geneid | 4600 |
---|---|
ensemblid | ENSG00000183486.14 |
hgncid | 7533 |
symbol | MX2 |
name | MX dynamin like GTPase 2 |
refseq_nuc | NM_002463.2 |
refseq_prot | NP_002454.1 |
ensembl_nuc | ENST00000330714.8 |
ensembl_prot | ENSP00000333657.3 |
mane_status | MANE Select |
chr | chr21 |
start | 41362027 |
end | 41409393 |
strand | + |
ver | v1.2 |
region | chr21:41362027-41409393 |
region5000 | chr21:41357027-41414393 |
regionname0 | MX2_chr21_41362027_41409393 |
regionname5000 | MX2_chr21_41357027_41414393 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 715 | 331 | 65 | 65 | 140 | 18 | 41 | 105 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002 | 0/0 | 715 | 26 | 15 | 3 | 7 | 0 | 1 | 6 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0003 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0004 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0005 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0006 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0007 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0008 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0009 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0010 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0011 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0012 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0013 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0014 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0015 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0016 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0017 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2148 | 279 | 52 | 63 | 107 | 17 | 38 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0002 | 0/0 | 2148 | 35 | 5 | 1 | 25 | 1 | 3 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0003 | 0/0 | 2148 | 19 | 11 | 1 | 6 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0004 | 0/0 | 2148 | 12 | 5 | 0 | 7 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0005 | 0/0 | 2148 | 4 | 2 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0006 | 0/0 | 2148 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0007 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0008 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0009 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0010 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0011 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0012 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0013 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0014 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0015 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0016 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0017 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0018 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0019 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0020 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0021 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0022 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0023 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0024 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0025 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0026 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0027 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
c0028 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
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 | 1259 | 246 | 44 | 62 | 94 | 15 | 30 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0002 | 1/0 | 1261 | 67 | 5 | 4 | 42 | 2 | 13 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0003 | 0/0 | 1259 | 17 | 8 | 2 | 7 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0004 | 0/0 | 1259 | 13 | 13 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0005 | 0/0 | 1259 | 8 | 8 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0006 | 0/0 | 1257 | 6 | 4 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0007 | 0/0 | 1259 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0008 | 0/0 | 1259 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0009 | 0/0 | 1259 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0010 | 0/0 | 1259 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0011 | 0/0 | 1259 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0012 | 0/0 | 1259 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0013 | 0/0 | 1259 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0014 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0015 | 0/0 | 1259 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0016 | 0/0 | 1259 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0017 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0018 | 0/0 | 1259 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
t0019 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
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 | 1 | 4 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2148 | 279 | 52 | 63 | 107 | 17 | 38 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0002 | 0/0 | 2148 | 35 | 5 | 1 | 25 | 1 | 3 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0004 | 0/0 | 2148 | 12 | 5 | 0 | 7 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0006 | 0/0 | 2148 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0024 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0025 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0026 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0003 | 0/0 | 2148 | 19 | 11 | 1 | 6 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0005 | 0/0 | 2148 | 4 | 2 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0010 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0013 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0014 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0003c0008 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0003c0009 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0004c0007 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0005c0028 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0006c0027 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0007c0023 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0008c0022 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0009c0020 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0010c0021 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0011c0019 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0012c0018 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0013c0017 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0014c0016 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0015c0015 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0016c0012 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0017c0011 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3406 | 210 | 31 | 59 | 77 | 14 | 28 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0002 | 1/0 | 3408 | 37 | 1 | 2 | 22 | 2 | 9 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0004 | 0/0 | 3406 | 9 | 9 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0005 | 0/0 | 3406 | 5 | 5 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0006 | 0/0 | 3404 | 5 | 3 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0007 | 0/0 | 3406 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0008 | 0/0 | 3406 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0009 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0010 | 0/0 | 3406 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0011 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0012 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0013 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0015 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0017 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0001t0018 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0002t0001 | 0/0 | 3406 | 8 | 0 | 0 | 7 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0002t0002 | 0/0 | 3408 | 26 | 4 | 1 | 18 | 0 | 3 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0002t0004 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0004t0003 | 0/0 | 3406 | 12 | 5 | 0 | 7 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0006t0001 | 0/0 | 3406 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0024t0006 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0025t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0001c0026t0009 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0003t0001 | 0/0 | 3406 | 12 | 6 | 1 | 4 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0003t0002 | 0/0 | 3408 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0003t0004 | 0/0 | 3406 | 3 | 3 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0003t0005 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0003t0019 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0005t0003 | 0/0 | 3406 | 4 | 2 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0010t0016 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0013t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0002c0014t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0003c0008t0003 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0003c0009t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0004c0007t0001 | 0/0 | 3406 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0005c0028t0001 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0006c0027t0005 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0007c0023t0014 | 0/0 | 3408 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0008c0022t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0009c0020t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0010c0021t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0011c0019t0002 | 0/0 | 3408 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0012c0018t0002 | 0/0 | 3408 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0013c0017t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0014c0016t0005 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0015c0015t0001 | 0/0 | 3406 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0016c0012t0001 | 0/0 | 3406 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
a0017c0011t0001 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | copy fasta | chr21 | 41357027 | 41414393 |
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 | 4 | 0 | 1 | 3 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0006g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0007g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0009g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0011g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0017g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0001t0018g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0006t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0024t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0025t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0001c0026t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0003t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0005t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0005t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0005t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0010t0016g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0013t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0002c0014t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0003c0008t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0003c0009t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0004c0007t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0004c0007t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0005c0028t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0006c0027t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0007c0023t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0008c0022t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0009c0020t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0010c0021t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0011c0019t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0012c0018t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0013c0017t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0014c0016t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0015c0015t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0016c0012t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
a0017c0011t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0338 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | FIN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00558 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00621 | hp1 | a0008 | c0022 | t0001 | g0048 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01069 | hp2 | a0012 | c0018 | t0002 | g0016 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01106 | hp1 | a0001 | c0006 | t0001 | g0239 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01109 | hp1 | a0016 | c0012 | t0001 | g0272 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0341 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0334 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0024 | AMR | PUR | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01257 | hp1 | a0002 | c0005 | t0003 | g0293 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01258 | hp2 | a0002 | c0005 | t0003 | g0294 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01516 | hp2 | a0001 | c0001 | t0011 | g0266 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01884 | hp1 | a0001 | c0004 | t0003 | g0321 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0263 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02055 | hp1 | a0002 | c0005 | t0003 | g0023 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0323 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02071 | hp1 | a0001 | c0026 | t0009 | g0172 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02074 | hp1 | a0002 | c0013 | t0001 | g0192 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | KHV | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02145 | hp1 | a0002 | c0005 | t0003 | g0023 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02155 | hp2 | a0009 | c0020 | t0001 | g0110 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | CDX | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02257 | hp1 | a0001 | c0006 | t0001 | g0140 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02257 | hp2 | a0017 | c0011 | t0001 | g0271 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02280 | hp1 | a0003 | c0009 | t0001 | g0333 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0072 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0320 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0250 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0297 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0322 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02723 | hp2 | a0002 | c0010 | t0016 | g0329 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02738 | hp2 | a0001 | c0001 | t0013 | g0092 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02809 | hp1 | a0002 | c0003 | t0004 | g0302 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0312 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02895 | hp2 | a0003 | c0008 | t0003 | g0292 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0311 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02922 | hp2 | a0001 | c0004 | t0003 | g0317 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02965 | hp2 | a0004 | c0007 | t0001 | g0328 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02970 | hp1 | a0002 | c0003 | t0001 | g0299 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02970 | hp2 | a0014 | c0016 | t0005 | g0279 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03041 | hp2 | a0002 | c0003 | t0005 | g0296 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0324 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0074 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03130 | hp2 | a0002 | c0003 | t0004 | g0269 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0291 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03209 | hp1 | a0001 | c0024 | t0006 | g0331 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03486 | hp2 | a0002 | c0014 | t0001 | g0071 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0011 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03540 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03579 | hp1 | a0007 | c0023 | t0014 | g0278 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03654 | hp1 | a0011 | c0019 | t0002 | g0223 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0289 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18522 | hp1 | a0001 | c0004 | t0003 | g0307 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18522 | hp2 | a0002 | c0003 | t0004 | g0301 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0179 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18906 | hp2 | a0001 | c0025 | t0001 | g0332 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18943 | hp1 | a0015 | c0015 | t0001 | g0035 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18943 | hp2 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18952 | hp2 | a0001 | c0004 | t0003 | g0124 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18957 | hp2 | a0001 | c0004 | t0003 | g0094 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18965 | hp1 | a0002 | c0003 | t0002 | g0225 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0326 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18966 | hp2 | a0013 | c0017 | t0001 | g0217 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18969 | hp1 | a0010 | c0021 | t0001 | g0185 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18972 | hp1 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18979 | hp1 | a0001 | c0004 | t0003 | g0242 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18984 | hp1 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18988 | hp2 | a0001 | c0004 | t0003 | g0227 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0335 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19030 | hp1 | a0002 | c0003 | t0019 | g0238 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0295 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19054 | hp2 | a0001 | c0004 | t0003 | g0128 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19078 | hp2 | a0001 | c0004 | t0003 | g0085 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19081 | hp1 | a0001 | c0004 | t0003 | g0086 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19083 | hp1 | a0001 | c0001 | t0018 | g0340 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0196 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | YRI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0298 | AFR | ASW | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | GIH | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20905 | hp2 | a0005 | c0028 | t0001 | g0304 | SAS | GIH | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG02559 | hp2 | a0006 | c0027 | t0005 | g0235 | AFR | ACB | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03471 | hp1 | a0004 | c0007 | t0001 | g0327 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0315 | AFR | MSL | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | USA | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | LWK | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0259 | REF | REF | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0257 | REF | REF | MX2_chr21_41357027_41414393 | MX2 | chr21 | 41357027 | 41414393 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41376962
|
G | A | 1 | a0003 | 2 | HG02280.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.56G>A | p.Arg19Gln | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 156/3408 | 56/2148 | 19/715 | chr21 | 41376962 | ||
chr21:41377007
|
C | T | 1 | a0005 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.101C>T | p.Pro34Leu | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 201/3408 | 101/2148 | 34/715 | chr21 | 41377007 | ||
chr21:41377025
|
C | T | 1 | a0006 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.119C>T | p.Pro40Leu | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 219/3408 | 119/2148 | 40/715 | chr21 | 41377025 | ||
chr21:41377123
|
C | G | 1 | a0004 | 2 | HG02965.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.217C>G | p.Pro73Ala | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 317/3408 | 217/2148 | 73/715 | chr21 | 41377123 | ||
chr21:41377154
|
T | C | 3 | a0002a0016a0017 | 28 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(25): Show |
