geneid | 65123 |
---|---|
ensemblid | ENSG00000143624.14 |
hgncid | 26153 |
symbol | INTS3 |
name | integrator complex subunit 3 |
refseq_nuc | NM_023015.5 |
refseq_prot | NP_075391.3 |
ensembl_nuc | ENST00000318967.7 |
ensembl_prot | ENSP00000318641.2 |
mane_status | MANE Select |
chr | chr1 |
start | 153728050 |
end | 153774808 |
strand | + |
ver | v1.2 |
region | chr1:153728050-153774808 |
region5000 | chr1:153723050-153779808 |
regionname0 | INTS3_chr1_153728050_153774808 |
regionname5000 | INTS3_chr1_153723050_153779808 |
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 | 1042 | 347 | 88 | 60 | 144 | 12 | 42 | 102 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0002 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0003 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
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 | 3129 | 298 | 53 | 55 | 141 | 11 | 37 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
c0002 | 0/0 | 3129 | 43 | 30 | 5 | 3 | 1 | 4 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
c0003 | 0/0 | 3129 | 4 | 4 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
c0004 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
c0005 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
c0006 | 0/0 | 3129 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
c0007 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2124 | 298 | 56 | 54 | 138 | 11 | 38 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0002 | 0/0 | 2124 | 29 | 17 | 4 | 3 | 1 | 4 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0003 | 0/0 | 2124 | 9 | 8 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0004 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0005 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0006 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0007 | 0/0 | 2102 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0008 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0009 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0010 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0011 | 0/0 | 2124 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0012 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
t0013 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
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 | 4 | 0 | 3 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
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 | 3129 | 298 | 53 | 55 | 141 | 11 | 37 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002 | 0/0 | 3129 | 43 | 30 | 5 | 3 | 1 | 4 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0003 | 0/0 | 3129 | 4 | 4 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0006 | 0/0 | 3129 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0007 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0002c0004 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0003c0005 | 0/0 | 3113 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5252 | 285 | 45 | 53 | 138 | 11 | 37 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0001t0003 | 0/0 | 5252 | 8 | 7 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0001t0007 | 0/0 | 5230 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0001t0009 | 0/0 | 5252 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0001t0010 | 0/0 | 5252 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0001t0011 | 0/0 | 5252 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0001t0013 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0001 | 0/0 | 5252 | 6 | 5 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0002 | 0/0 | 5252 | 29 | 17 | 4 | 3 | 1 | 4 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0004 | 0/0 | 5252 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0005 | 0/0 | 5252 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0006 | 0/0 | 5252 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0008 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0002t0012 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0003t0001 | 0/0 | 5252 | 4 | 4 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0006t0001 | 0/0 | 5252 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0001c0007t0003 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0002c0004t0001 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
a0003c0005t0001 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | copy fasta | chr1 | 153723050 | 153779808 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0009g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0011g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0002t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0001c0007t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0002c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
a0003c0005t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00558 | hp2 | a0001 | c0001 | t0009 | g0219 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01361 | hp2 | a0001 | c0001 | t0011 | g0183 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01891 | hp1 | a0001 | c0002 | t0005 | g0313 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02145 | hp1 | a0001 | c0002 | t0008 | g0319 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0286 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0038 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02622 | hp1 | a0001 | c0002 | t0006 | g0130 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02630 | hp1 | a0001 | c0002 | t0006 | g0129 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0320 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0229 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03139 | hp2 | a0003 | c0005 | t0001 | g0278 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03195 | hp1 | a0002 | c0004 | t0001 | g0148 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03209 | hp2 | a0001 | c0002 | t0005 | g0312 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0323 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0137 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03579 | hp1 | a0001 | c0002 | t0012 | g0013 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04204 | hp1 | a0001 | c0006 | t0001 | g0070 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18906 | hp2 | a0001 | c0007 | t0003 | g0321 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18998 | hp1 | a0001 | c0001 | t0010 | g0227 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0330 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19068 | hp2 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ASW | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0034 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | GIH | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0243 | REF | REF | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:153728720
|
G | A | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.86G>A | p.Gly29Glu | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/30 | 671/5252 | 86/3129 | 29/1042 | chr1 | 153728720 | ||
chr1:153770198
|
TTCAGAGC others(9): Show |
T | 1 | a0003 | 1 | HG03139.hp2 | frameshift_variant&splice_region_variant | HIGH | c.2391_2406delTCAGAG others(10): Show |
p.Ile797fs | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 24/30 | 2976/5252 | 2391/3129 | 797/1042 | chr1 | 153770198 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:153767809
|
G | A | 1 | a0001c0003 | 4 | HG02145.hp2 HG02258.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.2226G>A | p.Thr742Thr | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/30 | 2811/5252 | 2226/3129 | 742/1042 | chr1 | 153767809 | ||
chr1:153772397
|
C | T | 1 | a0001c0007 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2778C>T | p.His926His | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 27/30 | 3363/5252 | 2778/3129 | 926/1042 | chr1 | 153772397 | ||
chr1:153772652
|
G | C | 1 | a0001c0002 | 43 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(40): Show |
synonymous_variant | LOW | c.2835G>C | p.Thr945Thr | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 28/30 | 3420/5252 | 2835/3129 | 945/1042 | chr1 | 153772652 | ||
chr1:153773063
|
G | A | 1 | a0001c0006 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.3033G>A | p.Ser1011Ser | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 29/30 | 3618/5252 | 3033/3129 | 1011/1042 | chr1 | 153773063 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:153728115
|
C | T | 1 | a0001c0001t0013 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-520C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/30 | 520 | chr1 | 153728115 | |||||
chr1:153728365
|
A | G | 16 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(13): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
5_prime_UTR_variant | MODIFIER | c.-270A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/30 | 270 | chr1 | 153728365 | |||||
chr1:153773750
|
A | C | 1 | a0001c0002t0006 | 2 | HG02622.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*480A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 480 | chr1 | 153773750 | |||||
chr1:153773783
|
C | G | 2 | a0001c0002t0004a0001c0002t0012 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*513C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 513 | chr1 | 153773783 | |||||
chr1:153773849
|
G | T | 2 | a0001c0002t0004a0001c0002t0012 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*579G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 579 | chr1 | 153773849 | |||||
chr1:153773984
|
CTGTTTTT others(15): Show |
C | 1 | a0001c0001t0007 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727_*748delTGTTTT others(16): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 727 | INFO_REALIGN_3_PRIME | chr1 | 153773984 | ||||
chr1:153773998
|
G | T | 1 | a0001c0001t0011 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 728 | chr1 | 153773998 | |||||
chr1:153774134
|
G | A | 1 | a0001c0002t0002 | 29 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*864G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 864 | chr1 | 153774134 | |||||
chr1:153774145
|
C | T | 1 | a0001c0001t0010 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 875 | chr1 | 153774145 | |||||
chr1:153774148
|
C | T | 1 | a0001c0002t0005 | 2 | HG01891.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*878C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 878 | chr1 | 153774148 | |||||
chr1:153774305
|
G | A | 1 | a0001c0002t0002 | 29 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1035G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 1035 | chr1 | 153774305 | |||||
chr1:153774537
|
A | G | 1 | a0001c0001t0009 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 1267 | chr1 | 153774537 | |||||
chr1:153774619
|
A | C | 1 | a0001c0002t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 1349 | chr1 | 153774619 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:153728867
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+83G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153728867 | ||||||
chr1:153728900
|
G | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.150+116G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153728900 | ||||||
chr1:153729022
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.150+238T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729022 | ||||||
chr1:153729049
|
T | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01070.hp1 HG01071.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.150+265T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729049 | ||||||
chr1:153729280
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.150+496T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729280 | ||||||
chr1:153729337
|
G | T | 1 | a0001c0001t0001g0335 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.150+553G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729337 | ||||||
chr1:153729429
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.150+645G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729429 | ||||||
chr1:153729819
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.150+1035T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729819 | ||||||
chr1:153729865
|
C | CA | 304 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.150+1098dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153729865 | |||||
chr1:153729865
|
