12-551del others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 50895252 | |||||
chr18:50895308
|
T | G | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-501T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895308 | ||||||
chr18:50895334
|
G | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-12-475G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895334 | ||||||
chr18:50895357
|
G | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-12-452G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895357 | ||||||
chr18:50895501
|
C | T | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-308C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895501 | ||||||
chr18:50895582
|
C | T | 1 | a0001c0001t0076g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12-227C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 1/15 | chr18 | 50895582 | ||||||
chr18:50895983
|
T | C | 10 | a0001c0001t0010g0043a0001c0001t0027g0042a0001c0001t0027g0047others(7): Show | 10 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+55T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50895983 | ||||||
chr18:50895991
|
A | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+63A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50895991 | ||||||
chr18:50896067
|
G | A | 1 | a0001c0001t0015g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.108+139G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896067 | ||||||
chr18:50896347
|
C | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+419C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896347 | ||||||
chr18:50896366
|
T | C | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.108+438T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896366 | ||||||
chr18:50896529
|
T | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+601T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896529 | ||||||
chr18:50896615
|
A | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.108+687A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50896615 | ||||||
chr18:50897092
|
T | A | 1 | a0002c0002t0098g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108+1164T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897092 | ||||||
chr18:50897238
|
C | T | 2 | a0002c0002t0011g0154a0002c0002t0087g0153 | 2 | NA18990.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.108+1310C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897238 | ||||||
chr18:50897571
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.108+1643C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897571 | ||||||
chr18:50897582
|
C | T | 1 | a0002c0002t0120g0161 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+1654C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897582 | ||||||
chr18:50897831
|
C | A | 3 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200 | 3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.108+1903C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897831 | ||||||
chr18:50897861
|
A | G | 1 | a0001c0001t0046g0087 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.108+1933A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50897861 | ||||||
chr18:50897865
|
AAAAAAG | A | 81 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(78): Show | 82 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.108+1955_108+1960d others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50897865 | |||||
chr18:50898084
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(238): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.108+2156A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898084 | ||||||
chr18:50898621
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.108+2693T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898621 | ||||||
chr18:50898668
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.108+2740G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898668 | ||||||
chr18:50898671
|
G | A | 1 | a0001c0001t0004g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.108+2743G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898671 | ||||||
chr18:50898823
|
C | T | 1 | a0001c0001t0024g0286 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.108+2895C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898823 | ||||||
chr18:50898865
|
T | G | 1 | a0001c0001t0049g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.108+2937T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898865 | ||||||
chr18:50898869
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.108+2941C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898869 | ||||||
chr18:50898881
|
A | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.108+2953A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898881 | ||||||
chr18:50898955
|
T | G | 1 | a0001c0001t0007g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+3027T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50898955 | ||||||
chr18:50899092
|
G | A | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108+3164G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899092 | ||||||
chr18:50899160
|
T | C | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108+3232T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899160 | ||||||
chr18:50899376
|
G | A | 5 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0002g0010others(2): Show | 5 | HG01358.hp1 NA18955.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+3448G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899376 | ||||||
chr18:50899451
|
C | T | 2 | a0001c0001t0004g0008a0001c0001t0169g0192 | 3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108+3523C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899451 | ||||||
chr18:50899567
|
G | A | 1 | a0001c0001t0009g0072 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.108+3639G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899567 | ||||||
chr18:50899718
|
G | A | 1 | a0001c0001t0015g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.108+3790G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899718 | ||||||
chr18:50899796
|
T | C | 1 | a0002c0002t0122g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.108+3868T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899796 | ||||||
chr18:50899947
|
A | G | 61 | a0001c0001t0001g0014a0001c0001t0001g0217a0001c0001t0001g0219others(58): Show | 62 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.108+4019A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50899947 | ||||||
chr18:50900216
|
G | GT | 8 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0002g0257others(5): Show | 8 | HG02647.hp2 HG03704.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+4299dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900216 | |||||
chr18:50900270
|
T | TTTTA | 16 | a0001c0001t0003g0113a0001c0001t0006g0067a0001c0001t0010g0100others(13): Show | 17 | HG00408.hp2 HG00735.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.108+4381_108+4384d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900270 | |||||
chr18:50900270
|
TTTTA | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(200): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.108+4381_108+4384d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900270 | |||||
chr18:50900340
|
G | T | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.108+4412G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900340 | ||||||
chr18:50900363
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108+4435C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900363 | ||||||
chr18:50900443
|
T | C | 4 | a0002c0002t0042g0315a0002c0002t0042g0316a0002c0002t0173g0317others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+4515T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900443 | ||||||
chr18:50900463
|
T | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+4535T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900463 | ||||||
chr18:50900727
|
GT | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+4802delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50900727 | |||||
chr18:50900782
|
T | C | 1 | a0001c0001t0016g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.108+4854T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900782 | ||||||
chr18:50900922
|
A | G | 6 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200others(3): Show | 6 | HG02451.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+4994A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900922 | ||||||
chr18:50900975
|
CAAT | C | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+5048_108+5050d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50900975 | ||||||
chr18:50901071
|
T | C | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.108+5143T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901071 | ||||||
chr18:50901110
|
C | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.108+5182C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901110 | ||||||
chr18:50901309
|
C | T | 1 | a0001c0001t0124g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.108+5381C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901309 | ||||||
chr18:50901622
|
T | C | 1 | a0001c0001t0010g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108+5694T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901622 | ||||||
chr18:50901763
|
C | G | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.108+5835C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901763 | ||||||
chr18:50901824
|
A | C | 1 | a0002c0002t0157g0178 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.108+5896A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901824 | ||||||
chr18:50901940
|
C | T | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+6012C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50901940 | ||||||
chr18:50902043
|
A | T | 1 | a0001c0001t0008g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109-6020A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902043 | ||||||
chr18:50902219
|
T | C | 1 | a0001c0001t0004g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.109-5844T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902219 | ||||||
chr18:50902455
|
A | G | 4 | a0002c0002t0021g0005a0002c0002t0099g0158a0002c0002t0120g0161others(1): Show | 5 | HG01358.hp2 HG01993.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-5608A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902455 | ||||||
chr18:50902485
|
G | C | 1 | a0001c0001t0181g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.109-5578G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902485 | ||||||
chr18:50902543
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.109-5520A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902543 | ||||||
chr18:50902585
|
C | T | 64 | a0001c0001t0109g0157a0002c0002t0005g0127a0002c0002t0005g0129others(61): Show | 65 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.109-5478C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902585 | ||||||
chr18:50902597
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200 | 3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.109-5466G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902597 | ||||||
chr18:50902630
|
C | T | 1 | a0001c0001t0170g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109-5433C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902630 | ||||||
chr18:50902778
|
A | G | 49 | a0001c0001t0109g0157a0002c0002t0005g0127a0002c0002t0005g0129others(46): Show | 50 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.109-5285A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902778 | ||||||
chr18:50902809
|
A | G | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109-5254A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50902809 | ||||||
chr18:50903067
|
A | G | 1 | a0002c0002t0121g0150 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.109-4996A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903067 | ||||||
chr18:50903102
|
G | C | 8 | a0001c0001t0036g0191a0001c0001t0036g0201a0001c0001t0107g0202others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-4961G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903102 | ||||||
chr18:50903113
|
G | C | 1 | a0001c0001t0002g0233 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.109-4950G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903113 | ||||||
chr18:50903126
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(238): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.109-4937A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903126 | ||||||
chr18:50903234
|
T | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(220): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.109-4829T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903234 | ||||||
chr18:50903335
|
T | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-4728T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903335 | ||||||
chr18:50903455
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.109-4608G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903455 | ||||||
chr18:50903535
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.109-4528C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903535 | ||||||
chr18:50903695
|
C | T | 1 | a0001c0001t0014g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109-4368C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903695 | ||||||
chr18:50903697