missense_variant&splice_region_variant | MODERATE | c.248T>C | p.Met83Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 348/3408 | 248/2148 | 83/715 | chr21 | 41377154 | ||
chr21:41377819
|
G | A | 1 | a0015 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.280G>A | p.Glu94Lys | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/14 | 380/3408 | 280/2148 | 94/715 | chr21 | 41377819 | ||
chr21:41380103
|
G | A | 2 | a0014a0017 | 2 | HG02257.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.529G>A | p.Glu177Lys | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/14 | 629/3408 | 529/2148 | 177/715 | chr21 | 41380103 | ||
chr21:41390571
|
G | A | 1 | a0013 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.739G>A | p.Ala247Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/14 | 839/3408 | 739/2148 | 247/715 | chr21 | 41390571 | ||
chr21:41395721
|
A | G | 1 | a0007 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1006A>G | p.Arg336Gly | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/14 | 1106/3408 | 1006/2148 | 336/715 | chr21 | 41395721 | ||
chr21:41398951
|
G | A | 1 | a0016 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1204G>A | p.Glu402Lys | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 9/14 | 1304/3408 | 1204/2148 | 402/715 | chr21 | 41398951 | ||
chr21:41398969
|
G | A | 1 | a0012 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.1222G>A | p.Gly408Arg | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 9/14 | 1322/3408 | 1222/2148 | 408/715 | chr21 | 41398969 | ||
chr21:41403329
|
A | C | 1 | a0008 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1636A>C | p.Asn546His | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/14 | 1736/3408 | 1636/2148 | 546/715 | chr21 | 41403329 | ||
chr21:41403338
|
G | A | 1 | a0009 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1645G>A | p.Val549Ile | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/14 | 1745/3408 | 1645/2148 | 549/715 | chr21 | 41403338 | ||
chr21:41408106
|
G | A | 1 | a0010 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2021G>A | p.Arg674His | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 2121/3408 | 2021/2148 | 674/715 | chr21 | 41408106 | ||
chr21:41408141
|
G | A | 1 | a0011 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.2056G>A | p.Ala686Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 2156/3408 | 2056/2148 | 686/715 | chr21 | 41408141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41377008
|
G | A | 1 | a0001c0006 | 2 | HG01106.hp1 HG02257.hp1 |
synonymous_variant | LOW | c.102G>A | p.Pro34Pro | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 202/3408 | 102/2148 | 34/715 | chr21 | 41377008 | ||
chr21:41377077
|
T | G | 1 | a0002c0010 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.171T>G | p.Ala57Ala | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/14 | 271/3408 | 171/2148 | 57/715 | chr21 | 41377077 | ||
chr21:41377818
|
C | T | 2 | a0002c0010a0002c0014 | 2 | HG02723.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.279C>T | p.Tyr93Tyr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/14 | 379/3408 | 279/2148 | 93/715 | chr21 | 41377818 | ||
chr21:41382477
|
C | T | 1 | a0001c0026 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.645C>T | p.Ser215Ser | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/14 | 745/3408 | 645/2148 | 215/715 | chr21 | 41382477 | ||
chr21:41382555
|
C | T | 2 | a0001c0024a0001c0025 | 2 | HG03209.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.723C>T | p.Ile241Ile | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/14 | 823/3408 | 723/2148 | 241/715 | chr21 | 41382555 | ||
chr21:41399249
|
T | C | 3 | a0001c0002a0002c0013a0011c0019 | 37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
synonymous_variant | LOW | c.1326T>C | p.Val442Val | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/14 | 1426/3408 | 1326/2148 | 442/715 | chr21 | 41399249 | ||
chr21:41403313
|
C | T | 1 | a0001c0025 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1620C>T | p.Gly540Gly | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/14 | 1720/3408 | 1620/2148 | 540/715 | chr21 | 41403313 | ||
chr21:41406749
|
G | A | 3 | a0001c0004a0002c0005a0003c0008 | 17 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(14): Show |
synonymous_variant | LOW | c.1656G>A | p.Thr552Thr | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/14 | 1756/3408 | 1656/2148 | 552/715 | chr21 | 41406749 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41408267
|
G | T | 1 | a0002c0003t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*34G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 34 | chr21 | 41408267 | |||||
chr21:41408273
|
A | G | 4 | a0001c0001t0005a0002c0003t0005a0006c0027t0005others(1): Show | 8 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 40 | chr21 | 41408273 | |||||
chr21:41408286
|
G | A | 1 | a0001c0001t0011 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 53 | chr21 | 41408286 | |||||
chr21:41408417
|
C | T | 1 | a0001c0001t0010 | 2 | HG00558.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 184 | chr21 | 41408417 | |||||
chr21:41408452
|
C | T | 1 | a0001c0001t0018 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 219 | chr21 | 41408452 | |||||
chr21:41408604
|
G | C | 3 | a0001c0001t0004a0001c0002t0004a0002c0003t0004 | 13 | HG02145.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*371G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 371 | chr21 | 41408604 | |||||
chr21:41408606
|
C | A | 1 | a0001c0001t0012 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 373 | chr21 | 41408606 | |||||
chr21:41408683
|
T | C | 1 | a0001c0001t0013 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 450 | chr21 | 41408683 | |||||
chr21:41408746
|
C | A | 3 | a0001c0004t0003a0002c0005t0003a0003c0008t0003 | 17 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 513 | chr21 | 41408746 | |||||
chr21:41408775
|
C | T | 4 | a0001c0001t0006a0001c0001t0017a0001c0024t0006others(1): Show | 8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*542C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 542 | chr21 | 41408775 | |||||
chr21:41408818
|
C | T | 2 | a0001c0001t0006a0001c0024t0006 | 6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*585C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 585 | chr21 | 41408818 | |||||
chr21:41408940
|
C | T | 5 | a0001c0001t0006a0001c0001t0017a0001c0024t0006others(2): Show | 9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*707C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 707 | chr21 | 41408940 | |||||
chr21:41409056
|
C | A | 1 | a0001c0001t0007 | 2 | NA18974.hp2 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*823C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 823 | chr21 | 41409056 | |||||
chr21:41409075
|
T | A | 1 | a0001c0001t0008 | 2 | NA18943.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 842 | chr21 | 41409075 | |||||
chr21:41409117
|
C | T | 2 | a0001c0001t0015a0007c0023t0014 | 2 | HG01884.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*884C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 884 | chr21 | 41409117 | |||||
chr21:41409190
|
T | C | 5 | a0001c0001t0006a0001c0001t0017a0001c0024t0006others(2): Show | 9 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*957T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 957 | chr21 | 41409190 | |||||
chr21:41409236
|
TAC | T | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(35): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*1025_*1026delCA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 1025 | INFO_REALIGN_3_PRIME | chr21 | 41409236 | ||||
chr21:41409236
|
TACAC | T | 4 | a0001c0001t0006a0001c0001t0017a0001c0024t0006others(1): Show | 8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1026delCACA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 1023 | INFO_REALIGN_3_PRIME | chr21 | 41409236 | ||||
chr21:41409277
|
A | G | 2 | a0001c0001t0009a0001c0026t0009 | 2 | HG02071.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1044A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 14/14 | 1044 | chr21 | 41409277 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:41362064
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(34): Show | 40 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-72+9G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362064 | ||||||
chr21:41362136
|
A | G | 13 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(10): Show | 14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+81A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362136 | ||||||
chr21:41362138
|
C | T | 13 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(10): Show | 14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+83C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362138 | ||||||
chr21:41362186
|
C | T | 16 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(13): Show | 17 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+131C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362186 | ||||||
chr21:41362197
|
T | C | 1 | a0001c0001t0002g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-72+142T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362197 | ||||||
chr21:41362339
|
C | T | 1 | a0002c0003t0001g0326 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-72+284C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362339 | ||||||
chr21:41362367
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-72+312T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362367 | ||||||
chr21:41362402
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0004g0063a0001c0001t0005g0064 | 4 | HG02630.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+347G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362402 | ||||||
chr21:41362485
|
A | G | 16 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(13): Show | 17 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+430A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362485 | ||||||
chr21:41362487
|
T | G | 8 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0004g0063others(5): Show | 9 | HG02109.hp1 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-72+432T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362487 | ||||||
chr21:41362490
|
C | T | 1 | a0001c0002t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-72+435C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362490 | ||||||
chr21:41362491
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-72+436G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362491 | ||||||
chr21:41362524
|
G | A | 4 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+469G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362524 | ||||||
chr21:41362529
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0004g0063others(3): Show | 7 | HG02109.hp1 HG02630.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+474A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362529 | ||||||
chr21:41362533
|
C | T | 40 | a0001c0001t0001g0025a0001c0001t0001g0290a0001c0001t0001g0300others(37): Show | 43 | HG00140.hp1 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-72+478C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362533 | ||||||
chr21:41362564
|
C | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0002g0075 | 3 | HG01261.hp2 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-72+509C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362564 | ||||||
chr21:41362564
|
C | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0308a0001c0001t0001g0309others(16): Show | 20 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-72+509C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362564 | ||||||
chr21:41362720
|
A | G | 4 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+665A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362720 | ||||||
chr21:41362750
|
C | CT | 56 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0036others(53): Show | 61 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-72+721dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41362750 | |||||
chr21:41362750
|
C | CTT | 34 | a0001c0001t0001g0026a0001c0001t0001g0270a0001c0001t0001g0273others(31): Show | 35 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-72+720_-72+721dup others(2): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41362750 | |||||
chr21:41362750
|
CTTTTTTT others(4): Show |
C | 1 | a0006c0027t0005g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-72+711_-72+721del others(11): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41362750 | |||||
chr21:41362751
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0004g0063a0001c0001t0005g0064 | 4 | HG02630.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+696T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362751 | ||||||
chr21:41362757
|
T | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0308a0001c0001t0001g0309others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+702T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362757 | ||||||
chr21:41362762
|
T | TC | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-72+707_-72+708ins others(1): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362762 | ||||||
chr21:41362762
|
T | TCTTTTTT others(7): Show |
1 | a0001c0001t0001g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-72+707_-72+708ins others(14): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362762 | ||||||
chr21:41362763
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-72+708T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362763 | ||||||
chr21:41362763
|
T | TC | 4 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+708_-72+709ins others(1): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362763 | ||||||
chr21:41362820
|
G | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 5 | HG01074.hp2 HG01168.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+765G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362820 | ||||||
chr21:41362899
|
C | G | 17 | a0001c0001t0001g0026a0001c0001t0001g0288a0001c0001t0001g0336others(14): Show | 18 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+844C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41362899 | ||||||
chr21:41363006
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0236others(6): Show | 10 | HG02109.hp1 HG02630.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+951G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363006 | ||||||
chr21:41363039
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+984G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363039 | ||||||
chr21:41363060
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 305 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-72+1005T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363060 | ||||||
chr21:41363156
|
G | A | 4 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+1101G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363156 | ||||||
chr21:41363169
|
C | T | 1 | a0001c0001t0005g0320 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-72+1114C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363169 | ||||||
chr21:41363592
|
G | A | 2 | a0001c0004t0003g0085a0001c0004t0003g0086 | 2 | NA19078.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-72+1537G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363592 | ||||||
chr21:41363695
|
C | T | 5 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | HG01258.hp1 HG01981.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+1640C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363695 | ||||||
chr21:41363703
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-72+1648C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363703 | ||||||
chr21:41363743
|
G | A | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-72+1688G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363743 | ||||||
chr21:41363792
|
G | A | 69 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0270others(66): Show | 73 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.-72+1737G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363792 | ||||||
chr21:41363827
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 8 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.-72+1772C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363827 | ||||||
chr21:41363868
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0240a0001c0001t0001g0241 | 5 | HG02451.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+1813G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363868 | ||||||
chr21:41363906
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+1851G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363906 | ||||||
chr21:41363945
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0002g0075 | 3 | HG01261.hp2 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-72+1890C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41363945 | ||||||
chr21:41364130
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-72+2075T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364130 | ||||||
chr21:41364213
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-72+2158C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364213 | ||||||
chr21:41364271
|
C | G | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-72+2216C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364271 | ||||||
chr21:41364337
|
A | G | 1 | a0001c0004t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-72+2282A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364337 | ||||||
chr21:41364486
|
G | A | 13 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(10): Show | 14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+2431G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364486 | ||||||
chr21:41364499
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0002c0003t0001g0226others(1): Show | 4 | HG02922.hp1 NA18906.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+2444C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364499 | ||||||
chr21:41364540
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0240a0001c0001t0001g0241 | 5 | HG02451.hp2 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+2485T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364540 | ||||||
chr21:41364650
|
T | C | 4 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+2595T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364650 | ||||||
chr21:41364789
|
A | G | 1 | a0014c0016t0005g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-72+2734A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364789 | ||||||
chr21:41364877
|
C | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-72+2822C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364877 | ||||||
chr21:41364900
|
G | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0002g0075 | 3 | HG01261.hp2 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-72+2845G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41364900 | ||||||
chr21:41365010
|
C | T | 13 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(10): Show | 14 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-72+2955C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365010 | ||||||
chr21:41365047
|
A | G | 16 | a0001c0001t0001g0025a0001c0001t0001g0308a0001c0001t0001g0309others(13): Show | 18 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+2992A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365047 | ||||||
chr21:41365111
|
T | C | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-72+3056T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365111 | ||||||
chr21:41365125
|
A | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0036others(36): Show | 42 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.-72+3070A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365125 | ||||||
chr21:41365141
|
G | A | 1 | a0001c0002t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-72+3086G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365141 | ||||||
chr21:41365203
|
A | ATTTG | 20 | a0001c0001t0001g0270a0001c0001t0001g0273a0001c0001t0001g0275others(17): Show | 20 | HG01109.hp1 HG01258.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72+3176_-72+3179d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41365203 | |||||
chr21:41365203
|
ATTTG | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(262): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.-72+3176_-72+3179d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41365203 | |||||
chr21:41365245
|
T | C | 1 | a0001c0001t0004g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-72+3190T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365245 | ||||||
chr21:41365254
|
G | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0036others(37): Show | 43 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-72+3199G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365254 | ||||||