C | CAA | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00423.hp2 HG01175.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+1097_150+1098d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153729865 | |||||
chr1:153730184
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.150+1400A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730184 | ||||||
chr1:153730503
|
C | T | 9 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(6): Show | 9 | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+1719C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730503 | ||||||
chr1:153730537
|
C | T | 137 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(134): Show | 139 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.150+1753C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730537 | ||||||
chr1:153730541
|
ATTGTGTC others(5): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+1760_150+1771d others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153730541 | |||||
chr1:153730648
|
G | A | 27 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(24): Show | 28 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+1864G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730648 | ||||||
chr1:153730654
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0053 | 3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.150+1870G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730654 | ||||||
chr1:153730989
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.150+2205T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730989 | ||||||
chr1:153731066
|
A | G | 1 | a0001c0002t0002g0187 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.150+2282A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731066 | ||||||
chr1:153731414
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.150+2630C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731414 | ||||||
chr1:153731453
|
A | G | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+2669A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731453 | ||||||
chr1:153731480
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.150+2696C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731480 | ||||||
chr1:153731558
|
T | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.150+2774T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731558 | ||||||
chr1:153731577
|
C | CT | 146 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(143): Show | 151 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.150+2794dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731577 | |||||
chr1:153731577
|
C | CTT | 16 | a0001c0001t0001g0012a0001c0001t0001g0175a0001c0001t0001g0176others(13): Show | 17 | HG00597.hp1 HG01891.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.150+2794_150+2795i others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731577 | |||||
chr1:153731579
|
C | CT | 16 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(13): Show | 16 | HG00621.hp2 HG01496.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+2816dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731579 | |||||
chr1:153731579
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(159): Show | 168 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.150+2795C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731579 | ||||||
chr1:153731679
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.150+2895G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731679 | ||||||
chr1:153731680
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.150+2896G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731680 | ||||||
chr1:153731747
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+2963G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731747 | ||||||
chr1:153731901
|
C | CT | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(178): Show | 190 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.150+3141dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731901 | |||||
chr1:153731901
|
C | CTT | 23 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0149others(20): Show | 23 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.150+3140_150+3141d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731901 | |||||
chr1:153731901
|
CT | C | 25 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(22): Show | 26 | HG01081.hp1 HG01167.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.150+3141delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731901 | |||||
chr1:153731957
|
G | C | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+3173G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731957 | ||||||
chr1:153732193
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.150+3409G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732193 | ||||||
chr1:153732206
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.150+3422G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732206 | ||||||
chr1:153732242
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.150+3458A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732242 | ||||||
chr1:153732278
|
A | G | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+3494A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732278 | ||||||
chr1:153732296
|
A | G | 1 | a0003c0005t0001g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150+3512A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732296 | ||||||
chr1:153732299
|
T | C | 1 | a0001c0002t0004g0320 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150+3515T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732299 | ||||||
chr1:153732433
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+3649G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732433 | ||||||
chr1:153732447
|
A | AT | 7 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0121others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+3679dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732447 | |||||
chr1:153732447
|
AT | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0023others(14): Show | 19 | HG01256.hp1 HG01433.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.150+3679delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732447 | |||||
chr1:153732501
|
A | G | 2 | a0001c0002t0001g0147a0001c0002t0008g0319 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.150+3717A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732501 | ||||||
chr1:153732622
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.150+3838A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732622 | ||||||
chr1:153732706
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0182a0001c0001t0011g0183 | 4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3922C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732706 | ||||||
chr1:153732808
|
C | CT | 160 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(157): Show | 166 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.150+4037dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732808 | |||||
chr1:153732808
|
CT | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0053others(10): Show | 15 | HG01433.hp1 HG02257.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.150+4037delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732808 | |||||
chr1:153732810
|
T | G | 1 | a0001c0002t0002g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.150+4026T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732810 | ||||||
chr1:153733002
|
C | T | 2 | a0001c0002t0005g0312a0001c0002t0005g0313 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150+4218C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733002 | ||||||
chr1:153733130
|
C | T | 1 | a0001c0002t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+4346C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733130 | ||||||
chr1:153733134
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.150+4350C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733134 | ||||||
chr1:153733174
|
T | C | 3 | a0001c0002t0001g0008a0001c0002t0006g0129a0001c0002t0006g0130 | 4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+4390T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733174 | ||||||
chr1:153733197
|
CTT | C | 40 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0101others(37): Show | 40 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.150+4444_150+4445d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | |||||
chr1:153733197
|
CTTT | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.150+4443_150+4445d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | |||||
chr1:153733197
|
CTTTT | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(118): Show | 127 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.150+4442_150+4445d others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | |||||
chr1:153733197
|
CTTTTT | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0200others(22): Show | 27 | HG01081.hp1 HG01109.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.150+4441_150+4445d others(7): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | |||||
chr1:153733197
|
CTTTTTTT others(8): Show |
C | 9 | a0001c0001t0001g0007a0001c0001t0001g0122a0001c0001t0001g0124others(6): Show | 10 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.150+4431_150+4445d others(17): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | |||||
chr1:153733299
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+4515G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733299 | ||||||
chr1:153733369
|
C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+4585C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733369 | ||||||
chr1:153733622
|
T | G | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+4838T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733622 | ||||||
chr1:153733666
|
G | A | 12 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.150+4882G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733666 | ||||||
chr1:153733753
|
C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+4969C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733753 | ||||||
chr1:153733766
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.150+4982G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733766 | ||||||
chr1:153733820
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.150+5036C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733820 | ||||||
chr1:153733841
|
G | T | 1 | a0001c0001t0001g0056 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.150+5057G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733841 | ||||||
chr1:153733869
|
T | C | 1 | a0001c0001t0007g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.150+5085T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733869 | ||||||
chr1:153734209
|
T | C | 1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+5425T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734209 | ||||||
chr1:153734223
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(221): Show | 234 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.150+5439T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734223 | ||||||
chr1:153734375
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+5591T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734375 | ||||||
chr1:153734413
|
ACTT | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG03490.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.150+5633_150+5635d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153734413 | |||||
chr1:153734563
|
T | C | 1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+5779T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734563 | ||||||
chr1:153734616
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+5832G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734616 | ||||||
chr1:153734749
|
A | C | 1 | a0001c0001t0001g0293 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.151-5902A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734749 | ||||||
chr1:153734784
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151-5867A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734784 | ||||||
chr1:153734831
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.151-5820A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734831 | ||||||
chr1:153734884
|
A | G | 3 | a0001c0002t0001g0008a0001c0002t0006g0129a0001c0002t0006g0130 | 4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-5767A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734884 | ||||||
chr1:153734953