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.109-4366T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903697 | ||||||
chr18:50903787
|
A | G | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.109-4276A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903787 | ||||||
chr18:50903791
|
G | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-4272G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903791 | ||||||
chr18:50903937
|
G | A | 2 | a0001c0001t0003g0019a0001c0001t0009g0023 | 2 | NA18985.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.109-4126G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50903937 | ||||||
chr18:50904007
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.109-4056G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904007 | ||||||
chr18:50904194
|
G | A | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-3869G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904194 | ||||||
chr18:50904279
|
G | GT | 10 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0084g0099others(7): Show | 10 | HG01361.hp2 HG01884.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-3769dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr18 | 50904279 | |||||
chr18:50904280
|
T | C | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-3783T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904280 | ||||||
chr18:50904360
|
C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-3703C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904360 | ||||||
chr18:50904410
|
C | A | 74 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(71): Show | 75 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.109-3653C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904410 | ||||||
chr18:50904532
|
C | T | 1 | a0001c0001t0015g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.109-3531C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904532 | ||||||
chr18:50904717
|
C | T | 1 | a0002c0002t0150g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109-3346C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904717 | ||||||
chr18:50904819
|
A | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-3244A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50904819 | ||||||
chr18:50905073
|
G | A | 6 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200others(3): Show | 6 | HG02451.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-2990G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50905073 | ||||||
chr18:50905159
|
G | A | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-2904G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50905159 | ||||||
chr18:50905410
|
T | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-2653T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50905410 | ||||||
chr18:50906432
|
C | T | 14 | a0001c0001t0001g0013a0001c0001t0001g0245a0001c0001t0001g0287others(11): Show | 14 | HG00408.hp1 HG00544.hp2 HG03834.hp2 others(11): Show |
intron_variant | MODIFIER | c.109-1631C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906432 | ||||||
chr18:50906489
|
T | G | 9 | a0001c0001t0006g0067a0001c0001t0014g0090a0001c0001t0014g0115others(6): Show | 9 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-1574T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906489 | ||||||
chr18:50906714
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.109-1349G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906714 | ||||||
chr18:50906770
|
G | A | 2 | a0001c0003t0013g0207a0001c0003t0039g0208 | 2 | NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.109-1293G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50906770 | ||||||
chr18:50907124
|
C | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.109-939C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907124 | ||||||
chr18:50907213
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.109-850A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907213 | ||||||
chr18:50907386
|
G | A | 1 | a0001c0001t0002g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.109-677G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907386 | ||||||
chr18:50907509
|
C | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-554C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907509 | ||||||
chr18:50907635
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.109-428A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907635 | ||||||
chr18:50907655
|
G | A | 1 | a0001c0001t0092g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109-408G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907655 | ||||||
chr18:50907697
|
C | G | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.109-366C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907697 | ||||||
chr18:50907740
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.109-323G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907740 | ||||||
chr18:50907850
|
A | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-213A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907850 | ||||||
chr18:50907853
|
C | G | 1 | a0001c0001t0086g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.109-210C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907853 | ||||||
chr18:50907862
|
A | G | 1 | a0001c0001t0008g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109-201A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907862 | ||||||
chr18:50907909
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(135): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.109-154A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 2/15 | chr18 | 50907909 | ||||||
chr18:50908247
|
C | T | 1 | a0001c0001t0008g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.242+51C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908247 | ||||||
chr18:50908350
|
C | T | 1 | a0001c0001t0030g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.242+154C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908350 | ||||||
chr18:50908419
|
C | A | 57 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(54): Show | 58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.242+223C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908419 | ||||||
chr18:50908520
|
T | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.242+324T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908520 | ||||||
chr18:50908712
|
C | T | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242+516C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908712 | ||||||
chr18:50908786
|
G | A | 1 | a0001c0001t0015g0074 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.242+590G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908786 | ||||||
chr18:50908786
|
G | T | 57 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(54): Show | 58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.242+590G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908786 | ||||||
chr18:50908887
|
C | T | 1 | a0001c0001t0006g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.242+691C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908887 | ||||||
chr18:50908956
|
C | CT | 7 | a0001c0001t0010g0052a0001c0001t0025g0027a0001c0001t0025g0029others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.242+775dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50908956 | |||||
chr18:50908956
|
CT | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.242+775delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50908956 | |||||
chr18:50908961
|
T | C | 2 | a0001c0001t0015g0071a0001c0001t0076g0088 | 2 | HG00280.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.242+765T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50908961 | ||||||
chr18:50909166
|
A | G | 1 | a0001c0001t0082g0091 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.242+970A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909166 | ||||||
chr18:50909210
|
C | T | 1 | a0002c0002t0023g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.242+1014C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909210 | ||||||
chr18:50909371
|
C | T | 1 | a0001c0003t0039g0209 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.242+1175C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909371 | ||||||
chr18:50909389
|
G | A | 1 | a0001c0001t0007g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.242+1193G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909389 | ||||||
chr18:50909429
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0017g0280 | 2 | NA18998.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.242+1233A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909429 | ||||||
chr18:50909531
|
A | G | 13 | a0002c0002t0005g0127a0002c0002t0005g0149a0002c0002t0034g0147others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.242+1335A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909531 | ||||||
chr18:50909538
|
G | A | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.242+1342G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909538 | ||||||
chr18:50909553
|
C | T | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.242+1357C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909553 | ||||||
chr18:50909575
|
T | C | 1 | a0001c0001t0044g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.242+1379T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909575 | ||||||
chr18:50909606
|
G | A | 2 | a0001c0001t0068g0033a0006c0009t0069g0053 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.242+1410G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909606 | ||||||
chr18:50909625
|
A | G | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.242+1429A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909625 | ||||||
chr18:50909954
|
A | G | 9 | a0001c0001t0036g0191a0001c0001t0036g0201a0001c0001t0092g0189others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+1758A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50909954 | ||||||
chr18:50910045
|
G | T | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242+1849G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910045 | ||||||
chr18:50910192
|
G | A | 1 | a0002c0002t0089g0151 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.242+1996G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910192 | ||||||
chr18:50910268
|
C | CA | 117 | a0001c0001t0001g0230a0001c0001t0001g0244a0001c0001t0001g0245others(114): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.242+2096dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910268 | |||||
chr18:50910268
|
C | CAA | 62 | a0001c0001t0003g0076a0001c0001t0003g0113a0001c0001t0012g0006others(59): Show | 62 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.242+2095_242+2096d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910268 | |||||
chr18:50910268
|
C | CAAA | 17 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0020g0120others(14): Show | 18 | HG00423.hp2 HG01175.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.242+2094_242+2096d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910268 | |||||
chr18:50910355
|
C | A | 1 | a0001c0001t0022g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.242+2159C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910355 | ||||||
chr18:50910440
|
G | GA | 15 | a0001c0001t0002g0236a0001c0001t0004g0121a0001c0001t0004g0253others(12): Show | 15 | HG00621.hp2 HG00735.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.242+2261dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 50910440 | |||||
chr18:50910454
|
A | AG | 9 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(6): Show | 9 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+2258_242+2259i others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910454 | ||||||
chr18:50910454
|
A | G | 4 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326others(1): Show | 4 | HG01192.hp1 HG02071.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+2258A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910454 | ||||||
chr18:50910458
|
G | A | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.242+2262G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910458 | ||||||
chr18:50910459
|
A | G | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.242+2263A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910459 | ||||||
chr18:50910460
|
A | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.242+2264A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910460 | ||||||
chr18:50910720
|
C | T | 1 | a0001c0001t0029g0046 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.243-2081C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910720 | ||||||
chr18:50910987
|
G | A | 2 | a0001c0005t0024g0313a0001c0005t0130g0312 | 2 | HG02602.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.243-1814G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50910987 | ||||||
chr18:50911103
|
G | C | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.243-1698G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911103 | ||||||
chr18:50911196
|
C | T | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.243-1605C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911196 | ||||||
chr18:50911347
|
G | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.243-1454G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911347 | ||||||
chr18:50911453
|
A | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0309 | 2 | HG01109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.243-1348A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911453 | ||||||
chr18:50911814
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.243-987C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50911814 | ||||||
chr18:50912165
|
A | G | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.243-636A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912165 | ||||||
chr18:50912296
|
T | C | 9 | a0002c0002t0020g0120a0002c0002t0020g0322a0002c0002t0020g0323others(6): Show | 9 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.243-505T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912296 | ||||||
chr18:50912304
|
G | T | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.243-497G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912304 | ||||||
chr18:50912420
|
A | T | 1 | a0002c0004t0147g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.243-381A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 3/15 | chr18 | 50912420 | ||||||
chr18:50913074
|
C | T | 4 | a0001c0001t0002g0256a0001c0001t0018g0255a0001c0001t0018g0278others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+124C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913074 | ||||||
chr18:50913170
|
T | C | 1 | a0001c0001t0180g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.392+220T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913170 | ||||||
chr18:50913265
|
C | A | 57 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(54): Show | 58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.392+315C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913265 | ||||||
chr18:50913746
|
G | A | 1 | a0001c0001t0167g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.392+796G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913746 | ||||||
chr18:50913811
|
A | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.392+861A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913811 | ||||||
chr18:50913860
|
T | TACACAC | 18 | a0001c0001t0003g0077a0001c0001t0171g0212a0001c0003t0013g0009others(15): Show | 18 | HG00408.hp2 HG00738.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.392+936_392+941dup others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TACACACA others(1): Show |
37 | a0001c0001t0028g0057a0001c0001t0051g0118a0001c0001t0057g0058others(34): Show | 38 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.392+934_392+941dup others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TACACACA others(3): Show |
15 | a0001c0001t0028g0059a0001c0001t0108g0203a0002c0002t0011g0165others(12): Show | 15 | HG01934.hp2 HG02145.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.392+932_392+941dup others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TACACACA others(5): Show |
11 | a0001c0001t0052g0117a0002c0002t0020g0323a0002c0002t0023g0176others(8): Show | 11 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.392+930_392+941dup others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TACACACA others(7): Show |
12 | a0001c0001t0001g0295a0001c0001t0004g0121a0001c0001t0036g0191others(9): Show | 12 | HG01175.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.392+928_392+941dup others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TACACACA others(9): Show |
1 | a0002c0002t0020g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.392+926_392+941dup others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TACACACA others(13): Show |
3 | a0001c0001t0170g0193a0002c0002t0182g0015a0002c0002t0183g0015 | 3 | HG02818.hp1 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.392+922_392+941dup others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATAC | 4 | a0001c0001t0001g0232a0001c0001t0002g0256a0001c0001t0007g0220others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(1): Show |
3 | a0001c0001t0004g0195a0001c0001t0123g0326a0001c0001t0125g0196 | 3 | HG01192.hp1 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.392+911_392+912ins others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(3): Show |
10 | a0001c0001t0001g0199a0001c0001t0025g0027a0001c0001t0026g0002others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(5): Show |
6 | a0001c0001t0002g0236a0001c0001t0004g0008a0001c0001t0004g0205others(3): Show | 7 | HG01243.hp2 HG01433.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(7): Show |
25 | a0001c0001t0001g0014a0001c0001t0001g0273a0001c0001t0001g0276others(22): Show | 26 | HG00280.hp1 HG00621.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(9): Show |
73 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 75 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(11): Show |
21 | a0001c0001t0001g0245a0001c0001t0002g0010a0001c0001t0004g0305others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.392+911_392+912ins others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(13): Show |
3 | a0001c0001t0001g0279a0001c0001t0002g0235a0001c0001t0181g0197 | 3 | HG02280.hp1 NA18522.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.392+911_392+912ins others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913860
|
T | TATACACA others(17): Show |
2 | a0003c0007t0012g0184a0003c0007t0161g0311 | 2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.392+911_392+912ins others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50913860 | |||||
chr18:50913862
|
C | T | 1 | a0001c0001t0017g0283 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.392+912C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913862 | ||||||
chr18:50913892
|
T | C | 14 | a0001c0001t0001g0199a0001c0001t0001g0273a0001c0001t0041g0198others(11): Show | 14 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.392+942T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913892 | ||||||
chr18:50913997
|
G | A | 1 | a0001c0001t0008g0020 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.392+1047G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50913997 | ||||||
chr18:50914329
|
A | G | 6 | a0002c0002t0020g0120a0002c0002t0020g0322a0002c0002t0020g0323others(3): Show | 6 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+1379A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914329 | ||||||
chr18:50914454
|
A | T | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.392+1504A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914454 | ||||||
chr18:50914471
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.392+1521A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914471 | ||||||
chr18:50914474
|
G | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.392+1524G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914474 | ||||||
chr18:50914608
|
T | G | 1 | a0001c0001t0142g0294 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.393-1560T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914608 | ||||||
chr18:50914867
|
C | T | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.393-1301C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914867 | ||||||
chr18:50914972
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(147): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.393-1196T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50914972 | ||||||
chr18:50915089
|
C | CCCT | 5 | a0001c0001t0001g0240a0001c0001t0001g0279a0001c0001t0017g0280others(2): Show | 5 | HG02809.hp1 NA18940.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.393-1053_393-1051d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50915089 | |||||
chr18:50915089
|
CCCT | C | 72 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(69): Show | 73 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.393-1053_393-1051d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr18 | 50915089 | |||||
chr18:50915271
|
G | A | 1 | a0002c0004t0147g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.393-897G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915271 | ||||||
chr18:50915272
|
A | G | 1 | a0002c0004t0147g0130 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.393-896A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915272 | ||||||
chr18:50915292
|
C | T | 3 | a0001c0001t0043g0299a0001c0001t0043g0300a0001c0001t0172g0251 | 3 | NA18949.hp1 NA18974.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.393-876C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915292 | ||||||
chr18:50915315
|
C | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.393-853C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915315 | ||||||
chr18:50915324
|
A | G | 6 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.393-844A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915324 | ||||||
chr18:50915346
|
C | T | 10 | a0001c0001t0010g0043a0001c0001t0027g0042a0001c0001t0027g0047others(7): Show | 10 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.393-822C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915346 | ||||||
chr18:50915363
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.393-805C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915363 | ||||||
chr18:50915621
|
A | G | 4 | a0001c0001t0036g0201a0001c0001t0107g0202a0001c0001t0108g0203others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-547A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915621 | ||||||
chr18:50915685
|
T | A | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.393-483T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4/15 | chr18 | 50915685 | ||||||
chr18:50916269
|
C | T | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+26C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916269 | ||||||
chr18:50916539
|
A | T | 1 | a0002c0002t0011g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.468+296A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916539 | ||||||
chr18:50916580
|
T | C | 2 | a0002c0002t0023g0174a0002c0002t0150g0179 | 2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.468+337T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916580 | ||||||
chr18:50916772
|
A | G | 12 | a0001c0001t0003g0065a0001c0001t0003g0076a0001c0001t0006g0083others(9): Show | 12 | NA18954.hp1 NA18964.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.468+529A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50916772 | ||||||
chr18:50916925
|
CCTTTTT | C | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-414_469-409del others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr18 | 50916925 | |||||
chr18:50917010
|
C | A | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-337C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 5/15 | chr18 | 50917010 | ||||||
chr18:50917617
|
A | AT | 10 | a0002c0002t0020g0120a0002c0002t0020g0322a0002c0002t0020g0323others(7): Show | 10 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+118dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr18 | 50917617 | |||||
chr18:50917691
|
T | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+183T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | chr18 | 50917691 | ||||||
chr18:50917709
|
T | G | 1 | a0002c0002t0102g0122 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.630+201T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | chr18 | 50917709 | ||||||
chr18:50917919
|
C | T | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.631-191C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 6/15 | chr18 | 50917919 | ||||||
chr18:50918407
|
C | CT | 67 | a0001c0001t0017g0283a0001c0001t0059g0017a0001c0001t0109g0157others(64): Show | 68 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.734+195dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr18 | 50918407 | |||||
chr18:50918433
|
C | G | 50 | a0001c0001t0109g0157a0002c0002t0005g0127a0002c0002t0005g0129others(47): Show | 51 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.734+220C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918433 | ||||||
chr18:50918517
|
C | G | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.734+304C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918517 | ||||||
chr18:50918702
|
C | CT | 148 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(145): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.734+504dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr18 | 50918702 | |||||
chr18:50918704
|
T | C | 63 | a0001c0001t0003g0019a0001c0001t0003g0065a0001c0001t0003g0076others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.734+491T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918704 | ||||||
chr18:50918705
|
T | C | 1 | a0001c0001t0003g0111 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.734+492T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918705 | ||||||
chr18:50918879
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.734+666A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918879 | ||||||
chr18:50918898
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(228): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.734+685G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50918898 | ||||||
chr18:50919006
|
G | A | 1 | a0001c0001t0015g0071 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.734+793G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919006 | ||||||
chr18:50919062
|
C | CTCCCG | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.734+849_734+850ins others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919062 | ||||||
chr18:50919063
|
A | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.734+850A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919063 | ||||||
