geneid | 10747 |
---|---|
ensemblid | ENSG00000009724.18 |
hgncid | 6902 |
symbol | MASP2 |
name | MBL associated serine protease 2 |
refseq_nuc | NM_006610.4 |
refseq_prot | NP_006601.2 |
ensembl_nuc | ENST00000400897.8 |
ensembl_prot | ENSP00000383690.3 |
mane_status | MANE Select |
chr | chr1 |
start | 11026523 |
end | 11047239 |
strand | - |
ver | v1.2 |
region | chr1:11026523-11047239 |
region5000 | chr1:11021523-11052239 |
regionname0 | MASP2_chr1_11026523_11047239 |
regionname5000 | MASP2_chr1_11021523_11052239 |
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 | 0/1 | 686 | 171 | 20 | 46 | 72 | 5 | 27 | 49 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002 | 1/0 | 686 | 82 | 36 | 13 | 22 | 0 | 10 | 14 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003 | 0/0 | 686 | 53 | 15 | 3 | 28 | 1 | 6 | 23 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0004 | 0/0 | 686 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0005 | 0/0 | 686 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0006 | 0/0 | 686 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0007 | 0/0 | 686 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0008 | 0/0 | 686 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0009 | 0/0 | 686 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0010 | 0/0 | 686 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0011 | 0/0 | 686 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0012 | 0/0 | 686 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0013 | 0/0 | 686 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0014 | 0/0 | 686 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0015 | 0/0 | 686 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0016 | 0/0 | 686 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0017 | 0/0 | 686 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
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 | 0/1 | 2061 | 153 | 10 | 42 | 71 | 5 | 24 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0002 | 1/0 | 2061 | 48 | 5 | 12 | 22 | 0 | 8 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0003 | 0/0 | 2061 | 26 | 2 | 3 | 15 | 1 | 5 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0004 | 0/0 | 2061 | 16 | 15 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0005 | 0/0 | 2061 | 14 | 1 | 0 | 13 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0006 | 0/0 | 2061 | 12 | 11 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0007 | 0/0 | 2061 | 9 | 8 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0008 | 0/0 | 2061 | 6 | 6 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0009 | 0/0 | 2061 | 6 | 0 | 3 | 1 | 0 | 2 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0010 | 0/0 | 2061 | 6 | 5 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0011 | 0/0 | 2061 | 6 | 6 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0012 | 0/0 | 2061 | 5 | 5 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0013 | 0/0 | 2061 | 5 | 5 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0014 | 0/0 | 2061 | 5 | 0 | 0 | 5 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0015 | 0/0 | 2061 | 3 | 3 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0016 | 0/0 | 2061 | 3 | 0 | 0 | 3 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0017 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0018 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0019 | 0/0 | 2061 | 2 | 1 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0020 | 0/0 | 2061 | 2 | 0 | 2 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0021 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0022 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0023 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0024 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0025 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0026 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0027 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0028 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0029 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0030 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0031 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0032 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0033 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
c0034 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
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 | 0/1 | 395 | 232 | 35 | 52 | 104 | 6 | 34 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
t0002 | 1/0 | 395 | 107 | 57 | 14 | 26 | 0 | 9 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
t0003 | 0/0 | 395 | 3 | 3 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
t0004 | 0/0 | 395 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
t0005 | 0/0 | 395 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
t0006 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
t0007 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
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 | 5 | 0 | 0 | 4 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0002 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
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 | 0/1 | 2061 | 153 | 10 | 42 | 71 | 5 | 24 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0009 | 0/0 | 2061 | 6 | 0 | 3 | 1 | 0 | 2 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0010 | 0/0 | 2061 | 6 | 5 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0012 | 0/0 | 2061 | 5 | 5 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0026 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0002 | 1/0 | 2061 | 48 | 5 | 12 | 22 | 0 | 8 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0004 | 0/0 | 2061 | 16 | 15 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0006 | 0/0 | 2061 | 12 | 11 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0015 | 0/0 | 2061 | 3 | 3 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0023 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0024 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0025 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0003 | 0/0 | 2061 | 26 | 2 | 3 | 15 | 1 | 5 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0005 | 0/0 | 2061 | 14 | 1 | 0 | 13 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0011 | 0/0 | 2061 | 6 | 6 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0013 | 0/0 | 2061 | 5 | 5 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0030 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0033 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0004c0007 | 0/0 | 2061 | 9 | 8 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0005c0008 | 0/0 | 2061 | 6 | 6 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0006c0014 | 0/0 | 2061 | 5 | 0 | 0 | 5 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0007c0016 | 0/0 | 2061 | 3 | 0 | 0 | 3 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0007c0029 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0008c0021 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0009c0031 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0009c0032 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0010c0018 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0011c0017 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0012c0019 | 0/0 | 2061 | 2 | 1 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0013c0020 | 0/0 | 2061 | 2 | 0 | 2 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0014c0034 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0015c0027 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0016c0028 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0017c0022 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2455 | 148 | 7 | 42 | 69 | 5 | 24 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0001t0003 | 0/0 | 2455 | 3 | 3 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0001t0006 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0001t0007 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0009t0001 | 0/0 | 2455 | 6 | 0 | 3 | 1 | 0 | 2 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0010t0001 | 0/0 | 2455 | 6 | 5 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0012t0001 | 0/0 | 2455 | 5 | 5 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0001c0026t0001 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0002t0002 | 1/0 | 2455 | 47 | 5 | 12 | 22 | 0 | 7 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0002t0005 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0004t0002 | 0/0 | 2455 | 16 | 15 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0006t0001 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0006t0002 | 0/0 | 2455 | 11 | 10 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0015t0001 | 0/0 | 2455 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0015t0002 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0023t0001 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0024t0002 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0002c0025t0002 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0003t0001 | 0/0 | 2455 | 25 | 1 | 3 | 15 | 1 | 5 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0003t0004 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0005t0001 | 0/0 | 2455 | 14 | 1 | 0 | 13 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0011t0001 | 0/0 | 2455 | 6 | 6 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0013t0002 | 0/0 | 2455 | 5 | 5 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0030t0001 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0003c0033t0001 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0004c0007t0002 | 0/0 | 2455 | 9 | 8 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0005c0008t0002 | 0/0 | 2455 | 6 | 6 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0006c0014t0001 | 0/0 | 2455 | 5 | 0 | 0 | 5 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0007c0016t0002 | 0/0 | 2455 | 3 | 0 | 0 | 3 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0007c0029t0002 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0008c0021t0001 | 0/0 | 2455 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0009c0031t0002 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0009c0032t0001 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0010c0018t0002 | 0/0 | 2455 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0011c0017t0002 | 0/0 | 2455 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0012c0019t0001 | 0/0 | 2455 | 2 | 1 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0013c0020t0001 | 0/0 | 2455 | 2 | 0 | 2 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0014c0034t0001 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0015c0027t0001 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0016c0028t0002 | 0/0 | 2455 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
a0017c0022t0001 | 0/0 | 2455 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | copy fasta | chr1 | 11021523 | 11052239 |
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 | 5 | 0 | 0 | 4 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0002 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0009t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0009t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0009t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0009t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0009t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0009t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0010t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0010t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0010t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0012t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0012t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0012t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0012t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0001c0026t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0004t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0006t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0015t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0015t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0015t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0023t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0024t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0002c0025t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0003t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0011t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0011t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0011t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0011t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0011t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0013t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0013t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0013t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0013t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0013t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0030t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0003c0033t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0004c0007t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0005c0008t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0005c0008t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0005c0008t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0005c0008t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0005c0008t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0005c0008t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0006c0014t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0006c0014t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0006c0014t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0006c0014t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0006c0014t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0007c0016t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0007c0016t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0007c0029t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0008c0021t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0008c0021t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0009c0031t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0009c0032t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0010c0018t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0010c0018t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0011c0017t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0011c0017t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0012c0019t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0012c0019t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0013c0020t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0013c0020t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0014c0034t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0015c0027t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0016c0028t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
