geneid | 94031 |
---|---|
ensemblid | ENSG00000170801.10 |
hgncid | 30406 |
symbol | HTRA3 |
name | HtrA serine peptidase 3 |
refseq_nuc | NM_053044.5 |
refseq_prot | NP_444272.1 |
ensembl_nuc | ENST00000307358.7 |
ensembl_prot | ENSP00000303766.2 |
mane_status | MANE Select |
chr | chr4 |
start | 8269754 |
end | 8307098 |
strand | + |
ver | v1.2 |
region | chr4:8269754-8307098 |
region5000 | chr4:8264754-8312098 |
regionname0 | HTRA3_chr4_8269754_8307098 |
regionname5000 | HTRA3_chr4_8264754_8312098 |
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 | 1/0 | 453 | 370 | 90 | 67 | 150 | 15 | 47 | 111 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0002 | 0/1 | 453 | 9 | 3 | 4 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0003 | 0/0 | 28 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0004 | 0/0 | 453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0005 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0006 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0007 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0008 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0009 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0010 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0011 | 0/0 | 453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
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 | 1/0 | 1362 | 367 | 88 | 67 | 150 | 15 | 46 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0002 | 0/1 | 1362 | 9 | 3 | 4 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0003 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0004 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0005 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0006 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0007 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0008 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0009 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0010 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0011 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0012 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0013 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
c0014 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1178 | 329 | 55 | 68 | 143 | 16 | 45 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0002 | 0/0 | 1178 | 34 | 25 | 2 | 7 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0003 | 0/0 | 1178 | 3 | 3 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0004 | 0/0 | 1178 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0005 | 0/0 | 1178 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0006 | 0/0 | 1178 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0007 | 0/0 | 1178 | 2 | 1 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0008 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0009 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0010 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0011 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0012 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0013 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0014 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0015 | 0/0 | 1178 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0016 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0017 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0018 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0019 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0020 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
t0021 | 0/0 | 1178 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
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 | 1/0 | 1362 | 367 | 88 | 67 | 150 | 15 | 46 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0005 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0011 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0014 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0002c0002 | 0/1 | 1362 | 9 | 3 | 4 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0003c0003 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0004c0007 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0005c0013 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0006c0012 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0007c0010 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0008c0009 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0009c0008 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0010c0006 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0011c0004 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2539 | 311 | 52 | 63 | 137 | 15 | 43 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0002 | 0/0 | 2539 | 32 | 23 | 2 | 7 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0003 | 0/0 | 2539 | 3 | 3 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0004 | 0/0 | 2539 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0005 | 0/0 | 2539 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0006 | 0/0 | 2539 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0007 | 0/0 | 2539 | 2 | 1 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0008 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0009 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0011 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0012 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0013 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0014 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0015 | 0/0 | 2539 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0016 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0017 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0018 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0019 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0020 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0001t0021 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0005t0002 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0011t0001 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0001c0014t0001 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0002c0002t0001 | 0/1 | 2539 | 7 | 1 | 4 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0002c0002t0002 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0002c0002t0010 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0003c0003t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0004c0007t0001 | 0/0 | 2539 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0005c0013t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0006c0012t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0007c0010t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0008c0009t0001 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0009c0008t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0010c0006t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
a0011c0004t0001 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | copy fasta | chr4 | 8264754 | 8312098 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0009g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0012g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0014g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0015g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0016g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0018g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0019g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0020g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0001t0021g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0005t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0001c0014t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0001g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0002c0002t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0004c0007t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0005c0013t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0006c0012t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0007c0010t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0008c0009t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0009c0008t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0010c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
a0011c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0329 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0057 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0328 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00642 | hp1 | a0001 | c0001 | t0015 | g0205 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0181 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01975 | hp2 | a0004 | c0007 | t0001 | g0327 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02132 | hp1 | a0009 | c0008 | t0001 | g0111 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02165 | hp1 | a0001 | c0001 | t0009 | g0325 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0345 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0035 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0320 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02809 | hp1 | a0001 | c0001 | t0019 | g0348 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02809 | hp2 | a0002 | c0002 | t0010 | g0059 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02896 | hp2 | a0001 | c0005 | t0002 | g0155 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0174 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0175 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03209 | hp2 | a0008 | c0009 | t0001 | g0347 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0120 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03486 | hp1 | a0001 | c0014 | t0001 | g0346 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03669 | hp1 | a0001 | c0011 | t0001 | g0048 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04199 | hp1 | a0001 | c0001 | t0021 | g0248 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18967 | hp1 | a0001 | c0001 | t0006 | g0334 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18972 | hp2 | a0001 | c0001 | t0006 | g0335 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18980 | hp1 | a0001 | c0001 | t0018 | g0354 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18982 | hp1 | a0010 | c0006 | t0001 | g0064 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18984 | hp1 | a0001 | c0001 | t0020 | g0245 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18990 | hp2 | a0005 | c0013 | t0001 | g0097 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA18999 | hp2 | a0006 | c0012 | t0001 | g0242 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0112 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19067 | hp2 | a0007 | c0010 | t0001 | g0278 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0297 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ASW | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | ASW | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20905 | hp2 | a0011 | c0004 | t0001 | g0094 | SAS | GIH | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02486 | hp1 | a0001 | c0001 | t0017 | g0086 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03471 | hp1 | a0001 | c0001 | t0016 | g0131 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0061 | REF | REF | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0261 | REF | REF | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:8270048
|
C | G | 1 | a0002 | 9 | HG00140.hp1 HG00639.hp1 HG01074.hp1 others(6): Show |
missense_variant | MODERATE | c.80C>G | p.Ala27Gly | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 295/2539 | 80/1362 | 27/453 | chr4 | 8270048 | ||
chr4:8270055
|
C | A | 1 | a0003 | 1 | NA19070.hp1 | stop_gained | HIGH | c.87C>A | p.Cys29* | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 302/2539 | 87/1362 | 29/453 | chr4 | 8270055 | ||
chr4:8270146
|
G | A | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.178G>A | p.Glu60Lys | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 393/2539 | 178/1362 | 60/453 | chr4 | 8270146 | ||
chr4:8291399
|
C | A | 1 | a0010 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.738C>A | p.His246Gln | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 953/2539 | 738/1362 | 246/453 | chr4 | 8291399 | ||
chr4:8291466
|
G | A | 1 | a0004 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.805G>A | p.Val269Met | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 1020/2539 | 805/1362 | 269/453 | chr4 | 8291466 | ||
chr4:8291473
|
C | T | 1 | a0005 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.812C>T | p.Thr271Met | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 1027/2539 | 812/1362 | 271/453 | chr4 | 8291473 | ||
chr4:8291529
|
G | A | 1 | a0009 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.868G>A | p.Asp290Asn | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 1083/2539 | 868/1362 | 290/453 | chr4 | 8291529 | ||
chr4:8292333
|
G | A | 1 | a0008 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.916G>A | p.Gly306Arg | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/9 | 1131/2539 | 916/1362 | 306/453 | chr4 | 8292333 | ||
chr4:8304261
|
C | T | 1 | a0006 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1178C>T | p.Pro393Leu | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/9 | 1393/2539 | 1178/1362 | 393/453 | chr4 | 8304261 | ||
chr4:8306086
|
C | T | 1 | a0007 | 1 | NA19067.hp2 | missense_variant | MODERATE | c.1312C>T | p.Arg438Trp | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 1527/2539 | 1312/1362 | 438/453 | chr4 | 8306086 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:8270289
|
C | T | 1 | a0001c0014 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.321C>T | p.Ser107Ser | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 536/2539 | 321/1362 | 107/453 | chr4 | 8270289 | ||
chr4:8270316
|
G | A | 1 | a0001c0005 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.348G>A | p.Thr116Thr | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 563/2539 | 348/1362 | 116/453 | chr4 | 8270316 | ||
chr4:8306049
|
C | T | 1 | a0001c0011 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1275C>T | p.Ala425Ala | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 1490/2539 | 1275/1362 | 425/453 | chr4 | 8306049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:8269762
|
G | A | 2 | a0001c0001t0004a0001c0001t0008 | 3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-207G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 207 | chr4 | 8269762 | |||||
chr4:8306200
|
A | G | 1 | a0001c0001t0021 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 64 | chr4 | 8306200 | |||||
chr4:8306217
|
C | T | 1 | a0001c0001t0020 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 81 | chr4 | 8306217 | |||||
chr4:8306225
|
G | A | 1 | a0001c0001t0009 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 89 | chr4 | 8306225 | |||||
chr4:8306273
|
A | G | 3 | a0001c0001t0007a0001c0001t0008a0001c0001t0019 | 4 | HG01109.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 137 | chr4 | 8306273 | |||||
chr4:8306325
|
C | T | 1 | a0001c0001t0006 | 2 | NA18967.hp1 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*189C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 189 | chr4 | 8306325 | |||||
chr4:8306331
|
G | A | 1 | a0002c0002t0010 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 195 | chr4 | 8306331 | |||||
chr4:8306355
|
T | C | 1 | a0001c0001t0011 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 219 | chr4 | 8306355 | |||||
chr4:8306398
|
G | A | 1 | a0001c0001t0012 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 262 | chr4 | 8306398 | |||||
chr4:8306449
|
C | T | 1 | a0001c0001t0018 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 313 | chr4 | 8306449 | |||||
chr4:8306535
|
C | A | 1 | a0001c0001t0013 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 399 | chr4 | 8306535 | |||||
chr4:8306561
|
G | C | 1 | a0001c0001t0014 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 425 | chr4 | 8306561 | |||||
chr4:8306668
|
C | G | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(5): Show | 40 | HG00423.hp1 HG01109.hp2 HG01261.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*532C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 532 | chr4 | 8306668 | |||||
chr4:8306669
|
G | A | 1 | a0001c0001t0015 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 533 | chr4 | 8306669 | |||||
chr4:8306719
|
C | T | 1 | a0001c0001t0017 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 583 | chr4 | 8306719 | |||||
chr4:8306773
|
C | T | 1 | a0001c0001t0003 | 3 | HG02886.hp2 HG03486.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*637C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 637 | chr4 | 8306773 | |||||
chr4:8306784
|
C | T | 1 | a0001c0001t0011 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 648 | chr4 | 8306784 | |||||
chr4:8306946
|
G | T | 1 | a0001c0001t0016 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 810 | chr4 | 8306946 | |||||
chr4:8306976
|
C | T | 1 | a0001c0001t0005 | 2 | HG02738.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*840C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 840 | chr4 | 8306976 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:8270450
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG00741.hp1 HG02109.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+97G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270450 | ||||||
chr4:8270459
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0002g0005a0001c0001t0002g0033 | 4 | HG02559.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+106G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270459 | ||||||
chr4:8270594
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385+241C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270594 | ||||||
chr4:8270671
|
G | C | 2 | a0001c0001t0003g0036a0001c0001t0011g0035 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.385+318G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270671 | ||||||
chr4:8270712
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.385+359T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270712 | ||||||
chr4:8270935
|
C | T | 1 | a0001c0001t0001g0357 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.385+582C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270935 | ||||||
chr4:8270954
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.385+601C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270954 | ||||||
chr4:8271025
|
C | G | 1 | a0001c0001t0002g0005 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385+672C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271025 | ||||||
chr4:8271063
|
C | A | 1 | a0001c0001t0001g0038 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385+710C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271063 | ||||||
chr4:8271100
|
G | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.385+747G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271100 | ||||||
chr4:8271193
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.385+840C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271193 | ||||||
chr4:8271227
|
AT | A | 171 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.385+880delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8271227 | |||||
chr4:8271240
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.385+887T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271240 | ||||||
