geneid | 64399 |
---|---|
ensemblid | ENSG00000164161.10 |
hgncid | 14866 |
symbol | HHIP |
name | hedgehog interacting protein |
refseq_nuc | NM_022475.3 |
refseq_prot | NP_071920.1 |
ensembl_nuc | ENST00000296575.8 |
ensembl_prot | ENSP00000296575.3 |
mane_status | MANE Select |
chr | chr4 |
start | 144646156 |
end | 144745271 |
strand | + |
ver | v1.2 |
region | chr4:144646156-144745271 |
region5000 | chr4:144641156-144750271 |
regionname0 | HHIP_chr4_144646156_144745271 |
regionname5000 | HHIP_chr4_144641156_144750271 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 700 | 305 | 74 | 45 | 148 | 10 | 26 | 120 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0002 | 0/0 | 700 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0003 | 0/0 | 700 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0004 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2103 | 300 | 73 | 43 | 148 | 8 | 26 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
c0002 | 0/0 | 2103 | 8 | 7 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
c0003 | 0/0 | 2103 | 4 | 0 | 2 | 0 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
c0004 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
c0005 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
c0006 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7775 | 68 | 3 | 11 | 47 | 4 | 3 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0002 | 0/0 | 7773 | 67 | 12 | 8 | 44 | 0 | 3 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0003 | 0/0 | 7773 | 43 | 1 | 14 | 19 | 3 | 6 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0004 | 0/0 | 7773 | 15 | 14 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0005 | 0/0 | 7773 | 13 | 4 | 2 | 6 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0006 | 0/0 | 7772 | 7 | 6 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0007 | 0/0 | 7773 | 7 | 0 | 0 | 7 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0008 | 0/1 | 7775 | 6 | 0 | 1 | 2 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0009 | 0/0 | 7773 | 6 | 6 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0010 | 0/0 | 7775 | 5 | 4 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0011 | 0/0 | 7773 | 5 | 0 | 0 | 4 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0012 | 0/0 | 7773 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0013 | 0/0 | 7772 | 3 | 0 | 0 | 2 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0014 | 0/0 | 7774 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0015 | 0/0 | 7775 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0016 | 0/0 | 7773 | 3 | 0 | 0 | 3 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0017 | 0/0 | 7773 | 3 | 0 | 1 | 0 | 0 | 2 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0018 | 0/0 | 7781 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0019 | 0/0 | 7772 | 2 | 1 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0020 | 0/0 | 7772 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0021 | 0/0 | 7773 | 2 | 0 | 1 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0022 | 0/0 | 7774 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0023 | 0/0 | 7732 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0024 | 0/0 | 7772 | 2 | 1 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0025 | 0/0 | 7773 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0026 | 0/0 | 7772 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0027 | 0/0 | 7772 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0028 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0029 | 0/0 | 7773 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0030 | 0/0 | 7773 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0031 | 0/0 | 7773 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0032 | 0/0 | 7773 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0033 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0034 | 0/0 | 7775 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0035 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0036 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0037 | 0/0 | 7772 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0038 | 0/0 | 7772 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0039 | 0/0 | 7773 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0040 | 0/0 | 7772 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0041 | 0/0 | 7773 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0042 | 0/0 | 7771 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0043 | 0/0 | 7746 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0044 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0045 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0046 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0047 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0048 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0049 | 0/0 | 7775 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0050 | 0/0 | 7775 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0051 | 0/0 | 7800 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0052 | 0/0 | 7773 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0053 | 0/0 | 7775 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0054 | 1/0 | 7835 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0055 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0056 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0057 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0058 | 0/0 | 7777 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0059 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0060 | 0/0 | 7793 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0061 | 0/0 | 7773 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0062 | 0/0 | 7772 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0063 | 0/0 | 7774 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0064 | 0/0 | 7773 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
t0065 | 0/0 | 7773 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2103 | 300 | 73 | 43 | 148 | 8 | 26 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0003 | 0/0 | 2103 | 4 | 0 | 2 | 0 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0006 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0002c0002 | 0/0 | 2103 | 8 | 7 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0003c0004 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0004c0005 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9877 | 64 | 3 | 9 | 47 | 2 | 3 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0002 | 0/0 | 9875 | 67 | 12 | 8 | 44 | 0 | 3 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0003 | 0/0 | 9875 | 43 | 1 | 14 | 19 | 3 | 6 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0004 | 0/0 | 9875 | 14 | 13 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0005 | 0/0 | 9875 | 10 | 3 | 2 | 4 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0006 | 0/0 | 9874 | 7 | 6 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0007 | 0/0 | 9875 | 7 | 0 | 0 | 7 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0008 | 0/1 | 9877 | 6 | 0 | 1 | 2 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0010 | 0/0 | 9877 | 5 | 4 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0011 | 0/0 | 9875 | 5 | 0 | 0 | 4 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0012 | 0/0 | 9875 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0013 | 0/0 | 9874 | 3 | 0 | 0 | 2 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0014 | 0/0 | 9876 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0015 | 0/0 | 9877 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0016 | 0/0 | 9875 | 3 | 0 | 0 | 3 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0017 | 0/0 | 9875 | 3 | 0 | 1 | 0 | 0 | 2 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0018 | 0/0 | 9883 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0019 | 0/0 | 9874 | 2 | 1 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0020 | 0/0 | 9874 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0021 | 0/0 | 9875 | 2 | 0 | 1 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0022 | 0/0 | 9876 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0023 | 0/0 | 9834 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0024 | 0/0 | 9874 | 2 | 1 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0025 | 0/0 | 9875 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0026 | 0/0 | 9874 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0027 | 0/0 | 9874 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0028 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0029 | 0/0 | 9875 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0030 | 0/0 | 9875 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0031 | 0/0 | 9875 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0032 | 0/0 | 9875 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0033 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0034 | 0/0 | 9877 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0035 | 0/0 | 9874 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0036 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0037 | 0/0 | 9874 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0038 | 0/0 | 9874 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0039 | 0/0 | 9875 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0040 | 0/0 | 9874 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0041 | 0/0 | 9875 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0042 | 0/0 | 9873 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0043 | 0/0 | 9848 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0044 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0045 | 0/0 | 9876 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0046 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0047 | 0/0 | 9874 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0048 | 0/0 | 9876 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0049 | 0/0 | 9877 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0050 | 0/0 | 9877 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0051 | 0/0 | 9902 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0052 | 0/0 | 9875 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0053 | 0/0 | 9877 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0054 | 1/0 | 9937 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0055 | 0/0 | 9937 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0056 | 0/0 | 9908 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0057 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0058 | 0/0 | 9879 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0059 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0060 | 0/0 | 9895 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0061 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0062 | 0/0 | 9874 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0001t0065 | 0/0 | 9875 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0003t0001 | 0/0 | 9877 | 4 | 0 | 2 | 0 | 2 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0001c0006t0005 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0002c0002t0009 | 0/0 | 9875 | 6 | 6 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0002c0002t0063 | 0/0 | 9876 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0002c0002t0064 | 0/0 | 9875 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0003c0004t0005 | 0/0 | 9875 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
a0004c0005t0004 | 0/0 | 9875 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | copy fasta | chr4 | 144641156 | 144750271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0008g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0008g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0010g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0010g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0011g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0013g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0013g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0014g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0016g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0016g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0017g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0017g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0018g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0019g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0020g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0020g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0021g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0022g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0022g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0023g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0023g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0024g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0025g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0026g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0027g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0028g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0029g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0030g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0031g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0032g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0033g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0034g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0035g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0036g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0037g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0038g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0039g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0040g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0041g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0042g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0043g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0044g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0045g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0046g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0047g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0048g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0049g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0050g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0051g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0052g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0053g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0054g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0055g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0056g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0057g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0058g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0059g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0060g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0061g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0062g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0001t0065g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0001c0006t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0063g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0002c0002t0064g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0003c0004t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0003c0004t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
a0004c0005t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0113 | EUR | GBR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0183 | EUR | GBR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0102 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0153 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00408 | hp2 | a0001 | c0001 | t0008 | g0158 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00423 | hp2 | a0001 | c0001 | t0058 | g0249 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00621 | hp1 | a0001 | c0001 | t0011 | g0045 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0224 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00642 | hp2 | a0001 | c0001 | t0017 | g0089 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01074 | hp2 | a0001 | c0001 | t0021 | g0087 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01081 | hp2 | a0001 | c0001 | t0062 | g0110 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0292 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01106 | hp2 | a0001 | c0001 | t0008 | g0225 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01192 | hp1 | a0002 | c0002 | t0064 | g0138 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0161 | AMR | PUR | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01256 | hp1 | a0001 | c0001 | t0026 | g0223 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0080 | AMR | CLM | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0175 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01515 | hp2 | a0001 | c0001 | t0027 | g0168 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0297 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01891 | hp2 | a0001 | c0001 | t0036 | g0142 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01943 | hp2 | a0001 | c0001 | t0039 | g0060 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0177 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02015 | hp1 | a0001 | c0001 | t0038 | g0001 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02055 | hp2 | a0002 | c0002 | t0009 | g0136 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02056 | hp1 | a0001 | c0001 | t0030 | g0159 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02056 | hp2 | a0001 | c0001 | t0023 | g0261 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0122 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0147 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CDX | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02257 | hp1 | a0001 | c0001 | t0033 | g0199 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02258 | hp1 | a0002 | c0002 | t0063 | g0139 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02258 | hp2 | a0001 | c0001 | t0047 | g0281 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02572 | hp2 | a0001 | c0001 | t0056 | g0082 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0146 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02622 | hp2 | a0001 | c0001 | t0035 | g0079 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0214 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02630 | hp2 | a0002 | c0002 | t0009 | g0134 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02698 | hp1 | a0001 | c0001 | t0050 | g0017 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02723 | hp1 | a0001 | c0001 | t0019 | g0162 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02735 | hp1 | a0001 | c0001 | t0024 | g0090 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02809 | hp1 | a0001 | c0001 | t0015 | g0130 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02897 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02965 | hp2 | a0002 | c0002 | t0009 | g0135 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02970 | hp1 | a0001 | c0001 | t0028 | g0218 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02970 | hp2 | a0002 | c0002 | t0009 | g0137 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03041 | hp1 | a0002 | c0002 | t0009 | g0140 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03041 | hp2 | a0004 | c0005 | t0004 | g0118 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03130 | hp1 | a0002 | c0002 | t0009 | g0133 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03209 | hp1 | a0001 | c0001 | t0018 | g0149 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03209 | hp2 | a0001 | c0001 | t0046 | g0115 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03225 | hp1 | a0001 | c0001 | t0020 | g0119 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0278 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03239 | hp2 | a0001 | c0001 | t0013 | g0189 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03486 | hp1 | a0001 | c0001 | t0020 | g0072 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03516 | hp1 | a0001 | c0001 | t0061 | g0132 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03516 | hp2 | a0001 | c0001 | t0044 | g0144 | AFR | ESN | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0216 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03654 | hp2 | a0001 | c0001 | t0017 | g0083 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03669 | hp1 | a0001 | c0001 | t0021 | g0088 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03704 | hp1 | a0001 | c0001 | t0011 | g0295 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03831 | hp2 | a0001 | c0001 | t0017 | g0085 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03834 | hp1 | a0001 | c0001 | t0042 | g0065 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03927 | hp1 | a0001 | c0001 | t0041 | g0022 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03942 | hp1 | a0001 | c0001 | t0051 | g0095 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG04204 | hp2 | a0001 | c0001 | t0043 | g0040 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG04228 | hp1 | a0001 | c0001 | t0032 | g0217 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG04228 | hp2 | a0001 | c0001 | t0031 | g0165 | SAS | STU | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | CHB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18940 | hp2 | a0001 | c0001 | t0040 | g0027 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18942 | hp1 | a0001 | c0001 | t0034 | g0230 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18942 | hp2 | a0001 | c0001 | t0025 | g0157 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18944 | hp1 | a0001 | c0001 | t0023 | g0243 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18947 | hp2 | a0001 | c0001 | t0013 | g0211 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18948 | hp2 | a0003 | c0004 | t0005 | g0207 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18951 | hp1 | a0001 | c0001 | t0022 | g0250 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18953 | hp2 | a0001 | c0001 | t0022 | g0240 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18962 | hp1 | a0001 | c0001 | t0016 | g0048 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18965 | hp2 | a0001 | c0001 | t0011 | g0049 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18973 | hp1 | a0001 | c0001 | t0053 | g0006 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18983 | hp1 | a0001 | c0001 | t0029 | g0212 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18984 | hp1 | a0001 | c0001 | t0011 | g0259 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18986 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18988 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18991 | hp2 | a0001 | c0001 | t0049 | g0093 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18993 | hp1 | a0001 | c0001 | t0065 | g0180 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18994 | hp2 | a0001 | c0001 | t0016 | g0035 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19002 | hp2 | a0003 | c0004 | t0005 | g0206 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19005 | hp1 | a0001 | c0001 | t0037 | g0055 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19010 | hp1 | a0001 | c0001 | t0013 | g0210 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19030 | hp1 | a0001 | c0001 | t0012 | g0215 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19043 | hp1 | a0001 | c0001 | t0048 | g0279 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19043 | hp2 | a0001 | c0001 | t0018 | g0148 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19060 | hp2 | a0001 | c0001 | t0016 | g0030 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19068 | hp2 | a0001 | c0001 | t0008 | g0172 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19074 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19075 | hp1 | a0001 | c0001 | t0052 | g0057 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | YRI | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | ASW | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0296 | AFR | ASW | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02109 | hp1 | a0001 | c0001 | t0057 | g0270 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02486 | hp2 | a0001 | c0001 | t0045 | g0269 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02559 | hp1 | a0001 | c0001 | t0015 | g0127 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0226 | AFR | ACB | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03471 | hp1 | a0001 | c0001 | t0060 | g0075 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG03471 | hp2 | a0001 | c0001 | t0014 | g0285 | AFR | MSL | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG06807 | hp1 | a0001 | c0001 | t0059 | g0128 | AFR | USA | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