a0017c0022t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0304 | EUR | GBR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00438 | hp2 | a0003 | c0003 | t0001 | g0275 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00621 | hp2 | a0006 | c0014 | t0001 | g0167 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0306 | EAS | CHS | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0051 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00741 | hp1 | a0001 | c0010 | t0001 | g0225 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01099 | hp2 | a0001 | c0009 | t0001 | g0281 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01109 | hp2 | a0012 | c0019 | t0001 | g0273 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01167 | hp1 | a0002 | c0004 | t0002 | g0241 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0305 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01192 | hp1 | a0013 | c0020 | t0001 | g0324 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0292 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01243 | hp2 | a0004 | c0007 | t0002 | g0320 | AMR | PUR | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01261 | hp1 | a0013 | c0020 | t0001 | g0323 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01891 | hp1 | a0002 | c0015 | t0002 | g0079 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01891 | hp2 | a0003 | c0013 | t0002 | g0018 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01975 | hp1 | a0001 | c0009 | t0001 | g0283 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01978 | hp1 | a0001 | c0009 | t0001 | g0276 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0303 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02055 | hp1 | a0002 | c0004 | t0002 | g0247 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02055 | hp2 | a0002 | c0006 | t0002 | g0259 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02071 | hp1 | a0003 | c0005 | t0001 | g0165 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0175 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02145 | hp1 | a0004 | c0007 | t0002 | g0322 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02145 | hp2 | a0001 | c0012 | t0001 | g0013 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02257 | hp1 | a0004 | c0007 | t0002 | g0321 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02257 | hp2 | a0005 | c0008 | t0002 | g0034 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02258 | hp1 | a0005 | c0008 | t0002 | g0035 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02280 | hp1 | a0010 | c0018 | t0002 | g0243 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PEL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02451 | hp2 | a0005 | c0008 | t0002 | g0031 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02572 | hp1 | a0001 | c0010 | t0001 | g0224 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02572 | hp2 | a0002 | c0006 | t0002 | g0260 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02602 | hp1 | a0001 | c0009 | t0001 | g0250 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02602 | hp2 | a0002 | c0025 | t0002 | g0271 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02615 | hp1 | a0008 | c0021 | t0001 | g0326 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02615 | hp2 | a0002 | c0004 | t0002 | g0240 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02622 | hp1 | a0001 | c0010 | t0001 | g0223 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02622 | hp2 | a0002 | c0004 | t0002 | g0246 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02630 | hp1 | a0002 | c0004 | t0002 | g0237 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02630 | hp2 | a0002 | c0006 | t0002 | g0256 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02647 | hp1 | a0002 | c0004 | t0002 | g0245 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02647 | hp2 | a0003 | c0011 | t0001 | g0309 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02683 | hp2 | a0001 | c0009 | t0001 | g0300 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02698 | hp2 | a0017 | c0022 | t0001 | g0020 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02717 | hp1 | a0003 | c0013 | t0002 | g0017 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02717 | hp2 | a0011 | c0017 | t0002 | g0253 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02723 | hp1 | a0003 | c0030 | t0001 | g0310 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02723 | hp2 | a0010 | c0018 | t0002 | g0242 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02735 | hp2 | a0003 | c0003 | t0001 | g0297 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02809 | hp1 | a0005 | c0008 | t0002 | g0036 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02809 | hp2 | a0004 | c0007 | t0002 | g0318 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02818 | hp1 | a0002 | c0004 | t0002 | g0233 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02818 | hp2 | a0002 | c0006 | t0002 | g0265 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02886 | hp1 | a0003 | c0013 | t0002 | g0015 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02886 | hp2 | a0004 | c0007 | t0002 | g0319 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02895 | hp1 | a0001 | c0010 | t0001 | g0226 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02895 | hp2 | a0002 | c0004 | t0002 | g0249 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02896 | hp2 | a0003 | c0011 | t0001 | g0011 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02897 | hp1 | a0003 | c0011 | t0001 | g0011 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02897 | hp2 | a0002 | c0004 | t0002 | g0248 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02922 | hp2 | a0001 | c0012 | t0001 | g0012 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02965 | hp1 | a0002 | c0006 | t0002 | g0261 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02965 | hp2 | a0003 | c0003 | t0004 | g0302 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02970 | hp1 | a0002 | c0006 | t0002 | g0270 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02970 | hp2 | a0003 | c0013 | t0002 | g0016 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02976 | hp1 | a0002 | c0006 | t0002 | g0262 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02976 | hp2 | a0002 | c0024 | t0002 | g0255 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03041 | hp1 | a0004 | c0007 | t0002 | g0312 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0301 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03098 | hp2 | a0001 | c0012 | t0001 | g0003 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03130 | hp1 | a0002 | c0023 | t0001 | g0254 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03130 | hp2 | a0002 | c0004 | t0002 | g0239 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03139 | hp1 | a0004 | c0007 | t0002 | g0315 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03139 | hp2 | a0003 | c0011 | t0001 | g0308 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03195 | hp1 | a0002 | c0004 | t0002 | g0235 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03195 | hp2 | a0002 | c0004 | t0002 | g0236 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03209 | hp1 | a0005 | c0008 | t0002 | g0032 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03209 | hp2 | a0008 | c0021 | t0001 | g0325 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03225 | hp1 | a0001 | c0012 | t0001 | g0014 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03225 | hp2 | a0016 | c0028 | t0002 | g0264 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03453 | hp1 | a0002 | c0006 | t0002 | g0263 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03453 | hp2 | a0003 | c0005 | t0001 | g0229 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03486 | hp1 | a0004 | c0007 | t0002 | g0317 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03486 | hp2 | a0001 | c0010 | t0001 | g0228 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03491 | hp2 | a0002 | c0006 | t0002 | g0272 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03516 | hp1 | a0001 | c0012 | t0001 | g0003 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03516 | hp2 | a0002 | c0015 | t0001 | g0080 | AFR | ESN | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03540 | hp1 | a0003 | c0011 | t0001 | g0311 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03579 | hp2 | a0002 | c0006 | t0002 | g0258 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0285 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0298 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0045 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03704 | hp2 | a0003 | c0003 | t0001 | g0299 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03834 | hp1 | a0002 | c0002 | t0005 | g0049 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03927 | hp2 | a0003 | c0033 | t0001 | g0329 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04184 | hp1 | a0001 | c0026 | t0001 | g0055 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0041 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0137 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04228 | hp1 | a0003 | c0003 | t0001 | g0278 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18522 | hp1 | a0002 | c0015 | t0001 | g0081 | AFR | YRI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0269 | AFR | YRI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18612 | hp2 | a0007 | c0016 | t0002 | g0004 | EAS | CHB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18747 | hp1 | a0003 | c0005 | t0001 | g0145 | EAS | CHB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18906 | hp1 | a0002 | c0006 | t0001 | g0251 | AFR | YRI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0267 | AFR | YRI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18943 | hp2 | a0003 | c0005 | t0001 | g0147 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18946 | hp1 | a0007 | c0016 | t0002 | g0083 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18947 | hp1 | a0003 | c0005 | t0001 | g0161 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18947 | hp2 | a0006 | c0014 | t0001 | g0153 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18950 | hp2 | a0006 | c0014 | t0001 | g0173 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18956 | hp1 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18956 | hp2 | a0003 | c0005 | t0001 | g0162 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18957 | hp1 | a0007 | c0016 | t0002 | g0004 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18967 | hp2 | a0003 | c0005 | t0001 | g0192 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18969 | hp1 | a0003 | c0005 | t0001 | g0007 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18970 | hp1 | a0003 | c0005 | t0001 | g0160 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18975 | hp2 | a0003 | c0005 | t0001 | g0088 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0280 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18993 | hp2 | a0003 | c0005 | t0001 | g0214 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19030 | hp1 | a0009 | c0032 | t0001 | g0314 | AFR | LWK | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19030 | hp2 | a0002 | c0006 | t0002 | g0257 | AFR | LWK | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19043 | hp1 | a0002 | c0004 | t0002 | g0234 | AFR | LWK | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19043 | hp2 | a0005 | c0008 | t0002 | g0033 | AFR | LWK | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0289 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19055 | hp1 | a0003 | c0003 | t0001 | g0282 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19063 | hp2 | a0003 | c0005 | t0001 | g0007 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19067 | hp1 | a0007 | c0029 | t0002 | g0084 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19070 | hp2 | a0001 | c0009 | t0001 | g0287 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19079 | hp2 | a0015 | c0027 | t0001 | g0104 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19083 | hp2 | a0006 | c0014 | t0001 | g0218 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19085 | hp1 | a0003 | c0005 | t0001 | g0215 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19087 | hp2 | a0003 | c0005 | t0001 | g0171 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19088 | hp2 | a0006 | c0014 | t0001 | g0170 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0268 | AFR | YRI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA19240 | hp2 | a0002 | c0004 | t0002 | g0238 | AFR | YRI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ASW | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA20129 | hp2 | a0009 | c0031 | t0002 | g0313 | AFR | ASW | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | CLM | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02109 | hp1 | a0003 | c0013 | t0002 | g0019 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02109 | hp2 | a0014 | c0034 | t0001 | g0330 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02559 | hp1 | a0011 | c0017 | t0002 | g0252 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG02559 | hp2 | a0001 | c0010 | t0001 | g0227 | AFR | ACB | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03471 | hp1 | a0002 | c0004 | t0002 | g0244 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG03471 | hp2 | a0004 | c0007 | t0002 | g0316 | AFR | MSL | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG06807 | hp1 | a0003 | c0011 | t0001 | g0307 | AFR | USA | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
HG06807 | hp2 | a0002 | c0004 | t0002 | g0232 | AFR | USA | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18955 | hp1 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
NA21309 | hp2 | a0012 | c0019 | t0001 | g0274 | AFR | LWK | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0057 | REF | REF | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0038 | REF | REF | MASP2_chr1_11021523_11052239 | MASP2 | chr1 | 11021523 | 11052239 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11027215
|
T | G | 2 | a0006a0015 | 6 | HG00621.hp2 NA18947.hp2 NA18950.hp2 others(3): Show |
missense_variant | MODERATE | c.1731A>C | p.Gln577His | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1763/2455 | 1731/2061 | 577/686 | chr1 | 11027215 | ||
chr1:11027354
|
T | C | 1 | a0015 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.1592A>G | p.Asn531Ser | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1624/2455 | 1592/2061 | 531/686 | chr1 | 11027354 | ||
chr1:11027630
|
C | T | 2 | a0004a0010 | 11 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
missense_variant | MODERATE | c.1316G>A | p.Arg439His | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1348/2455 | 1316/2061 | 439/686 | chr1 | 11027630 | ||
chr1:11030230
|
C | T | 1 | a0011 | 2 | HG02559.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.1243G>A | p.Asp415Asn | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/11 | 1275/2455 | 1243/2061 | 415/686 | chr1 | 11030230 | ||
chr1:11030840
|
A | G | 3 | a0003a0008a0012 | 57 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(54): Show |
missense_variant | MODERATE | c.1130T>C | p.Val377Ala | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 9/11 | 1162/2455 | 1130/2061 | 377/686 | chr1 | 11030840 | ||
chr1:11030859
|
C | A | 5 | a0001a0006a0013others(2): Show | 180 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
missense_variant | MODERATE | c.1111G>T | p.Asp371Tyr | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 9/11 | 1143/2455 | 1111/2061 | 371/686 | chr1 | 11030859 | ||
chr1:11034851
|
T | A | 1 | a0016 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1064A>T | p.Asp355Val | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/11 | 1096/2455 | 1064/2061 | 355/686 | chr1 | 11034851 | ||
chr1:11045482
|
T | C | 1 | a0012 | 2 | HG01109.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.470A>G | p.His157Arg | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/11 | 502/2455 | 470/2061 | 157/686 | chr1 | 11045482 | ||
chr1:11045485
|
C | T | 1 | a0017 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.467G>A | p.Cys156Tyr | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/11 | 499/2455 | 467/2061 | 156/686 | chr1 | 11045485 | ||
chr1:11045488
|
T | C | 1 | a0007 | 4 | NA18612.hp2 NA18946.hp1 NA18957.hp1 others(1): Show |
missense_variant | MODERATE | c.464A>G | p.His155Arg | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/11 | 496/2455 | 464/2061 | 155/686 | chr1 | 11045488 | ||
chr1:11046591
|
G | A | 2 | a0004a0009 | 11 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