chr4:8271243
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 5 | HG01109.hp1 NA18947.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+890G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271243 | ||||||
chr4:8271295
|
C | T | 1 | a0001c0001t0018g0354 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.385+942C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271295 | ||||||
chr4:8271296
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0043 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.385+943G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271296 | ||||||
chr4:8271368
|
T | C | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+1015T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271368 | ||||||
chr4:8271520
|
C | G | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353 | 3 | NA18959.hp2 NA18972.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.385+1167C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271520 | ||||||
chr4:8271637
|
C | T | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | NA18944.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.385+1284C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271637 | ||||||
chr4:8271638
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0343a0001c0001t0001g0344others(4): Show | 8 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+1285C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271638 | ||||||
chr4:8271684
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.385+1331G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271684 | ||||||
chr4:8271743
|
TG | T | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.385+1391delG | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271743 | ||||||
chr4:8271752
|
C | G | 1 | a0001c0001t0001g0342 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.385+1399C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271752 | ||||||
chr4:8271989
|
A | G | 1 | a0001c0001t0004g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385+1636A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271989 | ||||||
chr4:8272015
|
A | T | 13 | a0001c0001t0001g0032a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+1662A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272015 | ||||||
chr4:8272100
|
C | T | 13 | a0001c0001t0001g0032a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+1747C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272100 | ||||||
chr4:8272225
|
C | T | 13 | a0001c0001t0001g0032a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+1872C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272225 | ||||||
chr4:8272351
|
C | G | 3 | a0001c0001t0004g0176a0001c0001t0004g0186a0001c0001t0008g0175 | 3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+1998C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272351 | ||||||
chr4:8272402
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0004g0186a0001c0001t0008g0175 | 3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+2049G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272402 | ||||||
chr4:8272403
|
TGG | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.385+2055_385+2056d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8272403 | |||||
chr4:8272404
|
G | T | 1 | a0001c0001t0001g0341 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.385+2051G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272404 | ||||||
chr4:8272435
|
G | C | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.385+2082G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272435 | ||||||
chr4:8272435
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.385+2082G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272435 | ||||||
chr4:8272491
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0279a0007c0010t0001g0278 | 3 | NA18942.hp2 NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.385+2138C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272491 | ||||||
chr4:8272521
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.385+2168G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272521 | ||||||
chr4:8272607
|
T | C | 24 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(21): Show | 25 | HG00733.hp2 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.385+2254T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272607 | ||||||
chr4:8272642
|
C | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0172others(3): Show | 8 | HG02280.hp2 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+2289C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272642 | ||||||
chr4:8272702
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.385+2349A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272702 | ||||||
chr4:8272773
|
C | T | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.385+2420C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272773 | ||||||
chr4:8272841
|
C | G | 3 | a0001c0001t0004g0176a0001c0001t0004g0186a0001c0001t0008g0175 | 3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+2488C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272841 | ||||||
chr4:8272881
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(74): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.385+2528G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272881 | ||||||
chr4:8272899
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0356 | 2 | HG01433.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.385+2546G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272899 | ||||||
chr4:8273167
|
C | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 114 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.385+2814C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273167 | ||||||
chr4:8273180
|
G | C | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 114 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.385+2827G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273180 | ||||||
chr4:8273233
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG01168.hp2 HG01257.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.385+2880G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273233 | ||||||
chr4:8273373
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.385+3020G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273373 | ||||||
chr4:8273377
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.385+3024A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273377 | ||||||
chr4:8273456
|
T | C | 1 | a0001c0011t0001g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.385+3103T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273456 | ||||||
chr4:8273522
|
TC | T | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(14): Show | 18 | HG00733.hp2 HG01109.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.385+3176delC | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8273522 | |||||
chr4:8273528
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385+3175C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273528 | ||||||
chr4:8273534
|
C | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.385+3181C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273534 | ||||||
chr4:8273534
|
C | G | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.385+3181C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273534 | ||||||
chr4:8273537
|
C | T | 117 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+3184C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273537 | ||||||
chr4:8273588
|
G | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(14): Show | 18 | HG00733.hp2 HG01109.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.385+3235G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273588 | ||||||
chr4:8273652
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.385+3299G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273652 | ||||||
chr4:8273888
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0160others(20): Show | 27 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.385+3535C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273888 | ||||||
chr4:8273894
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.385+3541T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273894 | ||||||
chr4:8273902
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.385+3549T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273902 | ||||||
chr4:8273909
|
C | CCCCTCCA others(44): Show |
13 | a0001c0001t0001g0032a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+3568_385+3569i others(53): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8273909 | |||||
chr4:8273909
|
C | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.385+3556C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273909 | ||||||
chr4:8274060
|
G | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.385+3707G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274060 | ||||||
chr4:8274083
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.385+3730C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274083 | ||||||
chr4:8274090
|
G | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.385+3737G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274090 | ||||||
chr4:8274380
|
G | C | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.385+4027G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274380 | ||||||
chr4:8274426
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385+4073T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274426 | ||||||
chr4:8274431
|
G | A | 6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0156others(3): Show | 8 | HG01433.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+4078G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274431 | ||||||
chr4:8274454
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(4): Show | 7 | HG01243.hp1 HG01261.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+4101C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274454 | ||||||
chr4:8274465
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0160others(20): Show | 27 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.385+4112C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274465 | ||||||
chr4:8274546
|
C | T | 6 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(3): Show | 6 | NA18952.hp2 NA18959.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+4193C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274546 | ||||||
chr4:8274612
|
C | T | 1 | a0001c0001t0003g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.385+4259C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274612 | ||||||
chr4:8274622
|
C | T | 118 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.385+4269C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274622 | ||||||
chr4:8274666
|
T | A | 1 | a0001c0001t0002g0196 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.385+4313T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274666 | ||||||
chr4:8274684
|
A | C | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.385+4331A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274684 | ||||||
chr4:8274698
|
T | A | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385+4345T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274698 | ||||||
chr4:8274765
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.385+4412A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274765 | ||||||
chr4:8274811
|
C | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0004g0176others(2): Show | 5 | HG02602.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+4458C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274811 | ||||||
chr4:8274812
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.385+4459G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274812 | ||||||
chr4:8274906
|
G | C | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0004g0176others(2): Show | 5 | HG02602.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+4553G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274906 | ||||||
chr4:8274916
|
A | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+4563A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274916 | ||||||
chr4:8274932
|
T | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 7 | HG02015.hp1 HG02027.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+4579T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274932 | ||||||
chr4:8274978
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG00741.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.385+4625T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274978 | ||||||
chr4:8275019
|
C | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0043others(64): Show | 70 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.385+4666C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275019 | ||||||
chr4:8275081
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.385+4728G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275081 | ||||||
chr4:8275088
|
G | C | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00733.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+4735G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275088 | ||||||
chr4:8275104
|
C | T | 2 | a0001c0001t0001g0148a0001c0005t0002g0155 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.385+4751C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275104 | ||||||
chr4:8275184
|
C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.385+4831C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275184 | ||||||
chr4:8275245
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+4892C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275245 | ||||||
chr4:8275374
|
T | G | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385+5021T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275374 | ||||||
chr4:8275415
|
A | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.385+5062A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275415 | ||||||
chr4:8275633
|
G | T | 2 | a0001c0001t0003g0036a0001c0001t0011g0035 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.385+5280G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275633 | ||||||
chr4:8275833
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.385+5480C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275833 | ||||||
chr4:8275905
|
T | C | 6 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(3): Show | 6 | NA18952.hp2 NA18959.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+5552T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275905 | ||||||
chr4:8276011
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.385+5658C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276011 | ||||||
chr4:8276033
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01243.hp2 HG01928.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+5680G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276033 | ||||||
chr4:8276108
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0160others(21): Show | 28 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.385+5755G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276108 | ||||||
chr4:8276296
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.385+5943C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276296 | ||||||
chr4:8276398
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.386-6039G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276398 | ||||||
chr4:8276441
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.386-5996C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276441 | ||||||
chr4:8276494
|
G | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0160others(19): Show | 26 | HG01081.hp1 HG01433.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.386-5943G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276494 | ||||||
chr4:8276666
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.386-5771C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276666 | ||||||
chr4:8276706
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | HG00733.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-5731G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276706 | ||||||
chr4:8276737
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.386-5700G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276737 | ||||||
chr4:8276813
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.386-5624G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276813 | ||||||
chr4:8276815
|
A | AGCAG | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0003g0036others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-5620_386-5617d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8276815 | |||||
chr4:8276826
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-5611C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276826 | ||||||
chr4:8276844
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-5593C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276844 | ||||||
chr4:8276876
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(66): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.386-5561G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276876 | ||||||
chr4:8276908
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-5529A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276908 | ||||||
chr4:8276989
|
C | T | 11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(8): Show | 11 | HG02056.hp2 HG02080.hp1 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-5448C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276989 | ||||||
chr4:8277013
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-5424C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277013 | ||||||
chr4:8277077
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.386-5360C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277077 | ||||||
chr4:8277141
|
G | A | 1 | a0001c0001t0018g0354 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.386-5296G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277141 | ||||||
chr4:8277199
|
C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(63): Show | 77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.386-5238C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277199 | ||||||
chr4:8277200
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.386-5237G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277200 | ||||||
chr4:8277206
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.386-5231G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277206 | ||||||
chr4:8277241
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.386-5196G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277241 | ||||||
chr4:8277306
|
G | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG00438.hp1 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.386-5131G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277306 | ||||||
chr4:8277345
|
C | A | 1 | a0001c0001t0004g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.386-5092C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277345 | ||||||
chr4:8277462
|
G | A | 2 | a0001c0001t0004g0176a0001c0001t0008g0175 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.386-4975G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277462 | ||||||
chr4:8277463
|
CT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(68): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.386-4971delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8277463 | |||||
