geneid | 11262 |
---|---|
ensemblid | ENSG00000079263.19 |
hgncid | 17133 |
symbol | SP140 |
name | SP140 nuclear body protein |
refseq_nuc | NM_007237.5 |
refseq_prot | NP_009168.4 |
ensembl_nuc | ENST00000392045.8 |
ensembl_prot | ENSP00000375899.3 |
mane_status | MANE Select |
chr | chr2 |
start | 230225736 |
end | 230313215 |
strand | + |
ver | v1.2 |
region | chr2:230225736-230313215 |
region5000 | chr2:230220736-230318215 |
regionname0 | SP140_chr2_230225736_230313215 |
regionname5000 | SP140_chr2_230220736_230318215 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 867 | 269 | 61 | 42 | 124 | 5 | 36 | 101 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0002 | 0/0 | 867 | 35 | 2 | 9 | 18 | 3 | 3 | 14 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003 | 0/0 | 867 | 25 | 2 | 15 | 0 | 5 | 3 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0004 | 0/0 | 867 | 16 | 14 | 0 | 1 | 0 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0005 | 1/0 | 867 | 9 | 0 | 2 | 1 | 4 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0006 | 0/0 | 867 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0007 | 0/0 | 867 | 3 | 2 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0008 | 0/0 | 867 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0009 | 0/0 | 867 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0010 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0011 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0012 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0013 | 0/0 | 867 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2604 | 255 | 55 | 41 | 123 | 3 | 32 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0002 | 0/0 | 2604 | 30 | 2 | 7 | 17 | 2 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0003 | 0/0 | 2604 | 16 | 14 | 0 | 1 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0004 | 0/0 | 2604 | 14 | 2 | 10 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0005 | 0/0 | 2604 | 11 | 0 | 5 | 0 | 5 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0006 | 0/0 | 2604 | 11 | 6 | 1 | 0 | 1 | 3 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0007 | 1/0 | 2604 | 9 | 0 | 2 | 1 | 4 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0008 | 0/0 | 2604 | 5 | 0 | 2 | 1 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0009 | 0/0 | 2604 | 4 | 4 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0010 | 0/0 | 2604 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0011 | 0/0 | 2604 | 2 | 0 | 0 | 1 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0012 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0013 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0014 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0015 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0016 | 0/0 | 2604 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0017 | 0/0 | 2604 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0018 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0019 | 0/0 | 2604 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
c0020 | 0/0 | 2604 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
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 | 1/1 | 641 | 293 | 68 | 48 | 127 | 13 | 35 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0002 | 0/0 | 641 | 43 | 15 | 6 | 17 | 0 | 5 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0003 | 0/0 | 641 | 23 | 1 | 14 | 0 | 5 | 3 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0004 | 0/0 | 641 | 5 | 5 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0005 | 0/0 | 641 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0006 | 0/0 | 641 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0007 | 0/0 | 641 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0008 | 0/0 | 641 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0009 | 0/0 | 641 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
t0010 | 0/0 | 641 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2604 | 255 | 55 | 41 | 123 | 3 | 32 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0006 | 0/0 | 2604 | 11 | 6 | 1 | 0 | 1 | 3 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0011 | 0/0 | 2604 | 2 | 0 | 0 | 1 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0016 | 0/0 | 2604 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0002c0002 | 0/0 | 2604 | 30 | 2 | 7 | 17 | 2 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0002c0008 | 0/0 | 2604 | 5 | 0 | 2 | 1 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003c0004 | 0/0 | 2604 | 14 | 2 | 10 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003c0005 | 0/0 | 2604 | 11 | 0 | 5 | 0 | 5 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0004c0003 | 0/0 | 2604 | 16 | 14 | 0 | 1 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0005c0007 | 1/0 | 2604 | 9 | 0 | 2 | 1 | 4 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0006c0009 | 0/0 | 2604 | 4 | 4 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0007c0012 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0007c0017 | 0/0 | 2604 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0008c0010 | 0/0 | 2604 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0008c0019 | 0/0 | 2604 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0009c0013 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0010c0018 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0011c0014 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0012c0015 | 0/0 | 2604 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0013c0020 | 0/0 | 2604 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3244 | 212 | 43 | 35 | 104 | 3 | 26 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0001t0002 | 0/0 | 3244 | 37 | 10 | 5 | 17 | 0 | 5 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0001t0004 | 0/0 | 3244 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0001t0005 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0001t0006 | 0/0 | 3244 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0001t0007 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0001t0009 | 0/0 | 3244 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0006t0001 | 0/0 | 3244 | 7 | 2 | 1 | 0 | 1 | 3 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0006t0002 | 0/0 | 3244 | 4 | 4 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0011t0001 | 0/0 | 3244 | 2 | 0 | 0 | 1 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0001c0016t0001 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0002c0002t0001 | 0/0 | 3244 | 30 | 2 | 7 | 17 | 2 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0002c0008t0001 | 0/0 | 3244 | 4 | 0 | 1 | 1 | 1 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0002c0008t0002 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003c0004t0003 | 0/0 | 3244 | 13 | 1 | 10 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003c0004t0010 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003c0005t0003 | 0/0 | 3244 | 10 | 0 | 4 | 0 | 5 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0003c0005t0008 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0004c0003t0001 | 0/0 | 3244 | 16 | 14 | 0 | 1 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0005c0007t0001 | 1/0 | 3244 | 9 | 0 | 2 | 1 | 4 | 1 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0006c0009t0002 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0006c0009t0004 | 0/0 | 3244 | 3 | 3 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0007c0012t0001 | 0/0 | 3244 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0007c0017t0001 | 0/0 | 3244 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0008c0010t0001 | 0/0 | 3244 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0008c0019t0001 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0009c0013t0001 | 0/0 | 3244 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0010c0018t0001 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0011c0014t0001 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0012c0015t0001 | 0/0 | 3244 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
a0013c0020t0001 | 0/0 | 3244 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | copy fasta | chr2 | 230220736 | 230318215 |
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 | 3 | 0 | 3 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0006t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0011t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0011t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0001c0016t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0008t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0008t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0008t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0008t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0002c0008t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0004t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0003c0005t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0004c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0005c0007t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0006c0009t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0006c0009t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0006c0009t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0006c0009t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0007c0012t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0007c0012t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0007c0017t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0008c0010t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0008c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0008c0019t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0009c0013t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0009c0013t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0010c0018t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0011c0014t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0012c0015t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
a0013c0020t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00140 | hp1 | a0001 | c0006 | t0001 | g0025 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00140 | hp2 | a0003 | c0005 | t0003 | g0098 | EUR | GBR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00280 | hp1 | a0005 | c0007 | t0001 | g0094 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00323 | hp1 | a0003 | c0005 | t0003 | g0162 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00323 | hp2 | a0007 | c0017 | t0001 | g0053 | EUR | FIN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00408 | hp1 | a0005 | c0007 | t0001 | g0058 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0326 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0347 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00597 | hp2 | a0001 | c0001 | t0009 | g0064 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00642 | hp2 | a0002 | c0008 | t0002 | g0351 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00738 | hp2 | a0003 | c0004 | t0003 | g0019 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01069 | hp1 | a0003 | c0005 | t0003 | g0186 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01070 | hp1 | a0005 | c0007 | t0001 | g0004 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0340 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01071 | hp1 | a0005 | c0007 | t0001 | g0004 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01071 | hp2 | a0003 | c0005 | t0003 | g0185 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01169 | hp1 | a0003 | c0004 | t0003 | g0032 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01175 | hp1 | a0003 | c0005 | t0003 | g0216 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01243 | hp1 | a0003 | c0004 | t0003 | g0024 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | PUR | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01255 | hp1 | a0003 | c0005 | t0003 | g0104 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01256 | hp1 | a0003 | c0004 | t0003 | g0016 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01256 | hp2 | a0003 | c0004 | t0003 | g0003 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01258 | hp1 | a0003 | c0004 | t0003 | g0003 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01261 | hp1 | a0013 | c0020 | t0001 | g0134 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01346 | hp2 | a0003 | c0004 | t0003 | g0030 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0345 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01358 | hp2 | a0001 | c0006 | t0001 | g0027 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01361 | hp1 | a0002 | c0008 | t0001 | g0339 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01433 | hp2 | a0003 | c0004 | t0003 | g0033 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01496 | hp1 | a0003 | c0004 | t0003 | g0020 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01515 | hp1 | a0005 | c0007 | t0001 | g0061 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0337 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0331 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01516 | hp2 | a0003 | c0005 | t0003 | g0006 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01517 | hp1 | a0005 | c0007 | t0001 | g0091 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01517 | hp2 | a0003 | c0005 | t0003 | g0006 | EUR | IBS | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01884 | hp1 | a0004 | c0003 | t0001 | g0271 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01884 | hp2 | a0004 | c0003 | t0001 | g0321 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0353 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0344 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01978 | hp1 | a0003 | c0005 | t0008 | g0215 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0332 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02145 | hp1 | a0009 | c0013 | t0001 | g0139 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02145 | hp2 | a0004 | c0003 | t0001 | g0045 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0342 | EAS | CDX | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02257 | hp1 | a0009 | c0013 | t0001 | g0140 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02257 | hp2 | a0006 | c0009 | t0004 | g0156 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0018 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02280 | hp1 | a0004 | c0003 | t0001 | g0310 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02300 | hp2 | a0008 | c0019 | t0001 | g0022 | AMR | PEL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0330 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02451 | hp2 | a0007 | c0012 | t0001 | g0012 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0322 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02602 | hp1 | a0001 | c0006 | t0001 | g0026 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02602 | hp2 | a0001 | c0001 | t0007 | g0181 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02615 | hp1 | a0004 | c0003 | t0001 | g0312 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02622 | hp2 | a0004 | c0003 | t0001 | g0270 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02717 | hp1 | a0004 | c0003 | t0001 | g0314 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02735 | hp1 | a0001 | c0006 | t0001 | g0023 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02738 | hp1 | a0005 | c0007 | t0001 | g0123 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02738 | hp2 | a0003 | c0004 | t0003 | g0034 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02809 | hp1 | a0004 | c0003 | t0001 | g0313 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02809 | hp2 | a0006 | c0009 | t0004 | g0155 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02818 | hp2 | a0001 | c0006 | t0001 | g0039 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02886 | hp1 | a0004 | c0003 | t0001 | g0269 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0038 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02970 | hp2 | a0007 | c0012 | t0001 | g0013 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03041 | hp1 | a0004 | c0003 | t0001 | g0315 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03195 | hp2 | a0004 | c0003 | t0001 | g0272 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03209 | hp2 | a0010 | c0018 | t0001 | g0254 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03225 | hp1 | a0004 | c0003 | t0001 | g0275 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03225 | hp2 | a0004 | c0003 | t0001 | g0311 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03239 | hp2 | a0003 | c0004 | t0003 | g0031 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03453 | hp2 | a0001 | c0006 | t0002 | g0028 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03486 | hp1 | a0012 | c0015 | t0001 | g0318 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03491 | hp1 | a0001 | c0006 | t0001 | g0037 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03516 | hp1 | a0001 | c0006 | t0002 | g0036 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ESN | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03831 | hp1 | a0003 | c0005 | t0003 | g0201 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03834 | hp2 | a0001 | c0016 | t0001 | g0284 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03927 | hp1 | a0004 | c0003 | t0001 | g0355 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0354 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | BEB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18522 | hp1 | a0006 | c0009 | t0002 | g0153 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18939 | hp1 | a0008 | c0010 | t0001 | g0111 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18944 | hp1 | a0001 | c0011 | t0001 | g0200 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18954 | hp2 | a0002 | c0008 | t0001 | g0333 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19002 | hp2 | a0004 | c0003 | t0001 | g0352 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19079 | hp1 | a0008 | c0010 | t0001 | g0066 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA19240 | hp2 | a0004 | c0003 | t0001 | g0227 | AFR | YRI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ASW | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20752 | hp1 | a0001 | c0011 | t0001 | g0165 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20752 | hp2 | a0005 | c0007 | t0001 | g0093 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20805 | hp1 | a0002 | c0008 | t0001 | g0334 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20805 | hp2 | a0003 | c0005 | t0003 | g0097 | EUR | TSI | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20905 | hp2 | a0002 | c0008 | t0001 | g0329 | SAS | GIH | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01123 | hp1 | a0003 | c0004 | t0003 | g0035 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | CLM | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02486 | hp1 | a0011 | c0014 | t0001 | g0267 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02559 | hp1 | a0006 | c0009 | t0004 | g0154 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
HG06807 | hp2 | a0003 | c0004 | t0010 | g0021 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA20300 | hp2 | a0001 | c0006 | t0002 | g0029 | AFR | USA | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
NA21309 | hp2 | a0001 | c0006 | t0002 | g0017 | AFR | LWK | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0213 | REF | REF | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
homoSapiens_grch38 | hp1 | a0005 | c0007 | t0001 | g0059 | REF | REF | SP140_chr2_230220736_230318215 | SP140 | chr2 | 230220736 | 230318215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230245054
|
C | T | 1 | a0013 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.638C>T | p.Ala213Val | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/27 | 747/3244 | 638/2604 | 213/867 | chr2 | 230245054 | ||
chr2:230245934
|
A | G | 1 | a0010 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.736A>G | p.Thr246Ala | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/27 | 845/3244 | 736/2604 | 246/867 | chr2 | 230245934 | ||
chr2:230248903
|
C | T | 1 | a0009 | 2 | HG02145.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.911C>T | p.Thr304Ile | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/27 | 1020/3244 | 911/2604 | 304/867 | chr2 | 230248903 | ||
chr2:230253326
|
A | C | 4 | a0002a0004a0007others(1): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
missense_variant | MODERATE | c.1068A>C | p.Leu356Phe | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/27 | 1177/3244 | 1068/2604 | 356/867 | chr2 | 230253326 | ||
chr2:230253394
|
G | A | 1 | a0011 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1136G>A | p.Ser379Asn | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/27 | 1245/3244 | 1136/2604 | 379/867 | chr2 | 230253394 | ||
chr2:230253406
|
G | T | 1 | a0011 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1148G>T | p.Gly383Val | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/27 | 1257/3244 | 1148/2604 | 383/867 | chr2 | 230253406 | ||
chr2:230255494
|
G | C | 1 | a0007 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1202G>C | p.Arg401Pro | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/27 | 1311/3244 | 1202/2604 | 401/867 | chr2 | 230255494 | ||
chr2:230255526
|
G | C | 1 | a0012 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1234G>C | p.Gly412Arg | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/27 | 1343/3244 | 1234/2604 | 412/867 | chr2 | 230255526 | ||
chr2:230284382
|
T | C | 2 | a0002a0008 | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
missense_variant | MODERATE | c.1535T>C | p.Met512Thr | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/27 | 1644/3244 | 1535/2604 | 512/867 | chr2 | 230284382 | ||
chr2:230284393
|
G | A | 12 | a0001a0002a0003others(9): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
missense_variant | MODERATE | c.1546G>A | p.Glu516Lys | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/27 | 1655/3244 | 1546/2604 | 516/867 | chr2 | 230284393 | ||
chr2:230287918
|
C | T | 1 | a0006 | 4 | HG02257.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
missense_variant | MODERATE | c.1672C>T | p.Arg558Cys | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/27 | 1781/3244 | 1672/2604 | 558/867 | chr2 | 230287918 | ||
chr2:230310834
|
T | C | 1 | a0003 | 25 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(22): Show |
missense_variant | MODERATE | c.2266T>C | p.Cys756Arg | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/27 | 2375/3244 | 2266/2604 | 756/867 | chr2 | 230310834 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230245867
|
C | T | 3 | a0001c0006a0003c0004a0008c0019 | 26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
synonymous_variant | LOW | c.669C>T | p.Ser223Ser | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/27 | 778/3244 | 669/2604 | 223/867 | chr2 | 230245867 | ||
chr2:230285801
|
C | T | 1 | a0001c0016 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1614C>T | p.Asn538Asn | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/27 | 1723/3244 | 1614/2604 | 538/867 | chr2 | 230285801 | ||
chr2:230311481
|
G | A | 5 | a0001c0011a0002c0002a0007c0017others(2): Show | 36 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(33): Show |
synonymous_variant | LOW | c.2391G>A | p.Glu797Glu | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/27 | 2500/3244 | 2391/2604 | 797/867 | chr2 | 230311481 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230225817
|
G | T | 1 | a0003c0004t0010 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/27 | 28 | chr2 | 230225817 | |||||
chr2:230312900
|
G | A | 1 | a0001c0001t0005 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 216 | chr2 | 230312900 | |||||
chr2:230312918
|
A | T | 1 | a0001c0001t0009 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 234 | chr2 | 230312918 | |||||
chr2:230312974
|
C | G | 1 | a0003c0005t0008 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 290 | chr2 | 230312974 | |||||
chr2:230313045
|
T | C | 1 | a0001c0001t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*361T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 361 | chr2 | 230313045 | |||||
chr2:230313107
|
G | A | 4 | a0001c0001t0002a0001c0006t0002a0002c0008t0002others(1): Show | 43 | HG00423.hp1 HG00642.hp1 HG00642.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*423G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 423 | chr2 | 230313107 | |||||
chr2:230313188
|
A | G | 1 | a0001c0001t0007 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 504 | chr2 | 230313188 | |||||
chr2:230313189
|
T | C | 4 | a0003c0004t0003a0003c0004t0010a0003c0005t0003others(1): Show | 25 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 505 | chr2 | 230313189 | |||||
chr2:230313191
|
T | C | 2 | a0001c0001t0004a0006c0009t0004 | 5 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*507T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 27/27 | 507 | chr2 | 230313191 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230225956
|
T | G | 2 | a0007c0012t0001g0012a0007c0012t0001g0013 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.59+53T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230225956 | ||||||
chr2:230226309
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015 | 4 | HG01106.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+406G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226309 | ||||||
chr2:230226362
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.59+459A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226362 | ||||||
chr2:230226508
|
T | G | 25 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(22): Show | 26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59+605T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226508 | ||||||
chr2:230226625
|
C | G | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+722C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226625 | ||||||
chr2:230226626
|