missense_variant | MODERATE | c.377C>T | p.Pro126Leu | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/11 | 409/2455 | 377/2061 | 126/686 | chr1 | 11046591 | ||
chr1:11046609
|
T | C | 1 | a0013 | 2 | HG01192.hp1 HG01261.hp1 |
missense_variant | MODERATE | c.359A>G | p.Asp120Gly | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/11 | 391/2455 | 359/2061 | 120/686 | chr1 | 11046609 | ||
chr1:11046672
|
C | T | 1 | a0005 | 6 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
missense_variant | MODERATE | c.296G>A | p.Arg99Gln | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/11 | 328/2455 | 296/2061 | 99/686 | chr1 | 11046672 | ||
chr1:11046705
|
G | A | 1 | a0008 | 2 | HG02615.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.263C>T | p.Thr88Met | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/11 | 295/2455 | 263/2061 | 88/686 | chr1 | 11046705 | ||
chr1:11047087
|
G | A | 1 | a0014 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.38C>T | p.Ser13Leu | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/11 | 70/2455 | 38/2061 | 13/686 | chr1 | 11047087 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11027008
|
C | T | 1 | a0002c0025 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.1938G>A | p.Arg646Arg | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1970/2455 | 1938/2061 | 646/686 | chr1 | 11027008 | ||
chr1:11027311
|
A | G | 1 | a0001c0026 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.1635T>C | p.Asn545Asn | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1667/2455 | 1635/2061 | 545/686 | chr1 | 11027311 | ||
chr1:11027329
|
A | G | 1 | a0001c0010 | 6 | HG00741.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.1617T>C | p.Asn539Asn | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1649/2455 | 1617/2061 | 539/686 | chr1 | 11027329 | ||
chr1:11027467
|
G | A | 16 | a0001c0001a0001c0009a0001c0010others(13): Show | 231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
synonymous_variant | LOW | c.1479C>T | p.Ser493Ser | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 1511/2455 | 1479/2061 | 493/686 | chr1 | 11027467 | ||
chr1:11037810
|
C | T | 6 | a0001c0009a0002c0004a0002c0024others(3): Show | 52 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
splice_region_variant&synonymous_variant | LOW | c.891G>A | p.Ala297Ala | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/11 | 923/2455 | 891/2061 | 297/686 | chr1 | 11037810 | ||
chr1:11042882
|
C | T | 4 | a0002c0024a0003c0011a0003c0030others(1): Show | 10 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
synonymous_variant | LOW | c.882G>A | p.Thr294Thr | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/11 | 914/2455 | 882/2061 | 294/686 | chr1 | 11042882 | ||
chr1:11043351
|
G | A | 5 | a0002c0006a0004c0007a0009c0031others(2): Show | 24 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(21): Show |
synonymous_variant | LOW | c.729C>T | p.Tyr243Tyr | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 5/11 | 761/2455 | 729/2061 | 243/686 | chr1 | 11043351 | ||
chr1:11043468
|
C | T | 2 | a0002c0023a0012c0019 | 3 | HG01109.hp2 HG03130.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.612G>A | p.Pro204Pro | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 5/11 | 644/2455 | 612/2061 | 204/686 | chr1 | 11043468 | ||
chr1:11043525
|
G | A | 2 | a0002c0015a0005c0008 | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
synonymous_variant | LOW | c.555C>T | p.Ser185Ser | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 5/11 | 587/2455 | 555/2061 | 185/686 | chr1 | 11043525 | ||
chr1:11045445
|
T | C | 1 | a0007c0029 | 1 | NA19067.hp1 | synonymous_variant | LOW | c.507A>G | p.Ala169Ala | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/11 | 539/2455 | 507/2061 | 169/686 | chr1 | 11045445 | ||
chr1:11046560
|
G | A | 3 | a0003c0011a0003c0030a0008c0021 | 9 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.408C>T | p.Ala136Ala | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/11 | 440/2455 | 408/2061 | 136/686 | chr1 | 11046560 | ||
chr1:11046972
|
T | C | 1 | a0003c0033 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.153A>G | p.Ala51Ala | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/11 | 185/2455 | 153/2061 | 51/686 | chr1 | 11046972 | ||
chr1:11047065
|
C | T | 1 | a0003c0013 | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
synonymous_variant | LOW | c.60G>A | p.Pro20Pro | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/11 | 92/2455 | 60/2061 | 20/686 | chr1 | 11047065 | ||
chr1:11047092
|
A | G | 1 | a0001c0012 | 5 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.33T>C | p.Cys11Cys | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/11 | 65/2455 | 33/2061 | 11/686 | chr1 | 11047092 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11026660
|
A | G | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(22): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*225T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 225 | chr1 | 11026660 | |||||
chr1:11026674
|
C | A | 1 | a0002c0002t0005 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 211 | chr1 | 11026674 | |||||
chr1:11026696
|
C | T | 1 | a0003c0003t0004 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 189 | chr1 | 11026696 | |||||
chr1:11026701
|
G | A | 1 | a0001c0001t0003 | 3 | HG02280.hp2 HG02451.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 184 | chr1 | 11026701 | |||||
chr1:11026714
|
T | G | 1 | a0001c0001t0006 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 171 | chr1 | 11026714 | |||||
chr1:11026856
|
T | C | 1 | a0001c0001t0007 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 11/11 | 29 | chr1 | 11026856 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11027718
|
C | T | 1 | a0014c0034t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1298-70G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11027718 | ||||||
chr1:11027778
|
T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(268): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1298-130A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11027778 | ||||||
chr1:11028159
|
T | G | 16 | a0002c0004t0002g0233a0002c0004t0002g0234a0002c0004t0002g0235others(13): Show | 16 | HG01167.hp1 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1298-511A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028159 | ||||||
chr1:11028179
|
C | G | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1298-531G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028179 | ||||||
chr1:11028217
|
C | CAG | 7 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(4): Show | 8 | HG02615.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1298-570_1298-569i others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028217 | ||||||
chr1:11028247
|
A | C | 6 | a0006c0014t0001g0153a0006c0014t0001g0167a0006c0014t0001g0170others(3): Show | 6 | HG00621.hp2 NA18947.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1298-599T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028247 | ||||||
chr1:11028497
|
C | A | 1 | a0004c0007t0002g0318 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1298-849G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028497 | ||||||
chr1:11028701
|
TTTTTC | T | 62 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(59): Show | 65 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1298-1058_1298-105 others(9): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028701 | ||||||
chr1:11028702
|
TTTTC | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1298-1058_1298-105 others(8): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028702 | ||||||
chr1:11028703
|
TTTC | T | 54 | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0001t0001g0180others(51): Show | 54 | HG00639.hp1 HG01123.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.1298-1058_1298-105 others(7): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028703 | ||||||
chr1:11028704
|
TTC | T | 8 | a0002c0002t0002g0039a0002c0002t0002g0070a0002c0002t0002g0073others(5): Show | 8 | HG00558.hp2 HG01361.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1298-1058_1298-105 others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028704 | ||||||
chr1:11028705
|
TC | T | 4 | a0002c0025t0002g0271a0005c0008t0002g0033a0005c0008t0002g0034others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1298-1058delG | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028705 | ||||||
chr1:11028706
|
C | CT | 9 | a0002c0002t0002g0041a0002c0002t0002g0043a0002c0002t0002g0046others(6): Show | 9 | HG00642.hp2 HG01192.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1298-1059dupA | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028706 | ||||||
chr1:11028706
|
C | T | 17 | a0002c0002t0002g0040a0002c0002t0002g0058a0002c0002t0002g0059others(14): Show | 17 | HG01891.hp1 HG02027.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1298-1058G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028706 | ||||||
chr1:11028707
|
T | G | 2 | a0002c0004t0002g0236a0002c0004t0002g0238 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1298-1059A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028707 | ||||||
chr1:11028708
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1298-1060A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028708 | ||||||
chr1:11028709
|
T | G | 49 | a0003c0003t0001g0275a0003c0003t0001g0277a0003c0003t0001g0278others(46): Show | 51 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1298-1061A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028709 | ||||||
chr1:11028711
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0001t0001g0180others(3): Show | 6 | HG00639.hp1 HG02602.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298-1063A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028711 | ||||||
chr1:11028712
|
T | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(190): Show | 205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1298-1064A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028712 | ||||||
chr1:11028713
|
T | G | 69 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(66): Show | 72 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1298-1065A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028713 | ||||||
chr1:11028715
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0001t0001g0180others(3): Show | 6 | HG00639.hp1 HG02602.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298-1067A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028715 | ||||||
chr1:11028716
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(149): Show | 164 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1298-1068A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028716 | ||||||
chr1:11028717
|
T | G | 111 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(108): Show | 114 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.1298-1069A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028717 | ||||||
chr1:11028719
|
T | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0001t0001g0180others(2): Show | 5 | HG00639.hp1 HG02602.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1298-1071A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028719 | ||||||
chr1:11028720
|
T | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 161 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1298-1072A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028720 | ||||||
chr1:11028721
|
T | G | 65 | a0001c0001t0001g0158a0001c0001t0003g0220a0001c0001t0003g0221others(62): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1298-1073A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028721 | ||||||
chr1:11028722
|
T | G | 42 | a0002c0004t0002g0232a0002c0004t0002g0233a0002c0004t0002g0234others(39): Show | 42 | HG01167.hp1 HG01243.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.1298-1074A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028722 | ||||||
chr1:11028724
|
T | G | 23 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 23 | HG00738.hp1 HG00738.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1298-1076A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028724 | ||||||
chr1:11028725
|
T | G | 12 | a0001c0001t0003g0220a0003c0003t0001g0294a0003c0003t0001g0295others(9): Show | 13 | HG02280.hp2 HG02615.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1298-1077A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028725 | ||||||
chr1:11028873
|
C | A | 5 | a0003c0013t0002g0015a0003c0013t0002g0016a0003c0013t0002g0017others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1298-1225G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028873 | ||||||
chr1:11028882
|
T | G | 1 | a0009c0032t0001g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1298-1234A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028882 | ||||||
chr1:11028937
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0139 | 2 | HG00639.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1297+1239A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028937 | ||||||
chr1:11028950
|
C | T | 1 | a0002c0002t0002g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1297+1226G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11028950 | ||||||
chr1:11029045
|
T | G | 16 | a0002c0004t0002g0233a0002c0004t0002g0234a0002c0004t0002g0235others(13): Show | 16 | HG01167.hp1 HG02055.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1297+1131A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029045 | ||||||
chr1:11029053
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1297+1123G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029053 | ||||||
chr1:11029165
|
TG | T | 3 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222 | 3 | HG02280.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1297+1010delC | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029165 | ||||||
chr1:11029168
|
AT | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1297+1007delA | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029168 | ||||||
chr1:11029191
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0127others(4): Show | 7 | HG01433.hp2 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297+985C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029191 | ||||||
chr1:11029386
|
C | T | 1 | a0002c0006t0002g0272 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1297+790G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029386 | ||||||
chr1:11029387
|
G | A | 1 | a0003c0003t0001g0306 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1297+789C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029387 | ||||||
chr1:11029394
|
C | T | 5 | a0003c0013t0002g0015a0003c0013t0002g0016a0003c0013t0002g0017others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297+782G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029394 | ||||||
chr1:11029406
|
T | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(266): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1297+770A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029406 | ||||||
chr1:11029409
|
T | A | 1 | a0002c0006t0002g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1297+767A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029409 | ||||||
chr1:11029553
|
A | T | 1 | a0002c0002t0002g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1297+623T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029553 | ||||||
chr1:11029634
|
C | CT | 62 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0012t0001g0013others(59): Show | 63 | HG00735.hp2 HG01168.hp1 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.1297+541dupA | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029634 | ||||||
chr1:11029634
|
C | CTT | 37 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0230others(34): Show | 37 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1297+540_1297+541d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029634 | ||||||