HG06807 | hp2 | a0001 | c0001 | t0055 | g0286 | AFR | USA | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA21309 | hp1 | a0001 | c0006 | t0005 | g0213 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0184 | REF | REF | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0054 | g0287 | REF | REF | HHIP_chr4_144641156_144750271 | HHIP | chr4 | 144641156 | 144750271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:144659714
|
G | A | 1 | a0002 | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
missense_variant | MODERATE | c.707G>A | p.Gly236Glu | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/13 | 1227/9937 | 707/2103 | 236/700 | chr4 | 144659714 | ||
chr4:144708220
|
G | A | 1 | a0004 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1210G>A | p.Val404Met | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/13 | 1730/9937 | 1210/2103 | 404/700 | chr4 | 144708220 | ||
chr4:144737949
|
A | G | 1 | a0003 | 2 | NA18948.hp2 NA19002.hp2 |
missense_variant | MODERATE | c.2095A>G | p.Ile699Val | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2615/9937 | 2095/2103 | 699/700 | chr4 | 144737949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:144715396
|
C | T | 1 | a0001c0006 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1644C>T | p.Ser548Ser | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/13 | 2164/9937 | 1644/2103 | 548/700 | chr4 | 144715396 | ||
chr4:144737912
|
T | C | 1 | a0001c0003 | 4 | HG00099.hp1 HG00280.hp1 HG01106.hp1 others(1): Show |
synonymous_variant | LOW | c.2058T>C | p.Ile686Ile | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2578/9937 | 2058/2103 | 686/700 | chr4 | 144737912 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:144646226
|
G | T | 1 | a0001c0001t0065 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-450G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | 450 | chr4 | 144646226 | |||||
chr4:144646243
|
C | T | 3 | a0002c0002t0009a0002c0002t0063a0002c0002t0064 | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-433C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | 433 | chr4 | 144646243 | |||||
chr4:144646319
|
T | A | 18 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(15): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-357T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | 357 | chr4 | 144646319 | |||||
chr4:144646536
|
T | G | 1 | a0001c0001t0034 | 1 | NA18942.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-140T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/13 | chr4 | 144646536 | ||||||
chr4:144738046
|
C | T | 2 | a0001c0001t0033a0001c0001t0062 | 2 | HG01081.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 89 | chr4 | 144738046 | |||||
chr4:144738143
|
A | G | 1 | a0001c0001t0061 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 186 | chr4 | 144738143 | |||||
chr4:144738268
|
T | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*311T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 311 | chr4 | 144738268 | |||||
chr4:144738373
|
T | A | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 416 | chr4 | 144738373 | |||||
chr4:144738438
|
A | G | 1 | a0001c0001t0060 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 481 | chr4 | 144738438 | |||||
chr4:144738495
|
A | G | 3 | a0001c0001t0059a0002c0002t0009a0002c0002t0064 | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*538A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 538 | chr4 | 144738495 | |||||
chr4:144738537
|
A | T | 1 | a0001c0001t0032 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 580 | chr4 | 144738537 | |||||
chr4:144738561
|
T | C | 1 | a0001c0001t0025 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 604 | chr4 | 144738561 | |||||
chr4:144738574
|
T | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 617 | chr4 | 144738574 | |||||
chr4:144739230
|
T | C | 2 | a0001c0001t0006a0001c0001t0035 | 8 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1273T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1273 | chr4 | 144739230 | |||||
chr4:144739399
|
A | G | 1 | a0001c0001t0031 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1442 | chr4 | 144739399 | |||||
chr4:144739582
|
A | T | 2 | a0001c0001t0006a0001c0001t0035 | 8 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1625A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1625 | chr4 | 144739582 | |||||
chr4:144739931
|
A | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1974A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 1974 | chr4 | 144739931 | |||||
chr4:144739985
|
T | C | 1 | a0001c0001t0014 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2028T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2028 | chr4 | 144739985 | |||||
chr4:144740224
|
A | C | 1 | a0001c0001t0058 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2267A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2267 | chr4 | 144740224 | |||||
chr4:144740328
|
A | T | 1 | a0001c0001t0057 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2371A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2371 | chr4 | 144740328 | |||||
chr4:144740499
|
G | C | 27 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(24): Show | 128 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2542G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2542 | chr4 | 144740499 | |||||
chr4:144740758
|
G | A | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*2801G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2801 | chr4 | 144740758 | |||||
chr4:144740763
|
G | T | 2 | a0001c0001t0017a0001c0001t0021 | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2806G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2806 | chr4 | 144740763 | |||||
chr4:144740816
|
G | A | 2 | a0001c0001t0021a0001c0001t0060 | 3 | HG01074.hp2 HG03471.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2859G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2859 | chr4 | 144740816 | |||||
chr4:144740923
|
T | C | 1 | a0001c0001t0036 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2966 | chr4 | 144740923 | |||||
chr4:144740946
|
G | C | 1 | a0001c0001t0045 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2989G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 2989 | chr4 | 144740946 | |||||
chr4:144740980
|
C | G | 2 | a0001c0001t0020a0001c0001t0044 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3023C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3023 | chr4 | 144740980 | |||||
chr4:144740980
|
CT | C | 2 | a0001c0001t0006a0001c0001t0035 | 8 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3025delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3025 | INFO_REALIGN_3_PRIME | chr4 | 144740980 | ||||
chr4:144741020
|
C | T | 1 | a0002c0002t0064 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3063 | chr4 | 144741020 | |||||
chr4:144741142
|
TA | T | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*3186delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3186 | chr4 | 144741142 | |||||
chr4:144741145
|
A | T | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*3188A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3188 | chr4 | 144741145 | |||||
chr4:144741363
|
GT | G | 12 | a0001c0001t0014a0001c0001t0020a0001c0001t0026others(9): Show | 15 | HG01081.hp2 HG01256.hp1 HG01515.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3422delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3422 | INFO_REALIGN_3_PRIME | chr4 | 144741363 | ||||
chr4:144741379
|
T | C | 1 | a0001c0001t0060 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3422T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3422 | chr4 | 144741379 | |||||
chr4:144741385
|
CT | C | 5 | a0001c0001t0013a0001c0001t0022a0001c0001t0038others(2): Show | 8 | HG02015.hp1 HG03209.hp2 HG03239.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3443delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3443 | INFO_REALIGN_3_PRIME | chr4 | 144741385 | ||||
chr4:144741465
|
C | T | 1 | a0001c0001t0053 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3508C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3508 | chr4 | 144741465 | |||||
chr4:144741541
|
G | A | 1 | a0001c0001t0010 | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3584G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3584 | chr4 | 144741541 | |||||
chr4:144741670
|
C | A | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*3713C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3713 | chr4 | 144741670 | |||||
chr4:144741678
|
A | G | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*3721A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3721 | chr4 | 144741678 | |||||
chr4:144741690
|
C | T | 12 | a0001c0001t0003a0001c0001t0011a0001c0001t0013others(9): Show | 60 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3733C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 3733 | chr4 | 144741690 | |||||
chr4:144742006
|
G | A | 2 | a0001c0001t0017a0001c0001t0021 | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4049G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4049 | chr4 | 144742006 | |||||
chr4:144742014
|
G | A | 1 | a0001c0001t0039 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4057G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4057 | chr4 | 144742014 | |||||
chr4:144742035
|
GTA | G | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*4088_*4089delAT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4088 | INFO_REALIGN_3_PRIME | chr4 | 144742035 | ||||
chr4:144742060
|
TAC | T | 2 | a0001c0001t0018a0001c0001t0056 | 4 | HG02145.hp2 HG02572.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4119_*4120delCA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4119 | INFO_REALIGN_3_PRIME | chr4 | 144742060 | ||||
chr4:144742062
|
C | T | 18 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(15): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4105C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4105 | chr4 | 144742062 | |||||
chr4:144742064
|
C | T | 1 | a0001c0001t0058 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4107C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4107 | chr4 | 144742064 | |||||
chr4:144742074
|
CACAT | C | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(42): Show | 211 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*4135_*4138delCATA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4135 | INFO_REALIGN_3_PRIME | chr4 | 144742074 | ||||
chr4:144742076
|
CAT | C | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(14): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*4121_*4122delTA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4121 | INFO_REALIGN_3_PRIME | chr4 | 144742076 | ||||
chr4:144742078
|
T | C | 2 | a0001c0001t0058a0001c0001t0060 | 2 | HG00423.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4121T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4121 | chr4 | 144742078 | |||||
chr4:144742261
|
A | G | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*4304A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4304 | chr4 | 144742261 | |||||
chr4:144742569
|
A | T | 1 | a0001c0001t0052 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4612A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4612 | chr4 | 144742569 | |||||
chr4:144742646
|
G | A | 12 | a0001c0001t0003a0001c0001t0011a0001c0001t0013others(9): Show | 60 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4689G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4689 | chr4 | 144742646 | |||||
chr4:144742663
|
T | A | 1 | a0001c0001t0040 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4706T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4706 | chr4 | 144742663 | |||||
chr4:144742832
|
GTTATATA others(20): Show |
G | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4892_*4918delATAT others(23): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4892 | INFO_REALIGN_3_PRIME | chr4 | 144742832 | ||||
chr4:144742849
|
A | T | 2 | a0001c0001t0018a0001c0001t0043 | 4 | HG02145.hp2 HG03209.hp1 HG04204.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4892A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4892 | chr4 | 144742849 | |||||
chr4:144742862
|
ATATATAT others(34): Show |
A | 1 | a0001c0001t0043 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4918_*4958delTTTA others(37): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4918 | INFO_REALIGN_3_PRIME | chr4 | 144742862 | ||||
chr4:144742872
|
C | A | 1 | a0001c0001t0016 | 3 | NA18962.hp1 NA18994.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4915C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4915 | chr4 | 144742872 | |||||
chr4:144742874
|
TTTTATAT others(45): Show |
T | 1 | a0001c0001t0018 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4945_*4996delTTTA others(48): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | INFO_REALIGN_3_PRIME | chr4 | 144742874 | ||||
chr4:144742889
|
ATATATAT others(7): Show |
A | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*4945_*4958delTTTA others(10): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | INFO_REALIGN_3_PRIME | chr4 | 144742889 | ||||
chr4:144742899
|
CTT | C | 2 | a0001c0001t0019a0001c0001t0060 | 3 | HG01243.hp2 HG02723.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4946_*4947delTT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4946 | INFO_REALIGN_3_PRIME | chr4 | 144742899 | ||||
chr4:144742899
|
CTTTTTAT others(8): Show |
C | 1 | a0001c0001t0040 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4944_*4958delTTTT others(11): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4944 | INFO_REALIGN_3_PRIME | chr4 | 144742899 | ||||
chr4:144742900
|
TTTTTATA others(9): Show |
T | 1 | a0001c0001t0042 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4945_*4960delTTTA others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | INFO_REALIGN_3_PRIME | chr4 | 144742900 | ||||
chr4:144742901
|
T | TATATATA others(4): Show |
1 | a0001c0001t0051 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4944_*4945insATAT others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | chr4 | 144742901 | |||||
chr4:144742901
|
TTTTATAT others(5): Show |
T | 1 | a0001c0001t0010 | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4947_*4958delTATA others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4947 | INFO_REALIGN_3_PRIME | chr4 | 144742901 | ||||
chr4:144742901
|
TTTTATAT others(90): Show |
T | 1 | a0001c0001t0023 | 2 | HG02056.hp2 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4945_*5041delTTTA others(93): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4945 | chr4 | 144742901 | |||||
chr4:144742914
|
T | A | 1 | a0001c0001t0010 | 5 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4957T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4957 | chr4 | 144742914 | |||||
chr4:144742927
|
TTTATATA others(54): Show |
T | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4972_*5032delTATA others(57): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 4972 | INFO_REALIGN_3_PRIME | chr4 | 144742927 | ||||
chr4:144742955
|
TACATATA others(36): Show |
T | 1 | a0001c0001t0024 | 2 | HG02559.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5000_*5042delCATA others(39): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5000 | INFO_REALIGN_3_PRIME | chr4 | 144742955 | ||||
chr4:144742964
|
GATATATG others(31): Show |
G | 1 | a0001c0001t0060 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5014_*5051delGTAT others(34): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5014 | INFO_REALIGN_3_PRIME | chr4 | 144742964 | ||||
chr4:144742971
|
G | A | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*5014G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5014 | chr4 | 144742971 | |||||
chr4:144742972
|
TATATATA others(33): Show |
T | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*5016_*5055delATAT others(36): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5016 | chr4 | 144742972 | |||||
chr4:144742993
|
T | C | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5036T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5036 | chr4 | 144742993 | |||||
chr4:144743000
|
T | G | 1 | a0001c0001t0019 | 2 | HG01243.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5043T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5043 | chr4 | 144743000 | |||||
chr4:144743009
|
A | C | 1 | a0001c0001t0023 | 2 | HG02056.hp2 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5052A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5052 | chr4 | 144743009 | |||||
chr4:144743024
|
T | G | 1 | a0001c0001t0024 | 2 | HG02559.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5067T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5067 | chr4 | 144743024 | |||||
chr4:144743120
|
A | T | 1 | a0001c0001t0055 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5163A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5163 | chr4 | 144743120 | |||||
chr4:144743220
|
T | C | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5263T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5263 | chr4 | 144743220 | |||||
chr4:144743360
|
A | G | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*5403A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5403 | chr4 | 144743360 | |||||
chr4:144743703
|
C | A | 1 | a0001c0001t0049 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5746C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5746 | chr4 | 144743703 | |||||
chr4:144743738
|
A | T | 1 | a0001c0001t0041 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5781A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5781 | chr4 | 144743738 | |||||
chr4:144743790
|
C | T | 1 | a0001c0001t0030 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5833C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5833 | chr4 | 144743790 | |||||
chr4:144743929
|
T | C | 1 | a0001c0001t0050 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5972T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 5972 | chr4 | 144743929 | |||||
chr4:144744082
|
G | T | 1 | a0001c0001t0050 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6125G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6125 | chr4 | 144744082 | |||||
chr4:144744112
|
T | C | 1 | a0001c0001t0029 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6155T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6155 | chr4 | 144744112 | |||||
chr4:144744143
|
A | G | 1 | a0001c0001t0006 | 7 | HG01496.hp2 HG02976.hp2 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6186A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6186 | chr4 | 144744143 | |||||
chr4:144744449
|
C | A | 1 | a0001c0001t0060 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6492C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6492 | chr4 | 144744449 | |||||
chr4:144744516
|
A | G | 1 | a0001c0001t0007 | 7 | NA18941.hp2 NA18960.hp1 NA18967.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6559A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6559 | chr4 | 144744516 | |||||
chr4:144744776
|
AG | A | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*6826delG | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6826 | INFO_REALIGN_3_PRIME | chr4 | 144744776 | ||||
chr4:144744800
|
G | A | 1 | a0001c0001t0018 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6843G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 6843 | chr4 | 144744800 | |||||
chr4:144745218
|
G | A | 1 | a0001c0001t0031 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7261G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 13/13 | 7261 | chr4 | 144745218 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:144647200
|
T | C | 225 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0070others(222): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.279+246T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647200 | ||||||
chr4:144647299
|
G | A | 63 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(60): Show | 67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+345G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647299 | ||||||
chr4:144647368
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.279+414G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647368 | ||||||
chr4:144647373
|
C | T | 1 | a0001c0001t0024g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.279+419C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647373 | ||||||
chr4:144647394
|
C | A | 1 | a0001c0001t0020g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+440C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647394 | ||||||
chr4:144647530
|
A | C | 63 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(60): Show | 67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+576A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647530 | ||||||
chr4:144647636
|
C | A | 1 | a0001c0001t0002g0015 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.279+682C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647636 | ||||||
chr4:144647692
|
T | TTAAC | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(75): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.279+741_279+742ins others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144647692 | |||||
chr4:144647704
|
A | C | 1 | a0001c0001t0008g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.279+750A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144647704 | ||||||
chr4:144647988
|
T | TA | 10 | a0001c0001t0004g0073a0001c0001t0006g0074a0001c0001t0006g0076others(7): Show | 10 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+1046dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144647988 | |||||
chr4:144647988
|
TA | T | 81 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.279+1046delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144647988 | |||||
chr4:144648202
|
T | C | 1 | a0001c0001t0003g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.279+1248T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648202 | ||||||
chr4:144648450
|
T | C | 10 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0153others(7): Show | 10 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+1496T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648450 | ||||||
chr4:144648529
|
C | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.279+1575C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648529 | ||||||
chr4:144648540
|
C | T | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(75): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.279+1586C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648540 | ||||||
chr4:144648680
|
C | A | 63 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(60): Show | 67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+1726C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144648680 | ||||||
chr4:144649235
|
G | GA | 36 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0071others(33): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.279+2292dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144649235 | |||||
chr4:144649353
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.279+2399T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144649353 | ||||||
chr4:144650135
|
G | A | 1 | a0001c0001t0010g0228 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.280-2470G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144650135 | ||||||
chr4:144650542
|
A | C | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-2063A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144650542 | ||||||
chr4:144650894
|
T | C | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-1711T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144650894 | ||||||
chr4:144651073
|
A | T | 1 | a0001c0001t0044g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.280-1532A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651073 | ||||||
chr4:144651183
|
A | C | 1 | a0001c0001t0002g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-1422A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651183 | ||||||
chr4:144651225
|
T | C | 1 | a0001c0001t0017g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.280-1380T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651225 | ||||||
chr4:144651331
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.280-1274C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651331 | ||||||