chr18:50919065
|
A | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.734+852A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919065 | ||||||
chr18:50919066
|
T | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.734+853T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919066 | ||||||
chr18:50919067
|
T | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.734+854T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919067 | ||||||
chr18:50919128
|
G | A | 76 | a0001c0001t0032g0004a0001c0001t0086g0116a0002c0002t0005g0127others(73): Show | 78 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.734+915G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919128 | ||||||
chr18:50919249
|
T | A | 333 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(330): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.734+1036T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919249 | ||||||
chr18:50919413
|
A | G | 9 | a0002c0002t0020g0120a0002c0002t0020g0322a0002c0002t0020g0323others(6): Show | 9 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.735-1043A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919413 | ||||||
chr18:50919433
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.735-1023T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919433 | ||||||
chr18:50919807
|
T | C | 6 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-649T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50919807 | ||||||
chr18:50920020
|
T | G | 1 | a0001c0001t0044g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735-436T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920020 | ||||||
chr18:50920225
|
G | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(238): Show | 246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.735-231G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920225 | ||||||
chr18:50920338
|
G | T | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.735-118G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920338 | ||||||
chr18:50920340
|
C | G | 1 | a0001c0001t0062g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.735-116C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 7/15 | chr18 | 50920340 | ||||||
chr18:50920573
|
A | C | 4 | a0002c0002t0042g0315a0002c0002t0042g0316a0002c0002t0173g0317others(1): Show | 4 | HG02572.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.844+8A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 8/15 | chr18 | 50920573 | ||||||
chr18:50920583
|
C | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.844+18C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 8/15 | chr18 | 50920583 | ||||||
chr18:50920794
|
C | T | 1 | a0001c0001t0008g0026 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.942+36C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 9/15 | chr18 | 50920794 | ||||||
chr18:50921035
|
T | G | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.943-39T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 9/15 | chr18 | 50921035 | ||||||
chr18:50921194
|
T | C | 1 | a0001c0001t0124g0228 | 1 | HG00323.hp1 | splice_region_variant&intron_variant | LOW | c.1056+7T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921194 | ||||||
chr18:50921384
|
A | G | 5 | a0002c0002t0005g0149a0002c0002t0101g0144a0002c0002t0116g0128others(2): Show | 5 | NA18612.hp1 NA18985.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056+197A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921384 | ||||||
chr18:50921406
|
T | TA | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1056+220dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr18 | 50921406 | |||||
chr18:50921500
|
T | C | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1056+313T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921500 | ||||||
chr18:50921641
|
A | G | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1056+454A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921641 | ||||||
chr18:50921701
|
C | A | 1 | a0001c0001t0167g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1056+514C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921701 | ||||||
chr18:50921702
|
G | T | 1 | a0001c0001t0167g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1056+515G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921702 | ||||||
chr18:50921711
|
G | C | 1 | a0001c0001t0007g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1056+524G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921711 | ||||||
chr18:50921940
|
G | C | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1056+753G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50921940 | ||||||
chr18:50922100
|
C | T | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+913C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922100 | ||||||
chr18:50922333
|
G | A | 10 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1056+1146G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922333 | ||||||
chr18:50922398
|
C | T | 4 | a0001c0001t0001g0272a0001c0001t0007g0262a0001c0001t0135g0277others(1): Show | 4 | NA18978.hp2 NA18999.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056+1211C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922398 | ||||||
chr18:50922425
|
T | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1056+1238T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922425 | ||||||
chr18:50922669
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1057-1429C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922669 | ||||||
chr18:50922816
|
T | C | 7 | a0001c0001t0109g0157a0002c0002t0131g0171a0002c0002t0132g0172others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-1282T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922816 | ||||||
chr18:50922870
|
T | C | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-1228T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922870 | ||||||
chr18:50922971
|
C | A | 4 | a0002c0002t0020g0322a0002c0002t0020g0323a0002c0002t0035g0325others(1): Show | 4 | HG00639.hp1 HG00642.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-1127C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50922971 | ||||||
chr18:50923052
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1057-1046T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923052 | ||||||
chr18:50923055
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1057-1043C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923055 | ||||||
chr18:50923056
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1057-1042T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923056 | ||||||
chr18:50923095
|
T | C | 2 | a0001c0001t0056g0082a0001c0001t0077g0093 | 2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1057-1003T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923095 | ||||||
chr18:50923320
|
CAA | C | 7 | a0001c0001t0014g0090a0001c0001t0014g0115a0001c0001t0015g0074others(4): Show | 7 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-776_1057-775d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr18 | 50923320 | |||||
chr18:50923435
|
C | T | 2 | a0001c0001t0030g0060a0001c0001t0030g0068 | 2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1057-663C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923435 | ||||||
chr18:50923457
|
A | G | 1 | a0001c0001t0022g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1057-641A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923457 | ||||||
chr18:50923676
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(16): Show | 20 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1057-422C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923676 | ||||||
chr18:50923800
|
A | G | 1 | a0002c0002t0122g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1057-298A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923800 | ||||||
chr18:50923852
|
G | A | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1057-246G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 10/15 | chr18 | 50923852 | ||||||
chr18:50924443
|
T | A | 1 | a0002c0002t0122g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1171+231T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924443 | ||||||
chr18:50924452
|
C | CTGTTGGA others(73): Show |
2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1171+243_1171+322d others(82): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50924452 | |||||
chr18:50924536
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1171+324G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924536 | ||||||
chr18:50924637
|
A | G | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+425A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924637 | ||||||
chr18:50924665
|
G | A | 1 | a0001c0001t0033g0248 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1171+453G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924665 | ||||||
chr18:50924703
|
G | GT | 18 | a0001c0001t0001g0232a0001c0001t0006g0025a0001c0001t0008g0110others(15): Show | 18 | HG00597.hp1 HG01358.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1171+502dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50924703 | |||||
chr18:50924704
|
T | TTTTTTG | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+497_1171+498i others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50924704 | |||||
chr18:50924830
|
C | T | 1 | a0001c0001t0051g0118 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1171+618C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924830 | ||||||
chr18:50924831
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1171+619G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924831 | ||||||
chr18:50924896
|
G | A | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171+684G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50924896 | ||||||
chr18:50925245
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1172-511G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925245 | ||||||
chr18:50925265
|
G | A | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1172-491G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925265 | ||||||
chr18:50925296
|
T | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1172-460T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925296 | ||||||
chr18:50925337
|
G | C | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1172-419G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | chr18 | 50925337 | ||||||
chr18:50925469
|
ACT | A | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1172-284_1172-283d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50925469 | |||||
chr18:50925575
|
TTTTTC | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1172-175_1172-171d others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 50925575 | |||||
chr18:50925937
|
C | T | 5 | a0001c0001t0014g0090a0001c0001t0014g0115a0001c0001t0015g0085others(2): Show | 5 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+39C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50925937 | ||||||
chr18:50926106
|
C | T | 2 | a0001c0001t0006g0067a0001c0001t0061g0069 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1314+208C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926106 | ||||||
chr18:50926301
|
CT | C | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+405delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50926301 | |||||
chr18:50926341
|
A | G | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1314+443A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926341 | ||||||
chr18:50926353
|
C | A | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1314+455C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926353 | ||||||
chr18:50926354
|
G | A | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1314+456G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926354 | ||||||
chr18:50926433
|
A | G | 1 | a0001c0001t0003g0081 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1314+535A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926433 | ||||||
chr18:50926475
|
A | G | 4 | a0001c0001t0036g0191a0001c0001t0110g0007a0001c0001t0111g0007others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+577A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926475 | ||||||
chr18:50926478
|
C | T | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+580C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926478 | ||||||
chr18:50926641
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0252 | 3 | HG00597.hp2 NA18960.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1314+743G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926641 | ||||||
chr18:50926690
|
A | G | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1314+792A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926690 | ||||||
chr18:50926732
|
G | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1314+834G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926732 | ||||||
chr18:50926897
|
A | G | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+999A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50926897 | ||||||
chr18:50927223
|
C | T | 2 | a0002c0002t0094g0177a0002c0002t0157g0178 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1314+1325C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927223 | ||||||
chr18:50927429
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1314+1531G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927429 | ||||||
chr18:50927443
|