chr1:11029634
|
C | CTTT | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(130): Show | 145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1297+539_1297+541d others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029634 | ||||||
chr1:11029634
|
C | CTTTT | 21 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0130others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1297+538_1297+541d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029634 | ||||||
chr1:11029634
|
CT | C | 21 | a0002c0006t0001g0251a0002c0015t0001g0080a0002c0015t0001g0081others(18): Show | 21 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1297+541delA | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029634 | ||||||
chr1:11029718
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1297+458G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029718 | ||||||
chr1:11029787
|
TACC | T | 13 | a0004c0007t0002g0312a0004c0007t0002g0315a0004c0007t0002g0316others(10): Show | 13 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1297+386_1297+388d others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029787 | ||||||
chr1:11029796
|
A | C | 2 | a0002c0002t0002g0043a0002c0002t0002g0044 | 2 | NA18981.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1297+380T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029796 | ||||||
chr1:11029915
|
C | T | 5 | a0003c0013t0002g0015a0003c0013t0002g0016a0003c0013t0002g0017others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297+261G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029915 | ||||||
chr1:11029957
|
A | G | 5 | a0005c0008t0002g0031a0005c0008t0002g0032a0005c0008t0002g0033others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1297+219T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11029957 | ||||||
chr1:11030028
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1297+148T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 10/10 | chr1 | 11030028 | ||||||
chr1:11030317
|
AC | A | 10 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1223-68delG | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 9/10 | chr1 | 11030317 | ||||||
chr1:11030330
|
ATGT | A | 7 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(4): Show | 8 | HG02615.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1223-83_1223-81del others(3): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 9/10 | chr1 | 11030330 | ||||||
chr1:11030419
|
G | A | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1223-169C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 9/10 | chr1 | 11030419 | ||||||
chr1:11030974
|
G | A | 46 | a0003c0003t0001g0275a0003c0003t0001g0277a0003c0003t0001g0278others(43): Show | 48 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1088-92C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11030974 | ||||||
chr1:11031148
|
G | A | 60 | a0002c0002t0002g0025a0002c0002t0002g0039a0002c0002t0002g0040others(57): Show | 61 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1088-266C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031148 | ||||||
chr1:11031236
|
A | G | 4 | a0002c0006t0001g0251a0002c0015t0001g0080a0002c0015t0001g0081others(1): Show | 4 | HG03130.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-354T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031236 | ||||||
chr1:11031245
|
C | T | 3 | a0002c0006t0002g0258a0002c0006t0002g0259a0002c0006t0002g0260 | 3 | HG02055.hp2 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1088-363G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031245 | ||||||
chr1:11031249
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0179 | 3 | HG01928.hp2 HG02083.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1088-367G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031249 | ||||||
chr1:11031261
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1088-379A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031261 | ||||||
chr1:11031290
|
G | A | 3 | a0003c0030t0001g0310a0012c0019t0001g0273a0012c0019t0001g0274 | 3 | HG01109.hp2 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1088-408C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031290 | ||||||
chr1:11031295
|
G | A | 1 | a0003c0013t0002g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1088-413C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031295 | ||||||
chr1:11031367
|
C | A | 13 | a0004c0007t0002g0312a0004c0007t0002g0315a0004c0007t0002g0316others(10): Show | 13 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088-485G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031367 | ||||||
chr1:11031367
|
C | CA | 10 | a0001c0001t0001g0143a0002c0002t0002g0076a0002c0006t0002g0270others(7): Show | 10 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-486dupT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031367 | ||||||
chr1:11031421
|
C | T | 1 | a0003c0003t0001g0305 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1088-539G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031421 | ||||||
chr1:11031472
|
A | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(274): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.1088-590T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031472 | ||||||
chr1:11031477
|
C | T | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1088-595G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031477 | ||||||
chr1:11031478
|
A | G | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1088-596T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031478 | ||||||
chr1:11031492
|
T | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(267): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1088-610A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031492 | ||||||
chr1:11031527
|
T | A | 1 | a0003c0005t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1088-645A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031527 | ||||||
chr1:11031528
|
T | A | 1 | a0003c0005t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1088-646A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031528
|
T | TAAAAAA | 8 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0010t0001g0225others(5): Show | 9 | HG00741.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1088-652_1088-647d others(8): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031528
|
T | TAAAAAAA | 157 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1088-653_1088-647d others(9): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031528
|
T | TAAAAAAA others(1): Show |
58 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(55): Show | 65 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1088-654_1088-647d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031528
|
T | TAAAAAAA others(2): Show |
25 | a0002c0004t0002g0233a0002c0004t0002g0234a0002c0004t0002g0235others(22): Show | 25 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1088-655_1088-647d others(11): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031528
|
T | TAAAAAAA others(3): Show |
14 | a0002c0004t0002g0236a0002c0004t0002g0240a0002c0004t0002g0245others(11): Show | 14 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1088-656_1088-647d others(12): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031528
|
T | TAAAAAAA others(4): Show |
3 | a0002c0004t0002g0247a0002c0015t0001g0080a0002c0025t0002g0271 | 3 | HG02055.hp1 HG02602.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1088-657_1088-647d others(13): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031528 | ||||||
chr1:11031547
|
G | A | 2 | a0001c0001t0001g0181a0003c0013t0002g0019 | 2 | HG01433.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1088-665C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031547 | ||||||
chr1:11031636
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1088-754C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031636 | ||||||
chr1:11031638
|
A | T | 1 | a0001c0001t0001g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1088-756T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031638 | ||||||
chr1:11031726
|
C | A | 13 | a0004c0007t0002g0312a0004c0007t0002g0315a0004c0007t0002g0316others(10): Show | 13 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088-844G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031726 | ||||||
chr1:11031832
|
G | C | 1 | a0003c0005t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1088-950C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031832 | ||||||
chr1:11031932
|
C | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1088-1050G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11031932 | ||||||
chr1:11032203
|
T | A | 1 | a0003c0030t0001g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1088-1321A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032203 | ||||||
chr1:11032215
|
G | A | 8 | a0002c0015t0001g0080a0002c0015t0001g0081a0003c0005t0001g0229others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088-1333C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032215 | ||||||
chr1:11032270
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0105 | 2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1088-1388A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032270 | ||||||
chr1:11032441
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1088-1559C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032441 | ||||||
chr1:11032496
|
G | A | 48 | a0003c0003t0001g0275a0003c0003t0001g0277a0003c0003t0001g0278others(45): Show | 50 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1088-1614C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032496 | ||||||
chr1:11032589
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(236): Show | 254 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.1088-1707A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032589 | ||||||
chr1:11032608
|
C | CAA | 10 | a0002c0004t0002g0232a0002c0004t0002g0233a0002c0004t0002g0235others(7): Show | 10 | HG01167.hp1 HG02615.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-1728_1088-172 others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032608 | ||||||
chr1:11032608
|
C | CAAA | 50 | a0002c0004t0002g0234a0002c0004t0002g0237a0002c0004t0002g0244others(47): Show | 52 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1088-1729_1088-172 others(7): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032608 | ||||||
chr1:11032700
|
G | A | 1 | a0002c0006t0002g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1088-1818C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11032700 | ||||||
chr1:11033046
|
C | T | 1 | a0001c0010t0001g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1087+1782G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033046 | ||||||
chr1:11033056
|
C | T | 1 | a0002c0004t0002g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1087+1772G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033056 | ||||||
chr1:11033139
|
A | G | 13 | a0003c0003t0001g0277a0003c0003t0001g0278a0003c0003t0001g0279others(10): Show | 13 | HG00609.hp2 HG00673.hp2 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087+1689T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033139 | ||||||
chr1:11033277
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(269): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1087+1551T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033277 | ||||||
chr1:11033284
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1087+1544G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033284 | ||||||
chr1:11033462
|
C | T | 14 | a0002c0006t0002g0270a0004c0007t0002g0312a0004c0007t0002g0315others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1087+1366G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033462 | ||||||
chr1:11033529
|
C | T | 64 | a0002c0002t0002g0293a0002c0004t0002g0232a0002c0004t0002g0233others(61): Show | 66 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1087+1299G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033529 | ||||||
chr1:11033572
|
C | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(270): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.1087+1256G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033572 | ||||||
chr1:11033644
|
C | G | 7 | a0002c0015t0001g0080a0002c0015t0001g0081a0003c0013t0002g0015others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+1184G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033644 | ||||||
chr1:11033684
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(275): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1087+1144T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033684 | ||||||
chr1:11033702
|
G | A | 1 | a0002c0006t0001g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1087+1126C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033702 | ||||||
chr1:11033718
|
G | A | 1 | a0001c0010t0001g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1087+1110C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033718 | ||||||
chr1:11033837
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(162): Show | 177 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1087+991C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033837 | ||||||
chr1:11033894
|
G | C | 1 | a0002c0002t0002g0039 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1087+934C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033894 | ||||||
chr1:11033926
|
G | GAC | 10 | a0002c0002t0002g0047a0002c0002t0002g0048a0002c0002t0002g0050others(7): Show | 10 | HG00642.hp2 HG00735.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1087+900_1087+901d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033926 | ||||||
chr1:11033926
|
GACACACA others(5): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1087+890_1087+901d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033926 | ||||||
chr1:11033926
|
GACACACA others(7): Show |
G | 2 | a0005c0008t0002g0036a0009c0031t0002g0313 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1087+888_1087+901d others(16): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033926 | ||||||
chr1:11033937
|
ACACACAC others(25): Show |
A | 14 | a0002c0002t0002g0293a0003c0003t0001g0277a0003c0003t0001g0278others(11): Show | 14 | HG00609.hp2 HG00673.hp2 HG03669.hp1 others(11): Show |
intron_variant | MODIFIER | c.1087+859_1087+890d others(34): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033937 | ||||||
chr1:11033949
|
ACACACAC others(13): Show |
A | 8 | a0002c0006t0002g0256a0002c0006t0002g0258a0002c0006t0002g0259others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087+859_1087+878d others(22): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033949 | ||||||
chr1:11033951
|
ACACACAC others(9): Show |
A | 2 | a0003c0003t0001g0301a0003c0003t0004g0302 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1087+861_1087+876d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033951 | ||||||
chr1:11033951
|
ACACACAC others(11): Show |
A | 4 | a0002c0004t0002g0239a0002c0004t0002g0240a0002c0006t0002g0257others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087+859_1087+876d others(20): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033951 | ||||||
chr1:11033953
|
ACACACAC others(7): Show |
A | 10 | a0004c0007t0002g0312a0004c0007t0002g0316a0004c0007t0002g0317others(7): Show | 10 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1087+861_1087+874d others(16): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033953 | ||||||
chr1:11033953
|
ACACACAC others(9): Show |
A | 24 | a0003c0003t0001g0292a0003c0003t0001g0294a0003c0003t0001g0295others(21): Show | 25 | HG00140.hp2 HG01175.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1087+859_1087+874d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033953 | ||||||
chr1:11033955
|
ACACACAC others(5): Show |