chr4:144651387
|
C | T | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.280-1218C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651387 | ||||||
chr4:144651449
|
A | T | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-1156A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651449 | ||||||
chr4:144651530
|
A | G | 1 | a0001c0001t0024g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-1075A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651530 | ||||||
chr4:144651761
|
A | AT | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-843dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 144651761 | |||||
chr4:144651785
|
A | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.280-820A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651785 | ||||||
chr4:144651901
|
C | G | 1 | a0001c0001t0002g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.280-704C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651901 | ||||||
chr4:144651979
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.280-626T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144651979 | ||||||
chr4:144652134
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.280-471T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144652134 | ||||||
chr4:144652476
|
T | C | 1 | a0001c0001t0046g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.280-129T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 1/12 | chr4 | 144652476 | ||||||
chr4:144652802
|
GA | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0071others(41): Show | 44 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.472+14delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144652802 | |||||
chr4:144653044
|
A | G | 11 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(8): Show | 11 | HG00735.hp2 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+247A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653044 | ||||||
chr4:144653087
|
G | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0071others(32): Show | 35 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.472+290G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653087 | ||||||
chr4:144653110
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.472+313T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653110 | ||||||
chr4:144653304
|
C | A | 1 | a0001c0001t0050g0017 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.472+507C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653304 | ||||||
chr4:144653442
|
A | G | 1 | a0001c0001t0006g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.472+645A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653442 | ||||||
chr4:144653692
|
A | G | 225 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0070others(222): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.472+895A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653692 | ||||||
chr4:144653698
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.472+901A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653698 | ||||||
chr4:144653722
|
T | C | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020 | 3 | HG00597.hp1 NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.472+925T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144653722 | ||||||
chr4:144654027
|
C | G | 2 | a0001c0001t0005g0224a0001c0001t0026g0223 | 2 | HG00642.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.472+1230C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654027 | ||||||
chr4:144654028
|
T | C | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.472+1231T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654028 | ||||||
chr4:144654097
|
T | C | 1 | a0001c0001t0002g0021 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.472+1300T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654097 | ||||||
chr4:144654256
|
G | A | 1 | a0001c0001t0017g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.472+1459G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654256 | ||||||
chr4:144654435
|
C | A | 1 | a0001c0001t0003g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.472+1638C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654435 | ||||||
chr4:144654536
|
T | G | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.472+1739T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654536 | ||||||
chr4:144654716
|
A | G | 1 | a0001c0001t0003g0150 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.472+1919A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654716 | ||||||
chr4:144654759
|
T | C | 63 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(60): Show | 67 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.472+1962T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654759 | ||||||
chr4:144654868
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0034g0230 | 3 | NA18942.hp1 NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.472+2071T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144654868 | ||||||
chr4:144655188
|
G | T | 1 | a0001c0001t0046g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.472+2391G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655188 | ||||||
chr4:144655403
|
A | G | 1 | a0001c0001t0005g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.472+2606A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655403 | ||||||
chr4:144655406
|
G | A | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(75): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.472+2609G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655406 | ||||||
chr4:144655504
|
T | C | 300 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.472+2707T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144655504 | ||||||
chr4:144655753
|
C | CTCTT | 186 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(183): Show | 194 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.472+2957_472+2958i others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144655753 | |||||
chr4:144656039
|
A | G | 1 | a0001c0001t0044g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.473-2751A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656039 | ||||||
chr4:144656056
|
C | T | 1 | a0001c0003t0001g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.473-2734C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656056 | ||||||
chr4:144656143
|
G | C | 1 | a0001c0001t0001g0232 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.473-2647G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656143 | ||||||
chr4:144656165
|
G | C | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-2625G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656165 | ||||||
chr4:144656218
|
A | G | 16 | a0001c0001t0001g0086a0001c0001t0006g0074a0001c0001t0006g0076others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.473-2572A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656218 | ||||||
chr4:144656241
|
G | A | 1 | a0001c0001t0044g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.473-2549G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656241 | ||||||
chr4:144656314
|
A | C | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.473-2476A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656314 | ||||||
chr4:144656379
|
C | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.473-2411C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656379 | ||||||
chr4:144656446
|
G | A | 6 | a0001c0001t0005g0219a0001c0001t0005g0220a0001c0001t0005g0221others(3): Show | 6 | HG01243.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.473-2344G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656446 | ||||||
chr4:144656484
|
T | C | 196 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(193): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.473-2306T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656484 | ||||||
chr4:144656766
|
A | G | 1 | a0001c0001t0046g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.473-2024A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656766 | ||||||
chr4:144656977
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.473-1813C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144656977 | ||||||
chr4:144657001
|
C | G | 1 | a0001c0001t0007g0066 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.473-1789C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657001 | ||||||
chr4:144657002
|
G | T | 1 | a0001c0001t0032g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.473-1788G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657002 | ||||||
chr4:144657389
|
T | C | 1 | a0002c0002t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.473-1401T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657389 | ||||||
chr4:144657515
|
T | C | 79 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(76): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.473-1275T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657515 | ||||||
chr4:144657647
|
C | T | 78 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(75): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.473-1143C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657647 | ||||||
chr4:144657661
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0284 | 3 | NA18947.hp1 NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.473-1129A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144657661 | ||||||
chr4:144658261
|
A | G | 2 | a0001c0001t0017g0085a0001c0001t0024g0090 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.473-529A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658261 | ||||||
chr4:144658351
|
G | GTATT | 28 | a0001c0001t0001g0092a0001c0001t0001g0288a0001c0001t0001g0289others(25): Show | 29 | HG00735.hp2 HG01192.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.473-409_473-406dup others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144658351 | |||||
chr4:144658351
|
G | GTATTTAT others(1): Show |
5 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0003g0163others(2): Show | 5 | HG03516.hp2 NA18952.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-413_473-406dup others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144658351 | |||||
chr4:144658351
|
GTATT | G | 93 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0111others(90): Show | 99 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.473-409_473-406del others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 144658351 | |||||
chr4:144658438
|
T | C | 186 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(183): Show | 194 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.473-352T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658438 | ||||||
chr4:144658439
|
G | C | 1 | a0001c0001t0020g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473-351G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658439 | ||||||
chr4:144658462
|
C | T | 1 | a0001c0001t0008g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.473-328C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658462 | ||||||
chr4:144658514
|
G | A | 4 | a0001c0001t0004g0114a0001c0001t0010g0145a0001c0001t0010g0146others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-276G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658514 | ||||||
chr4:144658755
|
G | A | 196 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(193): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.473-35G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 2/12 | chr4 | 144658755 | ||||||
chr4:144659020
|
T | C | 11 | a0001c0001t0001g0023a0001c0001t0003g0164a0001c0001t0003g0174others(8): Show | 11 | HG01074.hp1 HG01515.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.629+74T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659020 | ||||||
chr4:144659138
|
C | A | 69 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(66): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.629+192C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659138 | ||||||
chr4:144659216
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.629+270T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659216 | ||||||
chr4:144659319
|
G | T | 1 | a0001c0001t0042g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.630-318G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659319 | ||||||
chr4:144659433
|
A | C | 196 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(193): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.630-204A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659433 | ||||||
chr4:144659487
|
G | C | 4 | a0001c0001t0004g0114a0001c0001t0010g0145a0001c0001t0010g0146others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-150G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659487 | ||||||
chr4:144659535
|
A | T | 1 | a0001c0001t0002g0064 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.630-102A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 3/12 | chr4 | 144659535 | ||||||
chr4:144659907
|
A | G | 7 | a0001c0001t0003g0007a0001c0001t0003g0163a0001c0001t0003g0170others(4): Show | 8 | HG02165.hp1 NA18957.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+69A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144659907 | ||||||
chr4:144660033
|
A | G | 7 | a0002c0002t0009g0134a0002c0002t0009g0135a0002c0002t0009g0136others(4): Show | 7 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+195A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660033 | ||||||
chr4:144660306
|
C | A | 3 | a0001c0001t0008g0183a0001c0001t0008g0184a0001c0001t0008g0225 | 3 | HG00099.hp2 HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.831+468C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660306 | ||||||
chr4:144660403
|
C | T | 3 | a0001c0001t0010g0228a0001c0001t0010g0296a0001c0001t0010g0297 | 3 | HG01243.hp1 HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.831+565C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660403 | ||||||
chr4:144660444
|
T | C | 196 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(193): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.831+606T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660444 | ||||||
chr4:144660485
|
C | T | 5 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0062others(2): Show | 5 | HG01081.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+647C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660485 | ||||||
chr4:144660589
|
A | C | 2 | a0001c0001t0017g0085a0001c0001t0024g0090 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.831+751A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660589 | ||||||
chr4:144660679
|
G | A | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+841G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660679 | ||||||
chr4:144660748
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+910C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660748 | ||||||
chr4:144660761
|
A | G | 7 | a0001c0001t0001g0086a0001c0001t0017g0083a0001c0001t0017g0085others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+923A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660761 | ||||||
chr4:144660799
|
T | C | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+961T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660799 | ||||||
chr4:144660842
|
A | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(80): Show | 89 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.831+1004A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144660842 | ||||||
chr4:144661384
|
A | G | 196 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(193): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.831+1546A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661384 | ||||||
chr4:144661499
|
C | T | 1 | a0001c0001t0024g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.831+1661C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661499 | ||||||
chr4:144661583
|
C | T | 5 | a0001c0001t0003g0164a0001c0001t0003g0179a0001c0001t0003g0181others(2): Show | 5 | NA18944.hp2 NA18969.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+1745C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661583 | ||||||
chr4:144661668
|
T | C | 196 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0002g0001others(193): Show | 204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.831+1830T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661668 | ||||||
chr4:144661837
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.831+1999C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661837 | ||||||
chr4:144661920
|
C | T | 1 | a0001c0001t0042g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+2082C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144661920 | ||||||
chr4:144662114
|
A | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+2276A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144662114 | ||||||
chr4:144662689
|
GTGTGTGT others(3): Show |
G | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+2860_831+2869d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144662689 | |||||
chr4:144662710
|
C | A | 9 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(6): Show | 9 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+2872C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144662710 | ||||||
chr4:144662946
|
T | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+3108T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144662946 | ||||||
chr4:144663023
|
T | G | 16 | a0001c0001t0001g0086a0001c0001t0006g0074a0001c0001t0006g0076others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+3185T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663023 | ||||||
chr4:144663055
|
T | G | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+3217T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663055 | ||||||
chr4:144663512
|
C | A | 1 | a0001c0001t0020g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+3674C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663512 | ||||||
chr4:144663557
|
C | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+3719C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663557 | ||||||
chr4:144663893
|
G | T | 7 | a0001c0001t0001g0086a0001c0001t0017g0083a0001c0001t0017g0085others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+4055G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663893 | ||||||
chr4:144663960
|
C | A | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+4122C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144663960 | ||||||
chr4:144664179
|
G | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+4341G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664179 | ||||||
chr4:144664202
|
A | T | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+4364A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664202 | ||||||
chr4:144664210
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.831+4372G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664210 | ||||||
chr4:144664221
|
G | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+4383G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664221 | ||||||
chr4:144664300
|
G | A | 2 | a0001c0001t0004g0114a0004c0005t0004g0118 | 2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.831+4462G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664300 | ||||||
chr4:144664369
|
G | A | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+4531G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664369 | ||||||
chr4:144664531
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.831+4693G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664531 | ||||||
chr4:144664645
|
T | C | 10 | a0001c0001t0003g0007a0001c0001t0003g0163a0001c0001t0003g0166others(7): Show | 11 | HG02165.hp1 HG04228.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+4807T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664645 | ||||||
chr4:144664781
|
A | G | 1 | a0001c0001t0020g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+4943A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664781 | ||||||
chr4:144664791
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.831+4953C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664791 | ||||||
chr4:144664883
|
G | A | 2 | a0001c0001t0004g0073a0001c0001t0046g0115 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.831+5045G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664883 | ||||||
chr4:144664891
|
T | C | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+5053T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144664891 | ||||||
chr4:144665007
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | NA18950.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.831+5169G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665007 | ||||||
chr4:144665307
|
A | G | 101 | a0001c0001t0001g0086a0001c0001t0003g0007a0001c0001t0003g0008others(98): Show | 103 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.831+5469A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665307 | ||||||
chr4:144665400
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.831+5562A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665400 | ||||||
chr4:144665701
|
A | G | 7 | a0001c0001t0001g0086a0001c0001t0017g0083a0001c0001t0017g0085others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+5863A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665701 | ||||||
chr4:144665748
|
G | A | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+5910G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665748 | ||||||
chr4:144665761
|
C | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+5923C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665761 | ||||||
chr4:144665788
|
T | C | 3 | a0001c0001t0002g0236a0001c0001t0002g0237a0001c0001t0002g0238 | 3 | HG01346.hp1 HG01496.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.831+5950T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665788 | ||||||
chr4:144665830
|
C | A | 1 | a0001c0001t0003g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.831+5992C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665830 | ||||||
chr4:144665866
|
C | T | 1 | a0001c0001t0061g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.831+6028C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665866 | ||||||
chr4:144665963
|
G | C | 1 | a0001c0001t0004g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+6125G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144665963 | ||||||
chr4:144666217
|
C | T | 1 | a0001c0001t0002g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.831+6379C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666217 | ||||||
chr4:144666248
|
CGT | C | 11 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0005g0219others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+6456_831+6457d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGT | C | 15 | a0001c0001t0001g0084a0001c0001t0002g0015a0001c0001t0002g0052others(12): Show | 15 | HG02109.hp2 HG02451.hp1 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.831+6454_831+6457d others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGTGT | C | 107 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0001g0289others(104): Show | 112 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.831+6452_831+6457d others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGTGTG others(1): Show |
C | 69 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0267others(66): Show | 72 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.831+6450_831+6457d others(10): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGTGTG others(3): Show |
C | 81 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.831+6448_831+6457d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGTGTG others(5): Show |
C | 12 | a0001c0001t0002g0059a0001c0001t0002g0143a0001c0001t0006g0074others(9): Show | 12 | HG01081.hp1 HG01496.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+6446_831+6457d others(14): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0011g0234 | 3 | NA18952.hp2 NA18986.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.831+6444_831+6457d others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666248
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0010g0145a0001c0001t0010g0146 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.831+6442_831+6457d others(18): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144666248 | |||||
chr4:144666294
|
T | A | 3 | a0001c0001t0002g0026a0001c0001t0002g0052a0001c0001t0040g0027 | 3 | NA18940.hp2 NA19006.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.831+6456T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666294 | ||||||
chr4:144666549
|