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151-5698C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734953 | ||||||
chr1:153736002
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151-4649G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736002 | ||||||
chr1:153736063
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.151-4588C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736063 | ||||||
chr1:153736157
|
A | G | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.151-4494A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736157 | ||||||
chr1:153736276
|
T | G | 1 | a0001c0001t0001g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-4375T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736276 | ||||||
chr1:153736355
|
A | T | 1 | a0001c0001t0013g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151-4296A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736355 | ||||||
chr1:153736381
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151-4270T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736381 | ||||||
chr1:153736430
|
G | A | 29 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(26): Show | 30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-4221G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736430 | ||||||
chr1:153736451
|
C | CT | 162 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(159): Show | 168 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.151-4187dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153736451 | |||||
chr1:153736508
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0177a0001c0001t0001g0178others(7): Show | 11 | HG00621.hp2 HG00735.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.151-4143G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736508 | ||||||
chr1:153736571
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.151-4080C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736571 | ||||||
chr1:153736761
|
C | CT | 179 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(176): Show | 187 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.151-3870dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153736761 | |||||
chr1:153736761
|
C | CTT | 19 | a0001c0001t0001g0165a0001c0001t0001g0251a0001c0001t0001g0276others(16): Show | 19 | HG02055.hp2 HG02056.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.151-3871_151-3870d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153736761 | |||||
chr1:153736856
|
C | T | 2 | a0001c0002t0006g0129a0001c0002t0006g0130 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.151-3795C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736856 | ||||||
chr1:153736905
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-3746A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736905 | ||||||
chr1:153737213
|
C | T | 1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.151-3438C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737213 | ||||||
chr1:153737495
|
G | A | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.151-3156G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737495 | ||||||
chr1:153737500
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.151-3151C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737500 | ||||||
chr1:153737820
|
T | C | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-2831T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737820 | ||||||
chr1:153737841
|
T | A | 1 | a0001c0002t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.151-2810T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737841 | ||||||
chr1:153738072
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.151-2579G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738072 | ||||||
chr1:153738140
|
C | T | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.151-2511C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738140 | ||||||
chr1:153738220
|
T | C | 71 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(68): Show | 73 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.151-2431T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738220 | ||||||
chr1:153738326
|
C | T | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-2325C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738326 | ||||||
chr1:153738335
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151-2316A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738335 | ||||||
chr1:153738390
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.151-2261A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738390 | ||||||
chr1:153738442
|
T | C | 4 | a0001c0001t0001g0188a0001c0002t0001g0008a0001c0002t0006g0129others(1): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-2209T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738442 | ||||||
chr1:153738627
|
G | A | 1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.151-2024G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738627 | ||||||
chr1:153738634
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.151-2017T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738634 | ||||||
chr1:153738788
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.151-1863A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738788 | ||||||
chr1:153738792
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(159): Show | 168 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.151-1859T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738792 | ||||||
chr1:153738893
|
CT | C | 36 | a0001c0001t0001g0065a0001c0001t0001g0203a0001c0001t0001g0204others(33): Show | 38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.151-1741delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153738893 | |||||
chr1:153738927
|
C | T | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1724C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738927 | ||||||
chr1:153738940
|
C | G | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0113others(1): Show | 4 | HG01433.hp2 HG01952.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1711C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738940 | ||||||
chr1:153739189
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.151-1462G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739189 | ||||||
chr1:153739211
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1440G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739211 | ||||||
chr1:153739435
|
T | C | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.151-1216T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739435 | ||||||
chr1:153739467
|
C | T | 2 | a0001c0002t0001g0147a0001c0002t0008g0319 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.151-1184C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739467 | ||||||
chr1:153739486
|
A | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.151-1165A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739486 | ||||||
chr1:153739585
|
C | T | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1066C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739585 | ||||||
chr1:153739888
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.151-763G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739888 | ||||||
chr1:153739899
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.151-752A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739899 | ||||||
chr1:153739907
|
G | T | 16 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(13): Show | 17 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.151-744G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739907 | ||||||
chr1:153739914
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.151-737T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739914 | ||||||
chr1:153739949
|
C | A | 27 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(24): Show | 28 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-702C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739949 | ||||||
chr1:153740163
|
G | A | 3 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0309 | 3 | HG02647.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.151-488G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740163 | ||||||
chr1:153740204
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151-447A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740204 | ||||||
chr1:153740257
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.151-394G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740257 | ||||||
chr1:153740300
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-351G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740300 | ||||||
chr1:153740315
|
G | A | 29 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(26): Show | 30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-336G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740315 | ||||||
chr1:153740890
|
G | A | 1 | a0001c0002t0006g0130 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234+156G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 2/29 | chr1 | 153740890 | ||||||
chr1:153741143
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.235-142G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 2/29 | chr1 | 153741143 | ||||||
chr1:153741407
|
A | G | 1 | a0001c0002t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.318+39A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741407 | ||||||
chr1:153741454
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.318+86G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741454 | ||||||
chr1:153741703
|
T | C | 1 | a0001c0001t0003g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318+335T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741703 | ||||||
chr1:153741748
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.318+380G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741748 | ||||||
chr1:153741776
|
G | A | 128 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(125): Show | 130 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.318+408G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741776 | ||||||
chr1:153741942
|
C | T | 173 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(170): Show | 177 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.318+574C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741942 | ||||||
chr1:153741958
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.318+590C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741958 | ||||||
chr1:153742282
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+914G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742282 | ||||||
chr1:153742343
|
T | C | 7 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0251others(4): Show | 7 | NA18950.hp2 NA18953.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+975T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742343 | ||||||
chr1:153742425
|
G | T | 1 | a0001c0001t0010g0227 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.318+1057G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742425 | ||||||
chr1:153742478
|
C | CTCTGTGT others(3): Show |
1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.318+1111_318+1112i others(12): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTCTGTGT others(15): Show |
1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.318+1111_318+1112i others(24): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTG | 76 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(73): Show | 80 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.318+1139_318+1140d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTG | 5 | a0001c0001t0001g0128a0001c0001t0001g0226a0001c0001t0001g0268others(2): Show | 5 | HG01496.hp2 HG02080.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1137_318+1140d others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(1): Show |
3 | a0001c0002t0002g0046a0001c0002t0002g0049a0001c0002t0002g0050 | 3 | HG03130.hp2 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.318+1133_318+1140d others(10): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(3): Show |
2 | a0001c0002t0002g0047a0001c0002t0006g0129 | 2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.318+1131_318+1140d others(12): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(5): Show |
2 | a0001c0002t0002g0043a0001c0002t0002g0051 | 2 | HG01074.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.318+1129_318+1140d others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0188a0001c0002t0001g0008a0001c0002t0002g0029others(3): Show | 7 | HG02109.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1127_318+1140d others(16): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(9): Show |