A | 15 | a0001c0001t0001g0095a0001c0001t0001g0113a0001c0001t0001g0115others(12): Show | 15 | HG00323.hp1 HG00544.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1087+861_1087+872d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033955 | ||||||
chr1:11033955
|
ACACACAC others(7): Show |
A | 39 | a0001c0001t0001g0193a0001c0001t0003g0220a0001c0001t0003g0221others(36): Show | 41 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(38): Show |
intron_variant | MODIFIER | c.1087+859_1087+872d others(16): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033955 | ||||||
chr1:11033955
|
ACACACAC others(9): Show |
A | 1 | a0003c0003t0001g0275 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1087+857_1087+872d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033955 | ||||||
chr1:11033957
|
ACACACAC others(3): Show |
A | 2 | a0001c0001t0001g0021a0001c0001t0001g0148 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1087+861_1087+870d others(12): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033957 | ||||||
chr1:11033957
|
ACACACAC others(5): Show |
A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 143 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1087+859_1087+870d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033957 | ||||||
chr1:11033957
|
ACACACAC others(9): Show |
A | 1 | a0002c0004t0002g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1087+855_1087+870d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033957 | ||||||
chr1:11033959
|
ACACACAC others(3): Show |
A | 6 | a0001c0001t0001g0024a0001c0001t0001g0144a0001c0001t0001g0156others(3): Show | 6 | HG03017.hp2 HG03654.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1087+859_1087+868d others(12): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033959 | ||||||
chr1:11033959
|
ACACACAC others(5): Show |
A | 4 | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG00642.hp1 HG01069.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087+857_1087+868d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033959 | ||||||
chr1:11033961
|
ACACACTC others(1): Show |
A | 5 | a0001c0001t0001g0110a0001c0001t0001g0123a0001c0001t0001g0135others(2): Show | 5 | HG00639.hp2 HG01255.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087+859_1087+866d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033961 | ||||||
chr1:11033961
|
ACACACTC others(3): Show |
A | 1 | a0012c0019t0001g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1087+857_1087+866d others(12): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033961 | ||||||
chr1:11033965
|
A | ACACTCTC others(5): Show |
1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1087+862_1087+863i others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033965 | ||||||
chr1:11033965
|
A | T | 5 | a0002c0002t0002g0025a0002c0002t0002g0045a0005c0008t0002g0032others(2): Show | 5 | HG02132.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087+863T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033965 | ||||||
chr1:11033967
|
T | A | 17 | a0002c0002t0002g0059a0002c0002t0002g0060a0002c0002t0002g0061others(14): Show | 17 | HG01123.hp2 HG01361.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1087+861A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033967 | ||||||
chr1:11033969
|
T | A | 6 | a0002c0002t0002g0072a0002c0002t0002g0266a0002c0002t0002g0267others(3): Show | 6 | HG01943.hp1 HG03098.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1087+859A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033969 | ||||||
chr1:11033971
|
T | A | 2 | a0002c0002t0002g0039a0002c0002t0002g0073 | 2 | HG00558.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1087+857A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033971 | ||||||
chr1:11033973
|
T | A | 2 | a0003c0030t0001g0310a0012c0019t0001g0273 | 2 | HG01109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1087+855A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033973 | ||||||
chr1:11033985
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0107 | 3 | HG00544.hp2 HG02165.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1087+843A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11033985 | ||||||
chr1:11034099
|
G | A | 40 | a0002c0002t0002g0293a0003c0003t0001g0275a0003c0003t0001g0277others(37): Show | 41 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1087+729C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034099 | ||||||
chr1:11034141
|
G | A | 1 | a0002c0002t0002g0065 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1087+687C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034141 | ||||||
chr1:11034147
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(166): Show | 182 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1087+681C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034147 | ||||||
chr1:11034239
|
C | A | 1 | a0001c0009t0001g0276 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1087+589G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034239 | ||||||
chr1:11034243
|
G | GA | 15 | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0001t0001g0129others(12): Show | 15 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1087+584dupT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034243 | ||||||
chr1:11034243
|
GA | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0001g0180others(17): Show | 21 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1087+584delT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034243 | ||||||
chr1:11034243
|
GAA | G | 24 | a0002c0004t0002g0232a0002c0004t0002g0233a0002c0004t0002g0234others(21): Show | 24 | HG00438.hp2 HG01167.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1087+583_1087+584d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034243 | ||||||
chr1:11034243
|
GAAA | G | 49 | a0002c0002t0002g0293a0002c0004t0002g0248a0002c0015t0001g0080others(46): Show | 51 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1087+582_1087+584d others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034243 | ||||||
chr1:11034305
|
A | G | 24 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(21): Show | 24 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1087+523T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034305 | ||||||
chr1:11034397
|
TA | T | 7 | a0002c0015t0001g0080a0002c0015t0001g0081a0003c0013t0002g0015others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+430delT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034397 | ||||||
chr1:11034409
|
A | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG00642.hp1 HG01069.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087+419T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034409 | ||||||
chr1:11034435
|
C | T | 1 | a0002c0002t0002g0065 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1087+393G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034435 | ||||||
chr1:11034603
|
C | CAGGAGGA others(16): Show |
1 | a0003c0005t0001g0215 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1087+202_1087+224d others(25): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034603 | ||||||
chr1:11034608
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1087+220C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034608 | ||||||
chr1:11034661
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1087+167A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034661 | ||||||
chr1:11034700
|
G | GA | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(224): Show | 242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1087+127dupT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034700 | ||||||
chr1:11034700
|
G | GAA | 29 | a0001c0001t0001g0037a0002c0004t0002g0232a0002c0006t0001g0251others(26): Show | 29 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1087+126_1087+127d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034700 | ||||||
chr1:11034700
|
G | GAAA | 12 | a0001c0001t0001g0108a0001c0010t0001g0224a0002c0006t0002g0256others(9): Show | 12 | HG02055.hp2 HG02572.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1087+125_1087+127d others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034700 | ||||||
chr1:11034715
|
G | A | 7 | a0002c0015t0001g0080a0002c0015t0001g0081a0003c0013t0002g0015others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+113C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 8/10 | chr1 | 11034715 | ||||||
chr1:11034968
|
C | A | 5 | a0002c0006t0001g0251a0002c0023t0001g0254a0003c0030t0001g0310others(2): Show | 5 | HG01109.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009-62G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11034968 | ||||||
chr1:11034982
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(270): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.1009-76G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11034982 | ||||||
chr1:11035172
|
A | G | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1009-266T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035172 | ||||||
chr1:11035252
|
G | A | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1009-346C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035252 | ||||||
chr1:11035274
|
G | A | 60 | a0001c0009t0001g0250a0001c0009t0001g0287a0001c0009t0001g0300others(57): Show | 61 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1009-368C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035274 | ||||||
chr1:11035310
|
G | C | 1 | a0004c0007t0002g0320 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1009-404C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035310 | ||||||
chr1:11035367
|
A | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(174): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1009-461T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035367 | ||||||
chr1:11035485
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1009-579T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035485 | ||||||
chr1:11035528
|
A | AATC | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(229): Show | 244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1009-625_1009-623d others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035528 | ||||||
chr1:11035528
|
A | AATCATC | 16 | a0001c0001t0001g0005a0001c0001t0001g0103a0001c0001t0003g0220others(13): Show | 18 | HG00423.hp2 HG00741.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1009-628_1009-623d others(8): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035528 | ||||||
chr1:11035664
|
G | A | 65 | a0001c0001t0001g0085a0001c0009t0001g0250a0001c0009t0001g0276others(62): Show | 66 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1009-758C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035664 | ||||||
chr1:11035719
|
A | AC | 9 | a0002c0015t0001g0080a0002c0015t0001g0081a0002c0015t0002g0079others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1009-814dupG | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035719 | ||||||
chr1:11035757
|
G | A | 1 | a0012c0019t0001g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1009-851C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035757 | ||||||
chr1:11035826
|
G | A | 65 | a0001c0001t0001g0085a0001c0009t0001g0250a0001c0009t0001g0276others(62): Show | 66 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1009-920C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035826 | ||||||
chr1:11035894
|
CA | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0042a0002c0002t0002g0041others(25): Show | 29 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1009-989delT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035894 | ||||||
chr1:11035894
|
CAA | C | 28 | a0001c0026t0001g0055a0002c0002t0002g0025a0002c0002t0002g0039others(25): Show | 28 | HG00558.hp2 HG01123.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.1009-990_1009-989d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035894 | ||||||
chr1:11035894
|
CAAA | C | 7 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0130others(4): Show | 7 | HG01243.hp2 HG01255.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009-991_1009-989d others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035894 | ||||||
chr1:11035894
|
CAAAA | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1009-992_1009-989d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035894 | ||||||
chr1:11035894
|
CAAAAA | C | 70 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0206others(67): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1009-993_1009-989d others(7): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035894 | ||||||
chr1:11035974
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0098a0001c0001t0001g0163others(4): Show | 8 | HG00544.hp2 HG00621.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009-1068C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11035974 | ||||||
chr1:11036036
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0121others(3): Show | 7 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009-1130C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036036 | ||||||
chr1:11036069
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0103 | 3 | HG00423.hp2 NA18955.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1009-1163G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036069 | ||||||
chr1:11036232
|
C | T | 6 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(3): Show | 6 | HG02602.hp2 HG03098.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1009-1326G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036232 | ||||||
chr1:11036267
|
G | C | 1 | a0002c0006t0002g0259 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1009-1361C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036267 | ||||||
chr1:11036295
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1009-1389C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036295 | ||||||
chr1:11036365
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(172): Show | 189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1008+1328C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036365 | ||||||
chr1:11036367
|
G | A | 2 | a0001c0001t0003g0220a0001c0001t0003g0221 | 2 | HG02280.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1008+1326C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036367 | ||||||
chr1:11036396
|
C | G | 31 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(28): Show | 31 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.1008+1297G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036396 | ||||||
chr1:11036429
|
G | A | 3 | a0002c0023t0001g0254a0012c0019t0001g0273a0012c0019t0001g0274 | 3 | HG01109.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1008+1264C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036429 | ||||||
chr1:11036480
|
C | T | 8 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(5): Show | 9 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1213G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036480 | ||||||
chr1:11036498
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1008+1195C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036498 | ||||||
chr1:11036510
|
C | CA | 47 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0087others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1008+1182dupT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
C | CAA | 6 | a0002c0002t0002g0054a0003c0003t0001g0285a0003c0003t0001g0288others(3): Show | 6 | HG00609.hp2 HG01192.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008+1181_1008+118 others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
C | CAAA | 8 | a0001c0012t0001g0012a0002c0002t0002g0082a0002c0015t0001g0081others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008+1180_1008+118 others(7): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
CA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(73): Show | 85 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1008+1182delT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