G | C | 1 | a0002c0002t0152g0169 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1314+1545G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927443 | ||||||
chr18:50927470
|
G | A | 2 | a0002c0002t0120g0161a0002c0002t0149g0160 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1314+1572G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927470 | ||||||
chr18:50927482
|
C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1314+1584C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927482 | ||||||
chr18:50927633
|
C | T | 15 | a0002c0002t0020g0120a0002c0002t0020g0322a0002c0002t0020g0323others(12): Show | 15 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1314+1735C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927633 | ||||||
chr18:50927710
|
C | A | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+1812C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927710 | ||||||
chr18:50927721
|
C | CAT | 19 | a0001c0001t0008g0110a0001c0001t0010g0043a0001c0001t0010g0049others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1314+1853_1314+185 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATAT | 6 | a0001c0001t0002g0256a0001c0001t0018g0255a0001c0001t0065g0095others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+1851_1314+185 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATAT | 58 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1314+1849_1314+185 others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(1): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0199a0001c0001t0001g0217others(32): Show | 36 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1314+1847_1314+185 others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(3): Show |
20 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0289others(17): Show | 20 | HG01069.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1314+1845_1314+185 others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(5): Show |
13 | a0001c0001t0001g0279a0001c0001t0001g0281a0001c0001t0002g0235others(10): Show | 13 | HG01106.hp2 HG01261.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1314+1843_1314+185 others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(7): Show |
7 | a0001c0001t0001g0273a0001c0001t0002g0233a0001c0001t0032g0004others(4): Show | 8 | HG00621.hp1 HG00741.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1314+1841_1314+185 others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(9): Show |
4 | a0001c0001t0001g0272a0001c0001t0007g0229a0001c0001t0040g0269others(1): Show | 4 | HG00609.hp2 NA18978.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1839_1314+185 others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(11): Show |
5 | a0001c0001t0004g0121a0001c0001t0038g0185a0001c0001t0091g0270others(2): Show | 5 | HG00558.hp2 HG01074.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1314+1837_1314+185 others(22): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(13): Show |
1 | a0001c0001t0012g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1314+1835_1314+185 others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(17): Show |
1 | a0001c0001t0179g0260 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1314+1831_1314+185 others(28): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATATATA others(19): Show |
1 | a0001c0001t0024g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1314+1829_1314+185 others(30): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
C | CATGTATA others(11): Show |
1 | a0001c0001t0126g0275 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1314+1825_1314+182 others(22): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
CAT | C | 40 | a0001c0001t0003g0065a0001c0001t0003g0076a0001c0001t0003g0079others(37): Show | 40 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1314+1853_1314+185 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
CATATATA others(7): Show |
C | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+1841_1314+185 others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927721
|
CATATATA others(9): Show |
C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+1839_1314+185 others(20): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927721 | |||||
chr18:50927738
|
A | C | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+1840A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927738 | ||||||
chr18:50927751
|
T | C | 4 | a0001c0001t0003g0102a0001c0001t0051g0118a0001c0001t0052g0117others(1): Show | 4 | HG02486.hp2 HG03516.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1853T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927751 | ||||||
chr18:50927751
|
T | TATAC | 9 | a0002c0002t0005g0149a0002c0002t0023g0180a0002c0002t0096g0175others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATAC | 26 | a0001c0001t0164g0194a0002c0002t0005g0134a0002c0002t0020g0120others(23): Show | 27 | HG00639.hp1 HG00642.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATATA others(1): Show |
18 | a0002c0002t0005g0136a0002c0002t0005g0137a0002c0002t0005g0140others(15): Show | 18 | HG00609.hp1 HG02040.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATATA others(3): Show |
4 | a0002c0002t0005g0129a0002c0002t0011g0139a0002c0002t0100g0166others(1): Show | 4 | HG03704.hp1 NA18970.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATATA others(5): Show |
2 | a0002c0002t0005g0142a0007c0010t0088g0321 | 2 | NA19056.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(16): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATATA others(7): Show |
3 | a0002c0002t0005g0127a0002c0002t0182g0015a0002c0002t0183g0015 | 3 | HG00423.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(18): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATATA others(11): Show |
3 | a0002c0004t0005g0138a0002c0004t0011g0143a0002c0004t0147g0130 | 3 | NA18968.hp2 NA19058.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1314+1854_1314+185 others(22): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927751
|
T | TATATATA others(21): Show |
1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1314+1854_1314+185 others(32): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927751 | |||||
chr18:50927810
|
A | AT | 6 | a0001c0001t0003g0019a0001c0001t0030g0068a0001c0001t0053g0061others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1314+1934dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927810 | |||||
chr18:50927810
|
AT | A | 24 | a0001c0001t0003g0108a0001c0001t0004g0304a0001c0001t0025g0027others(21): Show | 24 | HG00408.hp2 HG00741.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1314+1934delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927810 | |||||
chr18:50927810
|
ATT | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(210): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1314+1933_1314+193 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50927810 | |||||
chr18:50927974
|
C | T | 1 | a0001c0001t0059g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1314+2076C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50927974 | ||||||
chr18:50928054
|
A | G | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+2156A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928054 | ||||||
chr18:50928081
|
G | A | 1 | a0001c0001t0007g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1314+2183G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928081 | ||||||
chr18:50928175
|
C | T | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1314+2277C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928175 | ||||||
chr18:50928241
|
C | CT | 11 | a0001c0001t0171g0212a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1314+2353dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50928241 | |||||
chr18:50928256
|
T | A | 6 | a0001c0001t0006g0083a0001c0001t0016g0073a0001c0001t0056g0082others(3): Show | 6 | NA18954.hp1 NA18967.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+2358T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928256 | ||||||
chr18:50928382
|
T | C | 12 | a0001c0001t0068g0033a0001c0001t0171g0212a0001c0003t0013g0009others(9): Show | 12 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1314+2484T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928382 | ||||||
chr18:50928426
|
T | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(239): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1314+2528T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928426 | ||||||
chr18:50928445
|
A | G | 1 | a0001c0001t0031g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1314+2547A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928445 | ||||||
chr18:50928515
|
G | A | 1 | a0002c0002t0005g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1314+2617G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928515 | ||||||
chr18:50928543
|
T | C | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1314+2645T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928543 | ||||||
chr18:50928750
|
A | G | 53 | a0001c0001t0048g0056a0002c0002t0005g0129a0002c0002t0005g0134others(50): Show | 54 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1314+2852A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928750 | ||||||
chr18:50928971
|
A | G | 69 | a0001c0001t0164g0194a0002c0002t0005g0127a0002c0002t0005g0129others(66): Show | 70 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1314+3073A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928971 | ||||||
chr18:50928978
|
A | G | 1 | a0001c0001t0154g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1314+3080A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50928978 | ||||||
chr18:50929030
|
G | A | 2 | a0001c0001t0018g0278a0001c0001t0166g0223 | 2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1314+3132G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929030 | ||||||
chr18:50929161
|
C | CT | 17 | a0001c0001t0018g0278a0001c0001t0025g0027a0001c0001t0031g0051others(14): Show | 17 | HG00408.hp2 HG00642.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1315-3083dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929161 | |||||
chr18:50929161
|
CT | C | 42 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(39): Show | 43 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1315-3083delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929161 | |||||
chr18:50929175
|
T | C | 2 | a0001c0001t0001g0284a0002c0002t0119g0131 | 2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1315-3083T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929175 | ||||||
chr18:50929246
|
A | T | 1 | a0001c0001t0014g0086 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1315-3012A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929246 | ||||||
chr18:50929485
|
C | CA | 147 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1315-2757dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929485 | |||||
chr18:50929485
|
C | CAA | 11 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0272others(8): Show | 12 | HG00735.hp2 HG01361.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1315-2758_1315-275 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929485 | |||||
chr18:50929485
|
CA | C | 11 | a0001c0001t0123g0326a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01192.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1315-2757delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50929485 | |||||
chr18:50929575
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(330): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1315-2683A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929575 | ||||||
chr18:50929656
|
A | G | 1 | a0001c0001t0006g0080 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1315-2602A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50929656 | ||||||
chr18:50930026
|
T | G | 1 | a0001c0001t0064g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1315-2232T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930026 | ||||||
chr18:50930027
|
A | C | 2 | a0001c0001t0056g0082a0001c0001t0077g0093 | 2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1315-2231A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930027 | ||||||
chr18:50930027
|
A | T | 1 | a0002c0002t0020g0322 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1315-2231A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930027 | ||||||
chr18:50930080
|
C | T | 68 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(65): Show | 69 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1315-2178C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930080 | ||||||
chr18:50930254
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0018g0010 | 2 | NA18955.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1315-2004C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930254 | ||||||
chr18:50930397
|
A | T | 2 | a0002c0002t0023g0180a0002c0002t0096g0175 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1315-1861A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930397 | ||||||
chr18:50930533
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1315-1725T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930533 | ||||||
chr18:50930607
|
G | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-1651G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930607 | ||||||
chr18:50930709
|
A | G | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1315-1549A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930709 | ||||||