chr4:8277466
|
T | G | 1 | a0001c0001t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.386-4971T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277466 | ||||||
chr4:8277469
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.386-4968G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277469 | ||||||
chr4:8277471
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.386-4966A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277471 | ||||||
chr4:8277650
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386-4787G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277650 | ||||||
chr4:8277692
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.386-4745G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277692 | ||||||
chr4:8277776
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.386-4661G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277776 | ||||||
chr4:8277782
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.386-4655C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277782 | ||||||
chr4:8277783
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(70): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.386-4654G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277783 | ||||||
chr4:8277829
|
T | C | 2 | a0001c0001t0003g0036a0001c0001t0011g0035 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.386-4608T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277829 | ||||||
chr4:8277860
|
A | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-4577A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277860 | ||||||
chr4:8277959
|
G | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0162others(20): Show | 27 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.386-4478G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277959 | ||||||
chr4:8278298
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG01109.hp1 NA18994.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.386-4139C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278298 | ||||||
chr4:8278313
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.386-4124C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278313 | ||||||
chr4:8278339
|
G | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.386-4098G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278339 | ||||||
chr4:8278390
|
G | GA | 12 | a0001c0001t0001g0008a0001c0001t0001g0088a0001c0001t0001g0089others(9): Show | 13 | HG00544.hp1 HG00609.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-4031dupA | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8278390 | |||||
chr4:8278390
|
GA | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(71): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.386-4031delA | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8278390 | |||||
chr4:8278533
|
C | T | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.386-3904C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278533 | ||||||
chr4:8278580
|
C | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | NA18941.hp1 NA18949.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-3857C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278580 | ||||||
chr4:8278604
|
C | T | 129 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.386-3833C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278604 | ||||||
chr4:8278630
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.386-3807G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278630 | ||||||
chr4:8278660
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.386-3777C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278660 | ||||||
chr4:8278769
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.386-3668C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278769 | ||||||
chr4:8278798
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.386-3639A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278798 | ||||||
chr4:8278866
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.386-3571G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278866 | ||||||
chr4:8279046
|
T | G | 1 | a0001c0001t0001g0293 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.386-3391T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279046 | ||||||
chr4:8279273
|
C | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02080.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.386-3164C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279273 | ||||||
chr4:8279419
|
C | G | 1 | a0002c0002t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386-3018C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279419 | ||||||
chr4:8279438
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.386-2999G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279438 | ||||||
chr4:8279459
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386-2978C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279459 | ||||||
chr4:8279490
|
G | A | 2 | a0001c0001t0001g0148a0001c0005t0002g0155 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.386-2947G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279490 | ||||||
chr4:8279542
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.386-2895C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279542 | ||||||
chr4:8279673
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.386-2764C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279673 | ||||||
chr4:8279734
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-2703T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279734 | ||||||
chr4:8279757
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.386-2680C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279757 | ||||||
chr4:8279913
|
C | G | 1 | a0001c0001t0017g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.386-2524C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279913 | ||||||
chr4:8279932
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0291a0001c0001t0001g0293others(5): Show | 9 | NA18942.hp1 NA18953.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-2505C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279932 | ||||||
chr4:8279961
|
AC | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(1): Show | 4 | HG02109.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-2475delC | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279961 | ||||||
chr4:8279964
|
A | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.386-2473A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279964 | ||||||
chr4:8279964
|
A | T | 2 | a0001c0001t0004g0176a0001c0001t0008g0175 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.386-2473A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279964 | ||||||
chr4:8280099
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.386-2338C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280099 | ||||||
chr4:8280126
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.386-2311A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280126 | ||||||
chr4:8280155
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.386-2282C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280155 | ||||||
chr4:8280274
|
G | T | 1 | a0001c0001t0001g0269 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.386-2163G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280274 | ||||||
chr4:8280333
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02080.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.386-2104G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280333 | ||||||
chr4:8280377
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.386-2060C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280377 | ||||||
chr4:8280383
|
T | C | 1 | a0001c0001t0007g0181 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.386-2054T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280383 | ||||||
chr4:8280397
|
A | C | 1 | a0001c0005t0002g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.386-2040A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280397 | ||||||
chr4:8280447
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.386-1990C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280447 | ||||||
chr4:8280483
|
C | T | 2 | a0001c0001t0006g0334a0001c0001t0006g0335 | 2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.386-1954C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280483 | ||||||
chr4:8280533
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-1904G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280533 | ||||||
chr4:8280563
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0206others(3): Show | 6 | HG02572.hp1 HG02965.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-1874G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280563 | ||||||
chr4:8280580
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.386-1857C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280580 | ||||||
chr4:8280615
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.386-1822T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280615 | ||||||
chr4:8280712
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1725G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280712 | ||||||
chr4:8280731
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.386-1706G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280731 | ||||||
chr4:8280735
|
G | GC | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.386-1700dupC | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8280735 | |||||
chr4:8280738
|
G | C | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-1699G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280738 | ||||||
chr4:8280740
|
C | G | 1 | a0001c0001t0002g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.386-1697C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280740 | ||||||
chr4:8280835
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-1602C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280835 | ||||||
chr4:8280896
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.386-1541T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280896 | ||||||
chr4:8280976
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | NA18952.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.386-1461G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280976 | ||||||
chr4:8281044
|
C | T | 23 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0038others(20): Show | 24 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.386-1393C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281044 | ||||||
chr4:8281084
|
A | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1353A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281084 | ||||||
chr4:8281150
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.386-1287G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281150 | ||||||
chr4:8281182
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.386-1255C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281182 | ||||||
chr4:8281265
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.386-1172C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281265 | ||||||
chr4:8281393
|
C | G | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-1044C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281393 | ||||||
chr4:8281396
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0015g0205 | 3 | HG00642.hp1 HG02109.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.386-1041G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281396 | ||||||
chr4:8281451
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.386-986G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281451 | ||||||
chr4:8281518
|
A | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.386-919A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281518 | ||||||
chr4:8281531
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-906A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281531 | ||||||
chr4:8281595
|
G | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.386-842G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281595 | ||||||
chr4:8281601
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386-836G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281601 | ||||||
chr4:8281660
|
C | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.386-777C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281660 | ||||||
chr4:8281695
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.386-742G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281695 | ||||||
chr4:8281748
|
T | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.386-689T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281748 | ||||||
chr4:8281766
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-671G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281766 | ||||||
chr4:8281767
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-670A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281767 | ||||||
chr4:8281784
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.386-653G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281784 | ||||||
chr4:8281806
|
A | G | 2 | a0001c0001t0001g0355a0001c0001t0007g0181 | 2 | HG01109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.386-631A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281806 | ||||||
chr4:8281903
|
C | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(82): Show | 95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.386-534C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281903 | ||||||
chr4:8282021
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0007g0181 | 2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.386-416G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282021 | ||||||
chr4:8282021
|
G | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.386-416G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282021 | ||||||
chr4:8282110
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.386-327T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282110 | ||||||
chr4:8282114
|
G | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0184a0001c0001t0001g0343others(4): Show | 8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-323G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282114 | ||||||
chr4:8282293
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.386-144G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282293 | ||||||
chr4:8282357
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(247): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.386-80T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282357 | ||||||
chr4:8282397
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.386-40G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282397 | ||||||
chr4:8282600
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.485+64G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282600 | ||||||
chr4:8282652
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.485+116C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282652 | ||||||
chr4:8282817
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0344a0001c0001t0012g0345others(2): Show | 6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+281A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282817 | ||||||
chr4:8282846
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.485+310G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282846 | ||||||
chr4:8282948
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0302 | 2 | HG01168.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.485+412G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282948 | ||||||
chr4:8283008
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.485+472G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283008 | ||||||
chr4:8283236
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.485+700G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283236 | ||||||
chr4:8283462
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.485+926G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283462 | ||||||
chr4:8283466
|
T | C | 1 | a0001c0001t0011g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485+930T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283466 | ||||||
chr4:8283603
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.485+1067G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283603 | ||||||
chr4:8283652
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.485+1116G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283652 | ||||||
chr4:8283665
|
A | G | 9 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(6): Show | 9 | HG00558.hp2 HG02004.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.485+1129A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283665 | ||||||
chr4:8283692
|
G | A | 1 | a0001c0001t0001g0349 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.485+1156G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283692 | ||||||
chr4:8283713
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0355 | 2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.485+1177C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283713 | ||||||
chr4:8283773
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+1237G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283773 | ||||||
chr4:8283807
|
C | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.485+1271C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283807 | ||||||
chr4:8283868
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.485+1332T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283868 | ||||||
chr4:8283892
|
C | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0287 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.485+1356C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283892 | ||||||
chr4:8283919
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.485+1383G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283919 | ||||||
chr4:8283967
|
C | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.485+1431C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283967 | ||||||
chr4:8283969
|
C | T | 1 | a0001c0005t0002g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.485+1433C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283969 | ||||||
chr4:8283996
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+1460C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283996 | ||||||
chr4:8284091
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0004g0176 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.485+1555G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284091 | ||||||
chr4:8284170
|
C | T | 1 | a0002c0002t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.485+1634C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284170 | ||||||
chr4:8284179
|
G | A | 25 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(22): Show | 28 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.485+1643G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284179 | ||||||
chr4:8284246
|
C | T | 1 | a0001c0001t0009g0325 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.485+1710C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284246 | ||||||
chr4:8284276
|
A | G | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.485+1740A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284276 | ||||||
chr4:8284361
|