C | T | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.831+6711C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666549 | ||||||
chr4:144666793
|
A | C | 1 | a0001c0001t0020g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+6955A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666793 | ||||||
chr4:144666964
|
A | T | 82 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(79): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.831+7126A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144666964 | ||||||
chr4:144667072
|
G | T | 7 | a0001c0001t0001g0086a0001c0001t0017g0083a0001c0001t0017g0085others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+7234G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667072 | ||||||
chr4:144667484
|
T | G | 1 | a0001c0001t0003g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.831+7646T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667484 | ||||||
chr4:144667753
|
T | A | 16 | a0001c0001t0001g0086a0001c0001t0006g0074a0001c0001t0006g0076others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+7915T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667753 | ||||||
chr4:144667819
|
A | G | 16 | a0001c0001t0001g0086a0001c0001t0006g0074a0001c0001t0006g0076others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.831+7981A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144667819 | ||||||
chr4:144667999
|
A | AATT | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+8180_831+8182d others(5): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144667999 | |||||
chr4:144668080
|
G | A | 5 | a0001c0001t0003g0151a0001c0001t0003g0153a0001c0001t0003g0155others(2): Show | 5 | HG00280.hp2 HG00609.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+8242G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668080 | ||||||
chr4:144668195
|
T | G | 6 | a0001c0001t0005g0219a0001c0001t0005g0220a0001c0001t0005g0221others(3): Show | 6 | HG01243.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+8357T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668195 | ||||||
chr4:144668454
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.831+8616G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668454 | ||||||
chr4:144668692
|
C | A | 75 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(72): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.831+8854C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668692 | ||||||
chr4:144668796
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0291 | 2 | HG00735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.831+8958C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668796 | ||||||
chr4:144668853
|
C | T | 195 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(192): Show | 203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.831+9015C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668853 | ||||||
chr4:144668864
|
T | C | 1 | a0001c0001t0012g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.831+9026T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668864 | ||||||
chr4:144668904
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0039g0060 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.831+9066G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144668904 | ||||||
chr4:144669022
|
T | C | 2 | a0001c0001t0017g0085a0001c0001t0024g0090 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.831+9184T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669022 | ||||||
chr4:144669279
|
A | C | 3 | a0001c0001t0012g0214a0001c0001t0012g0215a0001c0001t0012g0216 | 3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.831+9441A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669279 | ||||||
chr4:144669293
|
A | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 87 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.831+9455A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669293 | ||||||
chr4:144669411
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0241a0001c0001t0001g0267others(2): Show | 6 | NA18950.hp1 NA18953.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+9573G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669411 | ||||||
chr4:144669414
|
G | T | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0008g0172 | 3 | NA18961.hp2 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.831+9576G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669414 | ||||||
chr4:144669576
|
A | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+9738A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669576 | ||||||
chr4:144669639
|
A | C | 2 | a0001c0001t0004g0073a0001c0001t0046g0115 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.831+9801A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669639 | ||||||
chr4:144669710
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.831+9872C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669710 | ||||||
chr4:144669781
|
A | G | 185 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(182): Show | 193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.831+9943A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669781 | ||||||
chr4:144669805
|
AG | A | 81 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+9968delG | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669805 | ||||||
chr4:144669807
|
T | A | 81 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+9969T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669807 | ||||||
chr4:144669909
|
A | G | 81 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+10071A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669909 | ||||||
chr4:144669978
|
T | TA | 173 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(170): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.831+10156dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144669978 | |||||
chr4:144669989
|
A | G | 1 | a0001c0001t0048g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.831+10151A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144669989 | ||||||
chr4:144670059
|
G | A | 81 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+10221G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670059 | ||||||
chr4:144670106
|
A | G | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 87 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.831+10268A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670106 | ||||||
chr4:144670142
|
C | CA | 82 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(79): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.831+10315dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670142 | |||||
chr4:144670157
|
GAATTGGT others(10): Show |
G | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+10337_831+1035 others(21): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670157 | |||||
chr4:144670169
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.831+10331C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670169 | ||||||
chr4:144670274
|
C | A | 84 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.831+10436C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670274 | ||||||
chr4:144670289
|
C | T | 3 | a0001c0001t0003g0209a0001c0001t0013g0210a0001c0001t0013g0211 | 3 | NA18947.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.831+10451C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670289 | ||||||
chr4:144670455
|
C | CA | 102 | a0001c0001t0001g0233a0001c0001t0002g0001a0001c0001t0002g0002others(99): Show | 108 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.831+10633dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670455 | |||||
chr4:144670455
|
C | CAA | 84 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0003g0007others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.831+10632_831+1063 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670455 | |||||
chr4:144670543
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.831+10705C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670543 | ||||||
chr4:144670635
|
G | C | 1 | a0001c0001t0006g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.831+10797G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670635 | ||||||
chr4:144670707
|
G | GA | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(74): Show | 81 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+10883dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670707 | |||||
chr4:144670718
|
A | C | 5 | a0001c0001t0001g0266a0001c0001t0006g0074a0001c0001t0006g0078others(2): Show | 5 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+10880A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670718 | ||||||
chr4:144670722
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+10884C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670722 | ||||||
chr4:144670764
|
GA | G | 39 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0265others(36): Show | 42 | HG00099.hp1 HG00597.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.831+10950delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670764 | |||||
chr4:144670764
|
GAA | G | 64 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(61): Show | 68 | HG00423.hp1 HG00621.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.831+10949_831+1095 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670764 | |||||
chr4:144670764
|
GAAA | G | 85 | a0001c0001t0001g0023a0001c0001t0002g0021a0001c0001t0003g0007others(82): Show | 87 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.831+10948_831+1095 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144670764 | |||||
chr4:144670768
|
A | G | 1 | a0001c0001t0010g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.831+10930A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670768 | ||||||
chr4:144670769
|
A | G | 1 | a0001c0001t0010g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.831+10931A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670769 | ||||||
chr4:144670785
|
A | G | 7 | a0001c0001t0001g0232a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 7 | HG02145.hp2 HG03209.hp1 NA19043.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+10947A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144670785 | ||||||
chr4:144671207
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0005g0176a0001c0001t0005g0177others(1): Show | 4 | HG01515.hp1 HG01934.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+11369T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671207 | ||||||
chr4:144671226
|
A | G | 1 | a0004c0005t0004g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.831+11388A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671226 | ||||||
chr4:144671318
|
GT | G | 186 | a0001c0001t0001g0023a0001c0001t0001g0094a0001c0001t0001g0242others(183): Show | 194 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.831+11494delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144671318 | |||||
chr4:144671534
|
G | A | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+11696G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671534 | ||||||
chr4:144671703
|
T | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+11865T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671703 | ||||||
chr4:144671780
|
C | T | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+11942C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671780 | ||||||
chr4:144671809
|
C | G | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+11971C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671809 | ||||||
chr4:144671876
|
T | C | 82 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(79): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.831+12038T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671876 | ||||||
chr4:144671930
|
G | T | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+12092G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144671930 | ||||||
chr4:144672119
|
T | C | 2 | a0001c0001t0005g0193a0001c0001t0005g0222 | 2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.831+12281T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672119 | ||||||
chr4:144672522
|
G | C | 81 | a0001c0001t0001g0023a0001c0001t0003g0007a0001c0001t0003g0008others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.831+12684G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672522 | ||||||
chr4:144672549
|
G | C | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+12711G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672549 | ||||||
chr4:144672688
|
AT | A | 6 | a0001c0001t0005g0219a0001c0001t0005g0220a0001c0001t0005g0221others(3): Show | 6 | HG01243.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+12857delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144672688 | |||||
chr4:144672697
|
A | T | 1 | a0001c0001t0002g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+12859A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672697 | ||||||
chr4:144672728
|
G | A | 1 | a0001c0001t0004g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+12890G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672728 | ||||||
chr4:144672747
|
G | C | 1 | a0001c0001t0002g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+12909G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672747 | ||||||
chr4:144672748
|
C | G | 1 | a0001c0001t0002g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+12910C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672748 | ||||||
chr4:144672750
|
G | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+12912G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672750 | ||||||
chr4:144672801
|
A | G | 77 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(74): Show | 81 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+12963A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672801 | ||||||
chr4:144672836
|
G | A | 2 | a0001c0001t0002g0244a0001c0001t0023g0243 | 2 | NA18944.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.831+12998G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672836 | ||||||
chr4:144672851
|
G | T | 1 | a0001c0001t0016g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.831+13013G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144672851 | ||||||
chr4:144673082
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.831+13244T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673082 | ||||||
chr4:144673335
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.831+13497A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673335 | ||||||
chr4:144673448
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.831+13610C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673448 | ||||||
chr4:144673661
|
T | G | 1 | a0001c0001t0002g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.831+13823T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144673661 | ||||||
chr4:144674028
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.831+14190T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674028 | ||||||
chr4:144674130
|
T | C | 1 | a0001c0001t0004g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.831+14292T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674130 | ||||||
chr4:144674292
|
T | G | 1 | a0001c0001t0003g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.831+14454T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674292 | ||||||
chr4:144674312
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.831+14474G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674312 | ||||||
chr4:144674608
|
C | T | 80 | a0001c0001t0001g0263a0001c0001t0002g0001a0001c0001t0002g0002others(77): Show | 86 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.831+14770C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674608 | ||||||
chr4:144674873
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0020g0072 | 5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+15035G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144674873 | ||||||
chr4:144675041
|
C | T | 7 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+15203C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675041 | ||||||
chr4:144675253
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+15415C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675253 | ||||||
chr4:144675351
|
A | G | 13 | a0001c0001t0004g0073a0001c0001t0006g0074a0001c0001t0006g0076others(10): Show | 13 | HG01496.hp2 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.831+15513A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675351 | ||||||
chr4:144675541
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.831+15703G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675541 | ||||||
chr4:144675681
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+15843T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675681 | ||||||
chr4:144675733
|
A | C | 4 | a0001c0001t0003g0191a0001c0001t0003g0208a0001c0001t0005g0224others(1): Show | 4 | HG00323.hp2 HG00642.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+15895A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675733 | ||||||
chr4:144675910
|
A | G | 1 | a0001c0001t0023g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.831+16072A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675910 | ||||||
chr4:144675923
|
G | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(76): Show | 85 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.831+16085G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144675923 | ||||||
chr4:144676221
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.831+16383T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676221 | ||||||
chr4:144676395
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.831+16557A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676395 | ||||||
chr4:144676607
|
A | G | 194 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(191): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.831+16769A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676607 | ||||||
chr4:144676679
|
C | T | 2 | a0001c0001t0003g0166a0001c0001t0003g0167 | 2 | NA18939.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.831+16841C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676679 | ||||||
chr4:144676945
|
T | C | 1 | a0001c0001t0042g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.831+17107T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144676945 | ||||||
chr4:144677163
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(88): Show | 97 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.831+17325C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677163 | ||||||
chr4:144677316
|
C | G | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+17478C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677316 | ||||||
chr4:144677333
|
C | T | 10 | a0001c0001t0004g0073a0001c0001t0006g0074a0001c0001t0006g0076others(7): Show | 10 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+17495C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677333 | ||||||
chr4:144677382
|
TGTA | T | 3 | a0001c0001t0016g0030a0001c0001t0016g0035a0001c0001t0016g0048 | 3 | NA18962.hp1 NA18994.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.831+17546_831+1754 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144677382 | |||||
chr4:144677397
|
C | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+17559C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677397 | ||||||
chr4:144677774
|
C | T | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+17936C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677774 | ||||||
chr4:144677972
|
C | T | 2 | a0003c0004t0005g0206a0003c0004t0005g0207 | 2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.831+18134C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677972 | ||||||
chr4:144677977
|
G | A | 1 | a0001c0001t0003g0170 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.831+18139G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144677977 | ||||||
chr4:144678382
|
G | C | 194 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(191): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.831+18544G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678382 | ||||||
chr4:144678429
|
A | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+18591A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678429 | ||||||
chr4:144678539
|
C | G | 2 | a0001c0001t0001g0260a0001c0001t0011g0259 | 2 | HG00673.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.831+18701C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678539 | ||||||
chr4:144678756
|
G | A | 79 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(76): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.831+18918G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678756 | ||||||
chr4:144678928
|
G | A | 4 | a0001c0001t0003g0191a0001c0001t0003g0208a0001c0001t0005g0224others(1): Show | 4 | HG00323.hp2 HG00642.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+19090G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678928 | ||||||
chr4:144678928
|
G | C | 4 | a0001c0001t0017g0085a0001c0001t0021g0087a0001c0001t0021g0088others(1): Show | 4 | HG01074.hp2 HG02735.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+19090G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678928 | ||||||
chr4:144678976
|
A | G | 7 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+19138A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144678976 | ||||||
chr4:144679140
|
G | GT | 9 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(6): Show | 9 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+19312dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144679140 | |||||
chr4:144679223
|
G | A | 79 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(76): Show | 85 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.831+19385G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679223 | ||||||
chr4:144679618
|
A | G | 5 | a0001c0001t0010g0145a0001c0001t0010g0146a0001c0001t0012g0214others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+19780A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679618 | ||||||
chr4:144679623
|
T | C | 5 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0062others(2): Show | 5 | HG01081.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+19785T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679623 | ||||||
chr4:144679658
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.831+19820G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144679658 | ||||||
chr4:144680013
|
G | T | 1 | a0001c0001t0003g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.831+20175G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680013 | ||||||
chr4:144680040
|
T | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+20202T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680040 | ||||||
chr4:144680247
|
AC | A | 11 | a0001c0001t0004g0012a0001c0001t0004g0271a0001c0001t0004g0272others(8): Show | 12 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.831+20410delC | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680247 | ||||||
chr4:144680279
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.831+20441T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680279 | ||||||
chr4:144680289
|
A | G | 1 | a0001c0001t0002g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.831+20451A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680289 | ||||||
chr4:144680468
|
A | T | 1 | a0001c0001t0002g0033 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.831+20630A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680468 | ||||||
chr4:144680656
|
G | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+20818G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680656 | ||||||
chr4:144680711
|
A | G | 70 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(67): Show | 72 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.831+20873A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680711 | ||||||
chr4:144680820
|
G | A | 1 | a0001c0001t0006g0081 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.831+20982G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680820 | ||||||
chr4:144680972
|
C | A | 14 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(11): Show | 14 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+21134C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144680972 | ||||||
chr4:144681110
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.831+21272T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681110 | ||||||
chr4:144681237
|
T | C | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+21399T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681237 | ||||||
chr4:144681345
|