chr21:41365339
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+3284G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365339 | ||||||
chr21:41365511
|
T | G | 1 | a0001c0001t0009g0335 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-72+3456T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365511 | ||||||
chr21:41365609
|
C | T | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+3554C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365609 | ||||||
chr21:41365664
|
A | T | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-72+3609A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365664 | ||||||
chr21:41365665
|
T | A | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-72+3610T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365665 | ||||||
chr21:41365859
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-72+3804C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365859 | ||||||
chr21:41365919
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-72+3864C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365919 | ||||||
chr21:41365937
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-72+3882G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365937 | ||||||
chr21:41365958
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-72+3903G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365958 | ||||||
chr21:41365972
|
A | G | 1 | a0001c0002t0002g0220 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-72+3917A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41365972 | ||||||
chr21:41366029
|
CT | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(8): Show | 12 | HG00099.hp2 HG02080.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-72+3977delT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41366029 | |||||
chr21:41366296
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-72+4241G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366296 | ||||||
chr21:41366538
|
C | T | 1 | a0015c0015t0001g0035 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-72+4483C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366538 | ||||||
chr21:41366590
|
T | C | 3 | a0001c0001t0005g0324a0001c0001t0006g0322a0001c0004t0003g0321 | 3 | HG01884.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-72+4535T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366590 | ||||||
chr21:41366869
|
G | T | 1 | a0001c0001t0005g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72+4814G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41366869 | ||||||
chr21:41367173
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-72+5118G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367173 | ||||||
chr21:41367261
|
A | G | 2 | a0001c0001t0001g0288a0002c0003t0001g0289 | 2 | HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-72+5206A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367261 | ||||||
chr21:41367317
|
A | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0068others(14): Show | 19 | HG00099.hp2 HG01192.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-72+5262A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367317 | ||||||
chr21:41367319
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 7 | HG00738.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+5264T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367319 | ||||||
chr21:41367418
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-72+5363G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367418 | ||||||
chr21:41367422
|
G | C | 2 | a0001c0001t0005g0324a0001c0004t0003g0321 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-72+5367G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367422 | ||||||
chr21:41367506
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0036others(32): Show | 38 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.-72+5451T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367506 | ||||||
chr21:41367688
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-72+5633G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367688 | ||||||
chr21:41367696
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-72+5641A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367696 | ||||||
chr21:41367741
|
C | T | 4 | a0001c0001t0001g0300a0001c0001t0001g0303a0001c0001t0001g0305others(1): Show | 4 | HG00140.hp1 HG01070.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+5686C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367741 | ||||||
chr21:41367803
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+5748A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367803 | ||||||
chr21:41367843
|
G | A | 1 | a0006c0027t0005g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-72+5788G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367843 | ||||||
chr21:41367851
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0303 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-72+5796C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367851 | ||||||
chr21:41367894
|
C | T | 46 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0036others(43): Show | 49 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-72+5839C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41367894 | ||||||
chr21:41368052
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-72+5997A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368052 | ||||||
chr21:41368083
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+6028C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368083 | ||||||
chr21:41368287
|
C | T | 2 | a0001c0001t0006g0334a0001c0001t0006g0341 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-72+6232C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368287 | ||||||
chr21:41368348
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+6293C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368348 | ||||||
chr21:41368369
|
C | A | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-72+6314C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368369 | ||||||
chr21:41368561
|
A | G | 4 | a0001c0001t0001g0300a0001c0001t0001g0303a0001c0001t0001g0305others(1): Show | 4 | HG00140.hp1 HG01070.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+6506A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368561 | ||||||
chr21:41368572
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+6517C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368572 | ||||||
chr21:41368854
|
C | T | 1 | a0001c0002t0002g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-72+6799C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368854 | ||||||
chr21:41368897
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0211a0001c0001t0001g0215others(5): Show | 10 | HG00423.hp2 HG01358.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+6842C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41368897 | ||||||
chr21:41369022
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-72+6967G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369022 | ||||||
chr21:41369284
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-72+7229A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369284 | ||||||
chr21:41369304
|
G | A | 2 | a0001c0024t0006g0331a0001c0025t0001g0332 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-72+7249G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369304 | ||||||
chr21:41369305
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-72+7250G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369305 | ||||||
chr21:41369399
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-72+7344G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369399 | ||||||
chr21:41369492
|
G | A | 1 | a0002c0003t0019g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-71-7344G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369492 | ||||||
chr21:41369531
|
C | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG03239.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-71-7305C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369531 | ||||||
chr21:41369593
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-71-7243G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369593 | ||||||
chr21:41369617
|
G | C | 1 | a0001c0001t0011g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-71-7219G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369617 | ||||||
chr21:41369802
|
G | A | 5 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-7034G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369802 | ||||||
chr21:41369819
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-71-7017C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369819 | ||||||
chr21:41369823
|
A | ACCCCTGC others(8): Show |
1 | a0001c0001t0001g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-71-7009_-71-6995d others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41369823 | |||||
chr21:41369850
|
T | C | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-6986T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369850 | ||||||
chr21:41369883
|
G | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0336a0001c0001t0001g0338others(8): Show | 12 | HG00099.hp2 HG02080.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71-6953G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369883 | ||||||
chr21:41369998
|
A | G | 2 | a0003c0008t0003g0292a0003c0009t0001g0333 | 2 | HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-71-6838A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41369998 | ||||||
chr21:41370025
|
C | G | 1 | a0001c0001t0001g0005 | 3 | HG02451.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71-6811C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370025 | ||||||
chr21:41370089
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0002g0097 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-71-6747C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370089 | ||||||
chr21:41370109
|
C | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-71-6727C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370109 | ||||||
chr21:41370285
|
C | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.-71-6551C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370285 | ||||||
chr21:41370442
|
G | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-71-6394G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370442 | ||||||
chr21:41370489
|
C | T | 1 | a0007c0023t0014g0278 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71-6347C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370489 | ||||||
chr21:41370523
|
T | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-71-6313T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370523 | ||||||
chr21:41370537
|
G | A | 13 | a0001c0001t0001g0026a0001c0001t0001g0305a0001c0001t0001g0306others(10): Show | 14 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71-6299G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370537 | ||||||
chr21:41370602
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(302): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-71-6234A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370602 | ||||||
chr21:41370617
|
T | G | 1 | a0001c0001t0005g0280 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-6219T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370617 | ||||||
chr21:41370645
|
T | C | 1 | a0001c0001t0005g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-71-6191T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370645 | ||||||
chr21:41370748
|
G | C | 1 | a0001c0001t0004g0264 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-71-6088G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370748 | ||||||
chr21:41370907
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0303 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-71-5929C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41370907 | ||||||
chr21:41371184
|
G | C | 13 | a0001c0001t0001g0037a0001c0001t0001g0056a0001c0001t0001g0205others(10): Show | 14 | HG00423.hp1 HG00609.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71-5652G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371184 | ||||||
chr21:41371224
|
G | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0308a0001c0001t0001g0309others(13): Show | 17 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71-5612G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371224 | ||||||
chr21:41371343
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-71-5493G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371343 | ||||||
chr21:41371375
|
G | T | 3 | a0001c0002t0002g0073a0001c0002t0004g0074a0002c0003t0019g0238 | 3 | HG02451.hp1 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-71-5461G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371375 | ||||||
chr21:41371391
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-71-5445G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371391 | ||||||
chr21:41371397
|
C | T | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-5439C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371397 | ||||||
chr21:41371400
|
G | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-71-5436G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371400 | ||||||
chr21:41371569
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-71-5267C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371569 | ||||||
chr21:41371596
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0002g0330a0001c0001t0002g0339others(2): Show | 6 | HG02080.hp1 NA18965.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-5240C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371596 | ||||||
chr21:41371601
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-71-5235T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371601 | ||||||
chr21:41371841
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0004g0063others(6): Show | 10 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71-4995T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371841 | ||||||
chr21:41371869
|
G | T | 1 | a0001c0001t0005g0280 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-4967G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371869 | ||||||
chr21:41371894
|
A | G | 42 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0037others(39): Show | 44 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-71-4942A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41371894 | ||||||
chr21:41372337
|
A | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-71-4499A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372337 | ||||||
chr21:41372340
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-71-4496A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372340 | ||||||
chr21:41372529
|
T | TA | 5 | a0001c0001t0017g0072a0001c0002t0002g0073a0001c0002t0004g0074others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-4307_-71-4306i others(3): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372529 | ||||||
chr21:41372652
|
C | T | 1 | a0002c0003t0001g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-71-4184C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372652 | ||||||
chr21:41372678
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-71-4158A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372678 | ||||||
chr21:41372958
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(97): Show | 108 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-71-3878C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372958 | ||||||
chr21:41372984
|
C | A | 3 | a0001c0001t0004g0252a0001c0001t0005g0251a0001c0002t0002g0265 | 3 | HG02976.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-71-3852C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41372984 | ||||||
chr21:41373038
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-71-3798G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373038 | ||||||
chr21:41373078
|
G | T | 3 | a0001c0001t0005g0280a0004c0007t0001g0327a0004c0007t0001g0328 | 3 | HG02896.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-71-3758G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373078 | ||||||
chr21:41373138
|
A | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-71-3698A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373138 | ||||||
chr21:41373167
|
G | A | 1 | a0001c0002t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-71-3669G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373167 | ||||||
chr21:41373199
|
G | GA | 8 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0004g0063others(5): Show | 9 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-3635dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373199 | |||||
chr21:41373245
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0026others(59): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.-71-3591A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373245 | ||||||
chr21:41373424
|
G | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0068others(51): Show | 56 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.-71-3412G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373424 | ||||||
chr21:41373487
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-71-3349G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373487 | ||||||
chr21:41373521
|
G | A | 1 | a0001c0001t0011g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-71-3315G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373521 | ||||||
chr21:41373617
|
G | A | 2 | a0001c0024t0006g0331a0001c0025t0001g0332 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-71-3219G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373617 | ||||||
chr21:41373651
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-71-3185C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373651 | ||||||
chr21:41373663
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-71-3173C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373663 | ||||||
chr21:41373805
|
T | TA | 28 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0040others(25): Show | 31 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-71-3010dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373805 | |||||
chr21:41373805
|
T | TAAA | 45 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0100others(42): Show | 46 | HG01071.hp1 HG01109.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.-71-3012_-71-3010d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373805 | |||||
chr21:41373805
|
TA | T | 9 | a0001c0001t0001g0059a0001c0001t0001g0087a0001c0001t0001g0090others(6): Show | 9 | HG00140.hp2 HG01168.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-3010delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41373805 | |||||
chr21:41373846
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-71-2990G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373846 | ||||||
chr21:41373876
|
A | G | 1 | a0001c0001t0004g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-71-2960A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373876 | ||||||
chr21:41373887
|
C | G | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-2949C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373887 | ||||||
chr21:41373889
|
C | T | 1 | a0001c0001t0005g0280 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-2947C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373889 | ||||||
chr21:41373903
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0002g0145 | 3 | HG01109.hp2 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-2933G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373903 | ||||||
chr21:41373935
|
C | A | 1 | a0001c0004t0003g0307 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-71-2901C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373935 | ||||||
chr21:41373959
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00597.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-71-2877C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41373959 | ||||||
chr21:41374154
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-71-2682C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374154 | ||||||
chr21:41374229
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-71-2607T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374229 | ||||||
chr21:41374305
|
G | A | 2 | a0001c0001t0006g0334a0001c0001t0006g0341 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-71-2531G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374305 | ||||||
chr21:41374349
|
C | G | 114 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(111): Show | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-71-2487C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374349 | ||||||
chr21:41374394
|