A | C | 1 | a0001c0001t0001g0042 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.485+1825A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284361 | ||||||
chr4:8284395
|
G | A | 1 | a0001c0001t0007g0181 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.485+1859G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284395 | ||||||
chr4:8284547
|
G | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0132a0001c0001t0002g0133others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2011G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284547 | ||||||
chr4:8284575
|
C | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(19): Show | 25 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.486-1986C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284575 | ||||||
chr4:8284615
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.486-1946C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284615 | ||||||
chr4:8284683
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.486-1878G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284683 | ||||||
chr4:8284899
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | NA18962.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.486-1662G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284899 | ||||||
chr4:8285052
|
G | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-1509G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285052 | ||||||
chr4:8285071
|
G | C | 1 | a0001c0001t0008g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.486-1490G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285071 | ||||||
chr4:8285115
|
C | T | 1 | a0001c0001t0001g0356 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.486-1446C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285115 | ||||||
chr4:8285189
|
G | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.486-1372G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285189 | ||||||
chr4:8285311
|
T | A | 1 | a0001c0005t0002g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.486-1250T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285311 | ||||||
chr4:8285470
|
C | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-1091C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285470 | ||||||
chr4:8285625
|
G | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.486-936G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285625 | ||||||
chr4:8285725
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-836C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285725 | ||||||
chr4:8285734
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.486-827C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285734 | ||||||
chr4:8285760
|
A | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-801A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285760 | ||||||
chr4:8285767
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.486-794A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285767 | ||||||
chr4:8285836
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-725G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285836 | ||||||
chr4:8285940
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0156 | 3 | HG02145.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.486-621C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285940 | ||||||
chr4:8285959
|
G | A | 5 | a0001c0001t0001g0148a0001c0001t0001g0167a0001c0001t0003g0036others(2): Show | 5 | HG02630.hp2 HG02886.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-602G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285959 | ||||||
chr4:8286015
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.486-546C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286015 | ||||||
chr4:8286056
|
T | G | 128 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(125): Show | 138 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.486-505T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286056 | ||||||
chr4:8286088
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.486-473C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286088 | ||||||
chr4:8286115
|
G | A | 1 | a0001c0001t0001g0331 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.486-446G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286115 | ||||||
chr4:8286142
|
C | G | 1 | a0008c0009t0001g0347 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486-419C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286142 | ||||||
chr4:8286206
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.486-355G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286206 | ||||||
chr4:8286264
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.486-297G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286264 | ||||||
chr4:8286301
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.486-260G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286301 | ||||||
chr4:8286381
|
C | A | 2 | a0001c0001t0001g0330a0001c0001t0001g0355 | 2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.486-180C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286381 | ||||||
chr4:8286499
|
C | G | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.486-62C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286499 | ||||||
chr4:8286794
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.708+11G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286794 | ||||||
chr4:8286807
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0005g0120 | 2 | HG02965.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.708+24C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286807 | ||||||
chr4:8286854
|
A | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.708+71A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286854 | ||||||
chr4:8286885
|
A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.708+102A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286885 | ||||||
chr4:8286943
|
T | C | 278 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.708+160T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286943 | ||||||
chr4:8286980
|
T | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.708+197T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286980 | ||||||
chr4:8286986
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.708+203G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286986 | ||||||
chr4:8287094
|
G | C | 3 | a0001c0001t0001g0183a0001c0001t0002g0128a0001c0001t0002g0193 | 3 | HG01261.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.708+311G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287094 | ||||||
chr4:8287188
|
A | C | 1 | a0001c0001t0001g0280 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.708+405A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287188 | ||||||
chr4:8287231
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0074 | 2 | HG00642.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.708+448C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287231 | ||||||
chr4:8287270
|
C | G | 277 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.708+487C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287270 | ||||||
chr4:8287428
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.708+645A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287428 | ||||||
chr4:8287480
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.708+697G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287480 | ||||||
chr4:8287526
|
G | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.708+743G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287526 | ||||||
chr4:8287529
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.708+746A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287529 | ||||||
chr4:8287561
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.708+778G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287561 | ||||||
chr4:8287595
|
C | A | 2 | a0001c0001t0001g0194a0001c0001t0007g0181 | 2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.708+812C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287595 | ||||||
chr4:8287626
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.708+843C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287626 | ||||||
chr4:8287685
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.708+902C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287685 | ||||||
chr4:8287707
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.708+924A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287707 | ||||||
chr4:8287713
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.708+930T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287713 | ||||||
chr4:8287722
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0167a0001c0001t0003g0036others(2): Show | 5 | HG02630.hp2 HG02886.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+939C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287722 | ||||||
chr4:8287772
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.708+989C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287772 | ||||||
chr4:8287784
|
G | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0285a0001c0001t0001g0287others(1): Show | 4 | HG00438.hp1 HG02165.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+1001G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287784 | ||||||
chr4:8287816
|
C | T | 2 | a0001c0001t0001g0072a0001c0011t0001g0048 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.708+1033C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287816 | ||||||
chr4:8287819
|
C | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0355 | 2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.708+1036C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287819 | ||||||
chr4:8287909
|
T | G | 2 | a0001c0001t0008g0175a0001c0001t0019g0348 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.708+1126T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287909 | ||||||
chr4:8287990
|
G | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(18): Show | 24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+1207G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287990 | ||||||
chr4:8287991
|
A | G | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(18): Show | 24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+1208A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287991 | ||||||
chr4:8288080
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.708+1297A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288080 | ||||||
chr4:8288082
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.708+1299C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288082 | ||||||
chr4:8288170
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.708+1387T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288170 | ||||||
chr4:8288177
|
A | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.708+1394A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288177 | ||||||
chr4:8288188
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0083others(2): Show | 7 | HG01070.hp2 HG01168.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+1405T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288188 | ||||||
chr4:8288190
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.708+1407G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288190 | ||||||
chr4:8288231
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | NA18962.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.708+1448G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288231 | ||||||
chr4:8288261
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0182a0001c0001t0001g0184others(5): Show | 9 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.708+1478G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288261 | ||||||
chr4:8288310
|
G | T | 1 | a0001c0001t0001g0330 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.708+1527G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288310 | ||||||
chr4:8288313
|
G | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(19): Show | 25 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.708+1530G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288313 | ||||||
chr4:8288329
|
A | C | 1 | a0001c0001t0001g0284 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.708+1546A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288329 | ||||||
chr4:8288386
|
G | GCCTCAGC others(36): Show |
1 | a0001c0001t0001g0249 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.708+1605_708+1647d others(45): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288386 | |||||
chr4:8288574
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0323others(5): Show | 10 | HG00558.hp1 HG01175.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.708+1807dupT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | |||||
chr4:8288574
|
CT | C | 7 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0139others(4): Show | 7 | HG01167.hp2 HG01934.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+1807delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | |||||
chr4:8288574
|
CTT | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.708+1806_708+1807d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | |||||
chr4:8288574
|
CTTT | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0182a0001c0001t0001g0184others(8): Show | 12 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.708+1805_708+1807d others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | |||||
chr4:8288614
|
C | T | 2 | a0001c0001t0011g0035a0001c0001t0016g0131 | 2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.708+1831C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288614 | ||||||
chr4:8288707
|
T | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(18): Show | 24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+1924T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288707 | ||||||
chr4:8288853
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224 | 3 | NA18962.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.708+2070G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288853 | ||||||
chr4:8288864
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.708+2081C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288864 | ||||||
chr4:8288878
|
T | TTTCC | 27 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0028others(24): Show | 29 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.708+2108_708+2111d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | |||||
chr4:8288878
|
T | TTTCCTTC others(1): Show |
34 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0039others(31): Show | 37 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.708+2104_708+2111d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | |||||
chr4:8288878
|
T | TTTCCTTC others(5): Show |
31 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0055others(28): Show | 32 | HG00544.hp1 HG01433.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.708+2100_708+2111d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | |||||
chr4:8288878
|
T | TTTCCTTC others(9): Show |
24 | a0001c0001t0001g0060a0001c0001t0001g0068a0001c0001t0001g0072others(21): Show | 24 | HG00323.hp1 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+2096_708+2111d others(18): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | |||||
chr4:8288878
|
T | TTTCCTTC others(13): Show |
4 | a0001c0001t0001g0051a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG01074.hp2 HG02055.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.708+2111_708+2112i others(22): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | |||||
chr4:8288878
|
T | TTTCCTTC others(17): Show |
1 | a0001c0001t0001g0007 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.708+2111_708+2112i others(26): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | |||||
chr4:8288883
|
TTCCTTCC others(9): Show |
T | 2 | a0001c0001t0001g0163a0001c0001t0001g0262 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.708+2112_708+2127d others(18): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288883 | |||||
chr4:8288887
|
TTCCTTCC others(5): Show |
T | 14 | a0001c0001t0001g0021a0001c0001t0001g0056a0001c0001t0001g0101others(11): Show | 16 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.708+2112_708+2123d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288887 | |||||
chr4:8288891
|
TTCCG | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(76): Show | 86 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.708+2116_708+2119d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288891 | |||||
chr4:8288891
|
TTCCGTCC others(1): Show |
T | 24 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0038others(21): Show | 26 | HG00408.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.708+2112_708+2119d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288891 | |||||
chr4:8288895
|
G | T | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(142): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.708+2112G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288895 | ||||||
chr4:8288899
|
G | GTCCT | 5 | a0001c0001t0001g0160a0001c0001t0001g0293a0001c0001t0001g0321others(2): Show | 5 | HG00423.hp2 HG02647.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+2149_708+2152d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | |||||
chr4:8288899
|
G | GTCCTTCC others(1): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0167a0001c0001t0001g0184others(4): Show | 8 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+2145_708+2152d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | |||||
chr4:8288899
|
G | GTCCTTCC others(5): Show |
3 | a0001c0001t0001g0182a0001c0001t0002g0033a0001c0001t0002g0185 | 3 | HG02257.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.708+2141_708+2152d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | |||||
chr4:8288899
|
G | GTCCTTCC others(9): Show |
2 | a0001c0001t0003g0036a0001c0001t0004g0186 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.708+2137_708+2152d others(18): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | |||||
chr4:8288899
|
G | GTCCTTCC others(13): Show |
2 | a0001c0001t0001g0148a0001c0001t0004g0176 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.708+2133_708+2152d others(22): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | |||||
chr4:8288899
|
G | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(221): Show | 241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.708+2116G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288899 | ||||||
chr4:8288932
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.708+2149T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288932 | ||||||
chr4:8288935
|
T | TTCCTTCC others(3): Show |
1 | a0001c0001t0001g0091 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.708+2152_708+2153i others(12): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288935 | ||||||
chr4:8288936
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 5 | NA18947.hp1 NA18948.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+2153C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288936 | ||||||
chr4:8288937
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.708+2154C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288937 | ||||||
chr4:8288945
|
C | T | 2 | a0001c0001t0011g0035a0001c0001t0016g0131 | 2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.708+2162C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288945 | ||||||