CAA | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0139a0001c0001t0001g0219others(10): Show | 13 | HG00609.hp1 HG00639.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+1181_1008+118 others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0013t0002g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1008+1173_1008+118 others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
CAAAAAAA others(4): Show |
C | 4 | a0003c0013t0002g0016a0003c0013t0002g0017a0003c0013t0002g0018others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1172_1008+118 others(15): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036510
|
CAAAAAAA others(7): Show |
C | 14 | a0002c0006t0001g0251a0004c0007t0002g0312a0004c0007t0002g0315others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+1169_1008+118 others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036510 | ||||||
chr1:11036521
|
AAAAAAAA others(10): Show |
A | 5 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(2): Show | 5 | HG03098.hp1 HG03491.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008+1155_1008+117 others(21): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036521 | ||||||
chr1:11036523
|
AAAAAAAA others(8): Show |
A | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1008+1155_1008+116 others(19): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036523 | ||||||
chr1:11036526
|
A | C | 19 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(16): Show | 20 | HG02055.hp2 HG02572.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.1008+1167T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036526 | ||||||
chr1:11036527
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1008+1166T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036527 | ||||||
chr1:11036528
|
A | C | 3 | a0001c0001t0001g0132a0011c0017t0002g0252a0011c0017t0002g0253 | 3 | HG01256.hp2 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1008+1165T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036528 | ||||||
chr1:11036530
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1008+1163T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036530 | ||||||
chr1:11036533
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1008+1160T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036533 | ||||||
chr1:11036535
|
A | AC | 9 | a0003c0003t0001g0275a0003c0003t0001g0289a0003c0003t0001g0290others(6): Show | 9 | HG00438.hp2 HG02735.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1157_1008+115 others(5): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036535 | ||||||
chr1:11036537
|
A | AAC | 8 | a0002c0004t0002g0233a0002c0004t0002g0235a0002c0004t0002g0236others(5): Show | 8 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1155_1008+115 others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036537 | ||||||
chr1:11036538
|
C | A | 15 | a0001c0012t0001g0003a0001c0012t0001g0012a0001c0012t0001g0013others(12): Show | 16 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1008+1155G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036538 | ||||||
chr1:11036538
|
C | CA | 8 | a0002c0004t0002g0234a0002c0004t0002g0239a0002c0004t0002g0240others(5): Show | 8 | HG01167.hp1 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008+1154dupT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036538 | ||||||
chr1:11036539
|
A | C | 1 | a0003c0003t0001g0282 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1008+1154T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036539 | ||||||
chr1:11036541
|
A | C | 3 | a0003c0003t0001g0286a0003c0003t0001g0289a0003c0003t0001g0290 | 3 | NA18954.hp1 NA18956.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1008+1152T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036541 | ||||||
chr1:11036629
|
C | CT | 78 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0056others(75): Show | 80 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1008+1063dupA | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036629 | ||||||
chr1:11036629
|
C | CTT | 23 | a0002c0002t0002g0266a0002c0004t0002g0232a0002c0004t0002g0233others(20): Show | 24 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.1008+1062_1008+106 others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036629 | ||||||
chr1:11036629
|
CT | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0097a0001c0001t0003g0221others(8): Show | 11 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008+1063delA | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036629 | ||||||
chr1:11036631
|
T | C | 4 | a0002c0006t0002g0257a0002c0006t0002g0263a0002c0006t0002g0265others(1): Show | 4 | HG02818.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1062A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036631 | ||||||
chr1:11036632
|
T | C | 6 | a0002c0006t0002g0256a0002c0006t0002g0258a0002c0006t0002g0259others(3): Show | 6 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008+1061A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036632 | ||||||
chr1:11036786
|
G | A | 6 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(3): Show | 6 | HG02602.hp2 HG03098.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008+907C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11036786 | ||||||
chr1:11037177
|
C | T | 10 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1008+516G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037177 | ||||||
chr1:11037178
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1008+515C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037178 | ||||||
chr1:11037210
|
ATAATTTT others(35): Show |
A | 3 | a0002c0023t0001g0254a0012c0019t0001g0273a0012c0019t0001g0274 | 3 | HG01109.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1008+441_1008+482d others(44): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037210 | ||||||
chr1:11037368
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0174others(1): Show | 4 | HG02080.hp1 HG02523.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+325A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037368 | ||||||
chr1:11037380
|
C | A | 1 | a0003c0003t0001g0292 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1008+313G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037380 | ||||||
chr1:11037440
|
C | T | 1 | a0012c0019t0001g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1008+253G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037440 | ||||||
chr1:11037453
|
A | G | 1 | a0002c0002t0002g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1008+240T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037453 | ||||||
chr1:11037490
|
C | A | 52 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(49): Show | 52 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008+203G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037490 | ||||||
chr1:11037490
|
C | T | 3 | a0002c0015t0001g0080a0002c0015t0001g0081a0002c0015t0002g0079 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1008+203G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037490 | ||||||
chr1:11037491
|
G | A | 52 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(49): Show | 52 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008+202C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037491 | ||||||
chr1:11037493
|
G | A | 52 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(49): Show | 52 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008+200C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 7/10 | chr1 | 11037493 | ||||||
chr1:11037844
|
A | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG00741.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.890-33T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11037844 | ||||||
chr1:11037965
|
G | T | 1 | a0002c0006t0001g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890-154C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11037965 | ||||||
chr1:11038019
|
G | C | 1 | a0003c0003t0001g0292 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.890-208C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038019 | ||||||
chr1:11038209
|
C | T | 34 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(31): Show | 34 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.890-398G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038209 | ||||||
chr1:11038213
|
A | G | 54 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.890-402T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038213 | ||||||
chr1:11038214
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.890-403A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038214 | ||||||
chr1:11038275
|
C | T | 3 | a0002c0023t0001g0254a0012c0019t0001g0273a0012c0019t0001g0274 | 3 | HG01109.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.890-464G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038275 | ||||||
chr1:11038276
|
G | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.890-465C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038276 | ||||||
chr1:11038390
|
A | T | 1 | a0003c0003t0001g0275 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.890-579T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038390 | ||||||
chr1:11038567
|
G | A | 1 | a0002c0006t0001g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890-756C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038567 | ||||||
chr1:11038652
|
T | A | 1 | a0003c0003t0001g0288 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.890-841A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038652 | ||||||
chr1:11038654
|
A | C | 1 | a0003c0003t0001g0288 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.890-843T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038654 | ||||||
chr1:11038658
|
A | C | 1 | a0003c0003t0001g0288 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.890-847T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038658 | ||||||
chr1:11038659
|
G | C | 1 | a0003c0003t0001g0288 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.890-848C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038659 | ||||||
chr1:11038686
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.890-875G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038686 | ||||||
chr1:11038978
|
T | C | 1 | a0006c0014t0001g0167 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.890-1167A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11038978 | ||||||
chr1:11039014
|
A | T | 1 | a0003c0003t0001g0275 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.890-1203T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039014 | ||||||
chr1:11039017
|
TACTCTTC others(11): Show |
T | 55 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(52): Show | 55 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.890-1224_890-1207d others(20): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039017 | ||||||
chr1:11039059
|
G | A | 1 | a0002c0002t0002g0063 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.890-1248C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039059 | ||||||
chr1:11039160
|
C | G | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.890-1349G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039160 | ||||||
chr1:11039190
|
G | A | 17 | a0002c0002t0002g0039a0002c0002t0002g0040a0002c0002t0002g0058others(14): Show | 17 | HG00558.hp2 HG01123.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.890-1379C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039190 | ||||||
chr1:11039274
|
G | A | 11 | a0002c0006t0002g0256a0002c0006t0002g0258a0002c0006t0002g0259others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.890-1463C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039274 | ||||||
chr1:11039330
|
GTGGA | G | 63 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0057others(60): Show | 63 | HG00558.hp2 HG01123.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.890-1523_890-1520d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039330 | ||||||
chr1:11039330
|
GTGGATGG others(1): Show |
G | 33 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0009t0001g0250others(30): Show | 33 | HG00438.hp2 HG01109.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.890-1527_890-1520d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039330 | ||||||
chr1:11039330
|
GTGGATGG others(5): Show |
G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(189): Show | 206 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.890-1531_890-1520d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039330 | ||||||
chr1:11039330
|
GTGGATGG others(9): Show |
G | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-1535_890-1520d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039330 | ||||||
chr1:11039330
|
GTGGATGG others(17): Show |
G | 1 | a0002c0006t0001g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.890-1543_890-1520d others(26): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039330 | ||||||
chr1:11039364
|
GGATGGAT others(9): Show |
G | 3 | a0001c0001t0001g0098a0001c0001t0001g0204a0001c0001t0006g0189 | 3 | HG02135.hp1 NA18954.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.890-1569_890-1554d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039364 | ||||||
chr1:11039368
|
GGATGGAT others(5): Show |
G | 3 | a0003c0003t0001g0303a0003c0003t0001g0304a0003c0003t0001g0305 | 3 | HG00140.hp2 HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.890-1569_890-1558d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039368 | ||||||
chr1:11039374
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.890-1563T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039374 | ||||||
chr1:11039508
|
AGAAT | A | 17 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.890-1701_890-1698d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039508 | ||||||
chr1:11039522
|
AATGG | A | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-1715_890-1712d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039522 | ||||||
chr1:11039589
|
T | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.890-1778A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039589 | ||||||
chr1:11039731
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(169): Show | 186 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.890-1920C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039731 | ||||||
chr1:11039755
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.890-1944C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039755 | ||||||
chr1:11039776
|
T | A | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 345 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.890-1965A>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039776 | ||||||
chr1:11039777
|
C | T | 2 | a0012c0019t0001g0273a0012c0019t0001g0274 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.890-1966G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039777 | ||||||
chr1:11039815
|
G | GAAGGATG others(9): Show |
2 | a0005c0008t0002g0034a0005c0008t0002g0035 | 2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.890-2020_890-2005d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039815 | ||||||
chr1:11039865
|
A | AGGAT | 44 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0062others(41): Show | 45 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.890-2058_890-2055d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039865 | ||||||
chr1:11039865
|
A | AGGATGGA others(1): Show |
26 | a0001c0001t0001g0056a0001c0001t0001g0057a0002c0002t0002g0069others(23): Show | 27 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.890-2062_890-2055d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039865 | ||||||
chr1:11039865
|
A | AGGATGGA others(5): Show |
3 | a0003c0013t0002g0015a0003c0013t0002g0016a0014c0034t0001g0330 | 3 | HG02109.hp2 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.890-2066_890-2055d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039865 | ||||||