G | A | 1 | a0001c0002t0002g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-71-2442G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374394 | ||||||
chr21:41374441
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-71-2395G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374441 | ||||||
chr21:41374478
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-71-2358G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374478 | ||||||
chr21:41374565
|
G | A | 1 | a0001c0002t0002g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-71-2271G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374565 | ||||||
chr21:41374641
|
C | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-71-2195C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374641 | ||||||
chr21:41374651
|
GGCTGCCA others(8): Show |
G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-71-2182_-71-2168d others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41374651 | |||||
chr21:41374670
|
G | A | 1 | a0001c0001t0005g0280 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-2166G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374670 | ||||||
chr21:41374671
|
G | A | 5 | a0002c0003t0001g0295a0002c0003t0005g0296a0002c0005t0003g0023others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-2165G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374671 | ||||||
chr21:41374716
|
ACT | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 7 | HG02451.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-2117_-71-2116d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41374716 | |||||
chr21:41374725
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-71-2111G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41374725 | ||||||
chr21:41375069
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-71-1767C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375069 | ||||||
chr21:41375227
|
G | A | 3 | a0001c0001t0005g0324a0001c0001t0006g0322a0001c0004t0003g0321 | 3 | HG01884.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-71-1609G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375227 | ||||||
chr21:41375255
|
G | A | 1 | a0001c0001t0011g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-71-1581G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375255 | ||||||
chr21:41375308
|
C | G | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-71-1528C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375308 | ||||||
chr21:41375340
|
G | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0022others(58): Show | 66 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.-71-1496G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375340 | ||||||
chr21:41375454
|
G | T | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-1382G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375454 | ||||||
chr21:41375589
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-71-1247C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375589 | ||||||
chr21:41375615
|
G | T | 88 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0036others(85): Show | 93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.-71-1221G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375615 | ||||||
chr21:41375885
|
G | A | 1 | a0002c0014t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-71-951G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375885 | ||||||
chr21:41375920
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-71-916G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375920 | ||||||
chr21:41375949
|
T | C | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-71-887T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41375949 | ||||||
chr21:41376030
|
C | A | 1 | a0001c0002t0002g0011 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-71-806C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376030 | ||||||
chr21:41376305
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-71-531G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376305 | ||||||
chr21:41376308
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-71-528C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376308 | ||||||
chr21:41376390
|
A | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(307): Show | 339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-71-446A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376390 | ||||||
chr21:41376392
|
A | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.-71-444A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376392 | ||||||
chr21:41376438
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-71-398C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376438 | ||||||
chr21:41376546
|
TCAACAAC others(2): Show |
T | 48 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0037others(45): Show | 50 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-71-279_-71-271del others(9): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr21 | 41376546 | |||||
chr21:41376555
|
A | G | 1 | a0001c0001t0004g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-71-281A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376555 | ||||||
chr21:41376623
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0201 | 2 | HG01261.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-71-213G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376623 | ||||||
chr21:41376677
|
C | G | 1 | a0001c0004t0003g0321 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-71-159C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376677 | ||||||
chr21:41376702
|
A | G | 17 | a0001c0001t0002g0245a0001c0001t0004g0252a0001c0001t0006g0334others(14): Show | 19 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-71-134A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376702 | ||||||
chr21:41376776
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG00738.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-71-60G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376776 | ||||||
chr21:41376802
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0005g0064a0001c0001t0006g0067others(2): Show | 5 | HG02109.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-34C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376802 | ||||||
chr21:41376812
|
G | A | 3 | a0001c0001t0001g0303a0001c0001t0004g0252a0001c0002t0002g0265 | 3 | HG02717.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-71-24G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 1/13 | chr21 | 41376812 | ||||||
chr21:41377164
|
G | A | 4 | a0001c0002t0002g0315a0001c0006t0001g0239a0004c0007t0001g0327others(1): Show | 4 | HG01106.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+9G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377164 | ||||||
chr21:41377188
|
G | A | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+33G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377188 | ||||||
chr21:41377262
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 213 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.249+107A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377262 | ||||||
chr21:41377319
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.249+164A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377319 | ||||||
chr21:41377351
|
C | T | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+196C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377351 | ||||||
chr21:41377389
|
T | C | 1 | a0001c0002t0002g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.249+234T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377389 | ||||||
chr21:41377432
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+277G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377432 | ||||||
chr21:41377450
|
C | T | 40 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0037others(37): Show | 43 | HG00140.hp1 HG00423.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.249+295C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377450 | ||||||
chr21:41377489
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.250-300C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377489 | ||||||
chr21:41377634
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0002g0075 | 2 | HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.250-155G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377634 | ||||||
chr21:41377675
|
T | C | 8 | a0001c0001t0001g0308a0001c0001t0005g0251a0001c0001t0006g0067others(5): Show | 8 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-114T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377675 | ||||||
chr21:41377682
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250-107T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377682 | ||||||
chr21:41377719
|
C | T | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.250-70C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 2/13 | chr21 | 41377719 | ||||||
chr21:41377997
|
C | T | 2 | a0001c0024t0006g0331a0001c0025t0001g0332 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.442+16C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41377997 | ||||||
chr21:41378078
|
T | C | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442+97T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378078 | ||||||
chr21:41378125
|
AGAGAGAC others(10): Show |
A | 14 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(11): Show | 14 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.442+157_442+173del others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378125 | |||||
chr21:41378162
|
G | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.442+181G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378162 | ||||||
chr21:41378199
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442+218G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378199 | ||||||
chr21:41378225
|
A | AGAGACAG others(74): Show |
13 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.442+279_442+280ins others(81): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378225 | |||||
chr21:41378232
|
G | A | 2 | a0001c0024t0006g0331a0001c0025t0001g0332 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.442+251G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378232 | ||||||
chr21:41378239
|
G | GGGAGAGA others(93): Show |
1 | a0001c0001t0001g0254 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.442+285_442+286ins others(100): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378239 | |||||
chr21:41378239
|
G | GGGAGAGA others(76): Show |
19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(16): Show | 23 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.442+340_442+341ins others(83): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378239 | |||||
chr21:41378284
|
T | C | 15 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(12): Show | 15 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.442+303T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378284 | ||||||
chr21:41378302
|
A | ACTGGGAG others(10): Show |
16 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(13): Show | 16 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.442+338_442+354dup others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | |||||
chr21:41378302
|
A | ACTGGGAG others(93): Show |
92 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0056others(89): Show | 102 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.442+340_442+341ins others(100): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | |||||
chr21:41378302
|
A | ACTGGGAG others(323): Show |
6 | a0001c0001t0001g0273a0001c0001t0004g0264a0001c0001t0004g0274others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+340_442+341ins others(330): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | |||||
chr21:41378302
|
A | ACTGGGAG others(110): Show |
3 | a0001c0001t0001g0336a0001c0004t0003g0317a0001c0004t0003g0323 | 3 | HG02055.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442+340_442+341ins others(117): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | |||||
chr21:41378302
|
A | ACTGGGAG others(91): Show |
1 | a0001c0001t0015g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442+340_442+341ins others(98): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr21 | 41378302 | |||||
chr21:41378344
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0256 | 3 | HG00280.hp1 HG01243.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.442+363G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378344 | ||||||
chr21:41378385
|
T | C | 35 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(32): Show | 37 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.442+404T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378385 | ||||||
chr21:41378445
|
C | T | 2 | a0002c0010t0016g0329a0002c0014t0001g0071 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+464C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378445 | ||||||
chr21:41378485
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0056others(52): Show | 63 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.442+504A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378485 | ||||||
chr21:41378524
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0056others(52): Show | 63 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.442+543C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378524 | ||||||
chr21:41378525
|
G | A | 19 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+544G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378525 | ||||||
chr21:41378530
|
C | T | 2 | a0002c0010t0016g0329a0002c0014t0001g0071 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+549C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378530 | ||||||
chr21:41378604
|
C | A | 2 | a0002c0010t0016g0329a0002c0014t0001g0071 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+623C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378604 | ||||||
chr21:41378651
|
C | T | 19 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+670C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378651 | ||||||
chr21:41378652
|
A | C | 19 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(16): Show | 19 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.442+671A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378652 | ||||||
chr21:41378727
|
A | G | 13 | a0001c0001t0001g0254a0001c0001t0001g0275a0001c0001t0001g0288others(10): Show | 13 | HG01891.hp2 HG01952.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.442+746A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378727 | ||||||
chr21:41378807
|
A | G | 21 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 21 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.442+826A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378807 | ||||||
chr21:41378846
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0105 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.442+865G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378846 | ||||||
chr21:41378915
|
C | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0056others(97): Show | 110 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.442+934C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41378915 | ||||||
chr21:41379005
|
A | G | 21 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0054others(18): Show | 21 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.443-1012A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379005 | ||||||
chr21:41379031
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.443-986G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379031 | ||||||
chr21:41379325
|
C | T | 1 | a0002c0003t0004g0269 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.443-692C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379325 | ||||||
chr21:41379351
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-666G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379351 | ||||||
chr21:41379392
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.443-625C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379392 | ||||||
chr21:41379414
|
C | T | 3 | a0001c0001t0001g0336a0001c0004t0003g0317a0001c0004t0003g0323 | 3 | HG02055.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.443-603C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379414 | ||||||
chr21:41379415
|
G | A | 15 | a0001c0001t0001g0254a0001c0001t0001g0275a0001c0001t0001g0288others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.443-602G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379415 | ||||||
chr21:41379433
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-584G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379433 | ||||||
chr21:41379465
|
C | T | 16 | a0001c0001t0001g0254a0001c0001t0001g0275a0001c0001t0001g0288others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.443-552C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379465 | ||||||
chr21:41379506
|
C | T | 2 | a0001c0001t0001g0187a0001c0002t0002g0188 | 2 | NA18968.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.443-511C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379506 | ||||||
chr21:41379614
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.443-403A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379614 | ||||||
chr21:41379637
|
A | G | 2 | a0001c0001t0005g0064a0001c0006t0001g0239 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.443-380A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379637 | ||||||
chr21:41379651
|
T | C | 3 | a0001c0001t0005g0064a0001c0006t0001g0239a0002c0010t0016g0329 | 3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.443-366T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379651 | ||||||
chr21:41379656
|
A | G | 105 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0036others(102): Show | 113 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.443-361A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379656 | ||||||
chr21:41379681
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.443-336C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379681 | ||||||
chr21:41379732
|
A | G | 63 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0056others(60): Show | 67 | HG00423.hp1 HG00609.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.443-285A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379732 | ||||||
chr21:41379806
|
G | A | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0308others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-211G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379806 | ||||||
chr21:41379924
|
C | T | 1 | a0002c0014t0001g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443-93C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379924 | ||||||
chr21:41379931
|
G | A | 24 | a0001c0001t0001g0125a0001c0001t0001g0147a0001c0001t0001g0215others(21): Show | 28 | HG00280.hp2 HG00423.hp2 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.443-86G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379931 | ||||||
chr21:41379955
|
G | C | 2 | a0001c0001t0005g0064a0001c0006t0001g0239 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.443-62G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379955 | ||||||
chr21:41379960
|
G | A | 1 | a0001c0002t0001g0155 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.443-57G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379960 | ||||||
chr21:41379995
|
A | G | 3 | a0001c0001t0005g0064a0001c0006t0001g0239a0002c0010t0016g0329 | 3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.443-22A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41379995 | ||||||
chr21:41380011
|
G | A | 4 | a0001c0001t0006g0322a0001c0001t0006g0334a0001c0001t0006g0341others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.443-6G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41380011 | ||||||
chr21:41380011
|
G | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.443-6G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 3/13 | chr21 | 41380011 | ||||||
chr21:41380177
|
G | A | 3 | a0001c0001t0005g0064a0001c0006t0001g0239a0002c0010t0016g0329 | 3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.577+26G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380177 | ||||||
chr21:41380208
|
G | T | 3 | a0001c0001t0001g0336a0001c0004t0003g0317a0001c0004t0003g0323 | 3 | HG02055.hp2 HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.577+57G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380208 | ||||||
chr21:41380229
|
G | A | 3 | a0001c0001t0005g0064a0001c0006t0001g0239a0002c0010t0016g0329 | 3 | HG01106.hp1 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.577+78G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380229 | ||||||
chr21:41380324
|
G | A | 1 | a0001c0004t0003g0250 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.577+173G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380324 | ||||||
chr21:41380343
|