chr4:8288949
|
T | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(18): Show | 24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+2166T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288949 | ||||||
chr4:8288951
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.708+2168T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288951 | ||||||
chr4:8288981
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.708+2198G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288981 | ||||||
chr4:8289031
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.708+2248C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289031 | ||||||
chr4:8289037
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(17): Show | 23 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.708+2254A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289037 | ||||||
chr4:8289056
|
C | T | 1 | a0001c0001t0001g0350 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.708+2273C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289056 | ||||||
chr4:8289176
|
G | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(206): Show | 228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.709-2194G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289176 | ||||||
chr4:8289268
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.709-2102C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289268 | ||||||
chr4:8289348
|
C | G | 1 | a0002c0002t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.709-2022C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289348 | ||||||
chr4:8289358
|
A | T | 1 | a0001c0005t0002g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.709-2012A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289358 | ||||||
chr4:8289375
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(170): Show | 188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.709-1995C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289375 | ||||||
chr4:8289458
|
C | T | 5 | a0001c0001t0001g0194a0001c0001t0001g0355a0001c0001t0007g0181others(2): Show | 5 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.709-1912C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289458 | ||||||
chr4:8289460
|
T | C | 5 | a0001c0001t0001g0194a0001c0001t0001g0355a0001c0001t0007g0181others(2): Show | 5 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.709-1910T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289460 | ||||||
chr4:8289652
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0070 | 3 | HG02056.hp1 NA19000.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.709-1718C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289652 | ||||||
chr4:8289707
|
G | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 90 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.709-1663G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289707 | ||||||
chr4:8289794
|
A | ACCCTCCT others(112): Show |
21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(18): Show | 24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.709-1551_709-1433d others(121): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8289794 | |||||
chr4:8289898
|
TGGCCTCA others(53): Show |
T | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.709-1457_709-1398d others(62): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8289898 | |||||
chr4:8289954
|
T | C | 6 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(3): Show | 6 | HG00423.hp2 HG02074.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-1416T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289954 | ||||||
chr4:8289958
|
C | T | 6 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(3): Show | 6 | HG00423.hp2 HG02074.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-1412C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289958 | ||||||
chr4:8289973
|
A | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(17): Show | 23 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.709-1397A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289973 | ||||||
chr4:8289996
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0004g0176 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.709-1374C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289996 | ||||||
chr4:8290039
|
C | T | 16 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0132others(13): Show | 17 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.709-1331C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290039 | ||||||
chr4:8290060
|
C | T | 33 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0058others(30): Show | 35 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.709-1310C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290060 | ||||||
chr4:8290061
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0349 | 2 | HG02965.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.709-1309G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290061 | ||||||
chr4:8290124
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.709-1246C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290124 | ||||||
chr4:8290176
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.709-1194G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290176 | ||||||
chr4:8290183
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.709-1187G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290183 | ||||||
chr4:8290191
|
T | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.709-1179T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290191 | ||||||
chr4:8290254
|
T | C | 78 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0029others(75): Show | 84 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.709-1116T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290254 | ||||||
chr4:8290352
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.709-1018C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290352 | ||||||
chr4:8290466
|
G | A | 6 | a0001c0001t0001g0160a0001c0001t0002g0012a0001c0001t0002g0157others(3): Show | 7 | HG01433.hp2 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.709-904G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290466 | ||||||
chr4:8290475
|
C | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0182others(10): Show | 15 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.709-895C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290475 | ||||||
chr4:8290513
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0157a0001c0001t0002g0158others(2): Show | 6 | HG01433.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-857C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290513 | ||||||
chr4:8290534
|
C | T | 1 | a0001c0001t0004g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.709-836C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290534 | ||||||
chr4:8290637
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.709-733C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290637 | ||||||
chr4:8290819
|
G | A | 16 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0132others(13): Show | 17 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.709-551G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290819 | ||||||
chr4:8290830
|
T | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.709-540T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290830 | ||||||
chr4:8290875
|
G | A | 18 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0075others(15): Show | 19 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.709-495G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290875 | ||||||
chr4:8290886
|
C | T | 125 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(122): Show | 136 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.709-484C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290886 | ||||||
chr4:8290906
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.709-464G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290906 | ||||||
chr4:8290950
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0182a0001c0001t0001g0184others(5): Show | 9 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-420A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290950 | ||||||
chr4:8290974
|
A | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(18): Show | 24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.709-396A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290974 | ||||||
chr4:8291100
|
A | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(254): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.709-270A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291100 | ||||||
chr4:8291150
|
A | G | 1 | a0001c0001t0016g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.709-220A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291150 | ||||||
chr4:8291263
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.709-107G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291263 | ||||||
chr4:8291315
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.709-55G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291315 | ||||||
chr4:8291321
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0157a0001c0001t0002g0158others(2): Show | 6 | HG01433.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-49G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291321 | ||||||
chr4:8291629
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.903+65G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291629 | ||||||
chr4:8291652
|
C | A | 278 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.903+88C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291652 | ||||||
chr4:8291653
|
T | C | 50 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(47): Show | 52 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.903+89T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291653 | ||||||
chr4:8291671
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(196): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.903+107C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291671 | ||||||
chr4:8291675
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.903+111C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291675 | ||||||
chr4:8291691
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.903+127T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291691 | ||||||
chr4:8291716
|
T | C | 44 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(41): Show | 46 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.903+152T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291716 | ||||||
chr4:8291829
|
C | G | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(332): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.903+265C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291829 | ||||||
chr4:8291866
|
T | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0132a0001c0001t0001g0163others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+302T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291866 | ||||||
chr4:8291956
|
C | G | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.904-365C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291956 | ||||||
chr4:8292004
|
G | C | 1 | a0001c0001t0001g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.904-317G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292004 | ||||||
chr4:8292008
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0344a0001c0001t0012g0345others(2): Show | 6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-313C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292008 | ||||||
chr4:8292063
|
CTGCCTGG others(15): Show |
C | 2 | a0001c0001t0001g0079a0001c0001t0001g0124 | 2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.904-253_904-232del others(22): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 8292063 | |||||
chr4:8292072
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.904-249C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292072 | ||||||
chr4:8292075
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.904-246C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292075 | ||||||
chr4:8292247
|
C | T | 283 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.904-74C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292247 | ||||||
chr4:8292443
|
A | G | 6 | a0001c0001t0001g0038a0001c0001t0001g0132a0001c0001t0001g0163others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+90A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292443 | ||||||
chr4:8292469
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 106 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.936+116C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292469 | ||||||
chr4:8292524
|
C | T | 1 | a0001c0001t0001g0353 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.936+171C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292524 | ||||||
chr4:8292567
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.936+214C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292567 | ||||||
chr4:8292602
|
C | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0002g0016 | 4 | HG00558.hp2 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+249C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292602 | ||||||
chr4:8292612
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.936+259G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292612 | ||||||
chr4:8292688
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.936+335C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292688 | ||||||
chr4:8292822
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 102 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.936+469C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292822 | ||||||
chr4:8292823
|
G | A | 18 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(15): Show | 18 | HG02080.hp1 HG02109.hp2 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.936+470G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292823 | ||||||
chr4:8292824
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.936+471G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292824 | ||||||
chr4:8293020
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.936+667C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293020 | ||||||
chr4:8293152
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.936+799C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293152 | ||||||
chr4:8293283
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.937-804G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293283 | ||||||
chr4:8293293
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.937-794C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293293 | ||||||
chr4:8293330
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.937-757G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293330 | ||||||
chr4:8293403
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.937-684C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293403 | ||||||
chr4:8293559
|
T | A | 1 | a0009c0008t0001g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.937-528T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293559 | ||||||
chr4:8293607
|
G | A | 1 | a0001c0001t0001g0019 | 2 | NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.937-480G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293607 | ||||||
chr4:8293696
|
G | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0003g0036others(1): Show | 4 | HG00741.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-391G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293696 | ||||||
chr4:8293844
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.937-243G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293844 | ||||||
chr4:8293878
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.937-209A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293878 | ||||||
chr4:8294054
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0129others(7): Show | 11 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.937-33C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8294054 | ||||||
chr4:8294222
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0150others(2): Show | 7 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+21G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294222 | ||||||
chr4:8294415
|
G | A | 94 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(91): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1051+214G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294415 | ||||||
chr4:8294570
|
G | A | 3 | a0001c0001t0004g0186a0001c0001t0011g0035a0002c0002t0001g0067 | 3 | HG02451.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+369G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294570 | ||||||
chr4:8294574
|
G | A | 1 | a0001c0005t0002g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1051+373G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294574 | ||||||
chr4:8294578
|
G | A | 20 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0219others(17): Show | 22 | HG00423.hp1 HG01261.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051+377G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294578 | ||||||
chr4:8294582
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1051+381G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294582 | ||||||
chr4:8294612
|
C | CCATCCAT others(1108): Show |
1 | a0001c0001t0001g0101 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294612 | |||||
chr4:8294614
|
A | ACCCACCC others(149): Show |
2 | a0001c0001t0001g0148a0001c0001t0001g0179 | 2 | HG00733.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1051+413_1051+414i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294614 | ||||||
chr4:8294614
|
A | ACCCACCC others(153): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0129 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1051+413_1051+414i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294614 | ||||||
chr4:8294614
|
A | ATCCACCC others(149): Show |
1 | a0001c0001t0001g0110 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294614 | |||||
chr4:8294615
|
T | TCCACCCA others(129): Show |
1 | a0001c0001t0002g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+417_1051+418i others(138): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | |||||
chr4:8294615
|
T | TCCACCCA others(133): Show |
9 | a0001c0001t0001g0164a0001c0001t0002g0033a0001c0001t0002g0087others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(142): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | |||||
chr4:8294615
|
T | TCCACCCA others(25): Show |
9 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0002g0012others(6): Show | 11 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(34): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | |||||
chr4:8294615
|
T | TCCACCCA others(37): Show |
3 | a0001c0001t0001g0255a0001c0001t0002g0128a0001c0001t0002g0193 | 3 | HG01261.hp2 HG01891.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(46): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | |||||
chr4:8294616
|
C | CCACCCAC others(141): Show |
3 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0152 | 5 | HG02145.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(33): Show |
1 | a0009c0008t0001g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(42): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(1053): Show |