chr18:50930883
|
C | A | 1 | a0001c0001t0170g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1315-1375C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930883 | ||||||
chr18:50930934
|
T | C | 3 | a0001c0001t0010g0043a0001c0001t0031g0094a0001c0001t0072g0041 | 3 | NA19007.hp1 NA19067.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1315-1324T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930934 | ||||||
chr18:50930943
|
C | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1315-1315C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930943 | ||||||
chr18:50930988
|
A | G | 1 | a0001c0001t0136g0296 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1315-1270A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50930988 | ||||||
chr18:50931138
|
C | T | 4 | a0001c0001t0036g0201a0001c0001t0107g0202a0001c0001t0108g0203others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-1120C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931138 | ||||||
chr18:50931515
|
TA | T | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-740delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50931515 | |||||
chr18:50931603
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1315-655A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931603 | ||||||
chr18:50931682
|
C | CTTT | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-568_1315-566d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50931682 | |||||
chr18:50931770
|
G | A | 1 | a0001c0001t0181g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1315-488G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931770 | ||||||
chr18:50931819
|
C | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1315-439C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931819 | ||||||
chr18:50931840
|
AATTTTTT others(2): Show |
A | 4 | a0001c0001t0028g0057a0001c0001t0028g0059a0001c0001t0057g0058others(1): Show | 4 | HG00738.hp2 HG03225.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315-398_1315-390d others(11): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 50931840 | |||||
chr18:50931847
|
TG | T | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1315-410delG | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50931847 | ||||||
chr18:50932110
|
C | T | 1 | a0001c0001t0016g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1315-148C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50932110 | ||||||
chr18:50932111
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1315-147G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50932111 | ||||||
chr18:50932188
|
G | A | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1315-70G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 12/15 | chr18 | 50932188 | ||||||
chr18:50932614
|
G | T | 1 | a0001c0005t0130g0312 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1417+254G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932614 | ||||||
chr18:50932616
|
A | T | 1 | a0001c0005t0130g0312 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1417+256A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932616 | ||||||
chr18:50932645
|
C | G | 1 | a0001c0001t0018g0278 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1417+285C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932645 | ||||||
chr18:50932659
|
C | A | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1417+299C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50932659 | ||||||
chr18:50933102
|
G | A | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1417+742G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933102 | ||||||
chr18:50933136
|
T | C | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1417+776T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933136 | ||||||
chr18:50933154
|
A | G | 2 | a0001c0001t0051g0118a0001c0001t0052g0117 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1417+794A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933154 | ||||||
chr18:50933186
|
T | C | 1 | a0001c0001t0068g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1417+826T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933186 | ||||||
chr18:50933509
|
T | A | 1 | a0001c0001t0179g0260 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1417+1149T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933509 | ||||||
chr18:50933705
|
G | A | 2 | a0001c0001t0056g0082a0001c0001t0077g0093 | 2 | NA18978.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1417+1345G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933705 | ||||||
chr18:50933714
|
G | T | 1 | a0001c0001t0007g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1417+1354G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933714 | ||||||
chr18:50933744
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1417+1384A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933744 | ||||||
chr18:50933765
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1417+1405C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933765 | ||||||
chr18:50933812
|
T | C | 1 | a0001c0001t0135g0277 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1417+1452T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933812 | ||||||
chr18:50933813
|
C | T | 1 | a0001c0001t0135g0277 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1417+1453C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933813 | ||||||
chr18:50933816
|
G | A | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1456G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933816 | ||||||
chr18:50933853
|
C | G | 1 | a0001c0001t0003g0076 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1417+1493C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933853 | ||||||
chr18:50933907
|
A | G | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1417+1547A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933907 | ||||||
chr18:50933922
|
T | G | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+1562T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50933922 | ||||||
chr18:50934215
|
G | A | 1 | a0001c0001t0002g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1417+1855G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934215 | ||||||
chr18:50934363
|
C | G | 42 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(39): Show | 43 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1417+2003C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934363 | ||||||
chr18:50934680
|
C | T | 2 | a0001c0001t0004g0008a0001c0001t0169g0192 | 3 | HG02896.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1417+2320C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934680 | ||||||
chr18:50934787
|
C | T | 1 | a0001c0001t0032g0004 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1417+2427C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50934787 | ||||||
chr18:50935009
|
T | C | 1 | a0002c0002t0114g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1417+2649T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935009 | ||||||
chr18:50935108
|
G | T | 1 | a0001c0001t0125g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1417+2748G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935108 | ||||||
chr18:50935145
|
G | A | 1 | a0002c0002t0096g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1417+2785G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935145 | ||||||
chr18:50935146
|
C | T | 1 | a0001c0001t0036g0201 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1417+2786C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935146 | ||||||
chr18:50935277
|
C | T | 2 | a0001c0001t0016g0096a0001c0001t0053g0061 | 2 | HG00741.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1417+2917C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935277 | ||||||
chr18:50935394
|
A | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(328): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1417+3034A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935394 | ||||||
chr18:50935493
|
A | G | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1417+3133A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935493 | ||||||
chr18:50935584
|
A | T | 1 | a0001c0001t0077g0093 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1417+3224A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935584 | ||||||
chr18:50935586
|
T | A | 2 | a0001c0001t0077g0093a0005c0011t0002g0292 | 2 | HG01261.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1417+3226T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935586 | ||||||
chr18:50935586
|
T | TA | 135 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1417+3242dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935586 | |||||
chr18:50935586
|
TA | T | 17 | a0001c0001t0009g0072a0001c0001t0010g0049a0001c0001t0047g0055others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1417+3242delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935586 | |||||
chr18:50935586
|
TAA | T | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+3241_1417+324 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935586 | |||||
chr18:50935624
|
T | G | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1417+3264T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935624 | ||||||
chr18:50935703
|
G | A | 2 | a0001c0001t0002g0236a0001c0001t0022g0225 | 2 | HG01243.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1417+3343G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935703 | ||||||
chr18:50935751
|
C | CA | 48 | a0001c0001t0001g0219a0001c0001t0002g0256a0001c0001t0003g0108others(45): Show | 48 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1417+3412dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | |||||
chr18:50935751
|
C | CAA | 128 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(125): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1417+3411_1417+341 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | |||||
chr18:50935751
|
C | CAAA | 14 | a0001c0001t0001g0245a0001c0001t0001g0272a0001c0001t0001g0290others(11): Show | 15 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1417+3410_1417+341 others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | |||||
chr18:50935751
|
C | CAAAA | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+3409_1417+341 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935751 | |||||
chr18:50935770
|
A | AG | 48 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(45): Show | 49 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1417+3410_1417+341 others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935770 | ||||||
chr18:50935782
|
A | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1417+3422A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935782 | ||||||
chr18:50935840
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(233): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1417+3480G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935840 | ||||||
chr18:50935873
|
G | GA | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1417+3522dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50935873 | |||||
chr18:50935955
|
C | A | 1 | a0002c0002t0173g0317 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1417+3595C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50935955 | ||||||
chr18:50936019
|
A | G | 2 | a0001c0001t0071g0045a0001c0001t0075g0039 | 2 | NA19000.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1418-3551A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936019 | ||||||
chr18:50936380
|
C | G | 3 | a0001c0001t0001g0199a0001c0001t0041g0198a0001c0001t0041g0200 | 3 | HG02451.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1418-3190C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936380 | ||||||
chr18:50936453
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1418-3117T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936453 | ||||||
chr18:50936480
|
G | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-3090G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936480 | ||||||
chr18:50936531
|
A | G | 1 | a0001c0001t0007g0266 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1418-3039A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936531 | ||||||
chr18:50936536
|
T | G | 8 | a0001c0001t0015g0071a0001c0001t0016g0096a0001c0001t0053g0061others(5): Show | 8 | HG00741.hp1 HG01070.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1418-3034T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936536 | ||||||
chr18:50936575
|
A | T | 1 | a0001c0001t0156g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1418-2995A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936575 | ||||||
chr18:50936831
|
C | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-2739C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936831 | ||||||
chr18:50936883
|
G | C | 2 | a0001c0003t0013g0213a0001c0003t0141g0214 | 2 | HG00408.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1418-2687G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936883 | ||||||
chr18:50936952
|
C | T | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-2618C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50936952 | ||||||
chr18:50937163
|
G | A | 65 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(62): Show | 66 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1418-2407G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937163 | ||||||
chr18:50937369
|