G | A | 10 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0308others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.577+192G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380343 | ||||||
chr21:41380346
|
T | C | 6 | a0001c0001t0001g0336a0001c0001t0005g0064a0001c0004t0003g0317others(3): Show | 6 | HG01106.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.577+195T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380346 | ||||||
chr21:41380411
|
A | G | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 158 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.577+260A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380411 | ||||||
chr21:41380425
|
G | C | 7 | a0001c0001t0001g0336a0001c0001t0005g0064a0001c0004t0003g0317others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+274G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380425 | ||||||
chr21:41380431
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.577+280C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380431 | ||||||
chr21:41380432
|
G | A | 7 | a0001c0001t0001g0336a0001c0001t0005g0064a0001c0004t0003g0317others(4): Show | 7 | HG01257.hp1 HG01258.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+281G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380432 | ||||||
chr21:41380458
|
AG | A | 7 | a0001c0001t0001g0336a0001c0001t0005g0064a0001c0004t0003g0317others(4): Show | 7 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+310delG | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 41380458 | |||||
chr21:41380478
|
C | G | 2 | a0003c0008t0003g0292a0003c0009t0001g0333 | 2 | HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.577+327C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380478 | ||||||
chr21:41380612
|
T | C | 1 | a0001c0001t0005g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.577+461T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380612 | ||||||
chr21:41380638
|
C | T | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.577+487C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380638 | ||||||
chr21:41380688
|
T | G | 8 | a0001c0001t0001g0336a0001c0004t0003g0317a0001c0004t0003g0323others(5): Show | 8 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.577+537T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380688 | ||||||
chr21:41380702
|
G | A | 1 | a0001c0001t0015g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.577+551G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380702 | ||||||
chr21:41380780
|
T | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+629T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380780 | ||||||
chr21:41380785
|
C | T | 7 | a0001c0001t0001g0336a0001c0004t0003g0317a0001c0004t0003g0323others(4): Show | 7 | HG01106.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.577+634C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380785 | ||||||
chr21:41380827
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.577+676G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380827 | ||||||
chr21:41380877
|
A | G | 1 | a0001c0002t0002g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.577+726A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41380877 | ||||||
chr21:41381031
|
C | A | 1 | a0001c0001t0005g0324 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.577+880C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381031 | ||||||
chr21:41381070
|
C | G | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.577+919C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381070 | ||||||
chr21:41381111
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+960A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381111 | ||||||
chr21:41381127
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+976T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381127 | ||||||
chr21:41381136
|
C | A | 4 | a0001c0001t0001g0336a0001c0006t0001g0239a0002c0003t0019g0238others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+985C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381136 | ||||||
chr21:41381137
|
G | A | 25 | a0001c0001t0001g0125a0001c0001t0001g0147a0001c0001t0001g0215others(22): Show | 29 | HG00280.hp2 HG00423.hp2 HG01993.hp1 others(26): Show |
intron_variant | MODIFIER | c.577+986G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381137 | ||||||
chr21:41381144
|
C | T | 1 | a0001c0002t0002g0315 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.577+993C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381144 | ||||||
chr21:41381201
|
T | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0068others(32): Show | 38 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.577+1050T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381201 | ||||||
chr21:41381221
|
A | G | 4 | a0001c0001t0006g0322a0001c0001t0006g0334a0001c0001t0006g0341others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.577+1070A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381221 | ||||||
chr21:41381286
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.578-1124T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381286 | ||||||
chr21:41381295
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-1115A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381295 | ||||||
chr21:41381473
|
T | C | 342 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(339): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.578-937T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381473 | ||||||
chr21:41381513
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-897G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381513 | ||||||
chr21:41381521
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-889T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381521 | ||||||
chr21:41381542
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0002g0156 | 3 | NA18979.hp2 NA19010.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.578-868G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381542 | ||||||
chr21:41381548
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-862A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381548 | ||||||
chr21:41381610
|
G | T | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.578-800G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381610 | ||||||
chr21:41381640
|
G | A | 2 | a0001c0001t0002g0130a0002c0010t0016g0329 | 2 | HG02723.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.578-770G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381640 | ||||||
chr21:41381651
|
C | T | 1 | a0001c0001t0004g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.578-759C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381651 | ||||||
chr21:41381663
|
C | T | 3 | a0001c0001t0004g0274a0001c0001t0004g0277a0002c0010t0016g0329 | 3 | HG02723.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.578-747C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381663 | ||||||
chr21:41381672
|
G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.578-738G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381672 | ||||||
chr21:41381684
|
C | CA | 36 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0054others(33): Show | 36 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.578-703dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 41381684 | |||||
chr21:41381684
|
CA | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0033others(54): Show | 60 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.578-703delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr21 | 41381684 | |||||
chr21:41381878
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-532A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381878 | ||||||
chr21:41381957
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.578-453A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41381957 | ||||||
chr21:41382046
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-364T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382046 | ||||||
chr21:41382054
|
G | A | 1 | a0001c0004t0003g0307 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.578-356G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382054 | ||||||
chr21:41382269
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-141T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382269 | ||||||
chr21:41382327
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578-83G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 4/13 | chr21 | 41382327 | ||||||
chr21:41382636
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+72G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382636 | ||||||
chr21:41382926
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+362T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382926 | ||||||
chr21:41382995
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.732+431G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382995 | ||||||
chr21:41382999
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.732+435G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41382999 | ||||||
chr21:41383003
|
G | A | 1 | a0001c0001t0017g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.732+439G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383003 | ||||||
chr21:41383087
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.732+523G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383087 | ||||||
chr21:41383092
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+528C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383092 | ||||||
chr21:41383133
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.732+569A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383133 | ||||||
chr21:41383167
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+603C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383167 | ||||||
chr21:41383203
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+639A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383203 | ||||||
chr21:41383312
|
G | A | 1 | a0001c0001t0011g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.732+748G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383312 | ||||||
chr21:41383478
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+914C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383478 | ||||||
chr21:41383705
|
T | C | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.732+1141T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383705 | ||||||
chr21:41383733
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1169G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383733 | ||||||
chr21:41383761
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1197G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383761 | ||||||
chr21:41383799
|
G | A | 1 | a0001c0001t0006g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.732+1235G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383799 | ||||||
chr21:41383899
|
A | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1335A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383899 | ||||||
chr21:41383905
|
C | T | 2 | a0001c0024t0006g0331a0001c0025t0001g0332 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.732+1341C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383905 | ||||||
chr21:41383928
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1364T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383928 | ||||||
chr21:41383985
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.732+1421G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41383985 | ||||||
chr21:41384014
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1450G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384014 | ||||||
chr21:41384023
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1459T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384023 | ||||||
chr21:41384050
|
G | C | 1 | a0001c0001t0002g0330 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.732+1486G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384050 | ||||||
chr21:41384072
|
T | G | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1508T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384072 | ||||||
chr21:41384099
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.732+1535C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384099 | ||||||
chr21:41384139
|
A | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1575A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384139 | ||||||
chr21:41384150
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+1586C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384150 | ||||||
chr21:41384219
|
G | A | 1 | a0001c0002t0002g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.732+1655G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384219 | ||||||
chr21:41384251
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+1687A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384251 | ||||||
chr21:41384252
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+1688G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384252 | ||||||
chr21:41384348
|
T | C | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(145): Show | 161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.732+1784T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384348 | ||||||
chr21:41384393
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1829G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384393 | ||||||
chr21:41384420
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1856C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384420 | ||||||
chr21:41384458
|
T | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+1894T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384458 | ||||||
chr21:41384460
|
A | T | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(147): Show | 163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.732+1896A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384460 | ||||||
chr21:41384463
|
G | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0095a0001c0001t0001g0139others(6): Show | 9 | HG00099.hp1 HG01099.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.732+1899G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384463 | ||||||
chr21:41384494
|
T | C | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0002g0045others(2): Show | 5 | HG02071.hp2 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+1930T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384494 | ||||||
chr21:41384572
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2008T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384572 | ||||||
chr21:41384577
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2013C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384577 | ||||||
chr21:41384610
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG03654.hp2 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.732+2046G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384610 | ||||||
chr21:41384659
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.732+2095A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384659 | ||||||
chr21:41384685
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2121C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384685 | ||||||
chr21:41384708
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2144G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384708 | ||||||
chr21:41384732
|
T | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.732+2168T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384732 | ||||||
chr21:41384794
|
G | A | 2 | a0004c0007t0001g0327a0004c0007t0001g0328 | 2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.732+2230G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384794 | ||||||
chr21:41384810
|
G | A | 1 | a0001c0001t0008g0165 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.732+2246G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384810 | ||||||
chr21:41384838
|
C | CA | 147 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(144): Show | 160 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.732+2289dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41384838 | |||||
chr21:41384872
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.732+2308G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384872 | ||||||
chr21:41384927
|
A | T | 1 | a0002c0013t0001g0192 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.732+2363A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41384927 | ||||||
chr21:41385044
|
TGTGA | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0120others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+2484_732+2487d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41385044 | |||||
chr21:41385069
|
A | C | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(145): Show | 161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.732+2505A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385069 | ||||||
chr21:41385140
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+2576T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385140 | ||||||
chr21:41385157
|
G | C | 1 | a0001c0001t0001g0243 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.732+2593G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385157 | ||||||
chr21:41385162
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.732+2598C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385162 | ||||||
chr21:41385163
|
G | A | 3 | a0014c0016t0005g0279a0016c0012t0001g0272a0017c0011t0001g0271 | 3 | HG01109.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.732+2599G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385163 | ||||||
chr21:41385173
|
A | T | 19 | a0001c0001t0001g0125a0001c0001t0001g0215a0001c0001t0001g0288others(16): Show | 23 | HG00280.hp2 HG00423.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+2609A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385173 | ||||||
chr21:41385176
|
C | A | 46 | a0001c0001t0001g0095a0001c0001t0001g0125a0001c0001t0001g0215others(43): Show | 52 | HG00280.hp2 HG00423.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.732+2612C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385176 | ||||||
chr21:41385425
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0002g0060 | 4 | NA18963.hp1 NA19011.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+2861A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385425 | ||||||
chr21:41385554
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.732+2990G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385554 | ||||||
chr21:41385587
|
A | G | 1 | a0001c0025t0001g0332 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.732+3023A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385587 | ||||||
chr21:41385607
|
T | C | 1 | a0001c0025t0001g0332 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.732+3043T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385607 | ||||||
chr21:41385693
|
A | T | 49 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0021others(46): Show | 52 | HG00323.hp1 HG00621.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.732+3129A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41385693 | ||||||
chr21:41386005
|
C | A | 7 | a0001c0001t0001g0095a0001c0001t0015g0263a0001c0004t0003g0085others(4): Show | 7 | HG01884.hp2 NA18946.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+3441C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386005 | ||||||
chr21:41386175
|
A | G | 1 | a0001c0001t0015g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3611A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386175 | ||||||
chr21:41386199
|
A | G | 1 | a0001c0001t0015g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3635A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386199 | ||||||
chr21:41386219
|
C | CA | 47 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0031others(44): Show | 48 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.732+3685dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | |||||
chr21:41386219
|
CA | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 136 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.732+3685delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | |||||
chr21:41386219
|
CAA | C | 37 | a0001c0001t0001g0336a0001c0001t0002g0060a0001c0001t0004g0065others(34): Show | 42 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.732+3684_732+3685d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | |||||
chr21:41386219
|
CAAA | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0236others(8): Show | 12 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.732+3683_732+3685d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | |||||
chr21:41386219
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0004t0003g0323 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.732+3674_732+3685d others(14): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | |||||