T | C | 10 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0288others(7): Show | 10 | HG00735.hp2 HG01106.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+21507T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681345 | ||||||
chr4:144681421
|
CT | C | 106 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0097others(103): Show | 112 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.831+21605delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144681421 | |||||
chr4:144681421
|
CTT | C | 80 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(77): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.831+21604_831+2160 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144681421 | |||||
chr4:144681517
|
C | T | 1 | a0002c0002t0063g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.831+21679C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681517 | ||||||
chr4:144681545
|
C | T | 4 | a0001c0001t0004g0131a0001c0001t0020g0119a0001c0001t0044g0144others(1): Show | 4 | HG02451.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+21707C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681545 | ||||||
chr4:144681616
|
G | T | 14 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(11): Show | 14 | HG00642.hp2 HG01074.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+21778G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681616 | ||||||
chr4:144681624
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.831+21786C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681624 | ||||||
chr4:144681669
|
C | T | 2 | a0001c0001t0002g0053a0001c0001t0002g0056 | 2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.831+21831C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681669 | ||||||
chr4:144681675
|
G | A | 67 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(64): Show | 69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.831+21837G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681675 | ||||||
chr4:144681711
|
C | T | 1 | a0001c0001t0062g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.831+21873C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681711 | ||||||
chr4:144681946
|
T | C | 1 | a0001c0001t0015g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.831+22108T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144681946 | ||||||
chr4:144682216
|
C | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.831+22378C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682216 | ||||||
chr4:144682303
|
C | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.831+22465C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682303 | ||||||
chr4:144682549
|
AAG | A | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.831+22723_831+2272 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144682549 | |||||
chr4:144682577
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0020g0072 | 5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+22739C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682577 | ||||||
chr4:144682751
|
C | A | 1 | a0001c0001t0020g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.831+22913C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144682751 | ||||||
chr4:144683239
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.832-23292A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683239 | ||||||
chr4:144683442
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.832-23089C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683442 | ||||||
chr4:144683639
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.832-22892C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683639 | ||||||
chr4:144683683
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.832-22848T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683683 | ||||||
chr4:144683701
|
G | T | 194 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(191): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.832-22830G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683701 | ||||||
chr4:144683839
|
A | G | 2 | a0001c0001t0003g0192a0001c0001t0003g0205 | 2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.832-22692A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683839 | ||||||
chr4:144683873
|
A | G | 9 | a0001c0001t0001g0092a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 9 | HG00735.hp2 HG01106.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-22658A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683873 | ||||||
chr4:144683881
|
T | C | 68 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(65): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.832-22650T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683881 | ||||||
chr4:144683923
|
T | C | 194 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(191): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.832-22608T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683923 | ||||||
chr4:144683937
|
T | C | 1 | a0001c0001t0003g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.832-22594T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144683937 | ||||||
chr4:144684061
|
T | TA | 68 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(65): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.832-22460dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684061 | |||||
chr4:144684121
|
T | C | 194 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(191): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.832-22410T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684121 | ||||||
chr4:144684227
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.832-22304A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684227 | ||||||
chr4:144684232
|
A | ATT | 14 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0112others(11): Show | 14 | HG00741.hp1 HG02071.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.832-22256_832-2225 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
A | ATTT | 11 | a0001c0001t0001g0006a0001c0001t0001g0111a0001c0001t0001g0227others(8): Show | 11 | HG00597.hp2 HG00621.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-22257_832-2225 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA18946.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.832-22266_832-2225 others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
AT | A | 27 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(24): Show | 31 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.832-22255delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATT | A | 22 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0094others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.832-22256_832-2225 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTT | A | 8 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0289others(5): Show | 8 | HG01943.hp1 HG02056.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-22257_832-2225 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTT | A | 6 | a0001c0001t0006g0074a0001c0001t0006g0077a0001c0001t0006g0080others(3): Show | 6 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-22259_832-2225 others(9): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTT | A | 6 | a0001c0001t0004g0131a0001c0001t0006g0076a0001c0001t0006g0078others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-22260_832-2225 others(10): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832-22265_832-2225 others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0051 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.832-22266_832-2225 others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(6): Show |
A | 26 | a0001c0001t0001g0023a0001c0001t0002g0028a0001c0001t0002g0032others(23): Show | 26 | HG00621.hp1 HG01261.hp2 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.832-22267_832-2225 others(17): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(7): Show |
A | 41 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0005others(38): Show | 44 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.832-22268_832-2225 others(18): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(8): Show |
A | 38 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0015others(35): Show | 41 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.832-22269_832-2225 others(19): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(9): Show |
A | 37 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(34): Show | 39 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-22270_832-2225 others(20): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(10): Show |
A | 10 | a0001c0001t0003g0164a0001c0001t0003g0187a0001c0001t0004g0114others(7): Show | 10 | HG00642.hp2 HG01192.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-22271_832-2225 others(21): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(11): Show |
A | 12 | a0001c0001t0005g0220a0001c0001t0005g0221a0001c0001t0017g0083others(9): Show | 12 | HG01074.hp2 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-22272_832-2225 others(22): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(12): Show |
A | 2 | a0001c0001t0036g0142a0002c0002t0009g0134 | 2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.832-22273_832-2225 others(23): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(13): Show |
A | 3 | a0001c0001t0001g0235a0001c0001t0002g0117a0001c0006t0005g0213 | 3 | HG01884.hp2 NA18989.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.832-22274_832-2225 others(24): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(14): Show |
A | 1 | a0001c0001t0002g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.832-22275_832-2225 others(25): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(15): Show |
A | 2 | a0001c0001t0001g0233a0001c0001t0004g0073 | 2 | HG02717.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.832-22276_832-2225 others(26): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(18): Show |
A | 4 | a0001c0001t0002g0026a0001c0001t0002g0052a0001c0001t0016g0048others(1): Show | 4 | NA18940.hp2 NA18962.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-22279_832-2225 others(29): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684232
|
ATTTTTTT others(22): Show |
A | 1 | a0001c0003t0001g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.832-22283_832-2225 others(33): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144684232 | |||||
chr4:144684303
|
G | T | 1 | a0001c0001t0001g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.832-22228G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684303 | ||||||
chr4:144684320
|
G | A | 11 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162others(8): Show | 11 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-22211G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684320 | ||||||
chr4:144684419
|
C | T | 1 | a0001c0001t0007g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.832-22112C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684419 | ||||||
chr4:144684568
|
C | T | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-21963C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684568 | ||||||
chr4:144684647
|
C | G | 1 | a0001c0001t0046g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-21884C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684647 | ||||||
chr4:144684869
|
C | T | 194 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(191): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.832-21662C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684869 | ||||||
chr4:144684895
|
A | C | 1 | a0001c0003t0001g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832-21636A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144684895 | ||||||
chr4:144685157
|
A | C | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-21374A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685157 | ||||||
chr4:144685209
|
G | A | 2 | a0001c0001t0006g0076a0001c0001t0006g0081 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.832-21322G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685209 | ||||||
chr4:144685300
|
T | A | 1 | a0001c0001t0048g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.832-21231T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685300 | ||||||
chr4:144685432
|
G | A | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-21099G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685432 | ||||||
chr4:144685768
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0002g0282 | 2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.832-20763C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144685768 | ||||||
chr4:144686351
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0034g0230 | 3 | NA18942.hp1 NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.832-20180C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686351 | ||||||
chr4:144686542
|
A | G | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-19989A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686542 | ||||||
chr4:144686694
|
C | T | 192 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(189): Show | 200 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.832-19837C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686694 | ||||||
chr4:144686730
|
C | G | 1 | a0001c0001t0003g0171 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.832-19801C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686730 | ||||||
chr4:144686750
|
G | A | 176 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(173): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.832-19781G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144686750 | ||||||
chr4:144687713
|
T | A | 3 | a0001c0001t0004g0131a0001c0001t0020g0119a0001c0001t0044g0144 | 3 | HG02451.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-18818T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144687713 | ||||||
chr4:144687751
|
C | CT | 23 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0092others(20): Show | 24 | HG00597.hp2 HG00673.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.832-18752dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | |||||
chr4:144687751
|
CT | C | 23 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(20): Show | 23 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.832-18752delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | |||||
chr4:144687751
|
CTT | C | 144 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(141): Show | 152 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.832-18753_832-1875 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | |||||
chr4:144687751
|
CTTT | C | 17 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0039others(14): Show | 17 | HG01192.hp1 HG01884.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.832-18754_832-1875 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144687751 | |||||
chr4:144687848
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.832-18683C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144687848 | ||||||
chr4:144687921
|
C | T | 2 | a0001c0001t0004g0073a0004c0005t0004g0118 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-18610C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144687921 | ||||||
chr4:144688107
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0020g0072 | 5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-18424A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688107 | ||||||
chr4:144688367
|
G | A | 2 | a0001c0001t0004g0073a0004c0005t0004g0118 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-18164G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688367 | ||||||
chr4:144688775
|
AGAACGGA others(22): Show |
A | 14 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0124others(11): Show | 14 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.832-17755_832-1772 others(33): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688775 | ||||||
chr4:144688871
|
G | T | 2 | a0001c0001t0004g0073a0004c0005t0004g0118 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-17660G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688871 | ||||||
chr4:144688894
|
T | C | 3 | a0001c0001t0012g0214a0001c0001t0012g0215a0001c0001t0012g0216 | 3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.832-17637T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688894 | ||||||
chr4:144688907
|
A | C | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-17624A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688907 | ||||||
chr4:144688985
|
A | G | 1 | a0001c0001t0003g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.832-17546A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144688985 | ||||||
chr4:144689060
|
T | C | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-17471T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689060 | ||||||
chr4:144689255
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.832-17276T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689255 | ||||||
chr4:144689407
|
G | T | 1 | a0001c0001t0003g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.832-17124G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689407 | ||||||
chr4:144689427
|
G | C | 1 | a0001c0001t0014g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832-17104G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689427 | ||||||
chr4:144689590
|
A | C | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.832-16941A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689590 | ||||||
chr4:144689695
|
T | C | 12 | a0001c0001t0004g0073a0001c0001t0006g0074a0001c0001t0006g0076others(9): Show | 12 | HG01496.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-16836T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689695 | ||||||
chr4:144689874
|
T | C | 8 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.832-16657T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689874 | ||||||
chr4:144689982
|
T | C | 2 | a0001c0001t0003g0152a0001c0001t0008g0158 | 2 | HG00408.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.832-16549T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144689982 | ||||||
chr4:144690144
|
A | C | 2 | a0001c0001t0013g0210a0001c0001t0013g0211 | 2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.832-16387A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690144 | ||||||
chr4:144690315
|
G | T | 8 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-16216G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690315 | ||||||
chr4:144690394
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832-16137T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690394 | ||||||
chr4:144690616
|
A | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-15915A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690616 | ||||||
chr4:144690784
|
CTA | C | 159 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(156): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.832-15745_832-1574 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144690784 | |||||
chr4:144690925
|
A | G | 3 | a0001c0001t0004g0073a0001c0001t0004g0131a0004c0005t0004g0118 | 3 | HG02451.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-15606A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690925 | ||||||
chr4:144690967
|
A | C | 13 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(10): Show | 13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-15564A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690967 | ||||||
chr4:144690968
|
G | T | 13 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(10): Show | 13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-15563G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144690968 | ||||||
chr4:144691007
|
G | A | 3 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162 | 3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-15524G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691007 | ||||||
chr4:144691057
|
T | A | 2 | a0001c0001t0020g0119a0001c0001t0044g0144 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-15474T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691057 | ||||||
chr4:144691160
|
C | T | 16 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(13): Show | 16 | HG01496.hp2 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-15371C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691160 | ||||||
chr4:144691178
|
A | C | 13 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(10): Show | 13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-15353A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691178 | ||||||
chr4:144691192
|
A | T | 2 | a0001c0001t0003g0185a0001c0001t0003g0204 | 2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.832-15339A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691192 | ||||||
chr4:144691399
|
C | A | 154 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(151): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.832-15132C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691399 | ||||||
chr4:144691400
|
A | T | 154 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(151): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.832-15131A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691400 | ||||||
chr4:144691465
|
T | C | 1 | a0001c0001t0056g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.832-15066T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691465 | ||||||
chr4:144691593
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.832-14938G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691593 | ||||||
chr4:144691633
|
A | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0020g0072 | 5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-14898A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691633 | ||||||
chr4:144691790
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-14741C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691790 | ||||||
chr4:144691838
|
G | T | 1 | a0001c0001t0026g0223 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.832-14693G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144691838 | ||||||
chr4:144691896
|
GA | G | 71 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(68): Show | 75 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.832-14625delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144691896 | |||||
chr4:144691906
|
AT | A | 4 | a0001c0001t0002g0054a0001c0001t0004g0114a0001c0001t0019g0161others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-14621delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144691906 | |||||
chr4:144692028
|
A | G | 3 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162 | 3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-14503A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692028 | ||||||
chr4:144692098
|
C | T | 1 | a0001c0001t0002g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.832-14433C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692098 | ||||||
chr4:144692270
|
T | C | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-14261T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692270 | ||||||
chr4:144692309
|
C | T | 1 | a0002c0002t0009g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832-14222C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692309 | ||||||
chr4:144692399
|
A | G | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.832-14132A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692399 | ||||||
chr4:144692568
|
C | T | 3 | a0001c0001t0008g0183a0001c0001t0008g0184a0001c0001t0008g0225 | 3 | HG00099.hp2 HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.832-13963C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692568 | ||||||
chr4:144692607
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.832-13924G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692607 | ||||||
chr4:144692655
|
G | A | 154 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(151): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.832-13876G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692655 | ||||||
chr4:144692750
|
G | C | 5 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-13781G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692750 | ||||||
chr4:144692805
|
C | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-13726C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692805 | ||||||
chr4:144692891
|
A | AGAG | 193 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(190): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.832-13636_832-1363 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144692891 | |||||
chr4:144692949
|
C | A | 1 | a0001c0001t0005g0222 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.832-13582C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144692949 | ||||||
chr4:144693183
|