1 | a0001c0001t0001g0249 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(1062): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(1096): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 10 | HG01192.hp1 HG01255.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(1100): Show |
1 | a0001c0001t0016g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(137): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0089a0001c0001t0001g0119others(4): Show | 7 | HG01175.hp2 HG02040.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(146): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(141): Show |
52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0024others(49): Show | 59 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(145): Show |
15 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0039others(12): Show | 16 | HG02523.hp1 HG02735.hp2 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(137): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0132others(3): Show | 6 | HG00741.hp1 HG01243.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(146): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCACCCAC others(141): Show |
2 | a0001c0001t0003g0036a0001c0001t0003g0096 | 2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294616
|
C | CCATCCAT others(1104): Show |
1 | a0001c0001t0001g0289 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | |||||
chr4:8294618
|
A | ACCCACCC others(141): Show |
2 | a0001c0001t0001g0162a0001c0001t0015g0205 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | ||||||
chr4:8294618
|
A | ACCCACCC others(145): Show |
65 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 71 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | ||||||
chr4:8294618
|
A | ACCCACCC others(149): Show |
26 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0029others(23): Show | 28 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | ||||||
chr4:8294618
|
A | ACCCACCC others(153): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | ||||||
chr4:8294618
|
A | ACCCACCC others(141): Show |
1 | a0001c0001t0001g0113 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | ||||||
chr4:8294618
|
A | ATCCACCC others(145): Show |
1 | a0002c0002t0002g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | |||||
chr4:8294618
|
A | ATCCACCC others(149): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG01884.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1051+421_1051+422i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | |||||
chr4:8294618
|
A | ATCCACCC others(153): Show |
1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | |||||
chr4:8294618
|
A | ATCCATCC others(153): Show |
1 | a0001c0001t0011g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | |||||
chr4:8294619
|
T | C | 1 | a0009c0008t0001g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+418T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294619 | ||||||
chr4:8294619
|
T | TCCACCCA others(37): Show |
1 | a0001c0001t0002g0158 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(46): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294619 | |||||
chr4:8294619
|
T | TCCACCCA others(33): Show |
1 | a0001c0001t0001g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(42): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294619 | |||||
chr4:8294620
|
C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0106 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(1097): Show |
1 | a0001c0001t0001g0213 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1106): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(33): Show |
5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0157others(2): Show | 5 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051+421_1051+422i others(42): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(133): Show |
1 | a0001c0001t0001g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1051+421_1051+422i others(142): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(1084): Show |
1 | a0001c0001t0001g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1093): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(1096): Show |
28 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0104others(25): Show | 30 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1051+421_1051+422i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(1100): Show |
1 | a0001c0001t0007g0159 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(1104): Show |
2 | a0001c0001t0008g0175a0001c0001t0019g0348 | 2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1051+421_1051+422i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCACCCAC others(141): Show |
1 | a0001c0001t0007g0181 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCATCCAC others(1100): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0154a0001c0001t0001g0204others(13): Show | 17 | HG00738.hp2 HG01192.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCATCCAC others(1104): Show |
1 | a0001c0001t0001g0314 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294620
|
C | CCATCCAC others(1096): Show |
1 | a0006c0012t0001g0242 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | |||||
chr4:8294622
|
A | ACCCACCC others(145): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0071others(1): Show | 6 | HG01167.hp2 HG02280.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+421_1051+422i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294622 | ||||||
chr4:8294622
|
A | ACCCACCC others(149): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0303 | 2 | HG00609.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1051+421_1051+422i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294622 | ||||||
chr4:8294623
|
T | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0157others(2): Show | 5 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051+422T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294623 | ||||||
chr4:8294624
|
C | CCACCCAC others(133): Show |
1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(142): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1096): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0232 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1096): Show |
44 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0023others(41): Show | 47 | HG00408.hp1 HG01071.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1097): Show |
1 | a0001c0001t0001g0315 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1106): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1096): Show |
1 | a0001c0001t0001g0141 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1096): Show |
1 | a0001c0001t0001g0258 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1096): Show |
1 | a0001c0001t0001g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0290 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1097): Show |
1 | a0001c0001t0001g0353 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1106): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1092): Show |
3 | a0001c0001t0001g0237a0001c0001t0001g0263a0001c0001t0001g0265 | 3 | HG00280.hp2 HG00544.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1101): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCACCCAC others(1104): Show |
1 | a0001c0001t0001g0219 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCATCCAC others(1100): Show |
1 | a0001c0001t0001g0269 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1051+429_1051+430i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | CCATCCAT others(1104): Show |
1 | a0001c0001t0001g0259 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1051+433_1051+434i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | |||||
chr4:8294624
|
C | T | 19 | a0001c0001t0001g0117a0001c0001t0001g0164a0001c0001t0001g0202others(16): Show | 21 | HG00423.hp1 HG01891.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.1051+423C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294624 | ||||||
chr4:8294626
|
A | ACCCACCC others(153): Show |
2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+425_1051+426i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294626 | ||||||
chr4:8294626
|
A | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 89 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1051+425A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294626 | ||||||
chr4:8294627
|
T | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0002g0012others(6): Show | 11 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051+426T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294627 | ||||||
chr4:8294630
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1051+429A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294630 | ||||||
chr4:8294631
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1051+430T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294631 | ||||||
chr4:8294634
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+433A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294634 | ||||||
chr4:8294659
|
T | TCCA | 12 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0167others(9): Show | 16 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1051+459_1051+461d others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294659 | |||||
chr4:8294659
|
T | TCCACCAT others(85): Show |
1 | a0001c0001t0001g0101 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051+461_1051+462i others(94): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294659 | |||||
chr4:8294662
|
A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051+461_1051+462i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | ||||||
chr4:8294662
|
A | ACTTATCC others(1008): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 6 | HG02080.hp1 HG02886.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+461_1051+462i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | ||||||
chr4:8294662
|
A | ACTTATCC others(1012): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0162 | 2 | HG00609.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1051+461_1051+462i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | ||||||
chr4:8294662
|
A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1051+461_1051+462i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | ||||||
chr4:8294662
|
A | ACTTATCC others(1008): Show |
2 | a0001c0001t0002g0005a0001c0001t0002g0152 | 3 | HG02559.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1051+461_1051+462i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | ||||||
chr4:8294663
|
T | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0081a0001c0001t0001g0122others(8): Show | 13 | HG00609.hp2 HG00733.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1051+462T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294663 | ||||||
chr4:8294663
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+462T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294663 | ||||||
chr4:8294663
|
T | TCCACCAT others(85): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0138a0001c0001t0001g0204others(2): Show | 6 | HG00738.hp2 HG01192.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(94): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294663
|
T | TCCACTTA others(1008): Show |
1 | a0001c0001t0001g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294663
|
T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294663
|
T | TCCACTTA others(1015): Show |
1 | a0001c0001t0014g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1024): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294663
|
T | TCCACTTA others(1016): Show |
7 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0066others(4): Show | 9 | HG00642.hp2 HG01515.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294663
|
T | TCCACTTA others(1020): Show |
1 | a0001c0001t0001g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1029): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294663
|
T | TCCACTTA others(1020): Show |
1 | a0001c0001t0011g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1029): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | |||||
chr4:8294664
|
C | A | 1 | a0001c0001t0002g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1051+463C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294664 | ||||||
chr4:8294666
|
A | ACCATCCA others(81): Show |
28 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0073others(25): Show | 30 | HG00408.hp2 HG00558.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(90): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1049): Show |
1 | a0001c0001t0001g0244 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1058): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1005): Show |
1 | a0001c0001t0001g0331 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1014): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(989): Show |
1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(998): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1004): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0183 | 2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1013): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1008): Show |
1 | a0001c0001t0007g0181 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1008): Show |
12 | a0001c0001t0001g0027a0001c0001t0001g0091a0001c0001t0001g0230others(9): Show | 13 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1008): Show |
1 | a0001c0001t0001g0127 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1008): Show |
5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(2): Show | 5 | HG00140.hp2 HG02109.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1012): Show |
37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 40 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1016): Show |
1 | a0001c0001t0001g0060 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1012): Show |
2 | a0001c0001t0001g0126a0001c0001t0001g0169 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1008): Show |
1 | a0001c0001t0001g0333 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294666
|
A | ACTTATCC others(1008): Show |
2 | a0001c0001t0002g0011a0001c0001t0002g0151 | 3 | HG01891.hp1 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | ||||||
chr4:8294667
|
T | A | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(94): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1051+466T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294667 | ||||||
chr4:8294667
|
T | TACATCTG others(1137): Show |
1 | a0001c0001t0001g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1051+466_1051+467i others(1146): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294667 | ||||||
chr4:8294667
|
T | TACATCTG others(1112): Show |
1 | a0001c0001t0002g0128 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1051+466_1051+467i others(1121): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294667 | ||||||
chr4:8294667
|
T | TCCACCAT others(85): Show |
75 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0040others(72): Show | 77 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(94): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACCCA others(74): Show |
13 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0167others(10): Show | 17 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(83): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(993): Show |
1 | a0001c0001t0001g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1002): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1044): Show |
1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1053): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1048): Show |
1 | a0001c0001t0001g0343 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1057): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1012): Show |
66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(63): Show | 73 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1012): Show |
3 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0001g0053 | 3 | HG00741.hp2 HG01167.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1016): Show |
17 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 20 | HG00639.hp2 HG01261.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0071 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1020): Show |
2 | a0001c0001t0001g0194a0001c0001t0001g0286 | 2 | HG02155.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1029): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1012): Show |
9 | a0001c0001t0001g0026a0001c0001t0001g0123a0001c0001t0001g0277others(6): Show | 10 | NA18942.hp1 NA18953.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1012): Show |
8 | a0001c0001t0001g0164a0001c0001t0002g0033a0001c0001t0002g0095others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1016): Show |
1 | a0001c0001t0002g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCCACTTA others(1013): Show |
1 | a0001c0001t0001g0309 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1022): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294667
|
T | TCTGTCCA others(1108): Show |
1 | a0001c0001t0002g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1051+467_1051+468i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | |||||
chr4:8294668
|
C | A | 1 | a0009c0008t0001g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+467C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294668 | ||||||
chr4:8294670
|
A | ACCATCCA others(81): Show |
1 | a0001c0001t0001g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(90): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294670 | ||||||
chr4:8294670
|
A | ACTTATCC others(1012): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0145a0001c0001t0001g0160 | 3 | HG01074.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294670 | ||||||
chr4:8294671
|
T | A | 4 | a0001c0001t0001g0054a0001c0001t0001g0145a0001c0001t0001g0160others(1): Show | 4 | HG01074.hp2 HG02647.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+470T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294671 | ||||||
chr4:8294671
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+470T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294671 | ||||||
chr4:8294671
|
T | TCCACTTA others(1012): Show |
2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+473_1051+474i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294671 | |||||
chr4:8294671
|
T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1051+473_1051+474i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294671 | |||||
chr4:8294671
|
T | TCTGTCCA others(1108): Show |
1 | a0009c0008t0001g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+471_1051+472i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294671 | |||||
chr4:8294672
|
C | A | 8 | a0001c0001t0001g0117a0001c0001t0002g0049a0001c0001t0002g0050others(5): Show | 8 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1051+471C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294672 | ||||||
chr4:8294674
|
A | ACTTATCC others(1016): Show |
1 | a0001c0001t0001g0032 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1051+473_1051+474i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294674 | ||||||
chr4:8294675
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1051+474T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | ||||||
chr4:8294675
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+474T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | ||||||