chr21:41386219
|
CAAAAAAA others(6): Show |
C | 1 | a0002c0003t0001g0299 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.732+3673_732+3685d others(15): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386219 | |||||
chr21:41386236
|
A | C | 1 | a0001c0001t0002g0136 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.732+3672A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386236 | ||||||
chr21:41386237
|
A | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 66 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.732+3673A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386237 | ||||||
chr21:41386239
|
A | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0002g0060 | 4 | NA18963.hp1 NA19011.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+3675A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386239 | ||||||
chr21:41386239
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0015g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.732+3679_732+3689d others(13): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386239 | |||||
chr21:41386240
|
A | C | 2 | a0001c0001t0012g0291a0002c0014t0001g0071 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.732+3676A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386240 | ||||||
chr21:41386248
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.732+3684A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386248 | ||||||
chr21:41386300
|
G | A | 6 | a0001c0001t0001g0095a0001c0004t0003g0085a0001c0004t0003g0086others(3): Show | 6 | NA18946.hp2 NA18957.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+3736G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386300 | ||||||
chr21:41386368
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.732+3804T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386368 | ||||||
chr21:41386389
|
A | G | 1 | a0002c0013t0001g0192 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.732+3825A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386389 | ||||||
chr21:41386457
|
G | C | 1 | a0001c0001t0001g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.732+3893G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386457 | ||||||
chr21:41386500
|
A | G | 10 | a0001c0001t0001g0154a0001c0001t0001g0336a0001c0001t0004g0063others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+3936A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386500 | ||||||
chr21:41386783
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(69): Show | 81 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.733-3782T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386783 | ||||||
chr21:41386790
|
G | A | 2 | a0016c0012t0001g0272a0017c0011t0001g0271 | 2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.733-3775G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386790 | ||||||
chr21:41386850
|
G | A | 13 | a0001c0001t0001g0300a0001c0001t0001g0303a0001c0001t0002g0245others(10): Show | 15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.733-3715G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386850 | ||||||
chr21:41386916
|
C | T | 1 | a0001c0024t0006g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.733-3649C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41386916 | ||||||
chr21:41386995
|
GAAC | G | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 68 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.733-3555_733-3553d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41386995 | |||||
chr21:41387032
|
G | A | 8 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0004g0065others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-3533G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387032 | ||||||
chr21:41387067
|
C | T | 3 | a0002c0003t0001g0297a0002c0003t0001g0298a0002c0003t0001g0311 | 3 | HG02647.hp2 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.733-3498C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387067 | ||||||
chr21:41387089
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 68 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.733-3476C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387089 | ||||||
chr21:41387122
|
T | C | 1 | a0010c0021t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.733-3443T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387122 | ||||||
chr21:41387184
|
C | T | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(57): Show | 69 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.733-3381C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387184 | ||||||
chr21:41387206
|
G | C | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(155): Show | 174 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.733-3359G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387206 | ||||||
chr21:41387225
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733-3340G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387225 | ||||||
chr21:41387267
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733-3298T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387267 | ||||||
chr21:41387302
|
G | A | 2 | a0001c0001t0001g0154a0001c0024t0006g0331 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.733-3263G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387302 | ||||||
chr21:41387403
|
C | T | 3 | a0001c0001t0001g0336a0001c0001t0006g0334a0001c0001t0006g0341 | 3 | HG01167.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.733-3162C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387403 | ||||||
chr21:41387418
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.733-3147G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387418 | ||||||
chr21:41387551
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.733-3014T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387551 | ||||||
chr21:41387573
|
G | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(152): Show | 171 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.733-2992G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387573 | ||||||
chr21:41387665
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(153): Show | 172 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.733-2900C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387665 | ||||||
chr21:41387857
|
A | G | 5 | a0001c0001t0001g0336a0001c0001t0004g0063a0001c0001t0004g0252others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-2708A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387857 | ||||||
chr21:41387951
|
C | T | 29 | a0001c0001t0001g0121a0001c0001t0001g0288a0001c0001t0005g0251others(26): Show | 34 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.733-2614C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41387951 | ||||||
chr21:41388145
|
T | C | 3 | a0001c0001t0006g0067a0001c0001t0006g0322a0001c0001t0017g0072 | 3 | HG02280.hp2 HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.733-2420T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388145 | ||||||
chr21:41388154
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.733-2411G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388154 | ||||||
chr21:41388201
|
C | T | 1 | a0001c0001t0001g0005 | 3 | HG02451.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-2364C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388201 | ||||||
chr21:41388291
|
C | T | 1 | a0001c0002t0002g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.733-2274C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388291 | ||||||
chr21:41388324
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.733-2241G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388324 | ||||||
chr21:41388385
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.733-2180C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388385 | ||||||
chr21:41388600
|
G | A | 6 | a0001c0001t0001g0121a0001c0002t0001g0002a0001c0002t0001g0012others(3): Show | 9 | HG00280.hp2 HG00408.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-1965G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388600 | ||||||
chr21:41388636
|
G | T | 51 | a0001c0001t0001g0121a0001c0001t0001g0236a0001c0001t0001g0237others(48): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.733-1929G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388636 | ||||||
chr21:41388651
|
G | A | 32 | a0001c0001t0001g0095a0001c0001t0001g0161a0001c0001t0001g0275others(29): Show | 32 | HG01257.hp1 HG01258.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-1914G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388651 | ||||||
chr21:41388868
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.733-1697A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388868 | ||||||
chr21:41388906
|
A | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(58): Show | 70 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.733-1659A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41388906 | ||||||
chr21:41389021
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.733-1544C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389021 | ||||||
chr21:41389134
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.733-1431G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389134 | ||||||
chr21:41389152
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0026others(59): Show | 66 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.733-1413G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389152 | ||||||
chr21:41389157
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(90): Show | 107 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.733-1408G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389157 | ||||||
chr21:41389175
|
T | C | 32 | a0001c0001t0001g0121a0001c0001t0001g0154a0001c0001t0001g0288others(29): Show | 37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.733-1390T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389175 | ||||||
chr21:41389197
|
C | CA | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(88): Show | 105 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.733-1355dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr21 | 41389197 | |||||
chr21:41389231
|
A | C | 1 | a0001c0025t0001g0332 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733-1334A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389231 | ||||||
chr21:41389301
|
G | A | 5 | a0001c0001t0001g0336a0001c0001t0004g0063a0001c0001t0004g0252others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-1264G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389301 | ||||||
chr21:41389313
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0144 | 2 | NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.733-1252A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389313 | ||||||
chr21:41389317
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.733-1248C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389317 | ||||||
chr21:41389470
|
G | C | 1 | a0001c0001t0001g0006 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.733-1095G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389470 | ||||||
chr21:41389527
|
T | G | 1 | a0001c0001t0002g0339 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.733-1038T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389527 | ||||||
chr21:41389828
|
A | G | 2 | a0001c0001t0005g0280a0001c0001t0005g0324 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.733-737A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389828 | ||||||
chr21:41389865
|
G | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(121): Show | 140 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.733-700G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389865 | ||||||
chr21:41389888
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.733-677T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389888 | ||||||
chr21:41389910
|
T | C | 5 | a0002c0003t0001g0297a0002c0003t0001g0298a0002c0003t0001g0311others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-655T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41389910 | ||||||
chr21:41390105
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0100a0001c0001t0001g0200 | 4 | HG01358.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-460C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390105 | ||||||
chr21:41390230
|
G | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(121): Show | 140 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.733-335G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390230 | ||||||
chr21:41390276
|
T | C | 43 | a0001c0001t0001g0095a0001c0001t0001g0161a0001c0001t0001g0275others(40): Show | 45 | HG01109.hp1 HG01243.hp2 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.733-289T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390276 | ||||||
chr21:41390292
|
G | A | 2 | a0001c0001t0012g0291a0002c0014t0001g0071 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.733-273G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390292 | ||||||
chr21:41390338
|
G | C | 4 | a0001c0001t0006g0067a0001c0001t0006g0322a0001c0024t0006g0331others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-227G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390338 | ||||||
chr21:41390345
|
T | C | 147 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 163 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.733-220T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390345 | ||||||
chr21:41390436
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0051others(53): Show | 59 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.733-129T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390436 | ||||||
chr21:41390458
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733-107G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390458 | ||||||
chr21:41390478
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733-87C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390478 | ||||||
chr21:41390502
|
C | T | 1 | a0001c0002t0002g0129 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.733-63C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390502 | ||||||
chr21:41390512
|
A | G | 23 | a0001c0001t0001g0095a0001c0001t0001g0161a0001c0001t0001g0275others(20): Show | 23 | HG01496.hp1 HG01981.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-53A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390512 | ||||||
chr21:41390529
|
C | T | 1 | a0001c0001t0017g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.733-36C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 5/13 | chr21 | 41390529 | ||||||
chr21:41390719
|
C | A | 4 | a0001c0001t0001g0253a0001c0001t0001g0262a0001c0001t0002g0042others(1): Show | 4 | HG01192.hp1 HG02683.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+16C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390719 | ||||||
chr21:41390727
|
C | T | 15 | a0001c0001t0001g0290a0001c0001t0001g0300a0001c0001t0001g0303others(12): Show | 17 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.871+24C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390727 | ||||||
chr21:41390806
|
A | C | 27 | a0001c0001t0001g0121a0001c0001t0001g0288a0001c0001t0018g0340others(24): Show | 32 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.871+103A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390806 | ||||||
chr21:41390822
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0052a0008c0022t0001g0048 | 3 | HG00621.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.871+119G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390822 | ||||||
chr21:41390889
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.871+186C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390889 | ||||||
chr21:41390959
|
T | C | 34 | a0001c0001t0001g0121a0001c0001t0001g0288a0001c0001t0006g0067others(31): Show | 39 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.871+256T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41390959 | ||||||
chr21:41391005
|
C | CA | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(59): Show | 71 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.871+316dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391005 | |||||
chr21:41391008
|
A | C | 2 | a0001c0001t0004g0065a0001c0001t0004g0066 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.871+305A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391008 | ||||||
chr21:41391094
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.871+391C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391094 | ||||||
chr21:41391095
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.871+392G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391095 | ||||||
chr21:41391119
|
G | A | 47 | a0001c0001t0001g0121a0001c0001t0001g0288a0001c0001t0001g0290others(44): Show | 54 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.871+416G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391119 | ||||||
chr21:41391263
|
T | TA | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 68 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.871+568dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391263 | |||||
chr21:41391389
|
C | CT | 89 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0078others(86): Show | 96 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.871+701dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391389 | |||||
chr21:41391425
|
C | A | 13 | a0001c0001t0001g0290a0001c0001t0001g0300a0001c0001t0001g0303others(10): Show | 15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.871+722C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391425 | ||||||
chr21:41391461
|
ACTGTAAC others(2): Show |
A | 5 | a0001c0001t0012g0291a0001c0001t0015g0263a0001c0001t0017g0072others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.871+762_871+770del others(9): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391461 | |||||
chr21:41391503
|
C | T | 2 | a0001c0001t0005g0280a0001c0001t0005g0324 | 2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.871+800C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391503 | ||||||
chr21:41391530
|
A | G | 5 | a0001c0001t0012g0291a0001c0001t0015g0263a0001c0001t0017g0072others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.871+827A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391530 | ||||||
chr21:41391540
|
G | C | 4 | a0001c0001t0012g0291a0001c0001t0015g0263a0002c0014t0001g0071others(1): Show | 4 | HG01884.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+837G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391540 | ||||||
chr21:41391555
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.871+852T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391555 | ||||||
chr21:41391594
|
C | T | 1 | a0001c0025t0001g0332 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.871+891C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391594 | ||||||
chr21:41391712
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.871+1009A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391712 | ||||||
chr21:41391789
|
C | CT | 9 | a0001c0001t0001g0148a0001c0001t0001g0336a0001c0001t0004g0063others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.871+1100dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391789 | |||||
chr21:41391789
|
CT | C | 13 | a0001c0001t0001g0080a0001c0001t0001g0143a0001c0001t0001g0174others(10): Show | 13 | HG01168.hp1 HG01257.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.871+1100delT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391789 | |||||
chr21:41391789
|
CTTTT | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(102): Show | 121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.871+1097_871+1100d others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41391789 | |||||
chr21:41391861
|
C | T | 5 | a0001c0001t0012g0291a0001c0001t0015g0263a0001c0001t0017g0072others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.871+1158C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391861 | ||||||
chr21:41391904
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.871+1201G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391904 | ||||||
chr21:41391934
|
G | A | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.871+1231G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41391934 | ||||||
chr21:41392013
|
A | G | 18 | a0001c0001t0001g0290a0001c0001t0001g0300a0001c0001t0001g0303others(15): Show | 20 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.871+1310A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392013 | ||||||
chr21:41392028
|
T | C | 18 | a0001c0001t0001g0290a0001c0001t0001g0300a0001c0001t0001g0303others(15): Show | 20 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.871+1325T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392028 | ||||||
chr21:41392070
|