T | C | 2 | a0001c0001t0020g0119a0001c0001t0044g0144 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-13348T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693183 | ||||||
chr4:144693240
|
T | A | 1 | a0001c0001t0001g0013 | 2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.832-13291T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693240 | ||||||
chr4:144693472
|
C | T | 1 | a0001c0001t0017g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.832-13059C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693472 | ||||||
chr4:144693549
|
A | C | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.832-12982A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693549 | ||||||
chr4:144693738
|
G | A | 1 | a0001c0001t0023g0261 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.832-12793G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693738 | ||||||
chr4:144693832
|
G | A | 58 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(55): Show | 60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.832-12699G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693832 | ||||||
chr4:144693863
|
G | A | 1 | a0001c0001t0004g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.832-12668G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693863 | ||||||
chr4:144693884
|
A | G | 1 | a0001c0001t0013g0210 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.832-12647A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144693884 | ||||||
chr4:144694221
|
A | G | 7 | a0002c0002t0009g0133a0002c0002t0009g0134a0002c0002t0009g0135others(4): Show | 7 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-12310A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694221 | ||||||
chr4:144694246
|
T | G | 1 | a0001c0001t0002g0032 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.832-12285T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694246 | ||||||
chr4:144694273
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0241a0001c0001t0001g0267others(1): Show | 5 | NA18950.hp1 NA18953.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-12258T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694273 | ||||||
chr4:144694334
|
G | GT | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0003g0205others(7): Show | 10 | HG01192.hp1 HG01978.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-12187dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144694334 | |||||
chr4:144694434
|
T | C | 74 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(71): Show | 78 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.832-12097T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694434 | ||||||
chr4:144694518
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0120 | 4 | HG02257.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-12013A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694518 | ||||||
chr4:144694953
|
G | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-11578G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144694953 | ||||||
chr4:144695126
|
ACAAG | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0020g0072 | 5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-11404_832-1140 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695126 | ||||||
chr4:144695301
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-11230C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695301 | ||||||
chr4:144695590
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.832-10941T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695590 | ||||||
chr4:144695625
|
C | T | 3 | a0001c0001t0010g0228a0001c0001t0010g0296a0001c0001t0010g0297 | 3 | HG01243.hp1 HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.832-10906C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695625 | ||||||
chr4:144695803
|
C | T | 6 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.832-10728C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144695803 | ||||||
chr4:144696029
|
TACTTGAG others(27): Show |
T | 3 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162 | 3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-10500_832-1046 others(38): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144696029 | |||||
chr4:144696258
|
T | C | 1 | a0001c0001t0016g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.832-10273T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696258 | ||||||
chr4:144696266
|
T | G | 1 | a0001c0001t0052g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.832-10265T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696266 | ||||||
chr4:144696275
|
C | CT | 25 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0124others(22): Show | 25 | HG01192.hp1 HG01261.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.832-10246dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144696275 | |||||
chr4:144696549
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.832-9982G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696549 | ||||||
chr4:144696596
|
G | A | 193 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(190): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.832-9935G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696596 | ||||||
chr4:144696607
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.832-9924A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696607 | ||||||
chr4:144696794
|
C | T | 188 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(185): Show | 196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.832-9737C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144696794 | ||||||
chr4:144697414
|
T | A | 2 | a0001c0001t0003g0169a0001c0001t0027g0168 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.832-9117T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697414 | ||||||
chr4:144697456
|
C | T | 2 | a0001c0001t0048g0279a0002c0002t0063g0139 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832-9075C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697456 | ||||||
chr4:144697567
|
T | C | 164 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(161): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.832-8964T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697567 | ||||||
chr4:144697795
|
G | A | 1 | a0001c0001t0056g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.832-8736G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697795 | ||||||
chr4:144697991
|
G | T | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-8540G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144697991 | ||||||
chr4:144698044
|
G | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.832-8487G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698044 | ||||||
chr4:144698094
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-8437C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698094 | ||||||
chr4:144698181
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.832-8350C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698181 | ||||||
chr4:144698261
|
T | C | 154 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(151): Show | 160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.832-8270T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698261 | ||||||
chr4:144698288
|
T | A | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-8243T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698288 | ||||||
chr4:144698501
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.832-8030G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698501 | ||||||
chr4:144698589
|
A | G | 1 | a0002c0002t0063g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.832-7942A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698589 | ||||||
chr4:144698812
|
T | C | 13 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(10): Show | 13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-7719T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698812 | ||||||
chr4:144698888
|
A | C | 1 | a0001c0001t0011g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-7643A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144698888 | ||||||
chr4:144699141
|
T | C | 1 | a0001c0001t0011g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.832-7390T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699141 | ||||||
chr4:144699156
|
C | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0265 | 2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.832-7375C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699156 | ||||||
chr4:144699260
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832-7271T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699260 | ||||||
chr4:144699304
|
T | C | 1 | a0001c0001t0046g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.832-7227T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699304 | ||||||
chr4:144699402
|
G | A | 164 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(161): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.832-7129G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699402 | ||||||
chr4:144699447
|
A | T | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.832-7084A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699447 | ||||||
chr4:144699484
|
G | A | 5 | a0001c0001t0005g0193a0001c0001t0005g0195a0001c0001t0005g0222others(2): Show | 5 | HG02071.hp2 HG02074.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-7047G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699484 | ||||||
chr4:144699494
|
C | A | 3 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162 | 3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-7037C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144699494 | ||||||
chr4:144700153
|
A | G | 10 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162others(7): Show | 10 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-6378A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700153 | ||||||
chr4:144700176
|
G | A | 4 | a0001c0001t0062g0110a0001c0003t0001g0101a0001c0003t0001g0102others(1): Show | 4 | HG00099.hp1 HG00280.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-6355G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700176 | ||||||
chr4:144700367
|
G | A | 1 | a0001c0003t0001g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832-6164G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700367 | ||||||
chr4:144700585
|
G | A | 13 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(10): Show | 13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-5946G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700585 | ||||||
chr4:144700770
|
A | C | 1 | a0001c0001t0002g0015 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.832-5761A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700770 | ||||||
chr4:144700852
|
T | C | 3 | a0001c0001t0012g0214a0001c0001t0012g0215a0001c0001t0012g0216 | 3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.832-5679T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700852 | ||||||
chr4:144700881
|
G | C | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-5650G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144700881 | ||||||
chr4:144701004
|
CTT | C | 3 | a0001c0001t0004g0073a0001c0001t0004g0131a0004c0005t0004g0118 | 3 | HG02451.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-5523_832-5522d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144701004 | |||||
chr4:144701048
|
G | A | 2 | a0001c0001t0008g0183a0001c0001t0008g0184 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.832-5483G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701048 | ||||||
chr4:144701077
|
T | C | 8 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-5454T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701077 | ||||||
chr4:144701278
|
G | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-5253G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701278 | ||||||
chr4:144701291
|
T | A | 1 | a0001c0001t0002g0237 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.832-5240T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701291 | ||||||
chr4:144701323
|
C | CT | 173 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(170): Show | 179 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.832-5195dupT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144701323 | |||||
chr4:144701323
|
C | CTT | 17 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0004g0131others(14): Show | 19 | HG01496.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.832-5196_832-5195d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144701323 | |||||
chr4:144701499
|
T | C | 164 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(161): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.832-5032T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701499 | ||||||
chr4:144701646
|
A | G | 8 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-4885A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701646 | ||||||
chr4:144701649
|
T | C | 1 | a0001c0001t0044g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.832-4882T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701649 | ||||||
chr4:144701686
|
G | C | 2 | a0001c0001t0010g0145a0001c0001t0010g0146 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.832-4845G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701686 | ||||||
chr4:144701713
|
C | T | 3 | a0001c0001t0004g0073a0001c0001t0004g0131a0004c0005t0004g0118 | 3 | HG02451.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.832-4818C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701713 | ||||||
chr4:144701741
|
T | G | 1 | a0004c0005t0004g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.832-4790T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701741 | ||||||
chr4:144701798
|
C | G | 1 | a0001c0001t0001g0294 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.832-4733C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701798 | ||||||
chr4:144701800
|
C | T | 1 | a0001c0001t0005g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.832-4731C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701800 | ||||||
chr4:144701871
|
G | A | 13 | a0001c0001t0004g0073a0001c0001t0004g0131a0001c0001t0006g0074others(10): Show | 13 | HG01496.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-4660G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701871 | ||||||
chr4:144701955
|
G | A | 191 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(188): Show | 199 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.832-4576G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144701955 | ||||||
chr4:144702009
|
T | C | 181 | a0001c0001t0001g0023a0001c0001t0001g0111a0001c0001t0002g0001others(178): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.832-4522T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702009 | ||||||
chr4:144702681
|
T | G | 1 | a0001c0001t0007g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.832-3850T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702681 | ||||||
chr4:144702703
|
A | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0120a0001c0001t0020g0072 | 5 | HG02257.hp2 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.832-3828A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702703 | ||||||
chr4:144702837
|
A | C | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-3694A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702837 | ||||||
chr4:144702976
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.832-3555G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144702976 | ||||||
chr4:144703045
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.832-3486T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703045 | ||||||
chr4:144703082
|
CAAGTGCC others(3): Show |
C | 1 | a0001c0001t0010g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.832-3446_832-3437d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144703082 | |||||
chr4:144703163
|
G | A | 6 | a0002c0002t0009g0134a0002c0002t0009g0135a0002c0002t0009g0136others(3): Show | 6 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-3368G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703163 | ||||||
chr4:144703214
|
C | CA | 156 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(153): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.832-3305dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 144703214 | |||||
chr4:144703279
|
C | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.832-3252C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703279 | ||||||
chr4:144703295
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832-3236C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703295 | ||||||
chr4:144703332
|
T | G | 13 | a0001c0001t0004g0012a0001c0001t0004g0271a0001c0001t0004g0272others(10): Show | 14 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.832-3199T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703332 | ||||||
chr4:144703554
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.832-2977T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703554 | ||||||
chr4:144703729
|
C | T | 7 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(4): Show | 7 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-2802C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703729 | ||||||
chr4:144703748
|
C | A | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.832-2783C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703748 | ||||||
chr4:144703761
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.832-2770C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144703761 | ||||||
chr4:144704217
|
C | T | 1 | a0001c0001t0002g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.832-2314C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704217 | ||||||
chr4:144704561
|
A | G | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0006t0005g0213 | 3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.832-1970A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704561 | ||||||
chr4:144704578
|
C | T | 180 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.832-1953C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704578 | ||||||
chr4:144704799
|
A | G | 3 | a0001c0001t0020g0072a0001c0001t0020g0119a0001c0001t0044g0144 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.832-1732A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704799 | ||||||
chr4:144704944
|
C | G | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.832-1587C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144704944 | ||||||
chr4:144705182
|
C | T | 1 | a0001c0003t0001g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.832-1349C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705182 | ||||||
chr4:144705223
|
C | T | 2 | a0001c0001t0021g0087a0001c0001t0021g0088 | 2 | HG01074.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.832-1308C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705223 | ||||||
chr4:144705262
|
C | G | 163 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(160): Show | 169 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.832-1269C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705262 | ||||||
chr4:144705506
|
A | C | 1 | a0001c0001t0012g0216 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.832-1025A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705506 | ||||||
chr4:144705860
|
G | A | 178 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(175): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.832-671G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705860 | ||||||
chr4:144705881
|
G | A | 5 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-650G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144705881 | ||||||
chr4:144706245
|
C | T | 180 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.832-286C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706245 | ||||||
chr4:144706253
|
G | T | 180 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.832-278G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706253 | ||||||
chr4:144706306
|
A | G | 180 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.832-225A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706306 | ||||||
chr4:144706431
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-100T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706431 | ||||||
chr4:144706506
|
C | A | 1 | a0001c0001t0050g0017 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.832-25C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 4/12 | chr4 | 144706506 | ||||||
chr4:144706716
|
C | G | 1 | a0001c0001t0017g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.983+34C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 5/12 | chr4 | 144706716 | ||||||
chr4:144707464
|
G | A | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1157+204G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707464 | ||||||
chr4:144707576
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0006t0005g0213 | 3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1157+316C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707576 | ||||||
chr4:144707646
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0053a0001c0001t0002g0056 | 2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1157+389_1157+398d others(12): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707646
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1157+388_1157+398d others(13): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707646
|
C | CAAAAAAA others(5): Show |
15 | a0001c0001t0001g0099a0001c0001t0001g0262a0001c0001t0002g0116others(12): Show | 15 | HG01168.hp1 HG01243.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.1157+387_1157+398d others(14): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707646
|
C | CAAAAAAA others(6): Show |
106 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(103): Show | 112 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707646
|
C | CAAAAAAA others(7): Show |
146 | a0001c0001t0001g0023a0001c0001t0001g0098a0001c0001t0001g0108others(143): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707646
|
C | CAAAAAAA others(8): Show |
25 | a0001c0001t0001g0268a0001c0001t0002g0018a0001c0001t0002g0034others(22): Show | 25 | HG00621.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(17): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707646
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0044g0144a0002c0002t0009g0134a0002c0002t0009g0137others(1): Show | 4 | HG01192.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1157+398_1157+399i others(18): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707646 | |||||
chr4:144707649
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0008g0172 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1157+398_1157+399i others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 144707649 | |||||
chr4:144707709
|
G | T | 1 | a0001c0001t0039g0060 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1157+449G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707709 | ||||||
chr4:144707786
|
T | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1158-382T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707786 | ||||||
chr4:144707861
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0002g0282 | 2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1158-307C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707861 | ||||||
chr4:144707888
|
C | T | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1158-280C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707888 | ||||||
chr4:144707907
|
C | T | 3 | a0001c0001t0020g0072a0001c0001t0020g0119a0001c0001t0044g0144 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1158-261C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144707907 | ||||||
chr4:144708102
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1158-66A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 6/12 | chr4 | 144708102 | ||||||
chr4:144708478
|
A | T | 300 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(297): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1301+167A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708478 | ||||||
chr4:144708636
|
TAG | T | 3 | a0001c0001t0012g0214a0001c0001t0012g0215a0001c0001t0012g0216 | 3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1301+331_1301+332d others(4): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 144708636 | |||||
chr4:144708650
|
T | TTTTGA | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1301+344_1301+348d others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 144708650 | |||||
chr4:144708744
|
C | T | 1 | a0001c0001t0016g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1301+433C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708744 | ||||||
chr4:144708797
|