A | G | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+723A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226626 | ||||||
chr2:230226762
|
C | CAAAAAAA others(4): Show |
3 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0039 | 3 | HG02818.hp2 HG02896.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.59+868_59+878dupAA others(9): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | |||||
chr2:230226762
|
C | CAAAAAAA others(5): Show |
19 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(16): Show | 20 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.59+867_59+878dupAA others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | |||||
chr2:230226762
|
C | CAAAAAAA others(6): Show |
1 | a0003c0004t0003g0018 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.59+866_59+878dupAA others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | |||||
chr2:230226762
|
CA | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.59+878delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230226762 | |||||
chr2:230226941
|
G | A | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+1038G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226941 | ||||||
chr2:230226987
|
T | C | 1 | a0002c0002t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.59+1084T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230226987 | ||||||
chr2:230227037
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.59+1134C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227037 | ||||||
chr2:230227374
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357 | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+1471A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227374 | ||||||
chr2:230227451
|
A | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+1548A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227451 | ||||||
chr2:230227491
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.59+1588T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227491 | ||||||
chr2:230227792
|
C | T | 1 | a0001c0001t0004g0322 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59+1889C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227792 | ||||||
chr2:230227818
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.59+1915G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230227818 | ||||||
chr2:230228212
|
T | C | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.59+2309T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228212 | ||||||
chr2:230228238
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015 | 4 | HG01106.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+2335T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228238 | ||||||
chr2:230228287
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.59+2384G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228287 | ||||||
chr2:230228358
|
C | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+2455C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228358 | ||||||
chr2:230228453
|
C | G | 43 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(40): Show | 43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.59+2550C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228453 | ||||||
chr2:230228770
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015 | 4 | HG01106.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+2867A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228770 | ||||||
chr2:230228819
|
G | A | 1 | a0001c0006t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59+2916G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228819 | ||||||
chr2:230228866
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.59+2963T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228866 | ||||||
chr2:230228914
|
T | C | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | HG00423.hp1 NA18943.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.59+3011T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230228914 | ||||||
chr2:230229169
|
T | C | 1 | a0001c0001t0001g0356 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.59+3266T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229169 | ||||||
chr2:230229412
|
T | C | 1 | a0003c0004t0003g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.59+3509T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229412 | ||||||
chr2:230229421
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.59+3518G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229421 | ||||||
chr2:230229456
|
C | CT | 47 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(44): Show | 47 | HG00642.hp2 HG00673.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.59+3582dupT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
C | CTT | 9 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(6): Show | 9 | HG01884.hp2 HG01981.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.59+3581_59+3582dup others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
CT | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.59+3582delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
CTT | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+3581_59+3582del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.59+3572_59+3582del others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0002a0001c0001t0001g0014 | 3 | HG02615.hp2 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.59+3571_59+3582del others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357 | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.59+3570_59+3582del others(13): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229456
|
CTTTTTTT others(7): Show |
C | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+3569_59+3582del others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230229456 | |||||
chr2:230229536
|
C | T | 1 | a0004c0003t0001g0355 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.59+3633C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229536 | ||||||
chr2:230229994
|
G | T | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.59+4091G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230229994 | ||||||
chr2:230230384
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59+4481A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230384 | ||||||
chr2:230230451
|
C | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.59+4548C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230451 | ||||||
chr2:230230626
|
C | G | 1 | a0001c0001t0001g0213 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59+4723C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230626 | ||||||
chr2:230230872
|
T | C | 4 | a0001c0001t0005g0122a0007c0012t0001g0012a0007c0012t0001g0013others(1): Show | 4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+4969T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230872 | ||||||
chr2:230230963
|
T | C | 25 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(22): Show | 26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.59+5060T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230963 | ||||||
chr2:230230993
|
A | G | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.59+5090A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230230993 | ||||||
chr2:230231061
|
T | A | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+5158T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231061 | ||||||
chr2:230231237
|
A | G | 30 | a0001c0001t0001g0009a0001c0001t0001g0268a0001c0001t0001g0274others(27): Show | 31 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.59+5334A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231237 | ||||||
chr2:230231472
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0226a0004c0003t0001g0315 | 3 | HG01361.hp2 HG03041.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.59+5569C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231472 | ||||||
chr2:230231547
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357 | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-5536T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231547 | ||||||
chr2:230231556
|
C | T | 4 | a0001c0001t0005g0122a0007c0012t0001g0012a0007c0012t0001g0013others(1): Show | 4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-5527C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231556 | ||||||
chr2:230231561
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.60-5522A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231561 | ||||||
chr2:230231611
|
AG | A | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.60-5467delG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230231611 | |||||
chr2:230231629
|
A | G | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.60-5454A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231629 | ||||||
chr2:230231656
|
A | T | 3 | a0003c0004t0003g0030a0003c0004t0003g0031a0003c0004t0003g0032 | 3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.60-5427A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231656 | ||||||
chr2:230231711
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.60-5372T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231711 | ||||||
chr2:230231801
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.60-5282G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231801 | ||||||
chr2:230231899
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.60-5184C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230231899 | ||||||
chr2:230231948
|
ATCCACCC others(7): Show |
A | 1 | a0004c0003t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.60-5132_60-5119del others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230231948 | |||||
chr2:230232414
|
T | C | 39 | a0001c0001t0005g0122a0001c0006t0001g0023a0001c0006t0001g0025others(36): Show | 40 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.60-4669T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232414 | ||||||
chr2:230232466
|
GGTT | G | 4 | a0001c0001t0005g0122a0007c0012t0001g0012a0007c0012t0001g0013others(1): Show | 4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-4602_60-4600del others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230232466 | |||||
chr2:230232582
|
A | G | 1 | a0002c0002t0001g0350 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.60-4501A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232582 | ||||||
chr2:230232658
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.60-4425A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232658 | ||||||
chr2:230232701
|
T | G | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60-4382T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232701 | ||||||
chr2:230232845
|
G | C | 13 | a0001c0001t0005g0122a0004c0003t0001g0310a0004c0003t0001g0311others(10): Show | 13 | HG00323.hp2 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.60-4238G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232845 | ||||||
chr2:230232863
|
A | G | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.60-4220A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230232863 | ||||||
chr2:230233269
|
G | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(209): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.60-3814G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233269 | ||||||
chr2:230233325
|
A | G | 45 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(42): Show | 46 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.60-3758A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233325 | ||||||
chr2:230233356
|
C | A | 25 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(22): Show | 26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.60-3727C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233356 | ||||||
chr2:230233495
|
A | C | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-3588A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233495 | ||||||
chr2:230233670
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.60-3413G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233670 | ||||||
chr2:230233696
|
AAAT | A | 4 | a0001c0001t0005g0122a0007c0012t0001g0012a0007c0012t0001g0013others(1): Show | 4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-3381_60-3379del others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230233696 | |||||
chr2:230233745
|
T | C | 2 | a0007c0012t0001g0012a0007c0012t0001g0013 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.60-3338T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233745 | ||||||
chr2:230233763
|
C | T | 38 | a0001c0001t0005g0122a0001c0006t0001g0023a0001c0006t0001g0025others(35): Show | 39 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.60-3320C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233763 | ||||||
chr2:230233900
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.60-3183A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233900 | ||||||
chr2:230233987
|
G | A | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.60-3096G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230233987 | ||||||
chr2:230234197
|
G | A | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-2886G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234197 | ||||||
chr2:230234276
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.60-2807A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234276 | ||||||
chr2:230234427
|
A | T | 1 | a0001c0001t0002g0265 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.60-2656A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234427 | ||||||
chr2:230234444
|
A | G | 2 | a0001c0001t0002g0261a0001c0001t0002g0266 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.60-2639A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234444 | ||||||
chr2:230234455
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(131): Show | 140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.60-2628C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234455 | ||||||
chr2:230234489
|
C | T | 59 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0268others(56): Show | 61 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.60-2594C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230234489 | ||||||
chr2:230235324
|
A | G | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(353): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.60-1759A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235324 | ||||||
chr2:230235347
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(156): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.60-1736T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235347 | ||||||
chr2:230235367
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(156): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.60-1716T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235367 | ||||||
chr2:230235425
|
T | G | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.60-1658T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235425 | ||||||
chr2:230235860
|
T | C | 1 | a0005c0007t0001g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.60-1223T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235860 | ||||||
chr2:230235868
|
G | GT | 29 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0055others(26): Show | 30 | HG01175.hp2 HG02056.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.60-1190dupT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230235868 | |||||
chr2:230235868
|
GT | G | 49 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0060others(46): Show | 50 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.60-1190delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230235868 | |||||
chr2:230235868
|
GTT | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(119): Show | 128 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.60-1191_60-1190del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 230235868 | |||||
chr2:230235963
|
G | A | 1 | a0002c0002t0001g0348 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.60-1120G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230235963 | ||||||
chr2:230236035
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.60-1048C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236035 | ||||||
chr2:230236118
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357 | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-965G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236118 | ||||||
chr2:230236126
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0276 | 2 | HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.60-957C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236126 | ||||||
chr2:230236155
|
G | A | 1 | a0005c0007t0001g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.60-928G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236155 | ||||||
chr2:230236164
|
C | T | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.60-919C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236164 | ||||||
chr2:230236221
|
C | A | 1 | a0002c0002t0001g0324 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.60-862C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236221 | ||||||
chr2:230236265
|
A | G | 1 | a0002c0002t0001g0347 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.60-818A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236265 | ||||||
chr2:230236668
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60-415C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236668 | ||||||
chr2:230236683
|
C | T | 2 | a0002c0002t0001g0346a0002c0002t0001g0349 | 2 | NA18965.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.60-400C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236683 | ||||||
chr2:230236744
|
C | T | 6 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.60-339C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236744 | ||||||
chr2:230236834
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60-249G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 1/26 | chr2 | 230236834 | ||||||
chr2:230237720
|
C | G | 6 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+460C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230237720 | ||||||
chr2:230237833
|
T | TA | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(197): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.238-380_238-379ins others(1): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230237833 | ||||||
chr2:230237973
|
A | C | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.238-240A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230237973 | ||||||
chr2:230238104
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.238-109C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 2/26 | chr2 | 230238104 | ||||||
chr2:230238402
|
C | T | 1 | a0002c0002t0001g0354 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.406+21C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238402 | ||||||
chr2:230238470
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.406+89A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238470 | ||||||
chr2:230238493
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+112G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238493 | ||||||
chr2:230238631
|
G | A | 4 | a0006c0009t0002g0153a0006c0009t0004g0154a0006c0009t0004g0155others(1): Show | 4 | HG02257.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+250G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238631 | ||||||
chr2:230238936
|
G | A | 1 | a0007c0017t0001g0053 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.406+555G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238936 | ||||||
chr2:230238954
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.406+573G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238954 | ||||||
chr2:230238983
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.406+602A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230238983 | ||||||
chr2:230239081
|
A | T | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.406+700A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239081 | ||||||
chr2:230239099
|
G | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0207a0001c0001t0001g0208others(2): Show | 5 | HG02723.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+718G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239099 | ||||||
chr2:230239203
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+822C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239203 | ||||||
chr2:230239344
|
T | A | 43 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(40): Show | 43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.406+963T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239344 | ||||||
chr2:230239348
|
A | G | 5 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258others(2): Show | 5 | HG02717.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+967A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239348 | ||||||
chr2:230239371
|
T | C | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.406+990T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239371 | ||||||
chr2:230239418
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | NA18946.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.406+1037A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239418 | ||||||
chr2:230239645
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.406+1264C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239645 | ||||||
chr2:230239677
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.406+1296G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239677 | ||||||
chr2:230239764
|
C | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.406+1383C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239764 | ||||||
chr2:230239770
|
T | C | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.406+1389T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239770 | ||||||
chr2:230239775
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.406+1394C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239775 | ||||||
chr2:230239901
|
A | G | 1 | a0007c0017t0001g0053 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.407-1503A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230239901 | ||||||
chr2:230240019
|
G | A | 1 | a0007c0017t0001g0053 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.407-1385G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240019 | ||||||
chr2:230240043
|
A | G | 1 | a0004c0003t0001g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.407-1361A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240043 | ||||||
chr2:230240092
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.407-1312G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240092 | ||||||
chr2:230240129
|
C | T | 3 | a0001c0006t0002g0028a0001c0006t0002g0029a0001c0006t0002g0036 | 3 | HG03453.hp2 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.407-1275C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240129 | ||||||
chr2:230240158
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357 | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-1246A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240158 | ||||||
chr2:230240216
|
AAG | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.407-1184_407-1183d others(4): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 230240216 | |||||
chr2:230240357
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.407-1047C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240357 | ||||||
chr2:230240380
|
C | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.407-1024C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240380 | ||||||
chr2:230240486
|
A | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0144 | 2 | NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.407-918A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240486 | ||||||
chr2:230240512
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 42 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.407-892A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240512 | ||||||
chr2:230240555
|
A | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.407-849A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240555 | ||||||
chr2:230240568
|
CATT | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0268a0001c0001t0001g0274others(24): Show | 28 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.407-831_407-829del others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 230240568 | |||||
chr2:230240782
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407-622A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240782 | ||||||
chr2:230240897
|
C | A | 2 | a0002c0002t0001g0325a0002c0002t0001g0350 | 2 | NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.407-507C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240897 | ||||||
chr2:230240931
|
C | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.407-473C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240931 | ||||||
chr2:230240939
|
A | G | 4 | a0001c0001t0001g0157a0001c0001t0001g0191a0001c0001t0002g0190others(1): Show | 4 | NA18953.hp2 NA18979.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.407-465A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230240939 | ||||||
chr2:230241258
|
C | G | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG01109.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.407-146C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230241258 | ||||||
chr2:230241271
|
A | T | 1 | a0001c0001t0001g0320 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.407-133A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230241271 | ||||||
chr2:230241372
|
G | C | 1 | a0001c0006t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.407-32G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 3/26 | chr2 | 230241372 | ||||||
chr2:230241514
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490+27C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241514 | ||||||
chr2:230241529
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.490+42G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241529 | ||||||
chr2:230241567
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+80C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241567 | ||||||
chr2:230241652