CAT | C | 13 | a0001c0001t0001g0290a0001c0001t0001g0300a0001c0001t0001g0303others(10): Show | 15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.871+1368_871+1369d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392070 | ||||||
chr21:41392251
|
G | A | 48 | a0001c0001t0001g0121a0001c0001t0001g0154a0001c0001t0001g0288others(45): Show | 55 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.871+1548G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392251 | ||||||
chr21:41392266
|
G | A | 48 | a0001c0001t0001g0121a0001c0001t0001g0154a0001c0001t0001g0288others(45): Show | 55 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.871+1563G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392266 | ||||||
chr21:41392429
|
G | C | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.871+1726G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392429 | ||||||
chr21:41392526
|
T | C | 3 | a0001c0004t0003g0085a0001c0004t0003g0086a0001c0004t0003g0227 | 3 | NA18988.hp2 NA19078.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.871+1823T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392526 | ||||||
chr21:41392628
|
C | T | 3 | a0001c0001t0001g0290a0001c0001t0015g0263a0007c0023t0014g0278 | 3 | HG01884.hp2 HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.871+1925C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392628 | ||||||
chr21:41392644
|
T | C | 1 | a0001c0001t0011g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.871+1941T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392644 | ||||||
chr21:41392666
|
C | A | 1 | a0001c0025t0001g0332 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.871+1963C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392666 | ||||||
chr21:41392704
|
T | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0033others(30): Show | 36 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.871+2001T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392704 | ||||||
chr21:41392839
|
T | C | 9 | a0001c0001t0001g0336a0001c0001t0004g0063a0001c0001t0004g0252others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+2136T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392839 | ||||||
chr21:41392873
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0283a0001c0001t0001g0285others(1): Show | 4 | HG00140.hp2 HG02738.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+2170G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392873 | ||||||
chr21:41392924
|
G | A | 1 | a0014c0016t0005g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.871+2221G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41392924 | ||||||
chr21:41393021
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(56): Show | 68 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.871+2318G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393021 | ||||||
chr21:41393110
|
C | CA | 13 | a0001c0001t0001g0168a0001c0001t0001g0208a0001c0001t0001g0211others(10): Show | 14 | HG02083.hp2 HG02148.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.871+2428dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393110 | |||||
chr21:41393110
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0231 | 3 | HG01069.hp1 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.871+2407C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393110 | ||||||
chr21:41393110
|
CA | C | 68 | a0001c0001t0001g0039a0001c0001t0001g0095a0001c0001t0001g0154others(65): Show | 73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.871+2428delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393110 | |||||
chr21:41393110
|
CAA | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0033others(41): Show | 49 | HG00558.hp1 HG00673.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.871+2427_871+2428d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393110 | |||||
chr21:41393120
|
A | G | 1 | a0001c0001t0001g0020 | 2 | NA18950.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.871+2417A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393120 | ||||||
chr21:41393127
|
A | G | 21 | a0001c0001t0001g0095a0001c0001t0001g0161a0001c0001t0001g0275others(18): Show | 21 | HG01496.hp1 HG01981.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.871+2424A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393127 | ||||||
chr21:41393128
|
A | G | 3 | a0001c0001t0001g0338a0001c0001t0002g0207a0001c0025t0001g0332 | 3 | HG00099.hp2 HG04115.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.871+2425A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393128 | ||||||
chr21:41393145
|
GA | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 154 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.872-2432delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393145 | |||||
chr21:41393186
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.872-2401A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393186 | ||||||
chr21:41393217
|
A | G | 2 | a0001c0001t0004g0318a0001c0001t0004g0319 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.872-2370A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393217 | ||||||
chr21:41393257
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.872-2330G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393257 | ||||||
chr21:41393460
|
C | T | 1 | a0001c0001t0017g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.872-2127C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393460 | ||||||
chr21:41393544
|
C | T | 32 | a0001c0001t0001g0121a0001c0001t0001g0288a0001c0001t0017g0072others(29): Show | 37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.872-2043C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393544 | ||||||
chr21:41393577
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.872-2010T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393577 | ||||||
chr21:41393629
|
A | G | 2 | a0001c0001t0012g0291a0002c0014t0001g0071 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.872-1958A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393629 | ||||||
chr21:41393711
|
T | TG | 69 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(66): Show | 78 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.872-1875dupG | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41393711 | |||||
chr21:41393827
|
C | T | 1 | a0001c0001t0006g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.872-1760C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393827 | ||||||
chr21:41393828
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0002g0156a0001c0001t0002g0282 | 3 | NA18979.hp2 NA19000.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.872-1759G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393828 | ||||||
chr21:41393923
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.872-1664C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41393923 | ||||||
chr21:41394148
|
A | G | 1 | a0001c0025t0001g0332 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.872-1439A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394148 | ||||||
chr21:41394161
|
C | T | 5 | a0001c0001t0006g0067a0001c0001t0006g0322a0001c0001t0006g0334others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-1426C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394161 | ||||||
chr21:41394205
|
T | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(51): Show | 62 | HG00558.hp1 HG00673.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.872-1382T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394205 | ||||||
chr21:41394278
|
T | TC | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 206 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.872-1307dupC | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394278 | |||||
chr21:41394311
|
A | G | 1 | a0001c0002t0002g0212 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.872-1276A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394311 | ||||||
chr21:41394314
|
C | T | 4 | a0001c0001t0006g0067a0001c0001t0006g0322a0001c0024t0006g0331others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1273C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394314 | ||||||
chr21:41394394
|
C | A | 4 | a0001c0001t0006g0322a0001c0001t0006g0334a0001c0001t0006g0341others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1193C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394394 | ||||||
chr21:41394413
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.872-1174T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394413 | ||||||
chr21:41394429
|
C | A | 8 | a0001c0001t0001g0154a0001c0001t0006g0067a0001c0001t0006g0069others(5): Show | 8 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.872-1158C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394429 | ||||||
chr21:41394431
|
G | A | 4 | a0001c0001t0001g0154a0001c0001t0015g0263a0001c0006t0001g0239others(1): Show | 4 | HG01106.hp1 HG01884.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1156G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394431 | ||||||
chr21:41394431
|
G | T | 4 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0334others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-1156G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394431 | ||||||
chr21:41394479
|
C | T | 2 | a0001c0001t0015g0263a0007c0023t0014g0278 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.872-1108C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394479 | ||||||
chr21:41394539
|
T | C | 12 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0264others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.872-1048T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394539 | ||||||
chr21:41394541
|
C | A | 2 | a0001c0001t0002g0130a0001c0001t0002g0218 | 2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.872-1046C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394541 | ||||||
chr21:41394581
|
A | G | 6 | a0001c0001t0001g0154a0001c0001t0001g0336a0001c0004t0003g0317others(3): Show | 6 | HG01257.hp1 HG01258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-1006A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394581 | ||||||
chr21:41394652
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.872-935G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394652 | ||||||
chr21:41394680
|
T | C | 59 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(56): Show | 66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.872-907T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394680 | ||||||
chr21:41394731
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 139 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.872-856G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394731 | ||||||
chr21:41394865
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(178): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.872-722G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394865 | ||||||
chr21:41394872
|
C | T | 2 | a0001c0001t0015g0263a0007c0023t0014g0278 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.872-715C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394872 | ||||||
chr21:41394873
|
G | A | 1 | a0001c0001t0012g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.872-714G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394873 | ||||||
chr21:41394883
|
G | C | 17 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0290others(14): Show | 18 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.872-704G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394883 | ||||||
chr21:41394917
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0002g0118 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.872-670G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394917 | ||||||
chr21:41394929
|
C | CA | 49 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(46): Show | 55 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.872-652dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394929 | |||||
chr21:41394938
|
A | AAG | 25 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0290others(22): Show | 26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.872-629_872-628dup others(2): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394938 | |||||
chr21:41394938
|
A | AAGAG | 6 | a0001c0001t0001g0336a0001c0004t0003g0317a0002c0005t0003g0023others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.872-631_872-628dup others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394938 | |||||
chr21:41394982
|
A | AGAAG | 21 | a0001c0001t0001g0186a0001c0001t0001g0236a0001c0001t0001g0237others(18): Show | 22 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.872-585_872-582dup others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394982 | |||||
chr21:41394982
|
AGAAG | A | 10 | a0001c0001t0001g0095a0001c0001t0018g0340a0001c0004t0003g0085others(7): Show | 10 | NA18522.hp1 NA18946.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-585_872-582del others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41394982 | |||||
chr21:41394989
|
A | G | 1 | a0002c0003t0002g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.872-598A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41394989 | ||||||
chr21:41395006
|
A | G | 1 | a0001c0001t0008g0043 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.872-581A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395006 | ||||||
chr21:41395046
|
A | G | 1 | a0002c0003t0019g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.872-541A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395046 | ||||||
chr21:41395052
|
G | A | 1 | a0002c0003t0019g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.872-535G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395052 | ||||||
chr21:41395151
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(26): Show | 35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.872-436G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395151 | ||||||
chr21:41395155
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.872-432G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395155 | ||||||
chr21:41395206
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(151): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.872-381G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395206 | ||||||
chr21:41395263
|
AT | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.872-321delT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr21 | 41395263 | |||||
chr21:41395296
|
A | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(84): Show | 98 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.872-291A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395296 | ||||||
chr21:41395310
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.872-277T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395310 | ||||||
chr21:41395345
|
C | A | 285 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.872-242C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395345 | ||||||
chr21:41395352
|
T | C | 6 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-235T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395352 | ||||||
chr21:41395408
|
G | A | 5 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0264others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-179G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395408 | ||||||
chr21:41395486
|
A | G | 7 | a0001c0001t0001g0154a0001c0001t0005g0064a0001c0001t0005g0251others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.872-101A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 6/13 | chr21 | 41395486 | ||||||
chr21:41395806
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1070+21T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41395806 | ||||||
chr21:41395967
|
C | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1070+182C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41395967 | ||||||
chr21:41396013
|
G | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(46): Show | 55 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1070+228G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396013 | ||||||
chr21:41396189
|
G | A | 1 | a0001c0001t0011g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1070+404G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396189 | ||||||
chr21:41396208
|
G | A | 1 | a0002c0003t0002g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1070+423G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396208 | ||||||
chr21:41396258
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1070+473A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396258 | ||||||
chr21:41396265
|
A | G | 1 | a0001c0004t0003g0321 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1070+480A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396265 | ||||||
chr21:41396370
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(239): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1070+585C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396370 | ||||||
chr21:41396472
|
G | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0205others(1): Show | 4 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070+687G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396472 | ||||||
chr21:41396487
|
C | CAG | 332 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(329): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1070+702_1070+703i others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396487 | ||||||
chr21:41396634
|
T | C | 32 | a0001c0001t0001g0053a0001c0002t0001g0002a0001c0002t0001g0012others(29): Show | 37 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.1070+849T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396634 | ||||||
chr21:41396792
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(26): Show | 35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1071-821A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396792 | ||||||
chr21:41396859
|
C | T | 1 | a0001c0002t0002g0133 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1071-754C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396859 | ||||||
chr21:41396912
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1071-701C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396912 | ||||||
chr21:41396916
|
A | T | 5 | a0001c0004t0003g0317a0002c0005t0003g0023a0002c0005t0003g0293others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071-697A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396916 | ||||||
chr21:41396934
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(76): Show | 90 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1071-679G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396934 | ||||||
chr21:41396973
|
C | T | 1 | a0001c0002t0002g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1071-640C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41396973 | ||||||
chr21:41397045
|
T | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1071-568T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397045 | ||||||
chr21:41397109
|
T | C | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1071-504T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397109 | ||||||
chr21:41397136
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(152): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1071-477G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397136 | ||||||
chr21:41397140
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1071-473C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397140 | ||||||
chr21:41397190
|
G | C | 1 | a0001c0001t0002g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1071-423G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397190 | ||||||
chr21:41397267
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1071-346T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397267 | ||||||
chr21:41397313
|
A | G | 31 | a0001c0001t0001g0154a0001c0001t0001g0236a0001c0001t0001g0237others(28): Show | 32 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1071-300A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397313 | ||||||
chr21:41397353
|
T | A | 6 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071-260T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397353 | ||||||
chr21:41397432
|
TCCTGGCC others(8): Show |
T | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(26): Show | 35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1071-175_1071-161d others(17): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr21 | 41397432 | |||||
chr21:41397442
|
C | T | 3 | a0001c0006t0001g0140a0002c0003t0001g0295a0002c0003t0001g0299 | 3 | HG02257.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1071-171C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 7/13 | chr21 | 41397442 | ||||||
chr21:41398016
|
A | G | 6 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0205others(3): Show | 6 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+325A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398016 | ||||||