T | C | 3 | a0001c0001t0020g0072a0001c0001t0020g0119a0001c0001t0044g0144 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1301+486T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708797 | ||||||
chr4:144708838
|
G | T | 5 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1301+527G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708838 | ||||||
chr4:144708990
|
G | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1301+679G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144708990 | ||||||
chr4:144709141
|
A | T | 3 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162 | 3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1301+830A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144709141 | ||||||
chr4:144709243
|
T | A | 3 | a0001c0001t0020g0072a0001c0001t0020g0119a0001c0001t0044g0144 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1301+932T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144709243 | ||||||
chr4:144709931
|
C | T | 1 | a0001c0001t0041g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1301+1620C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144709931 | ||||||
chr4:144710131
|
C | T | 1 | a0002c0002t0009g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1302-1819C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710131 | ||||||
chr4:144710319
|
A | G | 1 | a0001c0001t0007g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1302-1631A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710319 | ||||||
chr4:144710416
|
G | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1302-1534G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710416 | ||||||
chr4:144710447
|
T | C | 5 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302-1503T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710447 | ||||||
chr4:144710496
|
T | G | 181 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(178): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1302-1454T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710496 | ||||||
chr4:144710637
|
T | C | 3 | a0001c0001t0002g0059a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01081.hp1 HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1302-1313T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710637 | ||||||
chr4:144710715
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1302-1235G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710715 | ||||||
chr4:144710845
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1302-1105T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144710845 | ||||||
chr4:144711028
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0284 | 3 | NA18947.hp1 NA18955.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1302-922T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711028 | ||||||
chr4:144711046
|
T | TCCTA | 181 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(178): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1302-901_1302-900i others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 144711046 | |||||
chr4:144711138
|
C | T | 1 | a0001c0001t0003g0187 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1302-812C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711138 | ||||||
chr4:144711373
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1302-577G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711373 | ||||||
chr4:144711540
|
C | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1302-410C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711540 | ||||||
chr4:144711926
|
T | C | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0006t0005g0213 | 3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1302-24T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 7/12 | chr4 | 144711926 | ||||||
chr4:144712280
|
G | C | 3 | a0001c0001t0004g0114a0001c0001t0019g0161a0001c0001t0019g0162 | 3 | HG01243.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1423+209G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712280 | ||||||
chr4:144712334
|
C | A | 1 | a0001c0001t0003g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1423+263C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712334 | ||||||
chr4:144712348
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1423+277T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712348 | ||||||
chr4:144712378
|
A | G | 1 | a0001c0001t0024g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1423+307A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712378 | ||||||
chr4:144712559
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1423+488C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712559 | ||||||
chr4:144712885
|
G | GGTGT | 167 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(164): Show | 175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.1423+834_1423+837d others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144712885 | |||||
chr4:144712885
|
G | GGTGTGT | 5 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0003g0178others(2): Show | 5 | HG01884.hp2 HG03831.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423+832_1423+837d others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144712885 | |||||
chr4:144712953
|
G | GA | 18 | a0001c0001t0001g0106a0001c0001t0004g0114a0001c0001t0004g0272others(15): Show | 18 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1423+897dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144712953 | |||||
chr4:144712962
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1423+891A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144712962 | ||||||
chr4:144713007
|
T | C | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1423+936T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144713007 | ||||||
chr4:144713250
|
A | C | 2 | a0001c0001t0021g0087a0001c0001t0021g0088 | 2 | HG01074.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1424-975A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144713250 | ||||||
chr4:144713336
|
G | T | 1 | a0001c0001t0041g0022 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1424-889G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144713336 | ||||||
chr4:144713890
|
GT | G | 6 | a0001c0001t0001g0267a0001c0001t0001g0294a0001c0001t0011g0045others(3): Show | 6 | HG00621.hp1 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1424-325delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 144713890 | |||||
chr4:144714035
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1424-190A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144714035 | ||||||
chr4:144714195
|
C | A | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1424-30C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 8/12 | chr4 | 144714195 | ||||||
chr4:144714358
|
C | G | 1 | a0004c0005t0004g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1547+10C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144714358 | ||||||
chr4:144714487
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1547+139T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144714487 | ||||||
chr4:144714861
|
C | T | 1 | a0001c0001t0035g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1548-439C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144714861 | ||||||
chr4:144715155
|
G | A | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1548-145G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 9/12 | chr4 | 144715155 | ||||||
chr4:144715580
|
T | C | 181 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(178): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1678+150T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715580 | ||||||
chr4:144715620
|
G | A | 5 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+190G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715620 | ||||||
chr4:144715767
|
A | T | 1 | a0001c0001t0002g0248 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1678+337A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715767 | ||||||
chr4:144715790
|
A | G | 1 | a0001c0001t0059g0128 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1678+360A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715790 | ||||||
chr4:144715923
|
A | T | 61 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(58): Show | 63 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1678+493A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144715923 | ||||||
chr4:144716217
|
C | T | 1 | a0001c0001t0003g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1678+787C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716217 | ||||||
chr4:144716263
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1678+833T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716263 | ||||||
chr4:144716297
|
T | C | 180 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1678+867T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716297 | ||||||
chr4:144716496
|
C | T | 4 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+1066C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716496 | ||||||
chr4:144716540
|
CAA | C | 4 | a0001c0001t0003g0150a0001c0001t0003g0190a0001c0001t0003g0200others(1): Show | 4 | HG00741.hp2 HG01192.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+1111_1678+111 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716540 | ||||||
chr4:144716657
|
G | A | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+1227G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716657 | ||||||
chr4:144716684
|
C | A | 1 | a0001c0001t0024g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1678+1254C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716684 | ||||||
chr4:144716721
|
C | G | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1678+1291C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716721 | ||||||
chr4:144716831
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0247others(1): Show | 6 | HG00609.hp2 NA18939.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+1401A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716831 | ||||||
chr4:144716854
|
G | GA | 11 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0104others(8): Show | 11 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1678+1458dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GA | G | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 65 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1678+1458delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAA | G | 41 | a0001c0001t0001g0096a0001c0001t0001g0257a0001c0001t0002g0026others(38): Show | 41 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1678+1457_1678+145 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAA | G | 103 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(100): Show | 111 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1678+1456_1678+145 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAA | G | 14 | a0001c0001t0002g0004a0001c0001t0002g0033a0001c0001t0002g0054others(11): Show | 14 | HG01168.hp2 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.1678+1455_1678+145 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(3): Show |
G | 3 | a0001c0001t0003g0192a0001c0001t0003g0205a0001c0001t0020g0119 | 3 | HG01978.hp2 HG02004.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1678+1449_1678+145 others(14): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(4): Show |
G | 9 | a0001c0001t0001g0268a0001c0001t0059g0128a0001c0001t0060g0075others(6): Show | 9 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+1448_1678+145 others(15): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(5): Show |
G | 1 | a0002c0002t0009g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1678+1447_1678+145 others(16): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(8): Show |
G | 9 | a0001c0001t0001g0264a0001c0001t0002g0236a0001c0001t0002g0237others(6): Show | 9 | HG01346.hp1 HG01496.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+1444_1678+145 others(19): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(9): Show |
G | 10 | a0001c0001t0002g0058a0001c0001t0003g0164a0001c0001t0006g0074others(7): Show | 10 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1678+1443_1678+145 others(20): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0029g0212 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1678+1442_1678+145 others(21): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(11): Show |
G | 1 | a0001c0001t0002g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1678+1441_1678+145 others(22): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716854
|
GAAAAAAA others(14): Show |
G | 1 | a0001c0001t0002g0032 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1678+1438_1678+145 others(25): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 144716854 | |||||
chr4:144716919
|
A | T | 1 | a0001c0001t0001g0289 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1678+1489A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716919 | ||||||
chr4:144716920
|
T | C | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+1490T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144716920 | ||||||
chr4:144717003
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1678+1573G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717003 | ||||||
chr4:144717026
|
C | T | 157 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(154): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1678+1596C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717026 | ||||||
chr4:144717043
|
A | C | 2 | a0001c0001t0002g0244a0001c0001t0023g0243 | 2 | NA18944.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1678+1613A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717043 | ||||||
chr4:144717111
|
C | A | 1 | a0001c0001t0035g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1678+1681C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717111 | ||||||
chr4:144717115
|
G | C | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1678+1685G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717115 | ||||||
chr4:144717576
|
T | C | 1 | a0001c0001t0021g0087 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1679-1299T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717576 | ||||||
chr4:144717881
|
G | T | 180 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1679-994G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144717881 | ||||||
chr4:144718166
|
G | A | 157 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(154): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1679-709G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718166 | ||||||
chr4:144718302
|
A | G | 1 | a0001c0001t0002g0031 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1679-573A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718302 | ||||||
chr4:144718557
|
G | A | 14 | a0001c0001t0004g0012a0001c0001t0004g0073a0001c0001t0004g0271others(11): Show | 15 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1679-318G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718557 | ||||||
chr4:144718578
|
A | G | 1 | a0001c0001t0003g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1679-297A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718578 | ||||||
chr4:144718748
|
T | C | 4 | a0001c0001t0003g0164a0001c0001t0003g0181a0001c0001t0003g0182others(1): Show | 4 | NA18944.hp2 NA18969.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-127T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 10/12 | chr4 | 144718748 | ||||||
chr4:144719002
|
C | T | 79 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(76): Show | 83 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1760+46C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719002 | ||||||
chr4:144719115
|
G | T | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1760+159G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719115 | ||||||
chr4:144719193
|
C | G | 189 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(186): Show | 197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1760+237C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719193 | ||||||
chr4:144719466
|
C | T | 4 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0021g0087others(1): Show | 4 | HG01074.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1760+510C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719466 | ||||||
chr4:144719550
|
G | C | 1 | a0001c0001t0047g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1760+594G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719550 | ||||||
chr4:144719833
|
A | G | 189 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(186): Show | 197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1760+877A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144719833 | ||||||
chr4:144720064
|
T | C | 1 | a0001c0001t0044g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1760+1108T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720064 | ||||||
chr4:144720089
|
T | A | 3 | a0001c0001t0020g0072a0001c0001t0020g0119a0001c0001t0044g0144 | 3 | HG03225.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1760+1133T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720089 | ||||||
chr4:144720137
|
A | G | 5 | a0001c0001t0005g0193a0001c0001t0005g0195a0001c0001t0005g0222others(2): Show | 5 | HG02071.hp2 HG02074.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1760+1181A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720137 | ||||||
chr4:144720336
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1760+1380A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720336 | ||||||
chr4:144720597
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1760+1641G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720597 | ||||||
chr4:144720676
|
G | T | 1 | a0001c0001t0049g0093 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1760+1720G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720676 | ||||||
chr4:144720679
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1760+1723C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720679 | ||||||
chr4:144720909
|
G | T | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0006t0005g0213 | 3 | HG01884.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1760+1953G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720909 | ||||||
chr4:144720985
|
A | T | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1760+2029A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144720985 | ||||||
chr4:144721522
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1760+2566T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721522 | ||||||
chr4:144721561
|
T | A | 3 | a0001c0001t0012g0214a0001c0001t0012g0215a0001c0001t0012g0216 | 3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1760+2605T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721561 | ||||||
chr4:144721563
|
GA | G | 6 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0004g0114others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1760+2611delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144721563 | |||||
chr4:144721594
|
GA | G | 171 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(168): Show | 177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1760+2656delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144721594 | |||||
chr4:144721771
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1760+2815C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721771 | ||||||
chr4:144721811
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+2855G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721811 | ||||||
chr4:144721820
|
T | C | 1 | a0001c0001t0014g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1760+2864T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721820 | ||||||
chr4:144721927
|
G | A | 189 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(186): Show | 197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1760+2971G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144721927 | ||||||
chr4:144722111
|
C | T | 1 | a0001c0001t0017g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1760+3155C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722111 | ||||||
chr4:144722174
|
G | C | 189 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(186): Show | 197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1760+3218G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722174 | ||||||
chr4:144722334
|
T | C | 198 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(195): Show | 206 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1760+3378T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722334 | ||||||
chr4:144722395
|
G | A | 1 | a0001c0001t0016g0035 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1760+3439G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722395 | ||||||
chr4:144722431
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1760+3475T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722431 | ||||||
chr4:144722548
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1760+3592G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722548 | ||||||
chr4:144722619
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1760+3663G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722619 | ||||||
chr4:144722728
|
C | T | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1760+3772C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144722728 | ||||||
chr4:144723010
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+4054G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723010 | ||||||
chr4:144723214
|
C | T | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1760+4258C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723214 | ||||||
chr4:144723651
|
C | T | 1 | a0001c0003t0001g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1760+4695C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723651 | ||||||
chr4:144723907
|
A | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+4951A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723907 | ||||||
chr4:144723971
|
C | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+5015C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144723971 | ||||||
chr4:144724074
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5118G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724074 | ||||||
chr4:144724086
|
T | C | 1 | a0001c0001t0002g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1760+5130T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724086 | ||||||
chr4:144724121
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1760+5165T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724121 | ||||||
chr4:144724338
|
A | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5382A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724338 | ||||||
chr4:144724358
|
G | A | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+5402G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724358 | ||||||
chr4:144724372
|
T | G | 1 | a0001c0001t0003g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1760+5416T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724372 | ||||||
chr4:144724385
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5429G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724385 | ||||||
chr4:144724401
|
A | C | 2 | a0001c0001t0001g0264a0001c0001t0002g0282 | 2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1760+5445A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724401 | ||||||
chr4:144724444
|
A | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5488A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724444 | ||||||
chr4:144724475
|
T | C | 14 | a0001c0001t0004g0012a0001c0001t0004g0073a0001c0001t0004g0271others(11): Show | 15 | HG00741.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1760+5519T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724475 | ||||||
chr4:144724598
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5642G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724598 | ||||||
chr4:144724611
|
A | G | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5655A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724611 | ||||||
chr4:144724648
|
T | TTG | 3 | a0001c0001t0001g0086a0001c0001t0004g0274a0001c0001t0057g0270 | 3 | HG02109.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1760+5712_1760+571 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144724648 | |||||
chr4:144724648
|
TTG | T | 113 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(110): Show | 119 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.1760+5712_1760+571 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144724648 | |||||
chr4:144724652
|
G | GTGTGTGT others(67): Show |