chr1:11039865
|
AGGAT | A | 54 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(51): Show | 54 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.890-2058_890-2055d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039865 | ||||||
chr1:11039902
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(186): Show | 202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.890-2091T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039902 | ||||||
chr1:11039902
|
AGATG | A | 7 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0188others(4): Show | 8 | HG01069.hp1 HG01074.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.890-2095_890-2092d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039902 | ||||||
chr1:11039906
|
G | A | 24 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(21): Show | 24 | HG00741.hp1 HG01243.hp2 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.890-2095C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039906 | ||||||
chr1:11039906
|
G | GGATA | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(142): Show | 158 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.890-2096_890-2095i others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039906 | ||||||
chr1:11039906
|
G | GGATGGAT others(1): Show |
21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0108others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.890-2103_890-2096d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039906 | ||||||
chr1:11039948
|
T | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(325): Show | 344 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.890-2137A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039948 | ||||||
chr1:11039959
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.890-2148C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039959 | ||||||
chr1:11039993
|
G | A | 5 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(2): Show | 5 | HG03098.hp1 HG03491.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-2182C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11039993 | ||||||
chr1:11040008
|
G | A | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-2197C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040008 | ||||||
chr1:11040032
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.890-2221C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040032 | ||||||
chr1:11040088
|
G | T | 1 | a0002c0006t0002g0270 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.890-2277C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040088 | ||||||
chr1:11040135
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.890-2324C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040135 | ||||||
chr1:11040229
|
G | A | 1 | a0002c0002t0002g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.890-2418C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040229 | ||||||
chr1:11040281
|
C | T | 1 | a0001c0009t0001g0283 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.890-2470G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040281 | ||||||
chr1:11040325
|
T | C | 12 | a0002c0006t0001g0251a0004c0007t0002g0312a0004c0007t0002g0315others(9): Show | 12 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.890-2514A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040325 | ||||||
chr1:11040389
|
T | TA | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 345 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.889+2485_889+2486i others(3): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040389 | ||||||
chr1:11040465
|
T | TA | 17 | a0002c0002t0002g0052a0002c0002t0002g0053a0002c0002t0002g0054others(14): Show | 17 | HG01192.hp2 HG02602.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.889+2409dupT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040465 | ||||||
chr1:11040465
|
T | TAA | 7 | a0001c0026t0001g0055a0003c0011t0001g0011a0003c0013t0002g0015others(4): Show | 8 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.889+2408_889+2409d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040465 | ||||||
chr1:11040465
|
TA | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(222): Show | 238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.889+2409delT | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040465 | ||||||
chr1:11040465
|
TAA | T | 15 | a0001c0001t0001g0116a0001c0001t0003g0220a0001c0001t0003g0221others(12): Show | 16 | HG00741.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.889+2408_889+2409d others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040465 | ||||||
chr1:11040687
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18950.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.889+2188T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040687 | ||||||
chr1:11040807
|
T | C | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.889+2068A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040807 | ||||||
chr1:11040841
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(297): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.889+2034T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040841 | ||||||
chr1:11040857
|
G | T | 1 | a0003c0003t0001g0275 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.889+2018C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040857 | ||||||
chr1:11040858
|
G | GTGGA | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+2013_889+2016d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040858 | ||||||
chr1:11040858
|
GTGGA | G | 4 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(1): Show | 4 | HG03098.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.889+2013_889+2016d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040858 | ||||||
chr1:11040882
|
G | GTAGGTAG others(5): Show |
1 | a0001c0012t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.889+1981_889+1992d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040882 | ||||||
chr1:11040934
|
G | A | 17 | a0002c0004t0002g0233a0002c0004t0002g0234a0002c0004t0002g0235others(14): Show | 17 | HG01167.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.889+1941C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040934 | ||||||
chr1:11040944
|
T | C | 1 | a0003c0013t0002g0016 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.889+1931A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040944 | ||||||
chr1:11040977
|
GGATA | G | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.889+1894_889+1897d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040977 | ||||||
chr1:11040981
|
A | G | 6 | a0005c0008t0002g0031a0005c0008t0002g0032a0005c0008t0002g0033others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.889+1894T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040981 | ||||||
chr1:11040998
|
G | A | 5 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(2): Show | 5 | HG03098.hp1 HG03491.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.889+1877C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11040998 | ||||||
chr1:11041096
|
A | AGGAT | 61 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0057others(58): Show | 62 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.889+1775_889+1778d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041096 | ||||||
chr1:11041096
|
A | AGGATGGA others(1): Show |
173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(170): Show | 186 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.889+1771_889+1778d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041096 | ||||||
chr1:11041096
|
A | AGGATGGA others(5): Show |
8 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG00558.hp1 HG00735.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.889+1778_889+1779i others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041096 | ||||||
chr1:11041096
|
AGGATGGA others(5): Show |
A | 9 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(6): Show | 10 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.889+1767_889+1778d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041096 | ||||||
chr1:11041097
|
GGATGGAT others(1): Show |
G | 3 | a0003c0003t0001g0303a0003c0003t0001g0304a0003c0003t0001g0305 | 3 | HG00140.hp2 HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.889+1770_889+1777d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041097 | ||||||
chr1:11041101
|
GGATA | G | 9 | a0001c0001t0001g0206a0002c0025t0002g0271a0005c0008t0002g0031others(6): Show | 9 | HG02080.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.889+1770_889+1773d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041101 | ||||||
chr1:11041105
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(305): Show | 323 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.889+1770T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041105 | ||||||
chr1:11041136
|
A | T | 7 | a0001c0001t0001g0213a0003c0003t0001g0294a0003c0003t0001g0295others(4): Show | 7 | HG02683.hp1 HG02735.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+1739T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041136 | ||||||
chr1:11041216
|
G | A | 7 | a0003c0003t0001g0275a0003c0003t0001g0294a0003c0003t0001g0295others(4): Show | 7 | HG00438.hp2 HG02735.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+1659C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041216 | ||||||
chr1:11041329
|
G | A | 2 | a0012c0019t0001g0273a0012c0019t0001g0274 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.889+1546C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041329 | ||||||
chr1:11041352
|
ATAGG | A | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.889+1519_889+1522d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041352 | ||||||
chr1:11041356
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(255): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.889+1519C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041356 | ||||||
chr1:11041373
|
C | CAGAT | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG01256.hp1 HG01258.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.889+1498_889+1501d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041373 | ||||||
chr1:11041374
|
A | AGATG | 3 | a0002c0004t0002g0232a0011c0017t0002g0252a0011c0017t0002g0253 | 3 | HG02559.hp1 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.889+1497_889+1500d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041374 | ||||||
chr1:11041374
|
A | AGATGGAT others(1): Show |
48 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(45): Show | 48 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.889+1493_889+1500d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041374 | ||||||
chr1:11041374
|
A | AGATGGAT others(5): Show |
4 | a0002c0002t0002g0293a0003c0003t0001g0294a0003c0003t0001g0295others(1): Show | 4 | NA18941.hp2 NA18955.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.889+1489_889+1500d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041374 | ||||||
chr1:11041378
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(166): Show | 183 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.889+1497C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041378 | ||||||
chr1:11041392
|
A | ATGGATGA others(1): Show |
5 | a0003c0013t0002g0015a0003c0013t0002g0016a0003c0013t0002g0017others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.889+1482_889+1483i others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041392 | ||||||
chr1:11041399
|
G | A | 8 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(5): Show | 9 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+1476C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041399 | ||||||
chr1:11041400
|
A | G | 8 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(5): Show | 9 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+1475T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041400 | ||||||
chr1:11041403
|
A | G | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.889+1472T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041403 | ||||||
chr1:11041404
|
G | A | 15 | a0001c0001t0001g0211a0002c0024t0002g0255a0003c0011t0001g0011others(12): Show | 16 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+1471C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041404 | ||||||
chr1:11041404
|
G | GTGGA | 52 | a0001c0001t0001g0028a0001c0001t0001g0111a0001c0001t0001g0112others(49): Show | 53 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.889+1467_889+1470d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041404 | ||||||
chr1:11041404
|
G | GTGGATGG others(1): Show |
192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(189): Show | 205 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.889+1463_889+1470d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041404 | ||||||
chr1:11041404
|
G | GTGGATGG others(5): Show |
16 | a0001c0001t0001g0024a0001c0001t0001g0209a0001c0001t0001g0210others(13): Show | 16 | HG00140.hp2 HG01175.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.889+1459_889+1470d others(14): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041404 | ||||||
chr1:11041404
|
G | GTGGATGG others(9): Show |
2 | a0002c0006t0002g0265a0009c0032t0001g0314 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.889+1455_889+1470d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041404 | ||||||
chr1:11041407
|
G | C | 9 | a0002c0002t0002g0039a0002c0002t0002g0069a0002c0002t0002g0070others(6): Show | 9 | HG00558.hp2 HG01123.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.889+1468C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041407 | ||||||
chr1:11041443
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.889+1432C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041443 | ||||||
chr1:11041588
|
G | A | 3 | a0002c0015t0001g0080a0002c0015t0001g0081a0002c0015t0002g0079 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889+1287C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041588 | ||||||
chr1:11041596
|
A | T | 2 | a0002c0015t0001g0080a0002c0015t0001g0081 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889+1279T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041596 | ||||||
chr1:11041597
|
T | G | 2 | a0002c0015t0001g0080a0002c0015t0001g0081 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889+1278A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041597 | ||||||
chr1:11041599
|
G | A | 2 | a0002c0015t0001g0080a0002c0015t0001g0081 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889+1276C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041599 | ||||||
chr1:11041599
|
G | GTGGA | 40 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0062others(37): Show | 41 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.889+1272_889+1275d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041599 | ||||||
chr1:11041599
|
GTGGA | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0090a0001c0001t0001g0098others(42): Show | 46 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.889+1272_889+1275d others(6): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041599 | ||||||
chr1:11041599
|
GTGGATGG others(1): Show |
G | 3 | a0003c0013t0002g0017a0003c0013t0002g0018a0003c0013t0002g0019 | 3 | HG01891.hp2 HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.889+1268_889+1275d others(10): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041599 | ||||||
chr1:11041599
|
GTGGATGG others(9): Show |
G | 2 | a0003c0013t0002g0015a0003c0013t0002g0016 | 2 | HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.889+1260_889+1275d others(18): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041599 | ||||||
chr1:11041736
|
T | TAGAAGAA others(248): Show |
1 | a0001c0001t0001g0097 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.889+1138_889+1139i others(257): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(259): Show |