2 | a0001c0002t0001g0314a0001c0002t0002g0036 | 2 | HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.318+1125_318+1140d others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(11): Show |
7 | a0001c0002t0001g0057a0001c0002t0002g0030a0001c0002t0002g0031others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+1123_318+1140d others(20): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(13): Show |
5 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0033others(2): Show | 6 | HG01081.hp1 HG01192.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+1121_318+1140d others(22): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | CTGTGTGT others(15): Show |
1 | a0001c0002t0002g0042 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318+1119_318+1140d others(24): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742478
|
C | G | 2 | a0001c0002t0001g0147a0001c0002t0008g0319 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.318+1110C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742478 | ||||||
chr1:153742478
|
CTG | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.318+1139_318+1140d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | |||||
chr1:153742505
|
T | TGTGTGTG others(9): Show |
1 | a0001c0002t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.318+1140_318+1141i others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742505 | |||||
chr1:153742507
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0185 | 2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.318+1139T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742507 | ||||||
chr1:153742507
|
T | TGTGTGTG others(9): Show |
1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.318+1140_318+1141i others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742507 | |||||
chr1:153742547
|
C | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.318+1179C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742547 | ||||||
chr1:153742559
|
C | CATCTCAG others(5): Show |
1 | a0001c0001t0001g0290 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.318+1193_318+1194i others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742559 | |||||
chr1:153742666
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.318+1298G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742666 | ||||||
chr1:153742925
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.318+1557C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742925 | ||||||
chr1:153743028
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0155a0001c0001t0001g0156others(11): Show | 17 | HG01069.hp1 HG01255.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.318+1660G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743028 | ||||||
chr1:153743605
|
CCTT | C | 137 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(134): Show | 139 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.318+2241_318+2243d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153743605 | |||||
chr1:153743646
|
T | A | 2 | a0001c0002t0006g0129a0001c0002t0006g0130 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.318+2278T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743646 | ||||||
chr1:153743710
|
C | G | 2 | a0001c0002t0006g0129a0001c0002t0006g0130 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.318+2342C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743710 | ||||||
chr1:153743759
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.318+2391C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743759 | ||||||
chr1:153743973
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0254 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.318+2605C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743973 | ||||||
chr1:153744007
|
T | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0280 | 3 | HG01081.hp2 HG01975.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.318+2639T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744007 | ||||||
chr1:153744038
|
C | CGT | 7 | a0001c0001t0001g0058a0001c0001t0001g0139a0001c0001t0001g0150others(4): Show | 7 | HG02055.hp1 HG02622.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+2713_318+2714d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
C | CGTGTGTG others(5): Show |
1 | a0001c0002t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+2703_318+2714d others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGT | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.318+2713_318+2714d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGTGT | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0053others(43): Show | 50 | HG00099.hp1 HG00621.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.318+2711_318+2714d others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGTGTGT | C | 124 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(121): Show | 126 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.318+2709_318+2714d others(8): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0250 | 3 | HG01123.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.318+2705_318+2714d others(12): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.318+2699_318+2714d others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0253 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.318+2697_318+2714d others(20): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744038
|
CGTGTGTG others(13): Show |
C | 8 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0096others(5): Show | 8 | HG02080.hp1 NA18982.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+2695_318+2714d others(22): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | |||||
chr1:153744046
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.318+2678T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744046 | ||||||
chr1:153744065
|
GTGTGTGT others(10): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.318+2699_318+2715d others(19): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744065 | |||||
chr1:153744088
|
C | A | 1 | a0001c0003t0001g0229 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.318+2720C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744088 | ||||||
chr1:153744396
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.319-2561T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744396 | ||||||
chr1:153744649
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0102 | 3 | HG00639.hp1 HG01074.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.319-2308G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744649 | ||||||
chr1:153744682
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.319-2275C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744682 | ||||||
chr1:153744706
|
G | A | 29 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(26): Show | 30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.319-2251G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744706 | ||||||
chr1:153744848
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0164a0001c0001t0001g0172 | 3 | HG00408.hp2 NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.319-2109C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744848 | ||||||
chr1:153745083
|
C | CAT | 4 | a0001c0001t0001g0188a0001c0002t0001g0008a0001c0002t0006g0129others(1): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1863_319-1862d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153745083 | |||||
chr1:153745083
|
CAT | C | 13 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1863_319-1862d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153745083 | |||||
chr1:153745161
|
C | CT | 195 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(192): Show | 201 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.319-1781dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153745161 | |||||
chr1:153745220
|
G | C | 2 | a0001c0002t0006g0129a0001c0002t0006g0130 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.319-1737G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745220 | ||||||
chr1:153745303
|
C | T | 13 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1654C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745303 | ||||||
chr1:153745304
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0290 | 2 | HG02300.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.319-1653G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745304 | ||||||
chr1:153745350
|
T | G | 1 | a0001c0002t0002g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319-1607T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745350 | ||||||
chr1:153745402
|
A | G | 44 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(41): Show | 45 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.319-1555A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745402 | ||||||
chr1:153745408
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0122a0001c0001t0001g0124others(8): Show | 12 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-1549C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745408 | ||||||
chr1:153745409
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0053 | 3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.319-1548G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745409 | ||||||
chr1:153745484
|
T | G | 18 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(15): Show | 18 | HG01433.hp2 HG01952.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.319-1473T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745484 | ||||||
chr1:153745547
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG02622.hp2 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-1410C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745547 | ||||||
chr1:153745593
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.319-1364G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745593 | ||||||
chr1:153745740
|
T | C | 2 | a0001c0002t0002g0033a0001c0002t0012g0013 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.319-1217T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745740 | ||||||
chr1:153745832
|
A | G | 14 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(11): Show | 14 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.319-1125A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745832 | ||||||
chr1:153745862
|
T | C | 32 | a0001c0001t0001g0188a0001c0002t0001g0035a0001c0002t0001g0057others(29): Show | 33 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.319-1095T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745862 | ||||||
chr1:153745864
|
A | G | 29 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(26): Show | 30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.319-1093A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745864 | ||||||
chr1:153745965
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-992C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745965 | ||||||
chr1:153745966
|
G | A | 3 | a0001c0001t0003g0322a0001c0002t0005g0312a0001c0002t0005g0313 | 3 | HG01891.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.319-991G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745966 | ||||||
chr1:153745996
|
G | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(184): Show | 191 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.319-961G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745996 | ||||||
chr1:153746034
|
C | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.319-923C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746034 | ||||||
chr1:153746270
|
G | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(172): Show | 179 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.319-687G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746270 | ||||||
chr1:153746421
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0184 | 3 | HG01106.hp1 HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.319-536G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746421 | ||||||
chr1:153746425
|
C | T | 147 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(144): Show | 150 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.319-532C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746425 | ||||||
chr1:153746463
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.319-494C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746463 | ||||||