|
G | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0207a0001c0001t0001g0208others(2): Show | 5 | HG02723.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+165G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241652 | ||||||
chr2:230241707
|
A | G | 2 | a0009c0013t0001g0139a0009c0013t0001g0140 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.490+220A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241707 | ||||||
chr2:230241906
|
A | G | 19 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(16): Show | 19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+419A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230241906 | ||||||
chr2:230242009
|
C | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+522C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242009 | ||||||
chr2:230242064
|
G | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0268a0001c0001t0001g0274others(24): Show | 28 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+577G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242064 | ||||||
chr2:230242143
|
G | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+656G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242143 | ||||||
chr2:230242220
|
G | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+733G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242220 | ||||||
chr2:230242229
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490+742G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242229 | ||||||
chr2:230242241
|
ATAAAGAG others(25): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490+756_490+787del others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 230242241 | |||||
chr2:230242270
|
A | AT | 168 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.490+783_490+784ins others(1): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242270 | ||||||
chr2:230242297
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490+810G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242297 | ||||||
chr2:230242339
|
A | AGACAACT others(22): Show |
1 | a0001c0001t0001g0138 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490+853_490+854ins others(29): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr2 | 230242339 | |||||
chr2:230242430
|
G | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.490+943G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242430 | ||||||
chr2:230242537
|
C | T | 31 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0268others(28): Show | 33 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.490+1050C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242537 | ||||||
chr2:230242543
|
T | C | 19 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(16): Show | 19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+1056T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242543 | ||||||
chr2:230242713
|
T | C | 1 | a0002c0002t0001g0326 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.491-1018T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242713 | ||||||
chr2:230242826
|
C | G | 19 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(16): Show | 19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.491-905C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242826 | ||||||
chr2:230242876
|
C | A | 1 | a0001c0006t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.491-855C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230242876 | ||||||
chr2:230243114
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(164): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.491-617G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243114 | ||||||
chr2:230243238
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(145): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.491-493C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243238 | ||||||
chr2:230243413
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(146): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.491-318A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243413 | ||||||
chr2:230243456
|
T | A | 15 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.491-275T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243456 | ||||||
chr2:230243476
|
A | G | 3 | a0003c0005t0003g0185a0003c0005t0003g0186a0003c0005t0003g0201 | 3 | HG01069.hp1 HG01071.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.491-255A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243476 | ||||||
chr2:230243511
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.491-220A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243511 | ||||||
chr2:230243523
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-208G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243523 | ||||||
chr2:230243631
|
A | T | 19 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(16): Show | 19 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.491-100A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243631 | ||||||
chr2:230243725
|
C | T | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.491-6C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 4/26 | chr2 | 230243725 | ||||||
chr2:230244038
|
A | T | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+227A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244038 | ||||||
chr2:230244195
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0136 | 2 | NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.571+384C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244195 | ||||||
chr2:230244213
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(204): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.571+402T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244213 | ||||||
chr2:230244222
|
T | C | 1 | a0001c0006t0001g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.571+411T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244222 | ||||||
chr2:230244553
|
G | A | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.572-435G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244553 | ||||||
chr2:230244591
|
C | A | 2 | a0009c0013t0001g0139a0009c0013t0001g0140 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.572-397C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244591 | ||||||
chr2:230244614
|
T | C | 49 | a0001c0001t0001g0152a0001c0001t0001g0207a0001c0001t0001g0208others(46): Show | 50 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.572-374T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244614 | ||||||
chr2:230244703
|
G | GAAAAGA | 4 | a0002c0002t0001g0325a0002c0002t0001g0327a0002c0002t0001g0328others(1): Show | 4 | NA18978.hp1 NA18982.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-278_572-273dup others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 230244703 | |||||
chr2:230244746
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357 | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-242C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244746 | ||||||
chr2:230244866
|
C | T | 15 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.572-122C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244866 | ||||||
chr2:230244918
|
C | T | 1 | a0004c0003t0001g0355 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.572-70C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244918 | ||||||
chr2:230244931
|
T | A | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.572-57T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244931 | ||||||
chr2:230244939
|
G | T | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.572-49G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244939 | ||||||
chr2:230244944
|
T | C | 1 | a0003c0004t0003g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.572-44T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244944 | ||||||
chr2:230244972
|
C | A | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.572-16C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 5/26 | chr2 | 230244972 | ||||||
chr2:230245125
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.664+45C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245125 | ||||||
chr2:230245284
|
G | T | 6 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.664+204G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245284 | ||||||
chr2:230245538
|
G | A | 1 | a0001c0006t0002g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-325G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245538 | ||||||
chr2:230245692
|
G | A | 2 | a0007c0012t0001g0012a0007c0012t0001g0013 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.665-171G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245692 | ||||||
chr2:230245774
|
C | G | 1 | a0002c0002t0001g0345 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.665-89C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245774 | ||||||
chr2:230245782
|
G | A | 30 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(27): Show | 30 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.665-81G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245782 | ||||||
chr2:230245782
|
G | T | 6 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-81G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 6/26 | chr2 | 230245782 | ||||||
chr2:230246022
|
C | T | 80 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(77): Show | 82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.742+82C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246022 | ||||||
chr2:230246074
|
C | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.742+134C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246074 | ||||||
chr2:230246268
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.742+328A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246268 | ||||||
chr2:230246307
|
C | T | 1 | a0001c0011t0001g0200 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.742+367C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246307 | ||||||
chr2:230246308
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.742+368G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246308 | ||||||
chr2:230246348
|
C | A | 80 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(77): Show | 82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.742+408C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246348 | ||||||
chr2:230246368
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.742+428T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246368 | ||||||
chr2:230246432
|
C | T | 1 | a0003c0005t0003g0104 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.742+492C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246432 | ||||||
chr2:230246707
|
A | G | 86 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(83): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.742+767A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230246707 | ||||||
chr2:230247030
|
C | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.743-886C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247030 | ||||||
chr2:230247057
|
C | G | 80 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(77): Show | 82 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.743-859C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247057 | ||||||
chr2:230247116
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743-800A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247116 | ||||||
chr2:230247180
|
C | T | 30 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(27): Show | 30 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.743-736C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247180 | ||||||
chr2:230247309
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-607C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247309 | ||||||
chr2:230247390
|
A | T | 86 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(83): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.743-526A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247390 | ||||||
chr2:230247540
|
C | T | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.743-376C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247540 | ||||||
chr2:230247653
|
G | A | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-263G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247653 | ||||||
chr2:230247661
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.743-255A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 7/26 | chr2 | 230247661 | ||||||
chr2:230248100
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0002g0206 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.892+35G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248100 | ||||||
chr2:230248219
|
A | G | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892+154A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248219 | ||||||
chr2:230248311
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.892+246A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248311 | ||||||
chr2:230248481
|
T | A | 1 | a0003c0004t0003g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.893-404T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248481 | ||||||
chr2:230248502
|
A | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.893-383A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248502 | ||||||
chr2:230248572
|
A | C | 6 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-313A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248572 | ||||||
chr2:230248663
|
T | A | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-222T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248663 | ||||||
chr2:230248690
|
T | C | 86 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(83): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.893-195T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248690 | ||||||
chr2:230248706
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.893-179C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248706 | ||||||
chr2:230248719
|
A | C | 1 | a0001c0006t0001g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.893-166A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248719 | ||||||
chr2:230248784
|
G | A | 25 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(22): Show | 26 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.893-101G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248784 | ||||||
chr2:230248853
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.893-32C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 8/26 | chr2 | 230248853 | ||||||
chr2:230249062
|
C | T | 5 | a0001c0001t0001g0282a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | NA18957.hp1 NA18989.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+94C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249062 | ||||||
chr2:230249195
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.976+227T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249195 | ||||||
chr2:230249234
|
C | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.976+266C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249234 | ||||||
chr2:230249267
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.976+299C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249267 | ||||||
chr2:230249287
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.976+319A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249287 | ||||||
chr2:230249408
|
T | G | 8 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0103others(5): Show | 8 | HG00558.hp1 HG01169.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.976+440T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249408 | ||||||
chr2:230249416
|
G | A | 31 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(28): Show | 32 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.976+448G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249416 | ||||||
chr2:230249465
|
A | G | 86 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(83): Show | 88 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.976+497A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249465 | ||||||
chr2:230249624
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(236): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.976+656G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249624 | ||||||
chr2:230249738
|
G | A | 84 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(81): Show | 86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.976+770G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249738 | ||||||
chr2:230249768
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.976+800G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249768 | ||||||
chr2:230249878
|
C | G | 78 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(75): Show | 80 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.976+910C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249878 | ||||||
chr2:230249974
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.976+1006C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230249974 | ||||||
chr2:230250005
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.977-976T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250005 | ||||||
chr2:230250028
|
A | T | 1 | a0002c0002t0001g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.977-953A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250028 | ||||||
chr2:230250084
|
A | G | 29 | a0001c0001t0001g0009a0001c0001t0001g0268a0001c0001t0001g0274others(26): Show | 30 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-897A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250084 | ||||||
chr2:230250092
|
C | T | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.977-889C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250092 | ||||||
chr2:230250167
|
C | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(3): Show | 6 | HG00639.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.977-814C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250167 | ||||||
chr2:230250275
|
C | G | 29 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(26): Show | 30 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-706C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250275 | ||||||
chr2:230250280
|
C | T | 29 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(26): Show | 30 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.977-701C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250280 | ||||||
chr2:230250298
|
A | G | 84 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(81): Show | 86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.977-683A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250298 | ||||||
chr2:230250481
|
T | G | 84 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(81): Show | 86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.977-500T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250481 | ||||||
chr2:230250491
|
C | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.977-490C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250491 | ||||||
chr2:230250518
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.977-463A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250518 | ||||||
chr2:230250530
|
C | G | 1 | a0004c0003t0001g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.977-451C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250530 | ||||||
chr2:230250558
|
G | C | 6 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.977-423G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250558 | ||||||
chr2:230250633
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.977-348G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250633 | ||||||
chr2:230250700
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.977-281A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250700 | ||||||
chr2:230250739
|
G | C | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.977-242G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250739 | ||||||
chr2:230250743
|
A | G | 8 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0119others(5): Show | 8 | HG00140.hp2 HG01099.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.977-238A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250743 | ||||||
chr2:230250809
|
A | T | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.977-172A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250809 | ||||||
chr2:230250888
|
T | C | 85 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(82): Show | 87 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.977-93T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250888 | ||||||
chr2:230250915
|
A | T | 30 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(27): Show | 31 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.977-66A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 9/26 | chr2 | 230250915 | ||||||
chr2:230251075
|
G | A | 21 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(18): Show | 22 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1057+14G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251075 | ||||||
chr2:230251170
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1057+109A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251170 | ||||||
chr2:230251261
|
C | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1057+200C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251261 | ||||||
chr2:230251265
|
A | G | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG01081.hp2 HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1057+204A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251265 | ||||||
chr2:230251304
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1057+243C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251304 | ||||||
chr2:230251442
|
C | A | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1057+381C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251442 | ||||||
chr2:230251508
|
C | T | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1057+447C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251508 | ||||||
chr2:230251645
|
T | C | 40 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(37): Show | 41 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1057+584T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251645 | ||||||
chr2:230251702
|
T | A | 30 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(27): Show | 31 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1057+641T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251702 | ||||||
chr2:230251805
|
C | T | 1 | a0005c0007t0001g0004 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1057+744C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251805 | ||||||
chr2:230251862
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1057+801C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230251862 | ||||||
chr2:230252080
|
T | A | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1057+1019T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252080 | ||||||
chr2:230252159
|
C | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1057+1098C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252159 | ||||||
chr2:230252271
|
A | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(3): Show | 6 | HG00639.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058-1045A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252271 | ||||||
chr2:230252396
|
G | A | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1058-920G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252396 | ||||||
chr2:230252418
|
C | A | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1058-898C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252418 | ||||||
chr2:230252421
|
G | A | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1058-895G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252421 | ||||||
chr2:230252454
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1058-862G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252454 | ||||||
chr2:230252751
|
T | TAGAAAAG others(318): Show |
3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1058-548_1058-547i others(327): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 230252751 | |||||
chr2:230252770
|
A | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(181): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1058-546A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252770 | ||||||
chr2:230252800
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(180): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1058-516G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252800 | ||||||
chr2:230252810
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(180): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1058-506G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252810 | ||||||
chr2:230252812
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(176): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1058-504C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252812 | ||||||
chr2:230252832
|
G | A | 52 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(49): Show | 53 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1058-484G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252832 | ||||||
chr2:230252864
|
G | T | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1058-452G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252864 | ||||||
chr2:230252952
|
C | T | 40 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(37): Show | 41 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1058-364C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230252952 | ||||||
chr2:230253049
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1058-267A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253049 | ||||||
chr2:230253155
|
C | T | 6 | a0004c0003t0001g0045a0004c0003t0001g0227a0004c0003t0001g0269others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058-161C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253155 | ||||||
chr2:230253156
|
G | A | 2 | a0001c0001t0002g0239a0001c0001t0002g0252 | 2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1058-160G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253156 | ||||||
chr2:230253209
|