C | T | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-2201C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937369 | ||||||
chr18:50937667
|
A | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418-1903A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937667 | ||||||
chr18:50937834
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1418-1736T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937834 | ||||||
chr18:50937893
|
A | G | 1 | a0002c0002t0011g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1418-1677A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50937893 | ||||||
chr18:50938002
|
A | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1418-1568A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938002 | ||||||
chr18:50938138
|
G | A | 10 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0111others(7): Show | 10 | HG00544.hp1 NA18940.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.1418-1432G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938138 | ||||||
chr18:50938187
|
G | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-1383G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938187 | ||||||
chr18:50938191
|
G | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-1379G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938191 | ||||||
chr18:50938243
|
G | A | 9 | a0001c0001t0036g0191a0001c0001t0036g0201a0001c0001t0092g0189others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1418-1327G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938243 | ||||||
chr18:50938255
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1418-1315G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938255 | ||||||
chr18:50938332
|
T | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1418-1238T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938332 | ||||||
chr18:50938436
|
A | C | 2 | a0002c0002t0023g0180a0002c0002t0096g0175 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1418-1134A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938436 | ||||||
chr18:50938658
|
T | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1418-912T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938658 | ||||||
chr18:50938728
|
A | G | 1 | a0001c0001t0024g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1418-842A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938728 | ||||||
chr18:50938747
|
G | A | 3 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0140g0009 | 3 | NA18955.hp1 NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1418-823G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938747 | ||||||
chr18:50938803
|
C | T | 12 | a0001c0001t0003g0019a0001c0001t0006g0025a0001c0001t0008g0020others(9): Show | 12 | HG00423.hp1 NA18965.hp2 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.1418-767C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938803 | ||||||
chr18:50938809
|
T | C | 1 | a0002c0002t0020g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1418-761T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938809 | ||||||
chr18:50938961
|
A | G | 42 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(39): Show | 43 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1418-609A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50938961 | ||||||
chr18:50939071
|
GGAAA | G | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1418-496_1418-493d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50939071 | |||||
chr18:50939128
|
CA | C | 87 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(84): Show | 89 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1418-431delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50939128 | |||||
chr18:50939139
|
A | G | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-431A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939139 | ||||||
chr18:50939140
|
G | A | 12 | a0001c0001t0018g0278a0001c0001t0036g0201a0001c0003t0013g0009others(9): Show | 12 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1418-430G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939140 | ||||||
chr18:50939140
|
G | GA | 137 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1418-419dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr18 | 50939140 | |||||
chr18:50939166
|
A | G | 10 | a0001c0001t0001g0272a0001c0003t0013g0009a0001c0003t0013g0206others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-404A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939166 | ||||||
chr18:50939194
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1418-376T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939194 | ||||||
chr18:50939219
|
A | G | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1418-351A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939219 | ||||||
chr18:50939266
|
T | G | 6 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418-304T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939266 | ||||||
chr18:50939407
|
G | A | 3 | a0001c0001t0008g0020a0001c0001t0060g0024a0001c0001t0166g0223 | 3 | HG03927.hp2 NA18994.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1418-163G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939407 | ||||||
chr18:50939457
|
G | A | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1418-113G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 13/15 | chr18 | 50939457 | ||||||
chr18:50939654
|
ATGT | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488+19_1488+21del others(3): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr18 | 50939654 | |||||
chr18:50939784
|
A | G | 1 | a0001c0001t0156g0267 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1488+144A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939784 | ||||||
chr18:50939899
|
C | A | 8 | a0002c0002t0023g0174a0002c0002t0023g0176a0002c0002t0023g0180others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488+259C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939899 | ||||||
chr18:50939903
|
A | G | 1 | a0001c0001t0016g0073 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1488+263A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939903 | ||||||
chr18:50939909
|
A | G | 1 | a0001c0001t0124g0228 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1488+269A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50939909 | ||||||
chr18:50940280
|
C | T | 3 | a0001c0001t0051g0118a0001c0001t0052g0117a0001c0001t0123g0326 | 3 | HG01192.hp1 HG02486.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.1489-8C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 14/15 | chr18 | 50940280 | ||||||
chr18:50940716
|
T | A | 2 | a0001c0001t0002g0256a0001c0001t0018g0255 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1587+330T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50940716 | ||||||
chr18:50940832
|
A | G | 48 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(45): Show | 49 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1587+446A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50940832 | ||||||
chr18:50941197
|
G | T | 2 | a0001c0001t0170g0193a0001c0001t0181g0197 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1587+811G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941197 | ||||||
chr18:50941261
|
C | CA | 10 | a0001c0001t0008g0020a0001c0001t0010g0049a0001c0001t0010g0052others(7): Show | 11 | HG00099.hp1 HG00642.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587+894dupA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941261 | |||||
chr18:50941261
|
CAA | C | 96 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0022g0225others(93): Show | 97 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1587+893_1587+894d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941261 | |||||
chr18:50941261
|
CAAA | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1587+892_1587+894d others(5): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941261 | |||||
chr18:50941300
|
G | A | 7 | a0001c0001t0004g0253a0001c0001t0004g0304a0001c0001t0004g0305others(4): Show | 7 | HG01109.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+914G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941300 | ||||||
chr18:50941353
|
C | CT | 47 | a0001c0001t0003g0019a0001c0001t0003g0076a0001c0001t0003g0077others(44): Show | 47 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1587+998dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTT | 13 | a0001c0001t0001g0199a0001c0001t0003g0111a0001c0001t0010g0100others(10): Show | 13 | HG00735.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1587+997_1587+998d others(4): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTT | 13 | a0001c0001t0092g0189a0002c0002t0005g0136a0002c0002t0005g0140others(10): Show | 13 | HG00609.hp1 HG01884.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1587+995_1587+998d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTT | 14 | a0002c0002t0005g0137a0002c0002t0011g0165a0002c0002t0021g0005others(11): Show | 15 | HG01993.hp2 HG02040.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1587+994_1587+998d others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTT | 14 | a0001c0001t0112g0204a0002c0002t0005g0129a0002c0002t0005g0134others(11): Show | 14 | HG01106.hp1 HG01358.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1587+993_1587+998d others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT | 7 | a0001c0001t0036g0201a0001c0001t0108g0203a0002c0002t0100g0166others(4): Show | 7 | HG00621.hp2 HG02630.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1587+992_1587+998d others(9): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(1): Show |
11 | a0001c0001t0110g0007a0001c0001t0111g0007a0002c0002t0020g0323others(8): Show | 11 | HG00639.hp1 HG02129.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1587+991_1587+998d others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0036g0191a0001c0001t0155g0190a0002c0002t0020g0120others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+990_1587+998d others(11): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(3): Show |
3 | a0002c0002t0005g0127a0002c0002t0104g0324a0002c0002t0175g0182 | 3 | HG00423.hp2 HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1587+989_1587+998d others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(4): Show |
1 | a0002c0002t0035g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1587+988_1587+998d others(13): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0086g0116a0001c0001t0107g0202 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1587+986_1587+998d others(15): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0181g0197a0002c0002t0042g0316 | 2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1587+984_1587+998d others(17): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0044g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1587+977_1587+998d others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0170g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1587+972_1587+998d others(29): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
CT | C | 10 | a0001c0001t0003g0065a0001c0001t0006g0084a0001c0001t0025g0029others(7): Show | 10 | HG00408.hp2 HG01891.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+998delT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
CTTTTTTT others(3): Show |
C | 69 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(66): Show | 71 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1587+989_1587+998d others(12): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
CTTTTTTT others(4): Show |
C | 47 | a0001c0001t0001g0014a0001c0001t0001g0217a0001c0001t0001g0219others(44): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1587+988_1587+998d others(13): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0066g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1587+987_1587+998d others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941353
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0035g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1587+984_1587+998d others(17): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941353 | |||||
chr18:50941406
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(235): Show | 243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1587+1020A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941406 | ||||||
chr18:50941420
|
G | A | 1 | a0001c0001t0158g0288 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1587+1034G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941420 | ||||||
chr18:50941536
|
G | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+1150G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941536 | ||||||
chr18:50941621
|
G | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+1235G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941621 | ||||||
chr18:50941671
|
G | A | 2 | a0001c0001t0032g0004a0001c0001t0086g0116 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1587+1285G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941671 | ||||||
chr18:50941682
|
G | GT | 216 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(213): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1587+1310dupT | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941682 | |||||
chr18:50941682
|
G | GTT | 24 | a0001c0001t0001g0232a0001c0001t0024g0271a0001c0001t0040g0269others(21): Show | 24 | HG00408.hp2 HG00609.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1587+1309_1587+131 others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50941682 | |||||