chr1:153746464
|
G | A | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.319-493G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746464 | ||||||
chr1:153746511
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.319-446C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746511 | ||||||
chr1:153746556
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.319-401G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746556 | ||||||
chr1:153746557
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.319-400T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746557 | ||||||
chr1:153746562
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-395G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746562 | ||||||
chr1:153746602
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.319-355C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746602 | ||||||
chr1:153746652
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0174a0001c0001t0001g0182others(1): Show | 5 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-305T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746652 | ||||||
chr1:153746653
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.319-304G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746653 | ||||||
chr1:153746692
|
C | T | 11 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-265C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746692 | ||||||
chr1:153746837
|
A | C | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-120A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746837 | ||||||
chr1:153746920
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.319-37C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746920 | ||||||
chr1:153747169
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0177a0001c0001t0001g0178others(7): Show | 11 | HG00621.hp2 HG00735.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+99T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 4/29 | chr1 | 153747169 | ||||||
chr1:153747582
|
T | C | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+219T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153747582 | ||||||
chr1:153747888
|
T | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.517+525T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153747888 | ||||||
chr1:153747943
|
C | G | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+580C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153747943 | ||||||
chr1:153748069
|
A | C | 4 | a0001c0001t0001g0188a0001c0002t0001g0008a0001c0002t0006g0129others(1): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-620A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748069 | ||||||
chr1:153748214
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 199 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.518-475G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748214 | ||||||
chr1:153748255
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-434G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748255 | ||||||
chr1:153748454
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.518-235G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748454 | ||||||
chr1:153748574
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-115G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748574 | ||||||
chr1:153748827
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.584+72G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153748827 | ||||||
chr1:153748863
|
T | C | 2 | a0001c0002t0005g0312a0001c0002t0005g0313 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.584+108T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153748863 | ||||||
chr1:153748919
|
A | T | 2 | a0001c0002t0005g0312a0001c0002t0005g0313 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.584+164A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153748919 | ||||||
chr1:153749129
|
G | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0151others(13): Show | 17 | HG00423.hp2 HG00673.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.584+374G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749129 | ||||||
chr1:153749131
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.584+376T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749131 | ||||||
chr1:153749158
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.584+403A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749158 | ||||||
chr1:153749232
|
T | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.584+477T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749232 | ||||||
chr1:153749543
|
G | A | 7 | a0001c0002t0002g0046a0001c0002t0002g0047a0001c0002t0002g0048others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+788G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749543 | ||||||
chr1:153749608
|
C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.584+853C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749608 | ||||||
chr1:153749706
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(3): Show | 7 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.584+951T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749706 | ||||||
chr1:153749791
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0135others(1): Show | 4 | HG02717.hp1 HG03540.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+1036C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749791 | ||||||
chr1:153750059
|
G | A | 1 | a0001c0002t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585-1036G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750059 | ||||||
chr1:153750229
|
A | G | 1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.585-866A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750229 | ||||||
chr1:153750276
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.585-819G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750276 | ||||||
chr1:153750561
|
T | C | 16 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(13): Show | 17 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.585-534T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750561 | ||||||
chr1:153750568
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.585-527C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750568 | ||||||
chr1:153750574
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.585-521G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750574 | ||||||
chr1:153750994
|
C | T | 8 | a0001c0002t0002g0041a0001c0002t0002g0046a0001c0002t0002g0047others(5): Show | 8 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-101C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750994 | ||||||
chr1:153751017
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.585-78C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153751017 | ||||||
chr1:153751354
|
C | G | 1 | a0001c0002t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.729+115C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153751354 | ||||||
chr1:153751414
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.729+175A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153751414 | ||||||
chr1:153751856
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.730-423T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153751856 | ||||||
chr1:153752252
|
G | A | 4 | a0001c0002t0002g0046a0001c0002t0002g0047a0001c0002t0002g0049others(1): Show | 4 | HG03130.hp2 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-27G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153752252 | ||||||
chr1:153752506
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0317others(3): Show | 7 | HG01433.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.859+98C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752506 | ||||||
chr1:153752769
|
C | T | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.859+361C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752769 | ||||||
chr1:153752770
|
G | A | 4 | a0001c0001t0001g0317a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+362G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752770 | ||||||
chr1:153752828
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.859+420G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752828 | ||||||
chr1:153752834
|
T | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0142others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+426T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752834 | ||||||
chr1:153752873
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.859+465C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752873 | ||||||
chr1:153753007
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.859+599C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753007 | ||||||
chr1:153753016
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.859+608G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753016 | ||||||
chr1:153753042
|
T | TAC | 35 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0061others(32): Show | 36 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.859+661_859+662dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | |||||
chr1:153753042
|
T | TACAC | 16 | a0001c0001t0001g0146a0001c0002t0001g0008a0001c0002t0002g0002others(13): Show | 18 | HG01081.hp1 HG01192.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.859+659_859+662dup others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | |||||
chr1:153753042
|
T | TACACAC | 4 | a0001c0002t0002g0036a0001c0002t0002g0038a0001c0002t0006g0129others(1): Show | 4 | HG01167.hp1 HG02602.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+657_859+662dup others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | |||||
chr1:153753042
|
TAC | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0178a0001c0001t0001g0193 | 3 | HG02897.hp2 HG03834.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.859+661_859+662del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | |||||
chr1:153753042
|
TACAC | T | 7 | a0001c0001t0001g0191a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG02056.hp1 NA18951.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.859+659_859+662del others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | |||||
chr1:153753077
|
T | G | 1 | a0001c0002t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.859+669T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753077 | ||||||
chr1:153753138
|
C | G | 1 | a0001c0002t0002g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.859+730C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753138 | ||||||
chr1:153753179
|
A | G | 7 | a0001c0001t0001g0192a0001c0001t0001g0223a0001c0001t0001g0262others(4): Show | 7 | NA18948.hp2 NA18962.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.859+771A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753179 | ||||||
chr1:153753287
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.859+879G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753287 | ||||||
chr1:153753314
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.859+906T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753314 | ||||||
chr1:153753325
|
G | T | 1 | a0001c0002t0002g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.859+917G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753325 | ||||||
chr1:153753329
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.859+921C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753329 | ||||||
chr1:153753341
|
G | A | 1 | a0001c0002t0002g0029 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.859+933G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753341 | ||||||
chr1:153753382
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.859+974C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753382 | ||||||
chr1:153753402
|
C | T | 3 | a0001c0001t0001g0248a0001c0001t0001g0308a0001c0001t0001g0310 | 3 | HG02559.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.859+994C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753402 | ||||||
chr1:153753476
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.859+1068G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753476 | ||||||
chr1:153753478
|
A | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.859+1070A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753478 | ||||||
chr1:153753512
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.859+1104G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753512 | ||||||
chr1:153753555
|