A | G | 1 | a0012c0015t0001g0318 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1058-107A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253209 | ||||||
chr2:230253286
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1058-30G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 10/26 | chr2 | 230253286 | ||||||
chr2:230253432
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1159+15C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253432 | ||||||
chr2:230253471
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1159+54G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253471 | ||||||
chr2:230253655
|
C | G | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1159+238C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253655 | ||||||
chr2:230253727
|
C | T | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1159+310C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253727 | ||||||
chr2:230253832
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1159+415G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253832 | ||||||
chr2:230253947
|
T | G | 1 | a0002c0008t0001g0329 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1159+530T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230253947 | ||||||
chr2:230254050
|
A | G | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+633A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254050 | ||||||
chr2:230254071
|
C | G | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159+654C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254071 | ||||||
chr2:230254169
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1159+752A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254169 | ||||||
chr2:230254177
|
A | G | 1 | a0001c0001t0001g0356 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1159+760A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254177 | ||||||
chr2:230254185
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1159+768A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254185 | ||||||
chr2:230254311
|
A | G | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1159+894A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254311 | ||||||
chr2:230254317
|
A | G | 1 | a0002c0002t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1159+900A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254317 | ||||||
chr2:230254395
|
C | A | 9 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0312others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+978C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254395 | ||||||
chr2:230254549
|
C | T | 55 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(52): Show | 56 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1160-903C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254549 | ||||||
chr2:230254848
|
C | T | 1 | a0003c0004t0003g0016 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1160-604C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254848 | ||||||
chr2:230254849
|
A | G | 1 | a0003c0004t0003g0016 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1160-603A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254849 | ||||||
chr2:230254952
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1160-500C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254952 | ||||||
chr2:230254968
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1160-484T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254968 | ||||||
chr2:230254984
|
C | G | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1160-468C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230254984 | ||||||
chr2:230255075
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1160-377T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255075 | ||||||
chr2:230255199
|
G | C | 24 | a0001c0001t0005g0122a0001c0006t0001g0023a0001c0006t0001g0025others(21): Show | 25 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1160-253G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255199 | ||||||
chr2:230255295
|
G | A | 1 | a0012c0015t0001g0318 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1160-157G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255295 | ||||||
chr2:230255327
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0193others(1): Show | 4 | HG02148.hp1 HG02602.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-125C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255327 | ||||||
chr2:230255353
|
G | A | 1 | a0002c0002t0001g0354 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1160-99G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255353 | ||||||
chr2:230255437
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1160-15C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 11/26 | chr2 | 230255437 | ||||||
chr2:230255540
|
CG | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(266): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1240+18delG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230255540 | |||||
chr2:230255540
|
CGG | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(61): Show | 65 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1240+17_1240+18del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230255540 | |||||
chr2:230255542
|
G | C | 4 | a0001c0001t0001g0211a0003c0005t0003g0006a0003c0005t0003g0216others(1): Show | 5 | HG01175.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+10G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255542 | ||||||
chr2:230255543
|
G | C | 11 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0001g0159others(8): Show | 11 | NA18940.hp2 NA18944.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240+11G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255543 | ||||||
chr2:230255543
|
G | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(54): Show | 58 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1240+11G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255543 | ||||||
chr2:230255544
|
G | C | 2 | a0001c0001t0001g0226a0003c0004t0010g0021 | 2 | HG06807.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1240+12G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255544 | ||||||
chr2:230255547
|
G | A | 1 | a0002c0002t0001g0348 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1240+15G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255547 | ||||||
chr2:230255548
|
G | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+16G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255548 | ||||||
chr2:230255549
|
G | T | 1 | a0012c0015t0001g0318 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+17G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230255549 | ||||||
chr2:230256004
|
C | T | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240+472C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256004 | ||||||
chr2:230256031
|
T | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(353): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1240+499T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256031 | ||||||
chr2:230256083
|
A | C | 1 | a0004c0003t0001g0355 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1240+551A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256083 | ||||||
chr2:230256287
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1240+755T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256287 | ||||||
chr2:230256287
|
T | G | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+755T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256287 | ||||||
chr2:230256344
|
TA | T | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+818delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230256344 | |||||
chr2:230256367
|
TTTGTAGG others(2): Show |
T | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+836_1240+844d others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256367 | ||||||
chr2:230256380
|
G | C | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+848G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256380 | ||||||
chr2:230256381
|
G | A | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+849G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256381 | ||||||
chr2:230256382
|
A | T | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+850A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256382 | ||||||
chr2:230256383
|
TGA | T | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+852_1240+853d others(4): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256383 | ||||||
chr2:230256386
|
A | T | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+854A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256386 | ||||||
chr2:230256482
|
T | C | 1 | a0002c0002t0001g0330 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+950T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256482 | ||||||
chr2:230256523
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1240+991T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256523 | ||||||
chr2:230256528
|
T | TG | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240+1001dupG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230256528 | |||||
chr2:230256534
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1240+1002A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256534 | ||||||
chr2:230256569
|
G | A | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1037G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256569 | ||||||
chr2:230256786
|
G | T | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1240+1254G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256786 | ||||||
chr2:230256791
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0203 | 2 | HG01257.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1240+1259T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256791 | ||||||
chr2:230256874
|
G | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+1342G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256874 | ||||||
chr2:230256913
|
T | C | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1381T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256913 | ||||||
chr2:230256965
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | NA18946.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1240+1433T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230256965 | ||||||
chr2:230257114
|
T | C | 62 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(59): Show | 63 | HG00140.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1240+1582T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257114 | ||||||
chr2:230257259
|
C | T | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1727C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257259 | ||||||
chr2:230257279
|
C | A | 3 | a0003c0004t0003g0030a0003c0004t0003g0031a0003c0004t0003g0032 | 3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1240+1747C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257279 | ||||||
chr2:230257342
|
T | G | 27 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(24): Show | 28 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+1810T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257342 | ||||||
chr2:230257374
|
CAGTA | C | 27 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(24): Show | 28 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+1845_1240+184 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230257374 | |||||
chr2:230257486
|
G | A | 38 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(35): Show | 38 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1240+1954G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257486 | ||||||
chr2:230257495
|
A | G | 66 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(63): Show | 67 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1240+1963A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257495 | ||||||
chr2:230257575
|
G | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1240+2043G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257575 | ||||||
chr2:230257650
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1240+2118C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257650 | ||||||
chr2:230257703
|
G | A | 4 | a0003c0005t0003g0162a0003c0005t0003g0185a0003c0005t0003g0186others(1): Show | 4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+2171G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257703 | ||||||
chr2:230257706
|
G | A | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1240+2174G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257706 | ||||||
chr2:230257792
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1240+2260C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257792 | ||||||
chr2:230257801
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1240+2269A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257801 | ||||||
chr2:230257833
|
G | A | 7 | a0004c0003t0001g0275a0004c0003t0001g0310a0004c0003t0001g0311others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+2301G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257833 | ||||||
chr2:230257910
|
C | T | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+2378C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257910 | ||||||
chr2:230257919
|
A | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0089 | 4 | HG02040.hp2 NA18957.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+2387A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230257919 | ||||||
chr2:230258227
|
T | G | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+2695T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258227 | ||||||
chr2:230258429
|
T | A | 7 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(4): Show | 7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+2897T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258429 | ||||||
chr2:230258527
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0145 | 2 | NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1240+2995T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258527 | ||||||
chr2:230258556
|
T | C | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+3024T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258556 | ||||||
chr2:230258649
|
T | G | 38 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(35): Show | 39 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1240+3117T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258649 | ||||||
chr2:230258745
|
A | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(56): Show | 62 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1240+3213A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258745 | ||||||
chr2:230258887
|
A | C | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+3355A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258887 | ||||||
chr2:230258895
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1240+3363G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258895 | ||||||
chr2:230258898
|
C | CT | 17 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 18 | HG00639.hp2 HG01106.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+3378dupT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230258898 | |||||
chr2:230258937
|
T | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0148a0001c0001t0001g0152others(8): Show | 12 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240+3405T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230258937 | ||||||
chr2:230259004
|
A | G | 42 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(39): Show | 43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1240+3472A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259004 | ||||||
chr2:230259081
|
GTTTA | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+3569_1240+357 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259081 | |||||
chr2:230259115
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+3583G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259115 | ||||||
chr2:230259194
|
A | G | 4 | a0001c0001t0005g0122a0007c0012t0001g0012a0007c0012t0001g0013others(1): Show | 4 | HG00323.hp2 HG01243.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+3662A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259194 | ||||||
chr2:230259211
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+3679C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259211 | ||||||
chr2:230259398
|
C | A | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1240+3866C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259398 | ||||||
chr2:230259405
|
C | T | 1 | a0004c0003t0001g0352 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1240+3873C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259405 | ||||||
chr2:230259430
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+3898C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259430 | ||||||
chr2:230259506
|
C | T | 7 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(4): Show | 7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+3974C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259506 | ||||||
chr2:230259512
|
C | T | 1 | a0001c0001t0004g0255 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1240+3980C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259512 | ||||||
chr2:230259515
|
TA | T | 27 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(24): Show | 28 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+3996delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259515 | |||||
chr2:230259612
|
G | A | 2 | a0001c0001t0001g0211a0012c0015t0001g0318 | 2 | HG03486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1240+4080G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259612 | ||||||
chr2:230259617
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4085G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259617 | ||||||
chr2:230259673
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0109others(11): Show | 14 | HG00558.hp1 HG01169.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240+4141C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259673 | ||||||
chr2:230259686
|
C | CA | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+4165dupA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259686 | |||||
chr2:230259686
|
CA | C | 7 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0095others(4): Show | 7 | HG02040.hp1 HG02080.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+4165delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259686 | |||||
chr2:230259726
|
A | G | 1 | a0001c0001t0002g0249 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1240+4194A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259726 | ||||||
chr2:230259770
|
TCATATAT others(20): Show |
T | 49 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 51 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1240+4241_1240+426 others(31): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259770 | |||||
chr2:230259771
|
C | CAT | 93 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1240+4263_1240+426 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATAT | 17 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0189others(14): Show | 17 | HG01109.hp2 HG01123.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1240+4261_1240+426 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATAT | 5 | a0001c0001t0001g0212a0001c0006t0001g0038a0001c0006t0001g0039others(2): Show | 5 | HG01361.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4259_1240+426 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(3): Show |
1 | a0012c0015t0001g0318 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+4255_1240+426 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(5): Show |
3 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0357 | 3 | HG03490.hp1 HG03492.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1240+4253_1240+426 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(7): Show |
9 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0224others(6): Show | 9 | HG00735.hp2 HG02074.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+4251_1240+426 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(9): Show |
17 | a0001c0001t0001g0009a0001c0001t0001g0199a0001c0001t0001g0282others(14): Show | 18 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+4249_1240+426 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(11): Show |
12 | a0001c0001t0001g0193a0001c0001t0001g0204a0001c0001t0001g0317others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240+4247_1240+426 others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(13): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0194a0001c0001t0001g0291others(10): Show | 15 | HG00323.hp2 HG00639.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+4245_1240+426 others(24): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(15): Show |
3 | a0001c0006t0001g0027a0003c0004t0003g0019a0007c0012t0001g0013 | 3 | HG00738.hp2 HG01358.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+4243_1240+426 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(17): Show |
7 | a0001c0001t0001g0293a0001c0001t0001g0304a0001c0006t0001g0037others(4): Show | 7 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+4241_1240+426 others(28): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(19): Show |
1 | a0001c0006t0001g0026 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1240+4264_1240+426 others(30): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(21): Show |
7 | a0001c0001t0001g0294a0001c0001t0001g0296a0003c0004t0003g0030others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+4264_1240+426 others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259771
|
C | CATATATA others(23): Show |
5 | a0001c0006t0002g0029a0001c0006t0002g0036a0003c0004t0003g0031others(2): Show | 5 | HG01123.hp1 HG01169.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4264_1240+426 others(34): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230259771 | |||||
chr2:230259805
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4273A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259805 | ||||||
chr2:230259847
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4315G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259847 | ||||||
chr2:230259856
|
G | C | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4324G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259856 | ||||||
chr2:230259959
|
G | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 51 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1240+4427G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230259959 | ||||||
chr2:230260037
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1240+4505G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260037 | ||||||
chr2:230260060
|
C | T | 1 | a0004c0003t0001g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1240+4528C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260060 | ||||||
chr2:230260061
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+4529A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260061 | ||||||
chr2:230260112
|
T | A | 46 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240+4580T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260112 | ||||||
chr2:230260134
|
C | A | 5 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4602C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260134 | ||||||
chr2:230260147
|
G | T | 42 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 44 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1240+4615G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260147 | ||||||
chr2:230260158
|
T | C | 2 | a0001c0001t0002g0238a0001c0001t0002g0248 | 2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1240+4626T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260158 | ||||||
chr2:230260188
|
T | C | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+4656T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260188 | ||||||
chr2:230260311
|
T | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+4779T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260311 | ||||||
chr2:230260369
|
A | G | 3 | a0003c0004t0003g0030a0003c0004t0003g0031a0003c0004t0003g0032 | 3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1240+4837A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260369 | ||||||
chr2:230260520
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+4988G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260520 | ||||||
chr2:230260781
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(90): Show | 96 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1240+5249G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260781 | ||||||
chr2:230260814
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1240+5282C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260814 | ||||||
chr2:230260870
|
G | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(38): Show | 43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1240+5338G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260870 | ||||||
chr2:230260872
|
G | C | 46 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1240+5340G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260872 | ||||||
chr2:230260972
|
T | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 52 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1240+5440T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260972 | ||||||
chr2:230260987
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 52 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1240+5455T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230260987 | ||||||
chr2:230261105
|
A | G | 7 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(4): Show | 7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+5573A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261105 | ||||||
chr2:230261265
|
G | A | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+5733G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261265 | ||||||
chr2:230261547
|
G | A | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1240+6015G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261547 | ||||||
chr2:230261612
|
C | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0242a0001c0001t0001g0244others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1240+6080C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261612 | ||||||
chr2:230261725
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1240+6193T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261725 | ||||||
chr2:230261727
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+6195T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261727 | ||||||
chr2:230261813
|
G | A | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1240+6281G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261813 | ||||||
chr2:230261819
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1240+6287G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261819 | ||||||
chr2:230261848
|
A | C | 4 | a0001c0006t0002g0028a0001c0006t0002g0029a0001c0006t0002g0036others(1): Show | 4 | HG03453.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+6316A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261848 | ||||||
chr2:230261923
|
C | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0242a0001c0001t0001g0244others(85): Show | 90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1240+6391C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261923 | ||||||
chr2:230261924
|
T | C | 1 | a0004c0003t0001g0310 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1240+6392T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261924 | ||||||
chr2:230261934
|
C | T | 5 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+6402C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230261934 | ||||||
chr2:230262000
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+6468A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262000 | ||||||
chr2:230262279
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1240+6747C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262279 | ||||||
chr2:230262397
|
C | G | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+6865C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262397 | ||||||
chr2:230262413
|
C | T | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+6881C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262413 | ||||||
chr2:230262511
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1240+6979G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262511 | ||||||
chr2:230262563
|
A | G | 36 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(33): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-6969A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262563 | ||||||
chr2:230262578
|
G | A | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1241-6954G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262578 | ||||||
chr2:230262667
|
A | G | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241-6865A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262667 | ||||||
chr2:230262705
|
C | T | 1 | a0004c0003t0001g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1241-6827C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262705 | ||||||
chr2:230262718
|
A | G | 38 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(35): Show | 38 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1241-6814A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262718 | ||||||
chr2:230262911
|
G | C | 2 | a0004c0003t0001g0312a0004c0003t0001g0313 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1241-6621G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262911 | ||||||
chr2:230262960
|
T | C | 1 | a0003c0004t0003g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1241-6572T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230262960 | ||||||
chr2:230263009
|
A | T | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1241-6523A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263009 | ||||||
chr2:230263172
|
G | A | 38 | a0001c0001t0001g0048a0002c0002t0001g0010a0002c0002t0001g0147others(35): Show | 39 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1241-6360G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263172 | ||||||
chr2:230263202
|
G | A | 2 | a0001c0001t0001g0199a0004c0003t0001g0275 | 2 | HG00280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1241-6330G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263202 | ||||||
chr2:230263279
|
C | A | 1 | a0003c0005t0003g0006 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1241-6253C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263279 | ||||||
chr2:230263346
|
G | A | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1241-6186G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263346 | ||||||
chr2:230263464
|
T | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(44): Show | 50 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1241-6068T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263464 | ||||||
chr2:230263716
|
C | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-5816C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263716 | ||||||
chr2:230263808
|
C | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0242a0001c0001t0001g0244others(85): Show | 90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1241-5724C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263808 | ||||||
chr2:230263911
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-5621T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263911 | ||||||
chr2:230263942
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1241-5590T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263942 | ||||||
chr2:230263952
|
C | T | 1 | a0002c0002t0001g0348 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1241-5580C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230263952 | ||||||
chr2:230264700
|
G | T | 4 | a0001c0006t0002g0028a0001c0006t0002g0029a0001c0006t0002g0036others(1): Show | 4 | HG03453.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-4832G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264700 | ||||||
chr2:230264748
|
G | T | 1 | a0008c0010t0001g0111 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1241-4784G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264748 | ||||||
chr2:230264760
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1241-4772C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264760 | ||||||
chr2:230264874
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1241-4658G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230264874 | ||||||
chr2:230265014
|
C | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1241-4518C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265014 | ||||||
chr2:230265015
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(132): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1241-4517A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265015 | ||||||
chr2:230265079
|
C | T | 33 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(30): Show | 34 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1241-4453C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265079 | ||||||
chr2:230265101
|
G | C | 38 | a0001c0001t0005g0122a0002c0002t0001g0010a0002c0002t0001g0147others(35): Show | 39 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1241-4431G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265101 | ||||||
chr2:230265123
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-4409G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265123 | ||||||
chr2:230265162
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1241-4370G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265162 | ||||||
chr2:230265442
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1241-4090G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265442 | ||||||
chr2:230265459
|
G | A | 6 | a0001c0001t0001g0274a0001c0001t0001g0282a0001c0001t0001g0298others(3): Show | 6 | NA18957.hp1 NA18986.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-4073G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265459 | ||||||
chr2:230265468
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-4064G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265468 | ||||||
chr2:230265585
|
T | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(55): Show | 60 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1241-3947T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265585 | ||||||
chr2:230265723
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1241-3809G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265723 | ||||||
chr2:230265790
|
CG | C | 111 | a0001c0001t0001g0011a0001c0001t0001g0148a0001c0001t0001g0152others(108): Show | 114 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1241-3733delG | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230265790 | |||||
chr2:230265793
|
G | T | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-3739G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265793 | ||||||
chr2:230265794
|
G | GT | 46 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(43): Show | 47 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1241-3738_1241-373 others(5): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265794 | ||||||
chr2:230265837
|
C | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0184a0001c0001t0001g0218 | 3 | NA18949.hp2 NA18983.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1241-3695C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265837 | ||||||
chr2:230265874
|
G | A | 2 | a0009c0013t0001g0139a0009c0013t0001g0140 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1241-3658G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230265874 | ||||||
chr2:230266012
|
T | C | 38 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(35): Show | 38 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1241-3520T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266012 | ||||||
chr2:230266172
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(129): Show | 136 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1241-3360C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266172 | ||||||
chr2:230266246
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1241-3286G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266246 | ||||||
chr2:230266306
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(58): Show | 63 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1241-3226A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266306 | ||||||
chr2:230266360
|
A | G | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-3172A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266360 | ||||||
chr2:230266431
|
A | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0242a0001c0001t0001g0244others(39): Show | 43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1241-3101A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266431 | ||||||
chr2:230266611
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1241-2921C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266611 | ||||||
chr2:230266659
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1241-2873C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266659 | ||||||
chr2:230266672
|
G | A | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-2860G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266672 | ||||||
chr2:230266806
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1241-2726A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266806 | ||||||
chr2:230266894
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1241-2638A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266894 | ||||||
chr2:230266988
|
C | G | 5 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-2544C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230266988 | ||||||
chr2:230267029
|
C | G | 2 | a0003c0005t0003g0098a0003c0005t0003g0104 | 2 | HG00140.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1241-2503C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267029 | ||||||
chr2:230267030
|
T | G | 2 | a0003c0005t0003g0098a0003c0005t0003g0104 | 2 | HG00140.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1241-2502T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267030 | ||||||
chr2:230267200
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1241-2332T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267200 | ||||||
chr2:230267382
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-2150T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267382 | ||||||
chr2:230267435
|
G | T | 4 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258others(1): Show | 4 | HG02717.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-2097G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267435 | ||||||
chr2:230267526
|
G | C | 9 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0230others(6): Show | 9 | HG00423.hp1 NA18943.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-2006G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267526 | ||||||
chr2:230267702
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1241-1830G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267702 | ||||||
chr2:230267844
|
T | G | 2 | a0001c0001t0001g0356a0004c0003t0001g0227 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1241-1688T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267844 | ||||||
chr2:230267885
|
A | T | 14 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(11): Show | 14 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1241-1647A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267885 | ||||||
chr2:230267908
|
A | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1241-1624A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230267908 | ||||||
chr2:230268006
|
C | T | 3 | a0003c0004t0003g0033a0003c0004t0003g0034a0003c0004t0003g0035 | 3 | HG01123.hp1 HG01433.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1241-1526C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268006 | ||||||
chr2:230268245
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1241-1287C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268245 | ||||||
chr2:230268279
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1241-1253T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268279 | ||||||
chr2:230268406
|
C | G | 6 | a0001c0001t0001g0274a0001c0001t0001g0282a0001c0001t0001g0298others(3): Show | 6 | NA18957.hp1 NA18986.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-1126C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268406 | ||||||
chr2:230268450
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(105): Show | 111 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1241-1082A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268450 | ||||||
chr2:230268524
|
T | TA | 10 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(7): Show | 10 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-993dupA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230268524 | |||||
chr2:230268663
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1241-869T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268663 | ||||||
chr2:230268813
|
T | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 43 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1241-719T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268813 | ||||||
chr2:230268863
|
C | T | 3 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020 | 3 | HG00738.hp2 HG01496.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1241-669C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230268863 | ||||||
chr2:230269144
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-388A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | chr2 | 230269144 | ||||||
chr2:230269363
|
AGCGTG | A | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-166_1241-162d others(7): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 230269363 | |||||
chr2:230270395
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-191T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 14/26 | chr2 | 230270395 | ||||||
chr2:230270852
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1498+213A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230270852 | ||||||
chr2:230270947
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 84 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1498+308A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230270947 | ||||||
chr2:230271350
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1498+711G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271350 | ||||||
chr2:230271362
|
G | C | 5 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 5 | HG02486.hp2 HG03209.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+723G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271362 | ||||||
chr2:230271372
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+733G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271372 | ||||||
chr2:230271442
|
G | A | 1 | a0007c0017t0001g0053 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1498+803G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271442 | ||||||
chr2:230271644
|
G | A | 3 | a0003c0004t0003g0030a0003c0004t0003g0031a0003c0004t0003g0032 | 3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1498+1005G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271644 | ||||||
chr2:230271686
|
G | A | 4 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498+1047G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271686 | ||||||
chr2:230271912
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+1273G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271912 | ||||||
chr2:230271958
|
T | A | 1 | a0001c0001t0001g0316 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1498+1319T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230271958 | ||||||
chr2:230272248
|
G | C | 1 | a0001c0006t0001g0037 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1498+1609G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272248 | ||||||
chr2:230272303
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1498+1664C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272303 | ||||||
chr2:230272446
|
G | A | 5 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0321others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+1807G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272446 | ||||||
chr2:230272627
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0136 | 2 | NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1498+1988A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272627 | ||||||
chr2:230272834
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0138 | 2 | NA18981.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1498+2195G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230272834 | ||||||
chr2:230273328
|
C | A | 5 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0321others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+2689C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273328 | ||||||
chr2:230273368
|
G | A | 5 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0321others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+2729G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273368 | ||||||
chr2:230273489
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1498+2850C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273489 | ||||||
chr2:230273530
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1498+2891C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273530 | ||||||
chr2:230273649
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1498+3010A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273649 | ||||||
chr2:230273830
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0301 | 2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1498+3191A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230273830 | ||||||
chr2:230274041
|
T | C | 10 | a0001c0001t0004g0255a0001c0001t0004g0322a0004c0003t0001g0312others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1498+3402T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274041 | ||||||
chr2:230274094
|
T | G | 2 | a0009c0013t0001g0139a0009c0013t0001g0140 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1498+3455T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274094 | ||||||
chr2:230274111
|
TA | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1498+3487delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230274111 | |||||
chr2:230274111
|
TAA | T | 61 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(58): Show | 63 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1498+3486_1498+348 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230274111 | |||||
chr2:230274478
|
T | C | 3 | a0001c0001t0004g0255a0001c0001t0004g0322a0010c0018t0001g0254 | 3 | HG02572.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1498+3839T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274478 | ||||||
chr2:230274610
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0006g0087 | 2 | NA18951.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1498+3971C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274610 | ||||||
chr2:230274645
|
G | A | 1 | a0002c0002t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1498+4006G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274645 | ||||||
chr2:230274655
|
A | T | 1 | a0001c0001t0002g0247 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1498+4016A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274655 | ||||||
chr2:230274664
|
A | T | 1 | a0002c0002t0001g0343 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1498+4025A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274664 | ||||||
chr2:230274667
|
C | T | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+4028C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274667 | ||||||
chr2:230274792
|
T | G | 3 | a0007c0012t0001g0012a0007c0012t0001g0013a0007c0017t0001g0053 | 3 | HG00323.hp2 HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1498+4153T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274792 | ||||||
chr2:230274803
|
C | T | 7 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(4): Show | 7 | HG00639.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498+4164C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230274803 | ||||||
chr2:230275062
|
T | C | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+4423T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275062 | ||||||
chr2:230275070
|
G | A | 1 | a0005c0007t0001g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1498+4431G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275070 | ||||||
chr2:230275199
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+4560T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275199 | ||||||
chr2:230275305
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+4666G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275305 | ||||||
chr2:230275307
|
C | CA | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1498+4675dupA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230275307 | |||||
chr2:230275342
|
A | G | 3 | a0003c0004t0003g0030a0003c0004t0003g0031a0003c0004t0003g0032 | 3 | HG01169.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1498+4703A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275342 | ||||||
chr2:230275350
|
AC | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+4712delC | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275350 | ||||||
chr2:230275497
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1498+4858G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275497 | ||||||
chr2:230275505
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498+4866T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275505 | ||||||
chr2:230275546
|
C | A | 1 | a0007c0012t0001g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1498+4907C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275546 | ||||||
chr2:230275785
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1498+5146A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275785 | ||||||
chr2:230275859
|
G | T | 2 | a0002c0002t0001g0344a0008c0019t0001g0022 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1498+5220G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275859 | ||||||
chr2:230275968
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+5329G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230275968 | ||||||
chr2:230276452
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1498+5813T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276452 | ||||||
chr2:230276481
|
C | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 32 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1498+5842C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276481 | ||||||
chr2:230276646
|
AAC | A | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1498+6011_1498+601 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230276646 | |||||
chr2:230276773
|
A | T | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1498+6134A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276773 | ||||||
chr2:230276857
|
C | G | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1498+6218C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276857 | ||||||
chr2:230276938
|
T | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | HG00673.hp2 HG02015.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498+6299T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230276938 | ||||||
chr2:230277260
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+6621C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277260 | ||||||
chr2:230277350
|
A | G | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498+6711A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277350 | ||||||
chr2:230277382
|
T | C | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1498+6743T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277382 | ||||||
chr2:230277427
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1498+6788C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277427 | ||||||
chr2:230277565
|
A | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03130.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1499-6781A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277565 | ||||||
chr2:230277804
|
G | A | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1499-6542G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230277804 | ||||||
chr2:230278274
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1499-6072G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278274 | ||||||
chr2:230278514
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1499-5832A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278514 | ||||||
chr2:230278573
|
C | G | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-5773C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278573 | ||||||
chr2:230278607
|
C | G | 1 | a0001c0001t0002g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1499-5739C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278607 | ||||||
chr2:230278731
|
T | A | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-5615T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278731 | ||||||
chr2:230278785
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-5561C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278785 | ||||||
chr2:230278924
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1499-5422C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278924 | ||||||
chr2:230278985
|
G | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0226 | 2 | HG01361.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1499-5361G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230278985 | ||||||
chr2:230279260
|
A | G | 2 | a0001c0001t0002g0239a0001c0001t0002g0252 | 2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1499-5086A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279260 | ||||||
chr2:230279388
|
G | C | 1 | a0008c0019t0001g0022 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1499-4958G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279388 | ||||||
chr2:230279513
|
T | C | 4 | a0002c0002t0001g0149a0002c0002t0001g0324a0002c0002t0001g0326others(1): Show | 4 | HG00408.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1499-4833T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279513 | ||||||
chr2:230279838
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1499-4508A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230279838 | ||||||
chr2:230279863
|
TCCTCCTG | T | 34 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(31): Show | 35 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1499-4478_1499-447 others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 230279863 | |||||
chr2:230280114
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1499-4232G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280114 | ||||||
chr2:230280220
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-4126A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280220 | ||||||
chr2:230280233
|
AT | A | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-4112delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280233 | ||||||
chr2:230280287
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1499-4059G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280287 | ||||||
chr2:230280363
|
C | T | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-3983C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280363 | ||||||
chr2:230280458
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1499-3888G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280458 | ||||||
chr2:230280469
|
A | G | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-3877A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280469 | ||||||
chr2:230280478
|
C | A | 5 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(2): Show | 5 | HG00639.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-3868C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280478 | ||||||
chr2:230280532
|
C | T | 4 | a0003c0005t0003g0162a0003c0005t0003g0185a0003c0005t0003g0186others(1): Show | 4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-3814C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280532 | ||||||
chr2:230280713
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1499-3633G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280713 | ||||||
chr2:230280793
|
C | T | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1499-3553C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280793 | ||||||
chr2:230280950
|
T | C | 1 | a0002c0002t0001g0324 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1499-3396T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230280950 | ||||||
chr2:230281160
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-3186G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230281160 | ||||||
chr2:230281710
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1499-2636T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230281710 | ||||||
chr2:230282313
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-2033G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282313 | ||||||
chr2:230282354
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-1992C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282354 | ||||||
chr2:230282528
|
G | A | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-1818G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282528 | ||||||
chr2:230282618
|
T | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(167): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1499-1728T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282618 | ||||||
chr2:230282674
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0081 | 2 | NA18944.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1499-1672C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282674 | ||||||
chr2:230282809
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1499-1537G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282809 | ||||||
chr2:230282809
|
G | C | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-1537G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230282809 | ||||||
chr2:230283060
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1499-1286C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283060 | ||||||
chr2:230283168
|
G | A | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1178G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283168 | ||||||
chr2:230283196
|
C | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(260): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1499-1150C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283196 | ||||||
chr2:230283222
|
A | G | 6 | a0004c0003t0001g0310a0004c0003t0001g0311a0004c0003t0001g0315others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1124A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283222 | ||||||
chr2:230283294
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1499-1052A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283294 | ||||||
chr2:230283413
|
A | G | 29 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(26): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1499-933A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283413 | ||||||
chr2:230283560
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(1): Show | 4 | HG00639.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-786G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283560 | ||||||
chr2:230283751
|
A | G | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1499-595A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283751 | ||||||
chr2:230283766
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1499-580A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283766 | ||||||
chr2:230283795
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1499-551C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230283795 | ||||||
chr2:230284023
|
A | T | 1 | a0002c0002t0001g0345 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1499-323A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284023 | ||||||
chr2:230284064
|
A | C | 45 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0207others(42): Show | 45 | HG00423.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1499-282A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284064 | ||||||
chr2:230284123
|
G | A | 37 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(34): Show | 37 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1499-223G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284123 | ||||||
chr2:230284172
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-174G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284172 | ||||||
chr2:230284173
|
G | T | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-173G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284173 | ||||||
chr2:230284181
|
T | G | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-165T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284181 | ||||||
chr2:230284182
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1499-164A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 15/26 | chr2 | 230284182 | ||||||
chr2:230284510
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0119 | 2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1564+99T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284510 | ||||||
chr2:230284655
|
C | T | 2 | a0002c0002t0001g0149a0002c0002t0001g0332 | 2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1564+244C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284655 | ||||||
chr2:230284834
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1564+423A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284834 | ||||||
chr2:230284856
|
A | G | 1 | a0001c0006t0001g0027 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1564+445A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284856 | ||||||
chr2:230284924
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+513T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230284924 | ||||||
chr2:230285252
|
C | G | 10 | a0001c0001t0004g0255a0001c0001t0004g0322a0004c0003t0001g0312others(7): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1565-500C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285252 | ||||||
chr2:230285337
|
T | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0182a0001c0001t0001g0183others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1565-415T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285337 | ||||||
chr2:230285378
|
G | A | 2 | a0001c0001t0001g0356a0004c0003t0001g0227 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1565-374G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285378 | ||||||
chr2:230285433
|
G | A | 1 | a0001c0001t0001g0005 | 2 | NA18957.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1565-319G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285433 | ||||||
chr2:230285676
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1565-76C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285676 | ||||||
chr2:230285683
|
G | A | 5 | a0004c0003t0001g0045a0004c0003t0001g0269a0004c0003t0001g0270others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1565-69G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 16/26 | chr2 | 230285683 | ||||||
chr2:230285851
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1645+19G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230285851 | ||||||
chr2:230285934
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1645+102G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230285934 | ||||||
chr2:230285969
|
G | T | 5 | a0001c0001t0004g0255a0001c0001t0004g0322a0004c0003t0001g0312others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645+137G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230285969 | ||||||
chr2:230286091
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(115): Show | 122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1645+259C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286091 | ||||||
chr2:230286138
|
G | A | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1645+306G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286138 | ||||||
chr2:230286216
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1645+384C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286216 | ||||||
chr2:230286231
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1645+399T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286231 | ||||||
chr2:230286263
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645+431T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286263 | ||||||
chr2:230286292
|
A | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0249 | 2 | HG02109.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1645+460A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286292 | ||||||
chr2:230286295
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | NA18956.hp2 NA19063.hp2 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645+463A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286295 | ||||||
chr2:230286300
|
T | C | 4 | a0001c0001t0002g0206a0001c0001t0002g0246a0001c0001t0002g0247others(1): Show | 4 | HG02109.hp2 HG03130.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645+468T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286300 | ||||||
chr2:230286398
|
T | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0088 | 2 | HG02040.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1645+566T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286398 | ||||||
chr2:230286431
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1645+599G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286431 | ||||||
chr2:230286491
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1645+659G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230286491 | ||||||
chr2:230287028
|
C | T | 151 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(148): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1646-864C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287028 | ||||||
chr2:230287152
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 93 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1646-740T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287152 | ||||||
chr2:230287238
|
T | C | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1646-654T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287238 | ||||||
chr2:230287256
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1646-636G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287256 | ||||||
chr2:230287411
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1646-481G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287411 | ||||||
chr2:230287475
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1646-417C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287475 | ||||||
chr2:230287484
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646-408C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287484 | ||||||
chr2:230287555
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1646-337A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287555 | ||||||
chr2:230287584
|
T | G | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1646-308T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 17/26 | chr2 | 230287584 | ||||||
chr2:230287984
|
A | G | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1720+18A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230287984 | ||||||
chr2:230288021
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1720+55C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288021 | ||||||
chr2:230288181
|
G | A | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1720+215G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288181 | ||||||
chr2:230288247
|
A | G | 11 | a0001c0001t0001g0148a0001c0001t0001g0273a0001c0001t0001g0277others(8): Show | 11 | HG00323.hp2 HG00639.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+281A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288247 | ||||||
chr2:230288268
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+302T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288268 | ||||||
chr2:230288345
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1720+379G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288345 | ||||||
chr2:230288455
|
A | ATCTT | 32 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0044others(29): Show | 33 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1720+555_1720+558d others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
A | ATCTTTCT others(1): Show |
15 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0067others(12): Show | 15 | HG01123.hp1 HG01433.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1720+551_1720+558d others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
A | ATCTTTCT others(5): Show |
5 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0180others(2): Show | 5 | HG00323.hp1 HG02055.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+547_1720+558d others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
A | ATCTTTCT others(13): Show |
2 | a0004c0003t0001g0310a0004c0003t0001g0321 | 2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1720+539_1720+558d others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
A | T | 1 | a0002c0002t0001g0346 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1720+489A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288455 | ||||||
chr2:230288455
|
ATCTT | A | 49 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0062others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1720+555_1720+558d others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
ATCTTTCT others(1): Show |
A | 23 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0046others(20): Show | 26 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1720+551_1720+558d others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
ATCTTTCT others(5): Show |
A | 13 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0090others(10): Show | 14 | HG00741.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+547_1720+558d others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
ATCTTTCT others(9): Show |
A | 7 | a0001c0001t0001g0084a0003c0004t0003g0018a0003c0004t0003g0019others(4): Show | 7 | HG00280.hp1 HG00738.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+543_1720+558d others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
ATCTTTCT others(13): Show |
A | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1720+539_1720+558d others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288455
|
ATCTTTCT others(17): Show |
A | 1 | a0001c0001t0001g0011 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1720+535_1720+558d others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288455 | |||||
chr2:230288489
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1720+523C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288489 | ||||||
chr2:230288503
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1720+537T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288503 | ||||||
chr2:230288505
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0001g0286 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1720+542_1720+554d others(15): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288505 | |||||
chr2:230288505
|
CTTTCTTT others(13): Show |
C | 1 | a0001c0001t0001g0146 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1720+543_1720+562d others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288505 | |||||
chr2:230288509
|
C | CTTTCTTT others(9): Show |
2 | a0001c0001t0001g0152a0009c0013t0001g0139 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1720+547_1720+562d others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288509 | |||||
chr2:230288509
|
C | CTTTCTTT others(5): Show |
2 | a0001c0001t0001g0209a0009c0013t0001g0140 | 2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1720+554_1720+555i others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288509 | |||||
chr2:230288509
|
CTTTCTTT others(2): Show |
C | 3 | a0001c0001t0001g0287a0001c0001t0001g0294a0001c0001t0001g0320 | 3 | HG02572.hp1 HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1720+546_1720+554d others(11): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288509 | |||||
chr2:230288513
|
CTTTCT | C | 14 | a0001c0001t0001g0285a0001c0001t0001g0301a0001c0001t0001g0306others(11): Show | 14 | HG01261.hp2 HG01516.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+550_1720+554d others(7): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288513 | |||||
chr2:230288513
|
CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1720+551_1720+562d others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288513 | |||||
chr2:230288517
|
CT | C | 29 | a0001c0001t0001g0199a0001c0001t0001g0224a0001c0001t0001g0290others(26): Show | 30 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.1720+554delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288517 | |||||
chr2:230288518
|
T | TTTC | 37 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0194others(34): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1720+555_1720+557d others(5): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | |||||
chr2:230288518
|
T | TTTCTTTC | 25 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(22): Show | 26 | HG00639.hp1 HG01081.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(9): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | |||||
chr2:230288518
|
T | TTTCTTTC others(4): Show |
14 | a0001c0001t0001g0245a0001c0001t0001g0299a0001c0001t0001g0300others(11): Show | 14 | HG01069.hp2 HG01081.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(13): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | |||||
chr2:230288518
|
T | TTTCTTTC others(12): Show |
3 | a0001c0001t0001g0204a0001c0001t0001g0297a0002c0002t0001g0348 | 3 | HG01099.hp1 HG01346.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1720+558_1720+559i others(21): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288518 | |||||
chr2:230288521
|
CT | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0196others(2): Show | 5 | HG00673.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+562delT | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288521 | |||||
chr2:230288522
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1720+556T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288522 | ||||||
chr2:230288522
|
T | TTTC | 4 | a0001c0001t0001g0128a0001c0001t0001g0214a0001c0006t0001g0025others(1): Show | 4 | HG00140.hp1 NA18949.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(5): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288522 | |||||
chr2:230288522
|
T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1720+558_1720+559i others(13): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288522 | |||||
chr2:230288522
|
T | TTTCTTTC others(7): Show |
1 | a0001c0001t0002g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1720+558_1720+559i others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288522 | |||||
chr2:230288523
|
T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1720+558_1720+559i others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 230288523 | |||||
chr2:230288524
|
T | TC | 4 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0263others(1): Show | 4 | HG00621.hp2 HG01071.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+558_1720+559i others(3): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288524 | ||||||
chr2:230288539
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 84 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1720+573T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288539 | ||||||
chr2:230288645
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0119 | 2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1720+679G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288645 | ||||||
chr2:230288671
|
C | T | 2 | a0009c0013t0001g0139a0009c0013t0001g0140 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1720+705C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288671 | ||||||
chr2:230288713
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1720+747T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288713 | ||||||
chr2:230288773
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG00741.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1720+807T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230288773 | ||||||
chr2:230289137
|
C | T | 1 | a0002c0002t0001g0335 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1720+1171C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289137 | ||||||
chr2:230289169
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+1203G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289169 | ||||||
chr2:230289297
|
A | G | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1721-1163A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289297 | ||||||
chr2:230289375
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1721-1085A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289375 | ||||||
chr2:230289694
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1721-766C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289694 | ||||||
chr2:230289986
|
A | C | 1 | a0002c0002t0001g0354 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1721-474A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230289986 | ||||||
chr2:230290412
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1721-48G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230290412 | ||||||
chr2:230290415
|
G | A | 3 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0001t0002g0266 | 3 | HG02258.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1721-45G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 18/26 | chr2 | 230290415 | ||||||
chr2:230290698
|
T | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 75 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1825+134T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230290698 | ||||||
chr2:230290823
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1825+259G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230290823 | ||||||
chr2:230290989