chr4:8294675
|
T | TACATCTG others(1111): Show |
1 | a0001c0001t0001g0117 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1051+474_1051+475i others(1120): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | ||||||
chr4:8294675
|
T | TACATCTG others(1112): Show |
7 | a0001c0001t0001g0202a0001c0001t0002g0012a0001c0001t0002g0016others(4): Show | 9 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+474_1051+475i others(1121): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | ||||||
chr4:8294675
|
T | TACATCTG others(1116): Show |
1 | a0001c0001t0002g0272 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1051+474_1051+475i others(1125): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | ||||||
chr4:8294675
|
T | TCTGTCCA others(1108): Show |
6 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0157others(3): Show | 6 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+475_1051+476i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294675 | |||||
chr4:8294678
|
A | ACTTATCC others(1012): Show |
1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1051+477_1051+478i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294678 | ||||||
chr4:8294679
|
T | A | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1051+478T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294679 | ||||||
chr4:8294683
|
T | TCTATCCA others(972): Show |
1 | a0001c0001t0001g0255 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+483_1051+484i others(981): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294683 | |||||
chr4:8294716
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1051+515T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294716 | ||||||
chr4:8294770
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0344a0001c0001t0012g0345others(2): Show | 6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+569C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294770 | ||||||
chr4:8294801
|
T | TCCAC | 134 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1051+612_1051+615d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294801 | |||||
chr4:8295055
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1051+854A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295055 | ||||||
chr4:8295194
|
C | T | 3 | a0001c0001t0004g0186a0001c0001t0011g0035a0002c0002t0001g0067 | 3 | HG02451.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+993C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295194 | ||||||
chr4:8295334
|
G | T | 3 | a0001c0001t0004g0186a0001c0001t0011g0035a0002c0002t0001g0067 | 3 | HG02451.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+1133G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295334 | ||||||
chr4:8295433
|
G | A | 2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+1232G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295433 | ||||||
chr4:8295843
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1051+1642G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295843 | ||||||
chr4:8296043
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 104 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1051+1842A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296043 | ||||||
chr4:8296120
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1051+1919G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296120 | ||||||
chr4:8296143
|
A | G | 1 | a0001c0001t0011g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+1942A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296143 | ||||||
chr4:8296152
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1051+1951G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296152 | ||||||
chr4:8296219
|
G | A | 2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+2018G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296219 | ||||||
chr4:8296269
|
A | G | 1 | a0001c0001t0007g0181 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1051+2068A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296269 | ||||||
chr4:8296330
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0083others(1): Show | 6 | HG01070.hp2 HG01255.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+2129C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296330 | ||||||
chr4:8296357
|
C | T | 14 | a0001c0001t0001g0164a0001c0001t0002g0005a0001c0001t0002g0011others(11): Show | 16 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+2156C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296357 | ||||||
chr4:8296557
|
G | T | 1 | a0001c0001t0017g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1051+2356G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296557 | ||||||
chr4:8296562
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1051+2361T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296562 | ||||||
chr4:8296563
|
G | A | 14 | a0001c0001t0001g0164a0001c0001t0002g0005a0001c0001t0002g0011others(11): Show | 16 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+2362G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296563 | ||||||
chr4:8296589
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0004g0186a0001c0001t0017g0086others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051+2388T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296589 | ||||||
chr4:8296891
|
T | C | 1 | a0001c0001t0017g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1051+2690T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296891 | ||||||
chr4:8296897
|
A | T | 2 | a0001c0001t0001g0184a0002c0002t0010g0059 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1051+2696A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296897 | ||||||
chr4:8296977
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1051+2776T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296977 | ||||||
chr4:8296993
|
G | A | 5 | a0001c0001t0001g0010a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 6 | HG01361.hp2 HG03490.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+2792G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296993 | ||||||
chr4:8297170
|
G | A | 16 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0002g0012others(13): Show | 18 | HG00423.hp1 HG01433.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1051+2969G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297170 | ||||||
chr4:8297171
|
C | G | 16 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0002g0012others(13): Show | 18 | HG00423.hp1 HG01433.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1051+2970C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297171 | ||||||
chr4:8297227
|
G | A | 2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+3026G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297227 | ||||||
chr4:8297382
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1051+3181G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297382 | ||||||
chr4:8297435
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 97 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.1051+3234T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297435 | ||||||
chr4:8297440
|
GCCAGAGG others(9): Show |
G | 1 | a0001c0001t0001g0216 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1051+3242_1051+325 others(20): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8297440 | |||||
chr4:8297495
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG02135.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1051+3294G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297495 | ||||||
chr4:8297563
|
G | A | 3 | a0001c0001t0001g0246a0001c0001t0001g0342a0001c0001t0001g0350 | 3 | NA18948.hp1 NA18995.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1051+3362G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297563 | ||||||
chr4:8297587
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0074 | 2 | HG00642.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1051+3386G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297587 | ||||||
chr4:8297619
|
C | T | 2 | a0001c0001t0006g0334a0001c0001t0006g0335 | 2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1051+3418C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297619 | ||||||
chr4:8297740
|
C | A | 2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+3539C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297740 | ||||||
chr4:8297840
|
C | G | 14 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(11): Show | 16 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1051+3639C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297840 | ||||||
chr4:8297849
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1051+3648G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297849 | ||||||
chr4:8297856
|
G | A | 1 | a0004c0007t0001g0327 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1051+3655G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297856 | ||||||
chr4:8297869
|
A | C | 13 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(10): Show | 15 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1051+3668A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297869 | ||||||
chr4:8297892
|
T | G | 14 | a0001c0001t0001g0194a0001c0001t0002g0005a0001c0001t0002g0011others(11): Show | 16 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+3691T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297892 | ||||||
chr4:8297913
|
C | T | 13 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(10): Show | 15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1051+3712C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297913 | ||||||
chr4:8297993
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(247): Show | 269 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1051+3792C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297993 | ||||||
chr4:8298000
|
A | G | 19 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0001g0292others(16): Show | 20 | HG00423.hp1 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051+3799A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298000 | ||||||
chr4:8298078
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1051+3877C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298078 | ||||||
chr4:8298134
|
A | G | 1 | a0001c0001t0017g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1051+3933A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298134 | ||||||
chr4:8298138
|
T | C | 12 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(9): Show | 14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051+3937T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298138 | ||||||
chr4:8298181
|
C | T | 1 | a0001c0001t0020g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1051+3980C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298181 | ||||||
chr4:8298310
|
T | C | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1051+4109T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298310 | ||||||
chr4:8298474
|
T | C | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3989T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298474 | ||||||
chr4:8298519
|
G | GT | 241 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 258 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1052-3933dupT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8298519 | |||||
chr4:8298709
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0002g0118 | 2 | NA18973.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1052-3754G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298709 | ||||||
chr4:8298788
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0330 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1052-3675G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298788 | ||||||
chr4:8298792
|
C | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0130others(3): Show | 6 | HG02818.hp2 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1052-3671C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298792 | ||||||
chr4:8298850
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1052-3613T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298850 | ||||||
chr4:8298866
|
C | T | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3597C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298866 | ||||||
chr4:8299069
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1052-3394T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299069 | ||||||
chr4:8299182
|
G | A | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3281G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299182 | ||||||
chr4:8299264
|
T | G | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3199T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299264 | ||||||
chr4:8299303
|
T | G | 1 | a0001c0001t0001g0020 | 2 | HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1052-3160T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299303 | ||||||
chr4:8299364
|
T | C | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3099T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299364 | ||||||
chr4:8299397
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1052-3066T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299397 | ||||||
chr4:8299548
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1052-2915G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299548 | ||||||
chr4:8299619
|
A | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 255 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1052-2844A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299619 | ||||||
chr4:8299654
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1052-2809T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299654 | ||||||
chr4:8299749
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1052-2714G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299749 | ||||||
chr4:8299841
|
C | CA | 132 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0020others(129): Show | 137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1052-2622_1052-262 others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299841 | ||||||
chr4:8299841
|
C | CAT | 4 | a0001c0001t0001g0022a0001c0001t0001g0257a0001c0001t0001g0306others(1): Show | 5 | HG02135.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-2622_1052-262 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299841 | ||||||
chr4:8299841
|
C | CT | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 105 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1052-2606dupT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8299841 | |||||
chr4:8299842
|
T | A | 7 | a0001c0001t0001g0082a0001c0001t0001g0343a0001c0001t0007g0159others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1052-2621T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299842 | ||||||
chr4:8299843
|
T | A | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-2620T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299843 | ||||||
chr4:8299913
|
C | T | 13 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(10): Show | 15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1052-2550C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299913 | ||||||
chr4:8299926
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0020others(133): Show | 142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1052-2537A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299926 | ||||||
chr4:8299966
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0199others(2): Show | 5 | HG02818.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-2497C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299966 | ||||||
chr4:8300021
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0180others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-2442G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300021 | ||||||
chr4:8300263
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1052-2200G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300263 | ||||||
chr4:8300414
|
T | C | 1 | a0001c0001t0011g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1052-2049T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300414 | ||||||
chr4:8300437
|
T | C | 7 | a0001c0001t0001g0123a0001c0001t0001g0255a0001c0001t0001g0277others(4): Show | 7 | NA18942.hp1 NA18951.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052-2026T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300437 | ||||||
chr4:8300509
|
C | T | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1954C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300509 | ||||||
chr4:8300516
|
A | C | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1947A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300516 | ||||||
chr4:8300542
|
T | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 110 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1052-1921T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300542 | ||||||
chr4:8300547
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1052-1916C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300547 | ||||||
chr4:8300602
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1052-1861T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300602 | ||||||
chr4:8300671
|
CTTTA | C | 3 | a0001c0001t0001g0306a0001c0001t0001g0307a0006c0012t0001g0242 | 3 | HG02135.hp2 NA18999.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1052-1788_1052-178 others(8): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8300671 | |||||
chr4:8300744
|
CATTG | C | 8 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0001t0002g0016others(5): Show | 9 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1052-1715_1052-171 others(8): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8300744 | |||||
chr4:8300827
|
C | T | 2 | a0001c0001t0001g0280a0002c0002t0002g0125 | 2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1052-1636C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300827 | ||||||
chr4:8300852
|
C | T | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1611C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300852 | ||||||
chr4:8300895
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0270others(1): Show | 4 | HG01109.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052-1568T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300895 | ||||||
chr4:8300985
|
A | ATTATTGA others(13): Show |
1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1452_1052-143 others(24): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8300985 | |||||
chr4:8301037
|
TCA | T | 142 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(139): Show | 149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1052-1422_1052-142 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301037 | |||||
chr4:8301131
|
ACT | A | 17 | a0001c0001t0001g0343a0001c0001t0002g0005a0001c0001t0002g0011others(14): Show | 19 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1052-1329_1052-132 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301131 | |||||
chr4:8301165
|
A | ACT | 320 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(317): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1052-1297_1052-129 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301165 | |||||
chr4:8301165
|
A | T | 2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1052-1298A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301165 | ||||||
chr4:8301168
|