chr18:50941839
|
C | T | 2 | a0002c0002t0182g0015a0002c0002t0183g0015 | 2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1587+1453C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941839 | ||||||
chr18:50941864
|
C | A | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1587+1478C>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941864 | ||||||
chr18:50941881
|
T | C | 1 | a0001c0001t0060g0024 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1587+1495T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941881 | ||||||
chr18:50941984
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1587+1598A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941984 | ||||||
chr18:50941985
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(237): Show | 245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1587+1599C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50941985 | ||||||
chr18:50942092
|
TA | T | 8 | a0001c0001t0036g0191a0001c0001t0036g0201a0001c0001t0107g0202others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1587+1708delA | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50942092 | |||||
chr18:50942179
|
T | C | 1 | a0001c0001t0053g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1587+1793T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942179 | ||||||
chr18:50942259
|
G | A | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+1873G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942259 | ||||||
chr18:50942352
|
A | G | 1 | a0001c0001t0009g0023 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1587+1966A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942352 | ||||||
chr18:50942411
|
T | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1587+2025T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942411 | ||||||
chr18:50942635
|
T | A | 12 | a0001c0001t0003g0019a0001c0001t0006g0025a0001c0001t0008g0020others(9): Show | 12 | HG00423.hp1 NA18965.hp2 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.1587+2249T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942635 | ||||||
chr18:50942782
|
TTGA | T | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+2400_1587+240 others(7): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50942782 | |||||
chr18:50942909
|
A | G | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1587+2523A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942909 | ||||||
chr18:50942978
|
T | A | 1 | a0001c0001t0019g0070 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1587+2592T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50942978 | ||||||
chr18:50943232
|
G | A | 1 | a0001c0001t0033g0248 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1587+2846G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943232 | ||||||
chr18:50943281
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0017g0280 | 2 | NA18998.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1587+2895A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943281 | ||||||
chr18:50943288
|
A | AATTT | 11 | a0001c0001t0156g0267a0001c0003t0013g0009a0001c0003t0013g0206others(8): Show | 11 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1587+2927_1587+293 others(8): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50943288 | |||||
chr18:50943326
|
G | A | 2 | a0001c0001t0040g0274a0001c0001t0162g0264 | 2 | HG00280.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1587+2940G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943326 | ||||||
chr18:50943344
|
G | A | 1 | a0002c0002t0106g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1587+2958G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943344 | ||||||
chr18:50943527
|
C | T | 1 | a0001c0001t0052g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1587+3141C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943527 | ||||||
chr18:50943546
|
T | G | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1587+3160T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943546 | ||||||
chr18:50943712
|
A | C | 12 | a0001c0001t0003g0065a0001c0001t0003g0076a0001c0001t0006g0083others(9): Show | 12 | NA18954.hp1 NA18964.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.1588-3305A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943712 | ||||||
chr18:50943812
|
G | A | 8 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(5): Show | 8 | HG01074.hp1 HG01106.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1588-3205G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943812 | ||||||
chr18:50943956
|
C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1588-3061C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943956 | ||||||
chr18:50943960
|
A | G | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1588-3057A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50943960 | ||||||
chr18:50944006
|
G | T | 1 | a0001c0001t0017g0280 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1588-3011G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944006 | ||||||
chr18:50944337
|
G | T | 68 | a0002c0002t0005g0127a0002c0002t0005g0129a0002c0002t0005g0134others(65): Show | 69 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1588-2680G>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944337 | ||||||
chr18:50944367
|
C | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-2650C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944367 | ||||||
chr18:50944583
|
C | T | 6 | a0001c0001t0025g0027a0001c0001t0025g0029a0001c0001t0026g0002others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-2434C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944583 | ||||||
chr18:50944606
|
A | G | 1 | a0001c0001t0010g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1588-2411A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944606 | ||||||
chr18:50944680
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1588-2337A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944680 | ||||||
chr18:50944726
|
C | G | 1 | a0001c0001t0003g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1588-2291C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944726 | ||||||
chr18:50944892
|
A | T | 1 | a0001c0001t0016g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1588-2125A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944892 | ||||||
chr18:50944947
|
G | A | 1 | a0001c0001t0004g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1588-2070G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50944947 | ||||||
chr18:50945015
|
A | G | 1 | a0002c0002t0005g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1588-2002A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945015 | ||||||
chr18:50945036
|
T | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 21 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1588-1981T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945036 | ||||||
chr18:50945319
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T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1588-1698T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945319 | ||||||
chr18:50945328
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GCCTGGTC others(26): Show |
G | 1 | a0001c0001t0146g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1588-1687_1588-165 others(37): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50945328 | |||||
chr18:50945411
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C | T | 1 | a0001c0001t0123g0326 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1588-1606C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945411 | ||||||
chr18:50945434
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T | C | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1588-1583T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945434 | ||||||
chr18:50945488
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C | T | 1 | a0001c0001t0010g0043 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1588-1529C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945488 | ||||||
chr18:50945497
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C | G | 1 | a0001c0001t0009g0072 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1588-1520C>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945497 | ||||||
chr18:50945712
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A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(139): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1588-1305A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945712 | ||||||
chr18:50945807
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C | T | 1 | a0001c0001t0066g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1588-1210C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945807 | ||||||
chr18:50945840
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G | C | 1 | a0001c0001t0159g0221 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1588-1177G>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945840 | ||||||
chr18:50945881
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A | C | 11 | a0001c0001t0012g0006a0001c0001t0012g0186a0001c0001t0012g0187others(8): Show | 11 | HG01074.hp1 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588-1136A>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945881 | ||||||
chr18:50945884
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T | A | 22 | a0002c0002t0005g0129a0002c0002t0005g0134a0002c0002t0005g0136others(19): Show | 22 | HG00609.hp1 HG01106.hp1 HG03704.hp1 others(19): Show |
intron_variant | MODIFIER | c.1588-1133T>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50945884 | ||||||
chr18:50946110
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T | TTAAA | 52 | a0001c0001t0001g0199a0001c0001t0006g0067a0001c0001t0025g0027others(49): Show | 53 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1588-878_1588-875d others(6): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50946110 | |||||
chr18:50946110
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T | TTAAATAA others(1): Show |
122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1588-882_1588-875d others(10): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50946110 | |||||
chr18:50946110
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T | TTAAATAA others(5): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0238a0001c0001t0001g0244others(21): Show | 24 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1588-886_1588-875d others(14): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 50946110 | |||||
chr18:50946161
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T | C | 1 | a0001c0001t0003g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1588-856T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946161 | ||||||
chr18:50946176
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G | A | 1 | a0007c0010t0088g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1588-841G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946176 | ||||||
chr18:50946196
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A | T | 10 | a0001c0003t0013g0009a0001c0003t0013g0206a0001c0003t0013g0207others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588-821A>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946196 | ||||||
chr18:50946314
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G | A | 10 | a0001c0001t0004g0195a0001c0001t0036g0191a0001c0001t0036g0201others(7): Show | 10 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1588-703G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946314 | ||||||
chr18:50946400
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C | T | 2 | a0001c0001t0030g0060a0001c0001t0030g0068 | 2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1588-617C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946400 | ||||||
chr18:50946408
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T | G | 5 | a0002c0002t0005g0149a0002c0002t0101g0144a0002c0002t0116g0128others(2): Show | 5 | NA18612.hp1 NA18985.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-609T>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946408 | ||||||
chr18:50946475
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T | C | 9 | a0002c0002t0020g0120a0002c0002t0020g0322a0002c0002t0020g0323others(6): Show | 9 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1588-542T>C | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946475 | ||||||
chr18:50946539
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G | A | 1 | a0001c0001t0066g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1588-478G>A | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946539 | ||||||
chr18:50946907
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A | G | 1 | a0002c0002t0122g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1588-110A>G | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946907 | ||||||
chr18:50946957
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C | T | 1 | a0006c0009t0069g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1588-60C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50946957 | ||||||
chr18:50947014
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C | T | 1 | a0001c0001t0091g0270 | 1 | HG00558.hp2 | splice_region_variant&intron_variant | LOW | c.1588-3C>T | ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | chr18 | 50947014 |