|
T | C | 155 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1825+425T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230290989 | ||||||
chr2:230291275
|
T | C | 1 | a0004c0003t0001g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1825+711T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291275 | ||||||
chr2:230291365
|
C | G | 1 | a0003c0004t0003g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1825+801C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291365 | ||||||
chr2:230291457
|
C | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0152a0001c0001t0001g0208others(8): Show | 12 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1825+893C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291457 | ||||||
chr2:230291719
|
T | C | 2 | a0001c0001t0004g0255a0001c0001t0004g0322 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-927T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291719 | ||||||
chr2:230291769
|
G | T | 17 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(14): Show | 18 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-877G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291769 | ||||||
chr2:230291959
|
C | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-687C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230291959 | ||||||
chr2:230292063
|
T | C | 4 | a0004c0003t0001g0269a0004c0003t0001g0270a0004c0003t0001g0271others(1): Show | 4 | HG01884.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-583T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292063 | ||||||
chr2:230292225
|
T | A | 3 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0020 | 3 | HG00738.hp2 HG01496.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1826-421T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292225 | ||||||
chr2:230292238
|
C | T | 1 | a0001c0011t0001g0200 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1826-408C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292238 | ||||||
chr2:230292452
|
C | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1826-194C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292452 | ||||||
chr2:230292556
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 83 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1826-90T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292556 | ||||||
chr2:230292599
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0114a0001c0001t0001g0214 | 3 | NA18949.hp1 NA18974.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1826-47C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 19/26 | chr2 | 230292599 | ||||||
chr2:230292797
|
A | G | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1968+9A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292797 | ||||||
chr2:230292812
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(261): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1968+24G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292812 | ||||||
chr2:230292835
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1968+47A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292835 | ||||||
chr2:230292853
|
T | A | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1968+65T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230292853 | ||||||
chr2:230293021
|
G | T | 1 | a0002c0002t0001g0347 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1968+233G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293021 | ||||||
chr2:230293198
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1968+410C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293198 | ||||||
chr2:230293283
|
A | G | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1968+495A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293283 | ||||||
chr2:230293395
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1968+607G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293395 | ||||||
chr2:230293509
|
G | T | 1 | a0001c0011t0001g0200 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1968+721G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293509 | ||||||
chr2:230293524
|
A | G | 3 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG01081.hp2 HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1968+736A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293524 | ||||||
chr2:230293575
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1969-696G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293575 | ||||||
chr2:230293607
|
G | A | 3 | a0001c0001t0001g0356a0001c0001t0001g0357a0004c0003t0001g0227 | 3 | HG03098.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1969-664G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293607 | ||||||
chr2:230293628
|
G | A | 1 | a0010c0018t0001g0254 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1969-643G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293628 | ||||||
chr2:230293926
|
G | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1969-345G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293926 | ||||||
chr2:230293935
|
G | C | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1969-336G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293935 | ||||||
chr2:230293995
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1969-276A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230293995 | ||||||
chr2:230294192
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1969-79T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230294192 | ||||||
chr2:230294216
|
A | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1969-55A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230294216 | ||||||
chr2:230294227
|
G | A | 4 | a0002c0002t0001g0149a0002c0002t0001g0324a0002c0002t0001g0326others(1): Show | 4 | HG00408.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1969-44G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 20/26 | chr2 | 230294227 | ||||||
chr2:230294320
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA19067.hp1 | splice_donor_variant&intron_variant | HIGH | c.2016+2T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294320 | ||||||
chr2:230294321
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19067.hp1 | splice_region_variant&intron_variant | LOW | c.2016+3G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294321 | ||||||
chr2:230294322
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19067.hp1 | splice_region_variant&intron_variant | LOW | c.2016+4A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294322 | ||||||
chr2:230294415
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2016+97T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294415 | ||||||
chr2:230294570
|
C | A | 1 | a0004c0003t0001g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2016+252C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294570 | ||||||
chr2:230294573
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2016+255G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294573 | ||||||
chr2:230294695
|
T | A | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2016+377T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294695 | ||||||
chr2:230294773
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(95): Show | 104 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.2016+455G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230294773 | ||||||
chr2:230295119
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2016+801T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295119 | ||||||
chr2:230295391
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016+1073A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295391 | ||||||
chr2:230295429
|
A | G | 2 | a0001c0001t0002g0190a0001c0001t0002g0192 | 2 | NA18953.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2016+1111A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295429 | ||||||
chr2:230295446
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0301 | 2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2016+1128G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295446 | ||||||
chr2:230295448
|
T | G | 2 | a0004c0003t0001g0311a0004c0003t0001g0321 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2016+1130T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295448 | ||||||
chr2:230295596
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0136 | 2 | NA18962.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2016+1278T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295596 | ||||||
chr2:230295806
|
A | G | 42 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(39): Show | 42 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.2016+1488A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230295806 | ||||||
chr2:230296003
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2017-1418C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296003 | ||||||
chr2:230296013
|
A | C | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2017-1408A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296013 | ||||||
chr2:230296076
|
CA | C | 155 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0088others(152): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2017-1330delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 230296076 | |||||
chr2:230296076
|
CAA | C | 7 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258others(4): Show | 7 | HG02258.hp2 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-1331_2017-133 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr2 | 230296076 | |||||
chr2:230296290
|
A | G | 37 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2017-1131A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296290 | ||||||
chr2:230296311
|
T | C | 26 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(23): Show | 27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.2017-1110T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296311 | ||||||
chr2:230296474
|
C | A | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2017-947C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296474 | ||||||
chr2:230296619
|
G | A | 2 | a0006c0009t0004g0154a0006c0009t0004g0156 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2017-802G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296619 | ||||||
chr2:230296622
|
T | A | 155 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2017-799T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296622 | ||||||
chr2:230296798
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2017-623G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296798 | ||||||
chr2:230296807
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2017-614A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296807 | ||||||
chr2:230296830
|
C | A | 10 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0074others(7): Show | 10 | NA18943.hp1 NA18949.hp1 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.2017-591C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230296830 | ||||||
chr2:230297128
|
G | C | 9 | a0001c0001t0004g0255a0001c0001t0004g0322a0004c0003t0001g0312others(6): Show | 9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2017-293G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297128 | ||||||
chr2:230297155
|
A | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-266A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297155 | ||||||
chr2:230297227
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2017-194A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297227 | ||||||
chr2:230297303
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2017-118T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297303 | ||||||
chr2:230297339
|
G | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017-82G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 21/26 | chr2 | 230297339 | ||||||
chr2:230297626
|
G | T | 152 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(149): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.2058+164G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297626 | ||||||
chr2:230297685
|
T | A | 1 | a0001c0001t0001g0131 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2058+223T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297685 | ||||||
chr2:230297898
|
T | C | 3 | a0004c0003t0001g0312a0004c0003t0001g0313a0004c0003t0001g0314 | 3 | HG02615.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2058+436T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297898 | ||||||
chr2:230297974
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2058+512T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230297974 | ||||||
chr2:230298040
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2058+578A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298040 | ||||||
chr2:230298211
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2058+749A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298211 | ||||||
chr2:230298240
|
G | A | 128 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.2058+778G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298240 | ||||||
chr2:230298283
|
C | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(259): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2058+821C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298283 | ||||||
chr2:230298284
|
G | A | 1 | a0005c0007t0001g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2058+822G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298284 | ||||||
chr2:230298383
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2058+921G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298383 | ||||||
chr2:230298474
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2058+1012T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298474 | ||||||
chr2:230298673
|
G | C | 163 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0088others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2058+1211G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298673 | ||||||
chr2:230298762
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 6 | HG00639.hp1 HG01074.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2058+1300G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298762 | ||||||
chr2:230298904
|
C | A | 2 | a0004c0003t0001g0311a0004c0003t0001g0321 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2058+1442C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298904 | ||||||
chr2:230298930
|
T | A | 1 | a0001c0001t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2058+1468T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298930 | ||||||
chr2:230298955
|
G | A | 10 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG00323.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2058+1493G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230298955 | ||||||
chr2:230299050
|
A | T | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0110others(1): Show | 4 | HG00621.hp2 HG02074.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+1588A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299050 | ||||||
chr2:230299219
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2058+1757G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299219 | ||||||
chr2:230299447
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058+1985G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299447 | ||||||
chr2:230299469
|
C | T | 1 | a0002c0002t0001g0326 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2058+2007C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299469 | ||||||
chr2:230299484
|
C | T | 3 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0001t0002g0266 | 3 | HG02258.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2058+2022C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299484 | ||||||
chr2:230299560
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2058+2098G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299560 | ||||||
chr2:230299833
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2058+2371C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299833 | ||||||
chr2:230299862
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2058+2400C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230299862 | ||||||
chr2:230300067
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2058+2605A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300067 | ||||||
chr2:230300221
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058+2759C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300221 | ||||||
chr2:230300413
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2058+2951A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300413 | ||||||
chr2:230300651
|
GCAGCTCT others(18): Show |
G | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2058+3190_2058+321 others(29): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300651 | ||||||
chr2:230300683
|
G | A | 1 | a0003c0005t0003g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2058+3221G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300683 | ||||||
chr2:230300836
|
C | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+3374C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230300836 | ||||||
chr2:230301124
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2058+3662A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301124 | ||||||
chr2:230301197
|
C | G | 1 | a0001c0001t0002g0232 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2058+3735C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301197 | ||||||
chr2:230301214
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2058+3752A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301214 | ||||||
chr2:230301220
|
G | A | 36 | a0002c0002t0001g0010a0002c0002t0001g0147a0002c0002t0001g0149others(33): Show | 37 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2058+3758G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301220 | ||||||
chr2:230301221
|
C | T | 41 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(38): Show | 41 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.2058+3759C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301221 | ||||||
chr2:230301392
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2058+3930G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301392 | ||||||
chr2:230301402
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2058+3940A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301402 | ||||||
chr2:230301653
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2058+4191A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301653 | ||||||
chr2:230301656
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(262): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.2058+4194T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230301656 | ||||||
chr2:230302125
|
C | T | 151 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(148): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2058+4663C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302125 | ||||||
chr2:230302229
|
CA | C | 7 | a0001c0001t0001g0164a0001c0001t0002g0247a0001c0001t0004g0322others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+4782delA | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230302229 | |||||
chr2:230302574
|
C | G | 2 | a0002c0002t0001g0330a0002c0002t0001g0331 | 2 | HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2058+5112C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302574 | ||||||
chr2:230302641
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2058+5179A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302641 | ||||||
chr2:230302863
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2058+5401G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230302863 | ||||||
chr2:230303094
|
A | T | 1 | a0004c0003t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2058+5632A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303094 | ||||||
chr2:230303219
|
G | A | 2 | a0002c0002t0001g0149a0002c0002t0001g0332 | 2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2058+5757G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303219 | ||||||
chr2:230303239
|
C | T | 1 | a0002c0002t0001g0345 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2058+5777C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303239 | ||||||
chr2:230303242
|
C | T | 7 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+5780C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303242 | ||||||
chr2:230303262
|
T | G | 2 | a0001c0001t0002g0238a0001c0001t0002g0248 | 2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2058+5800T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303262 | ||||||
chr2:230303419
|
A | C | 1 | a0002c0002t0001g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2058+5957A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303419 | ||||||
chr2:230303534
|
A | G | 2 | a0001c0001t0001g0356a0004c0003t0001g0227 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2058+6072A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303534 | ||||||
chr2:230303807
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2059-6117A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303807 | ||||||
chr2:230303977
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 6 | HG01106.hp2 HG02015.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059-5947G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230303977 | ||||||
chr2:230304050
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 84 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.2059-5874G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304050 | ||||||
chr2:230304185
|
G | A | 147 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2059-5739G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304185 | ||||||
chr2:230304287
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 5 | HG01106.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-5637G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304287 | ||||||
chr2:230304469
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2059-5455A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230304469 | ||||||
chr2:230305009
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 93 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2059-4915G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305009 | ||||||
chr2:230305046
|
A | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0159a0001c0001t0001g0161 | 3 | NA18980.hp1 NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2059-4878A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305046 | ||||||
chr2:230305146
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2059-4778T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305146 | ||||||
chr2:230305196
|
G | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2059-4728G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305196 | ||||||
chr2:230305459
|
T | A | 1 | a0001c0001t0001g0296 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2059-4465T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305459 | ||||||
chr2:230305548
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2059-4376G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305548 | ||||||
chr2:230305554
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 83 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.2059-4370A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305554 | ||||||
chr2:230305664
|
C | A | 42 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(39): Show | 42 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.2059-4260C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305664 | ||||||
chr2:230305674
|
G | A | 1 | a0003c0004t0003g0016 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2059-4250G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305674 | ||||||
chr2:230305685
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2059-4239C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305685 | ||||||
chr2:230305686
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2059-4238G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305686 | ||||||
chr2:230305700
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2059-4224A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305700 | ||||||
chr2:230305761
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2059-4163C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305761 | ||||||
chr2:230305789
|
G | A | 37 | a0001c0001t0001g0078a0002c0002t0001g0010a0002c0002t0001g0147others(34): Show | 38 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2059-4135G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305789 | ||||||
chr2:230305800
|
G | A | 4 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0002g0237others(1): Show | 4 | NA18956.hp1 NA18960.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2059-4124G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305800 | ||||||
chr2:230305817
|
G | A | 357 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(354): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2059-4107G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305817 | ||||||
chr2:230305916
|
C | T | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2059-4008C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230305916 | ||||||
chr2:230306479
|
C | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2059-3445C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306479 | ||||||
chr2:230306515
|
G | T | 2 | a0002c0002t0001g0340a0002c0008t0001g0329 | 2 | HG01070.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2059-3409G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306515 | ||||||
chr2:230306638
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-3286A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306638 | ||||||
chr2:230306708
|
C | T | 23 | a0001c0006t0001g0023a0001c0006t0001g0025a0001c0006t0001g0026others(20): Show | 24 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2059-3216C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306708 | ||||||
chr2:230306806
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-3118G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306806 | ||||||
chr2:230306848