1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5705_1760+570 others(78): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144724652 | |||||
chr4:144724668
|
G | A | 3 | a0001c0001t0003g0008a0001c0001t0013g0189a0001c0001t0017g0085 | 4 | HG01261.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760+5712G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724668 | ||||||
chr4:144724687
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5731T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724687 | ||||||
chr4:144724695
|
TAA | T | 180 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1760+5740_1760+574 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724695 | ||||||
chr4:144724696
|
A | G | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5740A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724696 | ||||||
chr4:144724697
|
A | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5741A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724697 | ||||||
chr4:144724698
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5742G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724698 | ||||||
chr4:144724738
|
C | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5782C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724738 | ||||||
chr4:144724768
|
G | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5812G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724768 | ||||||
chr4:144724773
|
C | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1760+5817C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724773 | ||||||
chr4:144724808
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5852T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724808 | ||||||
chr4:144724851
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1760+5895T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724851 | ||||||
chr4:144724859
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+5903T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144724859 | ||||||
chr4:144725031
|
G | T | 1 | a0001c0001t0051g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1760+6075G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725031 | ||||||
chr4:144725059
|
C | T | 1 | a0001c0001t0051g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1760+6103C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725059 | ||||||
chr4:144725257
|
C | T | 1 | a0001c0003t0001g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1760+6301C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725257 | ||||||
chr4:144725402
|
G | A | 180 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1760+6446G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725402 | ||||||
chr4:144725470
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6514T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725470 | ||||||
chr4:144725492
|
G | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6536G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725492 | ||||||
chr4:144725626
|
C | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6670C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725626 | ||||||
chr4:144725663
|
C | CGT | 9 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1760+6726_1760+672 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144725663 | |||||
chr4:144725663
|
C | T | 64 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0003g0007others(61): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1760+6707C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725663 | ||||||
chr4:144725663
|
CGT | C | 111 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(108): Show | 117 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.1760+6726_1760+672 others(6): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144725663 | |||||
chr4:144725782
|
C | T | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1760+6826C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725782 | ||||||
chr4:144725859
|
G | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6903G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725859 | ||||||
chr4:144725891
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1760+6935G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725891 | ||||||
chr4:144725916
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0034g0230 | 3 | NA18942.hp1 NA18962.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1760+6960C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725916 | ||||||
chr4:144725922
|
C | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+6966C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725922 | ||||||
chr4:144725969
|
G | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7013G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144725969 | ||||||
chr4:144726019
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7063T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726019 | ||||||
chr4:144726086
|
T | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1760+7130T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726086 | ||||||
chr4:144726092
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7136T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726092 | ||||||
chr4:144726224
|
A | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7268A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726224 | ||||||
chr4:144726286
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1760+7330T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726286 | ||||||
chr4:144726296
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1760+7340T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726296 | ||||||
chr4:144726791
|
G | T | 2 | a0001c0001t0036g0142a0001c0001t0060g0075 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1760+7835G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726791 | ||||||
chr4:144726867
|
A | G | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-7874A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726867 | ||||||
chr4:144726880
|
T | C | 190 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(187): Show | 198 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1761-7861T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144726880 | ||||||
chr4:144727020
|
C | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-7721C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727020 | ||||||
chr4:144727269
|
CACTTCTT others(9): Show |
C | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7470_1761-745 others(20): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144727269 | |||||
chr4:144727288
|
A | G | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7453A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727288 | ||||||
chr4:144727289
|
A | G | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7452A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727289 | ||||||
chr4:144727290
|
T | G | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7451T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727290 | ||||||
chr4:144727291
|
C | G | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7450C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727291 | ||||||
chr4:144727339
|
T | C | 2 | a0001c0001t0014g0014a0001c0001t0014g0285 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1761-7402T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727339 | ||||||
chr4:144727429
|
C | T | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1761-7312C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727429 | ||||||
chr4:144727485
|
G | A | 2 | a0003c0004t0005g0206a0003c0004t0005g0207 | 2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1761-7256G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727485 | ||||||
chr4:144727631
|
C | T | 180 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1761-7110C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727631 | ||||||
chr4:144727789
|
A | G | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-6952A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727789 | ||||||
chr4:144727818
|
T | C | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-6923T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727818 | ||||||
chr4:144727889
|
G | T | 5 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-6852G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144727889 | ||||||
chr4:144728090
|
C | T | 180 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1761-6651C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728090 | ||||||
chr4:144728208
|
G | T | 1 | a0001c0001t0046g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1761-6533G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728208 | ||||||
chr4:144728218
|
A | G | 6 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0004g0114others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-6523A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728218 | ||||||
chr4:144728324
|
G | A | 6 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0004g0114others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-6417G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728324 | ||||||
chr4:144728347
|
A | T | 2 | a0001c0001t0003g0152a0001c0001t0008g0158 | 2 | HG00408.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1761-6394A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728347 | ||||||
chr4:144728469
|
G | T | 2 | a0001c0001t0003g0185a0001c0001t0003g0204 | 2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1761-6272G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728469 | ||||||
chr4:144728508
|
T | C | 1 | a0001c0001t0020g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1761-6233T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728508 | ||||||
chr4:144728828
|
G | A | 2 | a0001c0001t0036g0142a0001c0001t0060g0075 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1761-5913G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728828 | ||||||
chr4:144728833
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1761-5908A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728833 | ||||||
chr4:144728869
|
G | A | 166 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(163): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1761-5872G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728869 | ||||||
chr4:144728943
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1761-5798C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144728943 | ||||||
chr4:144728983
|
GAAGA | G | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1761-5751_1761-574 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144728983 | |||||
chr4:144729165
|
G | T | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1761-5576G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729165 | ||||||
chr4:144729239
|
T | A | 1 | a0001c0001t0016g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1761-5502T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729239 | ||||||
chr4:144729469
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1761-5272A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729469 | ||||||
chr4:144729601
|
T | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1761-5140T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729601 | ||||||
chr4:144729815
|
C | CA | 190 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(187): Show | 198 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1761-4926_1761-492 others(5): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729815 | ||||||
chr4:144729852
|
C | T | 214 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(211): Show | 223 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1761-4889C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729852 | ||||||
chr4:144729995
|
A | G | 177 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(174): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1761-4746A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144729995 | ||||||
chr4:144730107
|
T | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1761-4634T>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730107 | ||||||
chr4:144730242
|
AT | A | 182 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(179): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1761-4492delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144730242 | |||||
chr4:144730511
|
A | G | 182 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(179): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1761-4230A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730511 | ||||||
chr4:144730541
|
G | A | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-4200G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730541 | ||||||
chr4:144730585
|
C | T | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1761-4156C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730585 | ||||||
chr4:144730826
|
T | C | 1 | a0001c0001t0011g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1761-3915T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730826 | ||||||
chr4:144730828
|
A | G | 1 | a0001c0001t0032g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1761-3913A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730828 | ||||||
chr4:144730989
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1761-3752C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144730989 | ||||||
chr4:144731280
|
C | T | 1 | a0001c0001t0036g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1761-3461C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731280 | ||||||
chr4:144731323
|
C | T | 1 | a0001c0001t0060g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761-3418C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731323 | ||||||
chr4:144731330
|
T | C | 6 | a0002c0002t0009g0134a0002c0002t0009g0135a0002c0002t0009g0136others(3): Show | 6 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-3411T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731330 | ||||||
chr4:144731443
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1761-3298G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731443 | ||||||
chr4:144731578
|
C | T | 1 | a0001c0001t0042g0065 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1761-3163C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144731578 | ||||||
chr4:144732011
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1761-2730G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732011 | ||||||
chr4:144732026
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0039g0060 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1761-2715G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732026 | ||||||
chr4:144732242
|
A | C | 7 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0004g0114others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1761-2499A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732242 | ||||||
chr4:144732480
|
A | C | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-2261A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732480 | ||||||
chr4:144732527
|
T | C | 1 | a0001c0001t0049g0093 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1761-2214T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732527 | ||||||
chr4:144732542
|
T | C | 163 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(160): Show | 171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.1761-2199T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732542 | ||||||
chr4:144732688
|
C | G | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-2053C>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732688 | ||||||
chr4:144732799
|
T | G | 1 | a0001c0001t0006g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1761-1942T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144732799 | ||||||
chr4:144733085
|
G | A | 1 | a0001c0006t0005g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1761-1656G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733085 | ||||||
chr4:144733108
|
T | G | 3 | a0001c0001t0005g0193a0001c0001t0005g0195a0001c0001t0005g0222 | 3 | HG02071.hp2 HG02074.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1761-1633T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733108 | ||||||
chr4:144733345
|
G | T | 61 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(58): Show | 63 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1761-1396G>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733345 | ||||||
chr4:144733546
|
A | G | 16 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0004g0114others(13): Show | 16 | HG00642.hp2 HG01074.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1761-1195A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733546 | ||||||
chr4:144733744
|
C | T | 2 | a0001c0001t0062g0110a0001c0003t0001g0113 | 2 | HG00099.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1761-997C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733744 | ||||||
chr4:144733761
|
T | C | 180 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1761-980T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733761 | ||||||
chr4:144733917
|
A | T | 8 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(5): Show | 8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1761-824A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733917 | ||||||
chr4:144733920
|
G | A | 1 | a0001c0001t0030g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1761-821G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733920 | ||||||
chr4:144733956
|
A | G | 14 | a0001c0001t0017g0083a0001c0001t0017g0085a0001c0001t0017g0089others(11): Show | 14 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761-785A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144733956 | ||||||
chr4:144734237
|
A | T | 172 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(169): Show | 180 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.1761-504A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734237 | ||||||
chr4:144734339
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0103 | 2 | HG01433.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1761-402T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734339 | ||||||
chr4:144734380
|
T | G | 181 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(178): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1761-361T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734380 | ||||||
chr4:144734490
|
G | A | 1 | a0001c0001t0024g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1761-251G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | chr4 | 144734490 | ||||||
chr4:144734617
|
T | TA | 85 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(82): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1761-111dupA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144734617 | |||||
chr4:144734617
|
TA | T | 6 | a0001c0001t0001g0109a0001c0001t0002g0042a0001c0001t0002g0051others(3): Show | 6 | HG02165.hp2 HG02622.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1761-111delA | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 144734617 | |||||
chr4:144734902
|
G | C | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+13G>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144734902 | ||||||
chr4:144735059
|
T | C | 180 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(177): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1909+170T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735059 | ||||||
chr4:144735149
|
A | C | 1 | a0001c0001t0017g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1909+260A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735149 | ||||||
chr4:144735268
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1909+379A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735268 | ||||||
chr4:144735426
|
G | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+537G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735426 | ||||||
chr4:144735462
|
A | C | 1 | a0001c0001t0002g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1909+573A>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735462 | ||||||
chr4:144735466
|
A | G | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1909+577A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735466 | ||||||
chr4:144735660
|
G | A | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1909+771G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735660 | ||||||
chr4:144735682
|
CT | C | 166 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(163): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1909+795delT | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144735682 | |||||
chr4:144735742
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1909+853C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735742 | ||||||
chr4:144735765
|
A | T | 1 | a0001c0001t0002g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+876A>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144735765 | ||||||
chr4:144736014
|
T | C | 183 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(180): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1909+1125T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736014 | ||||||
chr4:144736025
|
G | A | 2 | a0001c0001t0010g0145a0001c0001t0010g0146 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1909+1136G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736025 | ||||||
chr4:144736032
|
A | G | 9 | a0001c0001t0059g0128a0001c0001t0060g0075a0002c0002t0009g0133others(6): Show | 9 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1909+1143A>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736032 | ||||||
chr4:144736059
|
T | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1909+1170T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736059 | ||||||
chr4:144736136
|
C | CTTT | 165 | a0001c0001t0001g0023a0001c0001t0001g0264a0001c0001t0002g0001others(162): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1909+1262_1909+126 others(7): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736136 | |||||
chr4:144736136
|
C | CTTTT | 16 | a0001c0001t0002g0005a0001c0001t0002g0015a0001c0001t0002g0021others(13): Show | 17 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1909+1261_1909+126 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736136 | |||||
chr4:144736259
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1909+1370C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736259 | ||||||
chr4:144736342
|
G | A | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-1422G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736342 | ||||||
chr4:144736590
|
CTATA | C | 3 | a0001c0001t0018g0147a0001c0001t0018g0148a0001c0001t0018g0149 | 3 | HG02145.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1910-1169_1910-116 others(8): Show |
HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736590 | |||||
chr4:144736866
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1910-898C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736866 | ||||||
chr4:144736875
|
TC | T | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-886delC | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 144736875 | |||||
chr4:144736880
|
T | G | 8 | a0001c0001t0059g0128a0002c0002t0009g0133a0002c0002t0009g0134others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1910-884T>G | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736880 | ||||||
chr4:144736914
|
G | A | 7 | a0001c0001t0006g0074a0001c0001t0006g0076a0001c0001t0006g0077others(4): Show | 7 | HG01496.hp2 HG02622.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910-850G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144736914 | ||||||
chr4:144737134
|
C | T | 59 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0150others(56): Show | 61 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1910-630C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737134 | ||||||
chr4:144737184
|
C | T | 2 | a0001c0001t0019g0161a0001c0001t0019g0162 | 2 | HG01243.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1910-580C>T | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737184 | ||||||
chr4:144737277
|
T | C | 133 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1910-487T>C | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737277 | ||||||
chr4:144737671
|
C | A | 1 | a0001c0001t0002g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1910-93C>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737671 | ||||||
chr4:144737733
|
G | A | 3 | a0001c0001t0012g0214a0001c0001t0012g0215a0001c0001t0012g0216 | 3 | HG02630.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1910-31G>A | HHIP | ENSG00000164161.10 | transcript | ENST00000296575.8 | protein_coding | 12/12 | chr4 | 144737733 |