1 | a0002c0004t0002g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.889+1138_889+1139i others(268): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(255): Show |
11 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(8): Show | 11 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(264): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(263): Show |
32 | a0001c0009t0001g0250a0001c0009t0001g0276a0001c0009t0001g0281others(29): Show | 32 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(272): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(259): Show |
29 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0003g0220others(26): Show | 29 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(268): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(267): Show |
1 | a0003c0003t0001g0285 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.889+1138_889+1139i others(276): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(263): Show |
187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(184): Show | 202 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(272): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(267): Show |
47 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0056others(44): Show | 48 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(276): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(271): Show |
4 | a0002c0002t0002g0065a0002c0002t0002g0066a0002c0002t0002g0067others(1): Show | 4 | HG00423.hp1 HG02083.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(280): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(275): Show |
8 | a0002c0002t0002g0069a0002c0002t0002g0070a0002c0002t0002g0071others(5): Show | 8 | HG01123.hp2 HG01361.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.889+1138_889+1139i others(284): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(279): Show |
1 | a0002c0002t0002g0039 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.889+1138_889+1139i others(288): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(271): Show |
3 | a0002c0015t0001g0080a0002c0015t0001g0081a0002c0015t0002g0079 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.889+1138_889+1139i others(280): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(264): Show |
1 | a0001c0001t0001g0096 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.889+1138_889+1139i others(273): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(261): Show |
1 | a0003c0003t0001g0275 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.889+1138_889+1139i others(270): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041736
|
T | TAGAAGAA others(634): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18950.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.889+1138_889+1139i others(643): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041736 | ||||||
chr1:11041737
|
G | C | 1 | a0014c0034t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.889+1138C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041737 | ||||||
chr1:11041875
|
AGGATGGG others(5): Show |
A | 1 | a0014c0034t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.889+988_889+999del others(12): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041875 | ||||||
chr1:11041908
|
G | A | 1 | a0006c0014t0001g0218 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.889+967C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11041908 | ||||||
chr1:11042042
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.889+833T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042042 | ||||||
chr1:11042099
|
G | C | 3 | a0002c0023t0001g0254a0012c0019t0001g0273a0012c0019t0001g0274 | 3 | HG01109.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.889+776C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042099 | ||||||
chr1:11042180
|
A | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.889+695T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042180 | ||||||
chr1:11042218
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(271): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.889+657T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042218 | ||||||
chr1:11042300
|
A | G | 10 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.889+575T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042300 | ||||||
chr1:11042396
|
T | TTGGA | 17 | a0001c0009t0001g0287a0001c0010t0001g0228a0002c0002t0002g0077others(14): Show | 17 | HG00438.hp2 HG00609.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.889+475_889+478dup others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042396 | ||||||
chr1:11042396
|
TTGGA | T | 23 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(20): Show | 24 | HG00558.hp2 HG01109.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.889+475_889+478del others(4): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042396 | ||||||
chr1:11042396
|
TTGGATGG others(9): Show |
T | 1 | a0001c0001t0001g0219 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.889+463_889+478del others(16): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042396 | ||||||
chr1:11042396
|
TTGGATGG others(13): Show |
T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(156): Show | 172 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.889+459_889+478del others(20): Show |
MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042396 | ||||||
chr1:11042460
|
T | TG | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 345 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.889+414dupC | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042460 | ||||||
chr1:11042545
|
G | T | 1 | a0002c0006t0002g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.889+330C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042545 | ||||||
chr1:11042557
|
G | A | 14 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(11): Show | 15 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.889+318C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042557 | ||||||
chr1:11042559
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.889+316T>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042559 | ||||||
chr1:11042646
|
G | A | 7 | a0003c0003t0001g0275a0003c0003t0001g0294a0003c0003t0001g0295others(4): Show | 7 | HG00438.hp2 HG02735.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.889+229C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042646 | ||||||
chr1:11042680
|
G | T | 1 | a0002c0002t0002g0091 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.889+195C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042680 | ||||||
chr1:11042841
|
G | A | 1 | a0002c0006t0002g0272 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.889+34C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 6/10 | chr1 | 11042841 | ||||||
chr1:11043152
|
C | A | 5 | a0003c0013t0002g0015a0003c0013t0002g0016a0003c0013t0002g0017others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-130G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 5/10 | chr1 | 11043152 | ||||||
chr1:11043291
|
G | C | 8 | a0001c0009t0001g0250a0001c0009t0001g0300a0003c0003t0001g0301others(5): Show | 8 | HG00140.hp2 HG01175.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.741+48C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 5/10 | chr1 | 11043291 | ||||||
chr1:11043295
|
G | A | 1 | a0003c0003t0001g0291 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.741+44C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 5/10 | chr1 | 11043295 | ||||||
chr1:11043588
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.545-53C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11043588 | ||||||
chr1:11043727
|
G | A | 29 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(26): Show | 29 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.545-192C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11043727 | ||||||
chr1:11043852
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.545-317T>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11043852 | ||||||
chr1:11043910
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(212): Show | 230 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.545-375C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11043910 | ||||||
chr1:11043919
|
G | T | 17 | a0001c0009t0001g0276a0001c0009t0001g0281a0001c0009t0001g0283others(14): Show | 17 | HG00609.hp2 HG00673.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.545-384C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11043919 | ||||||
chr1:11043984
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.545-449C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11043984 | ||||||
chr1:11044011
|
C | T | 1 | a0011c0017t0002g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.545-476G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044011 | ||||||
chr1:11044025
|
C | T | 6 | a0005c0008t0002g0031a0005c0008t0002g0032a0005c0008t0002g0033others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.545-490G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044025 | ||||||
chr1:11044145
|
G | A | 1 | a0002c0006t0002g0270 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.545-610C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044145 | ||||||
chr1:11044164
|
A | T | 6 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(3): Show | 7 | HG02647.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.545-629T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044164 | ||||||
chr1:11044259
|
G | A | 8 | a0003c0011t0001g0011a0003c0011t0001g0307a0003c0011t0001g0308others(5): Show | 9 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.545-724C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044259 | ||||||
chr1:11044299
|
G | C | 1 | a0002c0025t0002g0271 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.545-764C>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044299 | ||||||
chr1:11044313
|
C | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(214): Show | 232 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.545-778G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044313 | ||||||
chr1:11044619
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(168): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.544+789C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044619 | ||||||
chr1:11044655
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(199): Show | 216 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.544+753C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044655 | ||||||
chr1:11044686
|
T | G | 15 | a0002c0006t0002g0272a0002c0024t0002g0255a0003c0011t0001g0011others(12): Show | 16 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.544+722A>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044686 | ||||||
chr1:11044707
|
T | C | 2 | a0004c0007t0002g0321a0004c0007t0002g0322 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.544+701A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044707 | ||||||
chr1:11044751
|
C | T | 1 | a0002c0024t0002g0255 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.544+657G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044751 | ||||||
chr1:11044775
|
C | T | 1 | a0003c0003t0001g0275 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.544+633G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044775 | ||||||
chr1:11044788
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.544+620A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044788 | ||||||
chr1:11044794
|
C | T | 10 | a0002c0006t0002g0256a0002c0006t0002g0257a0002c0006t0002g0258others(7): Show | 10 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.544+614G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11044794 | ||||||
chr1:11045007
|
C | T | 1 | a0004c0007t0002g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544+401G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045007 | ||||||
chr1:11045009
|
G | A | 15 | a0002c0006t0002g0272a0002c0024t0002g0255a0003c0011t0001g0011others(12): Show | 16 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.544+399C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045009 | ||||||
chr1:11045031
|
C | G | 1 | a0003c0005t0001g0229 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544+377G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045031 | ||||||
chr1:11045049
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(168): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.544+359G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045049 | ||||||
chr1:11045065
|
C | T | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(271): Show | 289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.544+343G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045065 | ||||||
chr1:11045180
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.544+228T>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045180 | ||||||
chr1:11045229
|
G | A | 1 | a0014c0034t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.544+179C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045229 | ||||||
chr1:11045321
|
C | T | 1 | a0002c0006t0002g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.544+87G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045321 | ||||||
chr1:11045328
|
C | G | 9 | a0002c0024t0002g0255a0003c0011t0001g0011a0003c0011t0001g0307others(6): Show | 10 | HG02615.hp1 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.544+80G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045328 | ||||||
chr1:11045383
|
T | C | 1 | a0005c0008t0002g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.544+25A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 4/10 | chr1 | 11045383 | ||||||
chr1:11045789
|
G | T | 1 | a0002c0023t0001g0254 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.413-250C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11045789 | ||||||
chr1:11045962
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.413-423C>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11045962 | ||||||
chr1:11046048
|
T | C | 2 | a0011c0017t0002g0252a0011c0017t0002g0253 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.412+508A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11046048 | ||||||
chr1:11046051
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.412+505G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11046051 | ||||||
chr1:11046170
|
G | A | 45 | a0002c0002t0002g0266a0002c0002t0002g0267a0002c0002t0002g0268others(42): Show | 46 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.412+386C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11046170 | ||||||
chr1:11046260
|
G | A | 33 | a0001c0009t0001g0276a0001c0009t0001g0281a0001c0009t0001g0283others(30): Show | 33 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.412+296C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11046260 | ||||||
chr1:11046302
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(272): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.412+254A>G | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11046302 | ||||||
chr1:11046333
|
C | A | 1 | a0003c0003t0001g0306 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.412+223G>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 3/10 | chr1 | 11046333 | ||||||
chr1:11046782
|
C | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | NA18941.hp1 NA18967.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.235-49G>C | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/10 | chr1 | 11046782 | ||||||
chr1:11046852
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00738.hp1 HG02132.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+39G>A | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/10 | chr1 | 11046852 | ||||||
chr1:11046878
|
G | A | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.234+13C>T | MASP2 | ENSG00000009724.18 | transcript | ENST00000400897.8 | protein_coding | 2/10 | chr1 | 11046878 |