chr21:41398224
|
G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0221 | 2 | HG02083.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1149+533G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398224 | ||||||
chr21:41398293
|
C | T | 1 | a0002c0003t0004g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149+602C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398293 | ||||||
chr21:41398586
|
T | C | 6 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-311T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398586 | ||||||
chr21:41398675
|
C | A | 1 | a0009c0020t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1150-222C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398675 | ||||||
chr21:41398677
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1150-220T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398677 | ||||||
chr21:41398740
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1150-157T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398740 | ||||||
chr21:41398745
|
A | G | 1 | a0001c0001t0007g0018 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1150-152A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398745 | ||||||
chr21:41398828
|
A | G | 1 | a0001c0002t0002g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1150-69A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 8/13 | chr21 | 41398828 | ||||||
chr21:41399435
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1414+98T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399435 | ||||||
chr21:41399507
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(170): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1414+170A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399507 | ||||||
chr21:41399519
|
A | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1414+182A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399519 | ||||||
chr21:41399605
|
G | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0144 | 2 | NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1414+268G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399605 | ||||||
chr21:41399626
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(25): Show | 34 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1414+289C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399626 | ||||||
chr21:41399627
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0284 | 3 | HG01261.hp2 HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1414+290G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399627 | ||||||
chr21:41399674
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1414+337T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399674 | ||||||
chr21:41399920
|
G | A | 2 | a0001c0001t0001g0273a0001c0006t0001g0239 | 2 | HG01106.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1414+583G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41399920 | ||||||
chr21:41400177
|
T | C | 6 | a0001c0001t0001g0336a0001c0004t0003g0317a0002c0005t0003g0023others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1414+840T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400177 | ||||||
chr21:41400286
|
A | G | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1414+949A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400286 | ||||||
chr21:41400312
|
A | G | 6 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414+975A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400312 | ||||||
chr21:41400387
|
C | T | 1 | a0001c0001t0012g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1414+1050C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400387 | ||||||
chr21:41400601
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1414+1264G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400601 | ||||||
chr21:41400605
|
A | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1414+1268A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400605 | ||||||
chr21:41400618
|
TA | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1414+1283delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41400618 | |||||
chr21:41400703
|
CTTTA | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1415-1251_1415-124 others(8): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41400703 | |||||
chr21:41400728
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1415-1242C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41400728 | ||||||
chr21:41401131
|
TACAATTT others(75): Show |
T | 1 | a0007c0023t0014g0278 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1415-817_1415-736d others(84): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401131 | |||||
chr21:41401161
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1415-809A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401161 | ||||||
chr21:41401323
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(44): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1415-647G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401323 | ||||||
chr21:41401461
|
C | T | 6 | a0001c0001t0005g0064a0001c0001t0005g0251a0001c0001t0005g0320others(3): Show | 6 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1415-509C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401461 | ||||||
chr21:41401491
|
T | G | 3 | a0002c0003t0001g0297a0002c0003t0001g0298a0002c0003t0001g0311 | 3 | HG02647.hp2 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1415-479T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401491 | ||||||
chr21:41401495
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1415-475T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401495 | ||||||
chr21:41401528
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1415-442C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401528 | ||||||
chr21:41401685
|
G | GT | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1415-272dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401685 | |||||
chr21:41401685
|
G | GTT | 7 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0103others(4): Show | 9 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415-273_1415-272d others(4): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401685 | |||||
chr21:41401685
|
G | GTTT | 36 | a0001c0001t0001g0006a0001c0001t0001g0095a0001c0001t0002g0042others(33): Show | 38 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1415-274_1415-272d others(5): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr21 | 41401685 | |||||
chr21:41401784
|
C | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(40): Show | 50 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1415-186C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401784 | ||||||
chr21:41401895
|
T | C | 30 | a0001c0001t0002g0032a0001c0001t0002g0045a0001c0001t0002g0061others(27): Show | 32 | HG00423.hp2 HG01993.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.1415-75T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 10/13 | chr21 | 41401895 | ||||||
chr21:41402238
|
C | T | 4 | a0001c0001t0005g0064a0001c0001t0005g0320a0002c0003t0005g0296others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+110C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402238 | ||||||
chr21:41402247
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1573+119G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402247 | ||||||
chr21:41402298
|
G | T | 1 | a0002c0005t0003g0023 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1573+170G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402298 | ||||||
chr21:41402402
|
C | T | 1 | a0001c0001t0012g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1573+274C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402402 | ||||||
chr21:41402614
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(205): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1573+486A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402614 | ||||||
chr21:41402686
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(194): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1573+558A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402686 | ||||||
chr21:41402709
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1574-558A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402709 | ||||||
chr21:41402864
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1574-403G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402864 | ||||||
chr21:41402998
|
C | A | 13 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(10): Show | 13 | HG01106.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1574-269C>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41402998 | ||||||
chr21:41403252
|
G | GT | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1574-15_1574-14ins others(1): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41403252 | ||||||
chr21:41403253
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1574-14C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 11/13 | chr21 | 41403253 | ||||||
chr21:41403437
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0146 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1650+94G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403437 | ||||||
chr21:41403597
|
G | A | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1650+254G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403597 | ||||||
chr21:41403597
|
G | T | 13 | a0001c0001t0004g0063a0001c0001t0004g0065a0001c0001t0004g0066others(10): Show | 13 | HG01106.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650+254G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403597 | ||||||
chr21:41403725
|
T | C | 2 | a0001c0001t0002g0245a0001c0002t0002g0265 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1650+382T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403725 | ||||||
chr21:41403760
|
C | T | 49 | a0001c0001t0001g0056a0001c0001t0002g0008a0001c0001t0002g0014others(46): Show | 53 | HG00423.hp2 HG00609.hp2 HG01993.hp1 others(50): Show |
intron_variant | MODIFIER | c.1650+417C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403760 | ||||||
chr21:41403905
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1650+562G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41403905 | ||||||
chr21:41404075
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1650+732G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404075 | ||||||
chr21:41404118
|
C | T | 1 | a0001c0004t0003g0321 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+775C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404118 | ||||||
chr21:41404356
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1650+1013G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404356 | ||||||
chr21:41404481
|
G | C | 2 | a0001c0001t0015g0263a0007c0023t0014g0278 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1650+1138G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404481 | ||||||
chr21:41404521
|
C | T | 1 | a0002c0010t0016g0329 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1650+1178C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404521 | ||||||
chr21:41404532
|
T | A | 6 | a0001c0001t0005g0064a0001c0001t0005g0251a0001c0001t0005g0320others(3): Show | 6 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+1189T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404532 | ||||||
chr21:41404642
|
G | C | 7 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+1299G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404642 | ||||||
chr21:41404719
|
C | T | 1 | a0001c0004t0003g0321 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+1376C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404719 | ||||||
chr21:41404744
|
C | T | 8 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+1401C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404744 | ||||||
chr21:41404745
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1650+1402G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404745 | ||||||
chr21:41404861
|
G | A | 9 | a0001c0001t0005g0064a0001c0001t0005g0251a0001c0001t0005g0280others(6): Show | 9 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1650+1518G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404861 | ||||||
chr21:41404873
|
C | CA | 14 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0121others(11): Show | 15 | HG00423.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1650+1548dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404873 | |||||
chr21:41404873
|
CA | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(55): Show | 66 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1650+1548delA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404873 | |||||
chr21:41404873
|
CAA | C | 19 | a0001c0001t0009g0335a0001c0001t0015g0263a0001c0004t0003g0085others(16): Show | 20 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1650+1547_1650+154 others(6): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404873 | |||||
chr21:41404886
|
A | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0284 | 3 | HG01261.hp2 HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1650+1543A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41404886 | ||||||
chr21:41404898
|
G | GA | 8 | a0001c0001t0005g0064a0001c0001t0005g0251a0001c0001t0005g0280others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+1565dupA | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41404898 | |||||
chr21:41405079
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0224 | 2 | NA18983.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1651-1665C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405079 | ||||||
chr21:41405162
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1651-1582T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405162 | ||||||
chr21:41405198
|
G | C | 1 | a0001c0002t0002g0126 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1651-1546G>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405198 | ||||||
chr21:41405272
|
A | T | 8 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-1472A>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405272 | ||||||
chr21:41405412
|
G | A | 1 | a0002c0003t0019g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1651-1332G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405412 | ||||||
chr21:41405418
|
G | A | 1 | a0001c0002t0002g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1651-1326G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405418 | ||||||
chr21:41405424
|
TCAG | T | 8 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-1319_1651-131 others(7): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405424 | ||||||
chr21:41405452
|
G | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 5 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-1292G>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405452 | ||||||
chr21:41405501
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1651-1243C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405501 | ||||||
chr21:41405502
|
G | A | 1 | a0001c0001t0004g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1651-1242G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405502 | ||||||
chr21:41405650
|
A | G | 17 | a0001c0001t0005g0064a0001c0001t0005g0251a0001c0001t0005g0280others(14): Show | 17 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1651-1094A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405650 | ||||||
chr21:41405701
|
C | CT | 18 | a0001c0001t0001g0019a0001c0001t0001g0096a0001c0001t0001g0125others(15): Show | 19 | HG01975.hp2 HG01978.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1651-1022dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405701 | |||||
chr21:41405701
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1651-1032_1651-102 others(15): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405701 | |||||
chr21:41405701
|
CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0005g0064a0001c0001t0005g0251a0001c0001t0005g0280others(6): Show | 9 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-1033_1651-102 others(16): Show |
MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405701 | |||||
chr21:41405754
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(209): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1651-990A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405754 | ||||||
chr21:41405773
|
C | T | 8 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651-971C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405773 | ||||||
chr21:41405897
|
G | GT | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1651-845dupT | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr21 | 41405897 | |||||
chr21:41405968
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1651-776T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41405968 | ||||||
chr21:41406002
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1651-742C>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406002 | ||||||
chr21:41406132
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1651-612G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406132 | ||||||
chr21:41406229
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1651-515C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406229 | ||||||
chr21:41406266
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1651-478G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406266 | ||||||
chr21:41406457
|
T | G | 18 | a0001c0001t0015g0263a0001c0004t0003g0085a0001c0004t0003g0086others(15): Show | 19 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1651-287T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406457 | ||||||
chr21:41406459
|
T | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(206): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1651-285T>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 12/13 | chr21 | 41406459 | ||||||
chr21:41407129
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(208): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1905+131T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407129 | ||||||
chr21:41407147
|
A | G | 2 | a0001c0002t0002g0133a0001c0002t0002g0197 | 2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1905+149A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407147 | ||||||
chr21:41407199
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 7 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1905+201A>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407199 | ||||||
chr21:41407201
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1905+203T>G | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407201 | ||||||
chr21:41407259
|
A | C | 1 | a0002c0003t0019g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1905+261A>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407259 | ||||||
chr21:41407283
|
G | A | 1 | a0013c0017t0001g0217 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1905+285G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407283 | ||||||
chr21:41407334
|
C | T | 1 | a0001c0002t0002g0038 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1905+336C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407334 | ||||||
chr21:41407481
|
C | T | 12 | a0001c0001t0001g0078a0001c0001t0001g0120a0001c0001t0001g0122others(9): Show | 12 | HG00642.hp2 HG01099.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1905+483C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407481 | ||||||
chr21:41407524
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1906-467T>C | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407524 | ||||||
chr21:41407548
|
C | T | 1 | a0002c0003t0019g0238 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906-443C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407548 | ||||||
chr21:41407604
|
C | T | 1 | a0001c0006t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1906-387C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407604 | ||||||
chr21:41407656
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1906-335G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407656 | ||||||
chr21:41407832
|
C | T | 6 | a0001c0001t0012g0291a0001c0025t0001g0332a0002c0003t0001g0297others(3): Show | 6 | HG02647.hp2 HG02896.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906-159C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407832 | ||||||
chr21:41407887
|
G | A | 7 | a0001c0001t0006g0067a0001c0001t0006g0069a0001c0001t0006g0322others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1906-104G>A | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407887 | ||||||
chr21:41407903
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0068a0001c0001t0001g0310others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906-88C>T | MX2 | ENSG00000183486.14 | transcript | ENST00000330714.8 | protein_coding | 13/13 | chr21 | 41407903 |