C | CA | 6 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0317others(3): Show | 7 | HG01433.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.860-1079dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753555 | |||||
chr1:153753655
|
C | CT | 14 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0110others(11): Show | 16 | HG00735.hp1 HG01106.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.860-969dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753655 | |||||
chr1:153753655
|
CT | C | 13 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0063others(10): Show | 13 | HG01070.hp2 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.860-969delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753655 | |||||
chr1:153753655
|
CTT | C | 12 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.860-970_860-969del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753655 | |||||
chr1:153753758
|
C | T | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.860-884C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753758 | ||||||
chr1:153753929
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0103others(1): Show | 5 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-713A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753929 | ||||||
chr1:153753939
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0103others(1): Show | 5 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-703G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753939 | ||||||
chr1:153753940
|
C | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0103others(1): Show | 5 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-702C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753940 | ||||||
chr1:153753956
|
CT | C | 178 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(175): Show | 182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.860-667delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753956 | |||||
chr1:153753956
|
CTT | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0271others(6): Show | 10 | HG01433.hp1 HG02145.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-668_860-667del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753956 | |||||
chr1:153754144
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.860-498G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153754144 | ||||||
chr1:153754280
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.860-362T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153754280 | ||||||
chr1:153754797
|
C | T | 2 | a0001c0002t0005g0312a0001c0002t0005g0313 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.957+58C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153754797 | ||||||
chr1:153754946
|
C | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.957+207C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153754946 | ||||||
chr1:153755060
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.957+321A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755060 | ||||||
chr1:153755086
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0211a0001c0001t0001g0218others(2): Show | 5 | HG00099.hp1 HG01258.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+347G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755086 | ||||||
chr1:153755156
|
T | C | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.957+417T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755156 | ||||||
chr1:153755249
|
G | GT | 12 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0059others(9): Show | 12 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.957+520dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr1 | 153755249 | |||||
chr1:153755327
|
G | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0247 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.957+588G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755327 | ||||||
chr1:153755332
|
C | T | 2 | a0001c0002t0001g0147a0001c0002t0008g0319 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.957+593C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755332 | ||||||
chr1:153755441
|
A | G | 1 | a0001c0002t0002g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.957+702A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755441 | ||||||
chr1:153755616
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.957+877G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755616 | ||||||
chr1:153755763
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(196): Show | 207 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.957+1024A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755763 | ||||||
chr1:153755854
|
C | T | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.957+1115C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755854 | ||||||
chr1:153755982
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(194): Show | 205 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.957+1243A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755982 | ||||||
chr1:153755982
|
A | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0267 | 2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.957+1243A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755982 | ||||||
chr1:153756100
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.957+1361C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756100 | ||||||
chr1:153756166
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.958-1406A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756166 | ||||||
chr1:153756229
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.958-1343G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756229 | ||||||
chr1:153756274
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0182a0001c0001t0011g0183 | 4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-1298A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756274 | ||||||
chr1:153756317
|
A | T | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-1255A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756317 | ||||||
chr1:153756476
|
C | T | 1 | a0001c0002t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.958-1096C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756476 | ||||||
chr1:153756544
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-1028G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756544 | ||||||
chr1:153756644
|
C | T | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.958-928C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756644 | ||||||
chr1:153756994
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-578G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756994 | ||||||
chr1:153757113
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.958-459T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153757113 | ||||||
chr1:153757186
|
T | G | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.958-386T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153757186 | ||||||
chr1:153757245
|
C | T | 8 | a0001c0002t0002g0041a0001c0002t0002g0046a0001c0002t0002g0047others(5): Show | 8 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-327C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153757245 | ||||||
chr1:153757847
|
C | G | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1149+84C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153757847 | ||||||
chr1:153757855
|
C | T | 3 | a0001c0002t0002g0045a0001c0002t0005g0312a0001c0002t0005g0313 | 3 | HG01891.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1149+92C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153757855 | ||||||
chr1:153758257
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1149+494T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758257 | ||||||
chr1:153758412
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1149+649T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758412 | ||||||
chr1:153758526
|
T | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0235a0001c0001t0001g0247 | 3 | HG01884.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1149+763T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758526 | ||||||
chr1:153758531
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1149+768A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758531 | ||||||
chr1:153758535
|
C | T | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1149+772C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758535 | ||||||
chr1:153758583
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0102 | 3 | HG00639.hp1 HG01074.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1149+820A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758583 | ||||||
chr1:153759059
|
G | A | 2 | a0001c0002t0006g0129a0001c0002t0006g0130 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1150-467G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759059 | ||||||
chr1:153759082
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1150-444G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759082 | ||||||
chr1:153759085
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1150-441C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759085 | ||||||
chr1:153759274
|
G | GA | 34 | a0001c0001t0001g0077a0001c0001t0001g0097a0001c0002t0001g0035others(31): Show | 35 | HG00544.hp2 HG01074.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1150-237dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 153759274 | |||||
chr1:153759274
|
GA | G | 138 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(135): Show | 140 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1150-237delA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 153759274 | |||||
chr1:153759295
|
G | A | 2 | a0001c0002t0006g0129a0001c0002t0006g0130 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1150-231G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759295 | ||||||
chr1:153759432
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1150-94C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759432 | ||||||
chr1:153759830
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1237+217G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153759830 | ||||||
chr1:153760095
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1238-216G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760095 | ||||||
chr1:153760164
|
A | G | 180 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(177): Show | 184 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1238-147A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760164 | ||||||
chr1:153760232
|
C | A | 5 | a0001c0001t0001g0202a0001c0001t0001g0232a0001c0001t0001g0238others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-79C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760232 | ||||||
chr1:153760232
|
C | CA | 16 | a0001c0001t0001g0028a0001c0001t0001g0100a0001c0001t0001g0110others(13): Show | 16 | HG00423.hp2 HG02080.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1238-53dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 153760232 | |||||
chr1:153760232
|
CA | C | 48 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0059others(45): Show | 49 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1238-53delA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 153760232 | |||||
chr1:153760232
|
CAAA | C | 6 | a0001c0002t0002g0046a0001c0002t0002g0048a0001c0002t0002g0049others(3): Show | 6 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-55_1238-53del others(3): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 153760232 | |||||
chr1:153760257
|
A | G | 2 | a0001c0001t0001g0287a0001c0002t0001g0008 | 3 | HG03098.hp2 HG03225.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1238-54A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760257 | ||||||
chr1:153760497
|
G | A | 28 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(25): Show | 29 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1317+107G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 12/29 | chr1 | 153760497 | ||||||
chr1:153760538
|
C | A | 8 | a0001c0001t0001g0097a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 8 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317+148C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 12/29 | chr1 | 153760538 | ||||||
chr1:153760540
|
T | C | 1 | a0001c0001t0003g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1317+150T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 12/29 | chr1 | 153760540 | ||||||
chr1:153761561
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1410-9C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 13/29 | chr1 | 153761561 | ||||||