T | C | 2 | a0001c0001t0001g0280a0002c0002t0010g0059 | 2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1052-1295T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301168 | ||||||
chr4:8301186
|
TTTA | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0108a0001c0001t0001g0119others(1): Show | 5 | HG01361.hp2 HG03490.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-1274_1052-127 others(7): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301186 | |||||
chr4:8301234
|
ATTATTGA others(13): Show |
A | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 124 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1052-1211_1052-119 others(24): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301234 | |||||
chr4:8301238
|
T | A | 140 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(137): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1052-1225T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301238 | ||||||
chr4:8301254
|
T | G | 4 | a0001c0001t0001g0343a0001c0001t0007g0159a0001c0001t0008g0175others(1): Show | 4 | HG02257.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-1209T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301254 | ||||||
chr4:8301257
|
A | T | 4 | a0001c0001t0001g0343a0001c0001t0007g0159a0001c0001t0008g0175others(1): Show | 4 | HG02257.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-1206A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301257 | ||||||
chr4:8301262
|
TTCACACT others(16): Show |
T | 2 | a0001c0001t0001g0132a0001c0001t0001g0163 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1052-1178_1052-115 others(27): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301262 | |||||
chr4:8301285
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1052-1178G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301285 | ||||||
chr4:8301285
|
GTCACACT others(16): Show |
G | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1155_1052-113 others(27): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301285 | |||||
chr4:8301412
|
A | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 125 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1052-1051A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301412 | ||||||
chr4:8301489
|
T | G | 1 | a0001c0001t0017g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1052-974T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301489 | ||||||
chr4:8301615
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0005g0120a0001c0001t0005g0320 | 3 | HG02738.hp1 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1052-848C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301615 | ||||||
chr4:8301632
|
G | C | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-831G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301632 | ||||||
chr4:8301830
|
G | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 273 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1052-633G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301830 | ||||||
chr4:8301872
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1052-591A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301872 | ||||||
chr4:8301877
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1052-586A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301877 | ||||||
chr4:8302014
|
C | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0353 | 2 | NA18972.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1052-449C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302014 | ||||||
chr4:8302311
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(294): Show | 319 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.1052-152T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302311 | ||||||
chr4:8302325
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1052-138A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302325 | ||||||
chr4:8302370
|
G | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(137): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1052-93G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302370 | ||||||
chr4:8302387
|
C | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0287 | 2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1052-76C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302387 | ||||||
chr4:8302407
|
A | G | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1052-56A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302407 | ||||||
chr4:8302408
|
G | A | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1052-55G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302408 | ||||||
chr4:8302410
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 98 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1052-53G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302410 | ||||||
chr4:8302436
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0249 | 2 | HG02293.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1052-27C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302436 | ||||||
chr4:8302444
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1052-19C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302444 | ||||||
chr4:8302670
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1100+159C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302670 | ||||||
chr4:8302810
|
G | A | 3 | a0001c0001t0001g0280a0001c0001t0001g0353a0002c0002t0002g0125 | 3 | HG02922.hp2 NA18972.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1100+299G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302810 | ||||||
chr4:8302929
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0350 | 2 | NA18948.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1100+418T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302929 | ||||||
chr4:8302943
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 306 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1100+432A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302943 | ||||||
chr4:8303087
|
A | T | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1100+576A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303087 | ||||||
chr4:8303137
|
G | A | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1100+626G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303137 | ||||||
chr4:8303172
|
C | T | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1100+661C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303172 | ||||||
chr4:8303266
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0003g0036a0001c0001t0003g0096 | 3 | HG03486.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1100+755C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303266 | ||||||
chr4:8303318
|
G | A | 1 | a0001c0001t0001g0002 | 3 | HG01515.hp2 HG01517.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1100+807G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303318 | ||||||
chr4:8303378
|
G | A | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1101-806G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303378 | ||||||
chr4:8303485
|
G | A | 142 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(139): Show | 150 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1101-699G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303485 | ||||||
chr4:8303512
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1101-672C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303512 | ||||||
chr4:8303537
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-647T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303537 | ||||||
chr4:8303742
|
TTG | T | 13 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(10): Show | 15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1101-440_1101-439d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 8303742 | |||||
chr4:8303776
|
CCGTTCCG others(19): Show |
C | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1101-382_1101-357d others(28): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 8303776 | |||||
chr4:8303777
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-407C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303777 | ||||||
chr4:8303802
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1101-382A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303802 | ||||||
chr4:8303805
|
T | A | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-379T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303805 | ||||||
chr4:8303827
|
TCC | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 152 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1101-356_1101-355d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303827 | ||||||
chr4:8303835
|
A | G | 144 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(141): Show | 152 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1101-349A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303835 | ||||||
chr4:8303900
|
T | C | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1101-284T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303900 | ||||||
chr4:8303900
|
T | TCATCCAT others(1): Show |
4 | a0001c0001t0001g0343a0001c0001t0007g0159a0001c0001t0007g0181others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101-262_1101-255d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 8303900 | |||||
chr4:8304054
|
G | T | 140 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(137): Show | 148 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1101-130G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8304054 | ||||||
chr4:8304301
|
C | T | 146 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(143): Show | 155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1196+22C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304301 | ||||||
chr4:8304319
|
G | A | 13 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0033others(10): Show | 15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1196+40G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304319 | ||||||
chr4:8304339
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1196+60G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304339 | ||||||
chr4:8304364
|
T | C | 146 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(143): Show | 155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1196+85T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304364 | ||||||
chr4:8304369
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1196+90C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304369 | ||||||
chr4:8304414
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1196+135T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304414 | ||||||
chr4:8304437
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0102 | 3 | HG01358.hp2 HG01943.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1196+158A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304437 | ||||||
chr4:8304534
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1196+255A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304534 | ||||||
chr4:8304572
|
G | A | 1 | a0001c0001t0001g0002 | 3 | HG01515.hp2 HG01517.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1196+293G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304572 | ||||||
chr4:8304608
|
T | C | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+329T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304608 | ||||||
chr4:8304610
|
C | T | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+331C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304610 | ||||||
chr4:8304622
|
G | A | 147 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(144): Show | 156 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1196+343G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304622 | ||||||
chr4:8304643
|
GT | G | 79 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(76): Show | 87 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(84): Show |
intron_variant | MODIFIER | c.1196+395delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304643
|
GTT | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(78): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1196+394_1196+395d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304643
|
GTTT | G | 11 | a0001c0001t0001g0117a0001c0001t0001g0169a0001c0001t0001g0280others(8): Show | 12 | HG00423.hp1 HG02027.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1196+393_1196+395d others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304643
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0316 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1196+384_1196+395d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304643
|
GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0002g0095a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG02572.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1196+383_1196+395d others(15): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304643
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0007g0159a0001c0001t0008g0175 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1196+382_1196+395d others(16): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304643
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+381_1196+395d others(17): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | |||||
chr4:8304648
|
T | TTG | 48 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(45): Show | 54 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1196+370_1196+371i others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304648 | |||||
chr4:8304649
|
T | TG | 80 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0023others(77): Show | 83 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1196+370_1196+371i others(3): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304649 | ||||||
chr4:8304649
|
T | TGTG | 13 | a0001c0001t0001g0101a0001c0001t0001g0191a0001c0001t0001g0200others(10): Show | 13 | HG00408.hp2 HG00558.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1196+370_1196+371i others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304649 | ||||||
chr4:8304650
|
T | G | 52 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(49): Show | 58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1196+371T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304650 | ||||||
chr4:8304651
|
T | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0023others(78): Show | 84 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.1196+372T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304651 | ||||||
chr4:8304652
|
T | G | 4 | a0001c0001t0001g0060a0001c0001t0001g0139a0001c0001t0001g0204others(1): Show | 4 | HG00323.hp1 HG03654.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196+373T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304652 | ||||||
chr4:8304653
|
T | G | 1 | a0001c0001t0002g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1196+374T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304653 | ||||||
chr4:8304654
|
T | G | 3 | a0001c0001t0001g0283a0001c0001t0001g0308a0002c0002t0001g0061 | 3 | HG00738.hp1 HG02074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1196+375T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304654 | ||||||
chr4:8304655
|
T | G | 24 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
intron_variant | MODIFIER | c.1196+376T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304655 | ||||||
chr4:8304701
|
C | A | 180 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(177): Show | 193 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1196+422C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304701 | ||||||
chr4:8304791
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1196+512G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304791 | ||||||
chr4:8304860
|
C | T | 356 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(353): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1196+581C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304860 | ||||||
chr4:8304896
|
C | G | 1 | a0001c0001t0001g0321 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1196+617C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304896 | ||||||
chr4:8305026
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1196+747A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305026 | ||||||
chr4:8305055
|
A | C | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+776A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305055 | ||||||
chr4:8305056
|
C | A | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+777C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305056 | ||||||
chr4:8305061
|
T | C | 151 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(148): Show | 160 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1196+782T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305061 | ||||||
chr4:8305221
|
G | A | 2 | a0001c0001t0004g0186a0002c0002t0001g0067 | 2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1197-750G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305221 | ||||||
chr4:8305247
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0180others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197-724G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305247 | ||||||
chr4:8305292
|
G | A | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-679G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305292 | ||||||
chr4:8305331
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1197-640A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305331 | ||||||
chr4:8305357
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0214 | 2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1197-614C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305357 | ||||||
chr4:8305364
|
C | T | 1 | a0001c0001t0017g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1197-607C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305364 | ||||||
chr4:8305394
|
C | T | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-577C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305394 | ||||||
chr4:8305513
|
T | C | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1197-458T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305513 | ||||||
chr4:8305515
|
C | T | 1 | a0001c0001t0019g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1197-456C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305515 | ||||||
chr4:8305580
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1197-391C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305580 | ||||||
chr4:8305596
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1197-375C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305596 | ||||||
chr4:8305650
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1197-321C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305650 | ||||||
chr4:8305674
|
T | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | NA18949.hp2 NA18975.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197-297T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305674 | ||||||
chr4:8305753
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1197-218C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305753 | ||||||
chr4:8305777
|
G | A | 137 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(134): Show | 145 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1197-194G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305777 | ||||||
chr4:8305811
|
T | C | 1 | a0002c0002t0010g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-160T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305811 |