|
C | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0316 | 2 | HG00099.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.2059-3076C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230306848 | ||||||
chr2:230307174
|
A | G | 10 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG00323.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2059-2750A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307174 | ||||||
chr2:230307195
|
C | T | 1 | a0002c0002t0001g0332 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2059-2729C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307195 | ||||||
chr2:230307260
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2059-2664G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307260 | ||||||
chr2:230307286
|
G | A | 2 | a0007c0012t0001g0012a0007c0012t0001g0013 | 2 | HG02451.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2059-2638G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307286 | ||||||
chr2:230307456
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2059-2468T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307456 | ||||||
chr2:230307589
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-2335T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307589 | ||||||
chr2:230307824
|
A | G | 48 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0182others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2059-2100A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307824 | ||||||
chr2:230307826
|
T | C | 1 | a0001c0001t0002g0264 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2059-2098T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307826 | ||||||
chr2:230307890
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2059-2034G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307890 | ||||||
chr2:230307927
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(247): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2059-1997T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307927 | ||||||
chr2:230307955
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1969G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307955 | ||||||
chr2:230307955
|
G | GTA | 21 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0077others(18): Show | 23 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.2059-1934_2059-193 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATA | 17 | a0001c0001t0001g0135a0001c0001t0001g0204a0001c0001t0001g0296others(14): Show | 18 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.2059-1936_2059-193 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATA | 8 | a0001c0001t0001g0100a0001c0001t0001g0297a0001c0001t0001g0306others(5): Show | 8 | HG00558.hp2 HG01346.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2059-1938_2059-193 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0040a0001c0001t0001g0274a0001c0001t0001g0291others(4): Show | 7 | HG00735.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-1940_2059-193 others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATAT others(3): Show |
13 | a0001c0001t0001g0088a0001c0001t0001g0187a0001c0001t0001g0189others(10): Show | 13 | HG00735.hp2 HG01109.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2059-1942_2059-193 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATAT others(5): Show |
9 | a0001c0001t0001g0009a0001c0001t0001g0198a0001c0001t0001g0202others(6): Show | 10 | HG02074.hp2 HG03490.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.2059-1944_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0070a0002c0002t0001g0335 | 2 | HG02523.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2059-1946_2059-193 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATAT others(9): Show |
7 | a0001c0001t0001g0183a0001c0001t0001g0286a0001c0001t0001g0287others(4): Show | 7 | HG00099.hp1 HG01123.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.2059-1948_2059-193 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2059-1956_2059-193 others(28): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
GTA | G | 12 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0071others(9): Show | 12 | HG02109.hp1 HG02486.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2059-1934_2059-193 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
GTATA | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0107others(5): Show | 8 | HG01109.hp1 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.2059-1936_2059-193 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
GTATATA | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 12 | HG00639.hp1 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.2059-1938_2059-193 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307955
|
GTATATAT others(3): Show |
G | 3 | a0001c0001t0001g0011a0001c0001t0002g0265a0004c0003t0001g0227 | 4 | HG02896.hp1 HG02897.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1942_2059-193 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307955 | |||||
chr2:230307957
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2059-1967A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307957 | ||||||
chr2:230307978
|
TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0175a0001c0001t0001g0356a0011c0014t0001g0267 | 3 | HG02486.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2059-1944_2059-193 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307978 | |||||
chr2:230307978
|
TATATATA others(15): Show |
T | 2 | a0004c0003t0001g0311a0004c0003t0001g0321 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2059-1944_2059-192 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307978 | |||||
chr2:230307980
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0002g0238a0001c0001t0002g0248 | 2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2059-1942_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | |||||
chr2:230307980
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0176 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2059-1942_2059-192 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | |||||
chr2:230307980
|
TATATATA others(9): Show |
T | 4 | a0002c0002t0001g0149a0002c0002t0001g0324a0002c0002t0001g0326others(1): Show | 4 | HG00408.hp2 HG01934.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1942_2059-192 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | |||||
chr2:230307980
|
TATATATA others(13): Show |
T | 3 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG02723.hp2 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2059-1942_2059-192 others(24): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307980 | |||||
chr2:230307982
|
TATATATA others(3): Show |
T | 30 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(27): Show | 30 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.2059-1940_2059-193 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307982 | |||||
chr2:230307982
|
TATATATA others(11): Show |
T | 2 | a0009c0013t0001g0139a0009c0013t0001g0140 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2059-1940_2059-192 others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307982 | |||||
chr2:230307984
|
TATATATA others(1): Show |
T | 5 | a0001c0001t0001g0115a0001c0001t0002g0243a0001c0001t0002g0256others(2): Show | 5 | HG02056.hp2 HG02683.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1938_2059-193 others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307984 | |||||
chr2:230307984
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0002g0206a0001c0001t0002g0239a0001c0001t0002g0252 | 3 | HG00642.hp1 HG01255.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2059-1938_2059-192 others(14): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307984 | |||||
chr2:230307986
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2059-1938T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307986 | ||||||
chr2:230307986
|
TATATAC | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0082a0001c0001t0001g0126others(19): Show | 23 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.2059-1936_2059-193 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307986 | |||||
chr2:230307986
|
TATATACA others(1): Show |
T | 9 | a0001c0001t0001g0007a0001c0001t0001g0170a0001c0001t0001g0178others(6): Show | 10 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2059-1936_2059-192 others(12): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307986 | |||||
chr2:230307988
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2059-1936T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307988 | ||||||
chr2:230307988
|
TATAC | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0042others(18): Show | 23 | HG00558.hp1 HG00741.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.2059-1934_2059-193 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307988 | |||||
chr2:230307988
|
TATACAC | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0172a0004c0003t0001g0269others(3): Show | 6 | HG00099.hp2 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2059-1934_2059-192 others(10): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307988 | |||||
chr2:230307989
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1935A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307989 | ||||||
chr2:230307990
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0014others(13): Show | 18 | HG01106.hp2 HG01109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2059-1934T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307990 | ||||||
chr2:230307990
|
T | TAC | 3 | a0001c0001t0001g0148a0001c0001t0001g0278a0007c0017t0001g0053 | 3 | HG00323.hp2 HG00639.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2059-1908_2059-190 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(5): Show |
1 | a0003c0005t0003g0097 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(5): Show |
5 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0006t0001g0037others(2): Show | 5 | HG01256.hp1 HG02148.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(16): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(7): Show |
3 | a0001c0001t0001g0301a0003c0005t0003g0185a0003c0005t0003g0186 | 3 | HG01069.hp1 HG01071.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(18): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(9): Show |
1 | a0001c0001t0007g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(9): Show |
2 | a0001c0001t0001g0194a0003c0004t0003g0003 | 3 | HG01106.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(20): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(11): Show |
5 | a0001c0006t0001g0026a0003c0004t0003g0024a0003c0004t0003g0031others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(22): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(13): Show |
3 | a0001c0006t0001g0025a0003c0004t0003g0030a0003c0004t0003g0032 | 3 | HG00140.hp1 HG01169.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(24): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(15): Show |
1 | a0004c0003t0001g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(15): Show |
3 | a0001c0006t0002g0017a0003c0005t0003g0098a0003c0005t0003g0162 | 3 | HG00140.hp2 HG00323.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(26): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(21): Show |
1 | a0003c0004t0003g0020 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2059-1933_2059-193 others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(17): Show |
3 | a0001c0006t0001g0023a0001c0006t0001g0027a0003c0004t0003g0018 | 3 | HG01358.hp2 HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(28): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(19): Show |
2 | a0003c0004t0003g0019a0003c0004t0010g0021 | 2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(30): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
T | TATATATA others(21): Show |
3 | a0001c0001t0001g0294a0003c0004t0003g0034a0003c0005t0003g0201 | 3 | HG02738.hp2 HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2059-1933_2059-193 others(32): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
TAC | T | 39 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0060others(36): Show | 40 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.2059-1908_2059-190 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307990
|
TACAC | T | 3 | a0001c0001t0001g0145a0002c0002t0001g0342a0002c0002t0001g0354 | 3 | HG02155.hp1 HG04115.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2059-1910_2059-190 others(8): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230307990 | |||||
chr2:230307992
|
C | T | 81 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0077others(78): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.2059-1932C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307992 | ||||||
chr2:230307994
|
C | T | 29 | a0001c0001t0004g0255a0001c0001t0004g0322a0001c0001t0005g0122others(26): Show | 30 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.2059-1930C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307994 | ||||||
chr2:230307996
|
C | T | 26 | a0001c0001t0005g0122a0002c0002t0001g0010a0002c0002t0001g0147others(23): Show | 27 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.2059-1928C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307996 | ||||||
chr2:230307998
|
C | T | 2 | a0001c0001t0005g0122a0002c0002t0001g0340 | 2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2059-1926C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230307998 | ||||||
chr2:230308000
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1924C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308000 | ||||||
chr2:230308002
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1922C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308002 | ||||||
chr2:230308004
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1920C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308004 | ||||||
chr2:230308006
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2059-1918C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308006 | ||||||
chr2:230308016
|
C | G | 43 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0245others(40): Show | 43 | HG00423.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.2059-1908C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308016 | ||||||
chr2:230308018
|
G | C | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2059-1906G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308018 | ||||||
chr2:230308020
|
GAC | G | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2059-1887_2059-188 others(6): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 230308020 | |||||
chr2:230308070
|
G | C | 2 | a0001c0001t0001g0285a0001c0001t0001g0317 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2059-1854G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308070 | ||||||
chr2:230308155
|
G | A | 1 | a0004c0003t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2059-1769G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308155 | ||||||
chr2:230308218
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1706T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308218 | ||||||
chr2:230308282
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0356a0001c0001t0001g0357others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2059-1642A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308282 | ||||||
chr2:230308308
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0076a0001c0001t0001g0130 | 3 | NA19063.hp2 NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2059-1616T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308308 | ||||||
chr2:230308493
|
G | A | 2 | a0001c0001t0001g0285a0001c0001t0001g0317 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2059-1431G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308493 | ||||||
chr2:230308542
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059-1382G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308542 | ||||||
chr2:230308571
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0174others(1): Show | 6 | HG01123.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2059-1353G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308571 | ||||||
chr2:230308592
|
G | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2059-1332G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308592 | ||||||
chr2:230308605
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1319G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308605 | ||||||
chr2:230308773
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1151T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308773 | ||||||
chr2:230308774
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1150A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308774 | ||||||
chr2:230308775
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-1149C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308775 | ||||||
chr2:230308775
|
C | T | 13 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0119others(10): Show | 13 | HG01099.hp2 HG01123.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2059-1149C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308775 | ||||||
chr2:230308782
|
C | G | 5 | a0003c0004t0003g0033a0003c0004t0003g0034a0003c0004t0003g0035others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2059-1142C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308782 | ||||||
chr2:230308792
|
G | A | 2 | a0004c0003t0001g0275a0011c0014t0001g0267 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2059-1132G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308792 | ||||||
chr2:230308825
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2059-1099C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308825 | ||||||
chr2:230308926
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2059-998T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308926 | ||||||
chr2:230308963
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-961A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230308963 | ||||||
chr2:230309139
|
G | A | 1 | a0002c0002t0001g0354 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2059-785G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309139 | ||||||
chr2:230309202
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2059-722T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309202 | ||||||
chr2:230309239
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 8 | HG01106.hp2 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2059-685C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309239 | ||||||
chr2:230309263
|
G | C | 2 | a0001c0001t0001g0179a0001c0016t0001g0284 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2059-661G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309263 | ||||||
chr2:230309322
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2059-602C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309322 | ||||||
chr2:230309374
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2059-550A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309374 | ||||||
chr2:230309382
|
T | C | 103 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(100): Show | 104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2059-542T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309382 | ||||||
chr2:230309386
|
C | G | 35 | a0001c0011t0001g0165a0001c0011t0001g0200a0002c0002t0001g0010others(32): Show | 36 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.2059-538C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309386 | ||||||
chr2:230309423
|
G | A | 1 | a0001c0001t0001g0356 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2059-501G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309423 | ||||||
chr2:230309423
|
G | C | 103 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(100): Show | 104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2059-501G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309423 | ||||||
chr2:230309590
|
C | T | 103 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(100): Show | 104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2059-334C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309590 | ||||||
chr2:230309688
|
T | C | 1 | a0002c0002t0001g0323 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2059-236T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309688 | ||||||
chr2:230309705
|
G | A | 123 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(120): Show | 126 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2059-219G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309705 | ||||||
chr2:230309708
|
T | G | 1 | a0003c0004t0003g0016 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2059-216T>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309708 | ||||||
chr2:230309847
|
G | A | 1 | a0001c0001t0002g0259 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2059-77G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309847 | ||||||
chr2:230309861
|
C | G | 2 | a0001c0001t0001g0063a0013c0020t0001g0134 | 2 | HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2059-63C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 22/26 | chr2 | 230309861 | ||||||
chr2:230310057
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2174+18G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310057 | ||||||
chr2:230310273
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2174+234C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310273 | ||||||
chr2:230310283
|
C | T | 5 | a0001c0001t0004g0255a0001c0001t0004g0322a0006c0009t0004g0154others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174+244C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310283 | ||||||
chr2:230310375
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2174+336A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310375 | ||||||
chr2:230310469
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2175-274C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310469 | ||||||
chr2:230310536
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2175-207G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310536 | ||||||
chr2:230310537
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2175-206A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310537 | ||||||
chr2:230310578
|
A | G | 1 | a0001c0001t0002g0240 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2175-165A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310578 | ||||||
chr2:230310637
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2175-106A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310637 | ||||||
chr2:230310670
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2175-73A>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310670 | ||||||
chr2:230310725
|
C | A | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175-18C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 23/26 | chr2 | 230310725 | ||||||
chr2:230310921
|
G | C | 2 | a0001c0001t0004g0255a0001c0001t0004g0322 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2283+70G>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230310921 | ||||||
chr2:230310956
|
C | T | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2283+105C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230310956 | ||||||
chr2:230311048
|
G | A | 123 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0208others(120): Show | 126 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2284-106G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311048 | ||||||
chr2:230311069
|
A | C | 1 | a0003c0004t0003g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2284-85A>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311069 | ||||||
chr2:230311080
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-74T>C | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311080 | ||||||
chr2:230311081
|
C | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02055.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-73C>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311081 | ||||||
chr2:230311098
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2284-56C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 24/26 | chr2 | 230311098 | ||||||
chr2:230311263
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2361+32C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311263 | ||||||
chr2:230311274
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2361+43T>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311274 | ||||||
chr2:230311325
|
G | A | 12 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0193others(9): Show | 12 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2361+94G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311325 | ||||||
chr2:230311344
|
C | T | 1 | a0011c0014t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2362-108C>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311344 | ||||||
chr2:230311448
|
C | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01081.hp2 HG01433.hp1 |
splice_region_variant&intron_variant | LOW | c.2362-4C>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 25/26 | chr2 | 230311448 | ||||||
chr2:230311767
|
G | T | 1 | a0001c0001t0005g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2505+172G>T | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | chr2 | 230311767 | ||||||
chr2:230311865
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0205 | 2 | NA18961.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2505+270A>G | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | chr2 | 230311865 | ||||||
chr2:230312297
|
G | A | 3 | a0004c0003t0001g0269a0004c0003t0001g0270a0004c0003t0001g0272 | 3 | HG02622.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2506-289G>A | SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | chr2 | 230312297 | ||||||
chr2:230312485
|
CTT | C | 20 | a0003c0004t0003g0003a0003c0004t0003g0016a0003c0004t0003g0018others(17): Show | 22 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2506-92_2506-91del others(2): Show |
SP140 | ENSG00000079263.19 | transcript | ENST00000392045.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 230312485 |