chr1:153762064
|
T | C | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1516+388T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762064 | ||||||
chr1:153762249
|
G | A | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1517-479G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762249 | ||||||
chr1:153762278
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0317others(5): Show | 9 | HG01433.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1517-450G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762278 | ||||||
chr1:153762373
|
C | G | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1517-355C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762373 | ||||||
chr1:153762961
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1636+114T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 15/29 | chr1 | 153762961 | ||||||
chr1:153763181
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1637-52C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 15/29 | chr1 | 153763181 | ||||||
chr1:153763529
|
G | A | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1766+167G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763529 | ||||||
chr1:153763590
|
C | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1766+228C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763590 | ||||||
chr1:153763595
|
G | C | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1766+233G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763595 | ||||||
chr1:153763672
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1767-160A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763672 | ||||||
chr1:153763804
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1767-28G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763804 | ||||||
chr1:153763904
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1821+18C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 17/29 | chr1 | 153763904 | ||||||
chr1:153764235
|
T | TCC | 13 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1925+16_1925+17dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr1 | 153764235 | |||||
chr1:153764285
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1925+64C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764285 | ||||||
chr1:153764520
|
G | A | 1 | a0001c0002t0012g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1926-170G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764520 | ||||||
chr1:153764538
|
C | A | 1 | a0001c0001t0001g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1926-152C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764538 | ||||||
chr1:153764634
|
G | A | 2 | a0001c0002t0002g0039a0001c0002t0002g0040 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1926-56G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764634 | ||||||
chr1:153764660
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1926-30G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764660 | ||||||
chr1:153765144
|
T | C | 1 | a0001c0002t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2090+81T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765144 | ||||||
chr1:153765182
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2090+119T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765182 | ||||||
chr1:153765252
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2090+189T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765252 | ||||||
chr1:153765257
|
C | T | 13 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2090+194C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765257 | ||||||
chr1:153765293
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0077a0001c0001t0001g0082others(4): Show | 8 | HG00544.hp2 NA18957.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.2090+230C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765293 | ||||||
chr1:153765515
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2090+452T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765515 | ||||||
chr1:153765789
|
C | T | 1 | a0001c0002t0002g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2090+726C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765789 | ||||||
chr1:153765986
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2090+923A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765986 | ||||||
chr1:153766021
|
G | C | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2090+958G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766021 | ||||||
chr1:153766079
|
T | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2090+1016T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766079 | ||||||
chr1:153766115
|
C | CT | 42 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(39): Show | 43 | HG00438.hp2 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2090+1076dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766115 | |||||
chr1:153766115
|
CT | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0073others(13): Show | 16 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2090+1076delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766115 | |||||
chr1:153766339
|
C | T | 3 | a0001c0002t0001g0008a0001c0002t0006g0129a0001c0002t0006g0130 | 4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2090+1276C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766339 | ||||||
chr1:153766347
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2090+1284G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766347 | ||||||
chr1:153766423
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0151others(14): Show | 18 | HG00423.hp2 HG00673.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.2091-1251G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766423 | ||||||
chr1:153766551
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0240 | 2 | HG00609.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2091-1123G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766551 | ||||||
chr1:153766591
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2091-1083G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766591 | ||||||
chr1:153766687
|
A | AT | 10 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(7): Show | 11 | HG01109.hp2 HG01433.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.2091-967dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766687 | |||||
chr1:153766687
|
AT | A | 36 | a0001c0001t0001g0180a0001c0001t0001g0200a0001c0001t0001g0334others(33): Show | 38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2091-967delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766687 | |||||
chr1:153766793
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(200): Show | 211 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.2091-881A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766793 | ||||||
chr1:153766883
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2091-791G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766883 | ||||||
chr1:153766999
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2091-675C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766999 | ||||||
chr1:153767005
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2091-669C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767005 | ||||||
chr1:153767343
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2091-331T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767343 | ||||||
chr1:153767479
|
G | A | 30 | a0001c0002t0001g0035a0001c0002t0001g0057a0001c0002t0001g0314others(27): Show | 31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2091-195G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767479 | ||||||
chr1:153767552
|
G | A | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2091-122G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767552 | ||||||
chr1:153767611
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2091-63C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767611 | ||||||
chr1:153767831
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA19064.hp2 | splice_region_variant&intron_variant | LOW | c.2244+4A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153767831 | ||||||
chr1:153768018
|
C | T | 36 | a0001c0002t0001g0008a0001c0002t0001g0035a0001c0002t0001g0057others(33): Show | 38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2244+191C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768018 | ||||||
chr1:153768021
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0053 | 3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2244+194T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768021 | ||||||
chr1:153768177
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2244+350C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768177 | ||||||
chr1:153768215
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2244+388G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768215 | ||||||
chr1:153768566
|
C | T | 3 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0329 | 3 | HG01243.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2245-327C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768566 | ||||||
chr1:153768580
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2245-313A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768580 | ||||||
chr1:153768661
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0317others(3): Show | 7 | HG01433.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2245-232A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768661 | ||||||
chr1:153768817
|
TAAGG | T | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2245-70_2245-67del others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 153768817 | |||||
chr1:153768836
|
A | G | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2245-57A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768836 | ||||||
chr1:153769036
|
C | A | 33 | a0001c0002t0001g0008a0001c0002t0001g0035a0001c0002t0001g0057others(30): Show | 35 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.2313+75C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769036 | ||||||
chr1:153769350
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0109others(2): Show | 5 | NA18947.hp2 NA18963.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2313+389G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769350 | ||||||
chr1:153769419
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2314-350G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769419 | ||||||
chr1:153769597
|
C | A | 1 | a0001c0002t0002g0002 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2314-172C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769597 | ||||||
chr1:153769613
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2314-156C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769613 | ||||||
chr1:153769666
|
AT | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0122a0001c0001t0001g0124others(40): Show | 46 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.2314-92delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr1 | 153769666 | |||||
chr1:153769894
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2389+50G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769894 | ||||||
chr1:153769961
|
T | C | 37 | a0001c0001t0001g0203a0001c0002t0001g0008a0001c0002t0001g0035others(34): Show | 39 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.2389+117T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769961 | ||||||
chr1:153769979
|
C | T | 6 | a0001c0001t0003g0322a0001c0001t0003g0326a0001c0001t0003g0327others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2389+135C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769979 | ||||||
chr1:153769980
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389+136G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769980 | ||||||
chr1:153769993
|
A | G | 36 | a0001c0002t0001g0008a0001c0002t0001g0035a0001c0002t0001g0057others(33): Show | 38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2389+149A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769993 | ||||||
chr1:153770058
|
G | GGT | 4 | a0001c0001t0001g0056a0001c0001t0001g0092a0001c0001t0001g0120others(1): Show | 4 | HG01167.hp2 HG02055.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2390-96_2390-95dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770058
|
GGT | G | 46 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0055others(43): Show | 46 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2390-96_2390-95del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770058
|
GGTGT | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(32): Show | 37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2390-98_2390-95del others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770058
|
GGTGTGT | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0054others(23): Show | 28 | HG00408.hp1 HG01106.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.2390-100_2390-95de others(7): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770058
|
GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0085 | 4 | HG00639.hp2 HG01433.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2390-102_2390-95de others(9): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770058
|
GGTGTGTG others(9): Show |
G | 2 | a0001c0002t0001g0147a0001c0002t0008g0319 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2390-110_2390-95de others(17): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770058
|
GGTGTGTG others(25): Show |
G | 36 | a0001c0002t0001g0008a0001c0002t0001g0035a0001c0002t0001g0057others(33): Show | 38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2390-126_2390-95de others(33): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | |||||
chr1:153770059
|
GT | G | 13 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(10): Show | 13 | HG00673.hp2 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2390-138delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | ||||||
chr1:153770059
|
GTGT | G | 66 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(63): Show | 68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2390-138_2390-136d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | ||||||
chr1:153770059
|
GTGTGT | G | 42 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(39): Show | 43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.2390-138_2390-134d others(7): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | ||||||
chr1:153770059
|
GTGTGTGT | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0027others(27): Show | 33 | HG00558.hp2 HG01069.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.2390-138_2390-132d others(9): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | ||||||
chr1:153770059
|
GTGTGTGT others(4): Show |
G | 2 | a0001c0001t0001g0263a0001c0001t0001g0287 | 2 | HG04199.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2390-138_2390-128d others(13): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | ||||||
chr1:153770059
|
GTGTGTGT others(12): Show |
G | 1 | a0001c0001t0001g0268 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2390-138_2390-120d others(21): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | ||||||
chr1:153770062
|
T | G | 2 | a0001c0001t0001g0059a0001c0002t0002g0069 | 2 | NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2390-136T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770062 | ||||||
chr1:153770064
|
T | G | 2 | a0001c0001t0001g0281a0001c0002t0002g0104 | 2 | HG00673.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2390-134T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770064 | ||||||
chr1:153770066
|
T | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0246a0001c0002t0002g0187 | 3 | HG00408.hp1 HG03017.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2390-132T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770066 | ||||||
chr1:153770100
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2390-98T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770100 | ||||||
chr1:153770102
|
T | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0064others(41): Show | 47 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.2390-96T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770102 | ||||||
chr1:153770121
|
G | A | 1 | a0001c0002t0001g0008 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2390-77G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770121 | ||||||
chr1:153770127
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2390-71T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770127 | ||||||
chr1:153770127
|
T | TG | 23 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0056others(20): Show | 23 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.2390-63dupG | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770127 | |||||
chr1:153770132
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2390-66G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770132 | ||||||
chr1:153770134
|
G | GGT | 15 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG01978.hp2 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2390-47_2390-46dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770134 | |||||
chr1:153770134
|
G | T | 9 | a0001c0001t0001g0097a0001c0001t0001g0207a0001c0001t0001g0211others(6): Show | 9 | HG00099.hp1 HG01258.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2390-64G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770134 | ||||||
chr1:153770134
|
GGT | G | 25 | a0001c0002t0001g0035a0001c0002t0002g0002a0001c0002t0002g0029others(22): Show | 26 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.2390-47_2390-46del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770134 | |||||
chr1:153770136
|
T | G | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0141others(1): Show | 4 | HG04199.hp1 NA18957.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2390-62T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770136 | ||||||
chr1:153770555
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2504-130G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 24/29 | chr1 | 153770555 | ||||||
chr1:153770758
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(166): Show | 175 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.2552+25T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770758 | ||||||
chr1:153770779
|
C | T | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2552+46C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770779 | ||||||
chr1:153770813
|
C | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 122 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.2552+80C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770813 | ||||||
chr1:153770841
|
G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 106 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2552+108G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770841 | ||||||
chr1:153770924
|
T | G | 1 | a0001c0007t0003g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2552+191T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770924 | ||||||
chr1:153770926
|
C | G | 5 | a0001c0002t0001g0057a0001c0002t0001g0314a0001c0002t0004g0320others(2): Show | 5 | HG02615.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2552+193C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770926 | ||||||
chr1:153770964
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2552+231G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770964 | ||||||
chr1:153771043
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2552+310C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771043 | ||||||
chr1:153771068
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2552+335C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771068 | ||||||
chr1:153771117
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2552+384G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771117 | ||||||
chr1:153771147
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0211a0001c0001t0001g0268 | 3 | HG00099.hp1 HG01496.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2552+414C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771147 | ||||||
chr1:153771185
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0142others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2552+452G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771185 | ||||||
chr1:153771219
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2552+486G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771219 | ||||||
chr1:153771304
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2553-492T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771304 | ||||||
chr1:153771376
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2553-420T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771376 | ||||||
chr1:153771451
|
A | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0203others(42): Show | 48 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2553-345A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771451 | ||||||
chr1:153771473
|
T | C | 42 | a0001c0001t0001g0203a0001c0001t0001g0317a0001c0001t0001g0332others(39): Show | 44 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2553-323T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771473 | ||||||
chr1:153771541
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2553-255G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771541 | ||||||
chr1:153771582
|
T | C | 4 | a0001c0001t0001g0317a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2553-214T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771582 | ||||||
chr1:153771662
|
T | C | 2 | a0001c0002t0001g0057a0001c0002t0001g0314 | 2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2553-134T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771662 | ||||||
chr1:153771768
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2553-28A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771768 | ||||||
chr1:153772020
|
C | CGGT | 6 | a0001c0001t0001g0124a0001c0001t0001g0136a0001c0001t0001g0150others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2720+86_2720+88dup others(3): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | |||||
chr1:153772020
|
CGG | C | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2720+58_2720+59del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772020 | ||||||
chr1:153772020
|
CGGT | C | 34 | a0001c0002t0001g0008a0001c0002t0001g0035a0001c0002t0001g0057others(31): Show | 36 | HG00408.hp1 HG01074.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2720+86_2720+88del others(3): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | |||||
chr1:153772020
|
CGGTGGTG others(8): Show |
C | 1 | a0001c0002t0008g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2720+74_2720+88del others(15): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | |||||
chr1:153772020
|
CGGTGGTG others(11): Show |
C | 9 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0224others(6): Show | 9 | HG02056.hp1 NA18941.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.2720+71_2720+88del others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | |||||
chr1:153772023
|
T | C | 3 | a0001c0002t0004g0320a0001c0002t0004g0323a0001c0002t0012g0013 | 3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2720+60T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772023 | ||||||
chr1:153772032
|
T | C | 7 | a0001c0002t0002g0046a0001c0002t0002g0047a0001c0002t0002g0048others(4): Show | 7 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2720+69T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772032 | ||||||
chr1:153772119
|
C | T | 1 | a0001c0002t0004g0323 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2720+156C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772119 | ||||||
chr1:153772139
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2720+176C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772139 | ||||||
chr1:153772140
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2720+177T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772140 | ||||||
chr1:153772238
|
T | C | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0109others(2): Show | 5 | NA18947.hp2 NA18963.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-102T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772238 | ||||||
chr1:153772306
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2721-34C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772306 | ||||||
chr1:153772839
|
C | T | 1 | a0001c0002t0002g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2895-86C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 28/29 | chr1 | 153772839 | ||||||
chr1:153772904
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0282 | 2 | HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2895-21G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 28/29 | chr1 | 153772904 |