geneid | 257218 |
---|---|
ensemblid | ENSG00000146414.17 |
hgncid | 19336 |
symbol | SHPRH |
name | SNF2 histone linker PHD RING helicase |
refseq_nuc | NM_001042683.3 |
refseq_prot | NP_001036148.2 |
ensembl_nuc | ENST00000275233.12 |
ensembl_prot | ENSP00000275233.7 |
mane_status | MANE Select |
chr | chr6 |
start | 145884807 |
end | 145964358 |
strand | - |
ver | v1.2 |
region | chr6:145884807-145964358 |
region5000 | chr6:145879807-145969358 |
regionname0 | SHPRH_chr6_145884807_145964358 |
regionname5000 | SHPRH_chr6_145879807_145969358 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1683 | 300 | 61 | 53 | 141 | 12 | 31 | 116 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0002 | 0/0 | 1683 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0003 | 0/0 | 1683 | 16 | 0 | 0 | 16 | 0 | 0 | 9 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0004 | 0/0 | 1683 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0005 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0006 | 0/0 | 1683 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0007 | 0/0 | 1683 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0008 | 0/0 | 1683 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0009 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0010 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0011 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0012 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0013 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 5052 | 203 | 36 | 44 | 91 | 9 | 22 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0002 | 1/0 | 5052 | 69 | 3 | 8 | 46 | 3 | 8 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0003 | 0/0 | 5052 | 22 | 21 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0004 | 0/0 | 5052 | 17 | 15 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0005 | 0/0 | 5052 | 16 | 0 | 0 | 16 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0006 | 0/0 | 5052 | 6 | 0 | 0 | 6 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0007 | 0/0 | 5052 | 4 | 4 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0008 | 0/0 | 5052 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0009 | 0/0 | 5052 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0010 | 0/0 | 5052 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0011 | 0/0 | 5052 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0012 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0013 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0014 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0015 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0016 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0017 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0018 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0019 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
c0020 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2545 | 177 | 26 | 35 | 98 | 5 | 13 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0002 | 0/1 | 2546 | 90 | 14 | 11 | 48 | 3 | 13 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0003 | 0/0 | 2546 | 26 | 23 | 3 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0004 | 0/0 | 2546 | 21 | 1 | 3 | 12 | 2 | 3 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0005 | 0/0 | 2546 | 15 | 14 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0006 | 0/0 | 2545 | 8 | 0 | 3 | 0 | 1 | 4 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0007 | 0/0 | 2545 | 6 | 0 | 0 | 6 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0008 | 0/0 | 2545 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0009 | 1/0 | 2545 | 2 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0010 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0011 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0012 | 0/0 | 2546 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0013 | 0/0 | 2546 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0014 | 0/0 | 2546 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0015 | 0/0 | 2546 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
t0016 | 0/0 | 2546 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
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 | 8 | 0 | 0 | 8 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0013 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5052 | 203 | 36 | 44 | 91 | 9 | 22 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0002 | 1/0 | 5052 | 69 | 3 | 8 | 46 | 3 | 8 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0003 | 0/0 | 5052 | 22 | 21 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0009 | 0/0 | 5052 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0014 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0015 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0019 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0020 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0002c0004 | 0/0 | 5052 | 17 | 15 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0003c0005 | 0/0 | 5052 | 16 | 0 | 0 | 16 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0004c0006 | 0/0 | 5052 | 6 | 0 | 0 | 6 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0005c0007 | 0/0 | 5052 | 4 | 4 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0006c0008 | 0/0 | 5052 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0007c0010 | 0/0 | 5052 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0008c0011 | 0/0 | 5052 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0009c0012 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0010c0013 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0011c0018 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0012c0017 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0013c0016 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7596 | 149 | 22 | 35 | 77 | 5 | 10 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0002 | 0/1 | 7597 | 21 | 11 | 3 | 1 | 0 | 5 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0004 | 0/0 | 7597 | 21 | 1 | 3 | 12 | 2 | 3 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0006 | 0/0 | 7596 | 8 | 0 | 3 | 0 | 1 | 4 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0010 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0012 | 0/0 | 7597 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0015 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0001t0016 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0002t0002 | 0/0 | 7597 | 68 | 3 | 8 | 46 | 3 | 8 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0002t0009 | 1/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0003t0003 | 0/0 | 7597 | 7 | 7 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0003t0005 | 0/0 | 7597 | 14 | 13 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0003t0009 | 0/0 | 7596 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0009t0001 | 0/0 | 7596 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0014t0001 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0015t0014 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0019t0001 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0001c0020t0001 | 0/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0002c0004t0003 | 0/0 | 7597 | 17 | 15 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0003c0005t0001 | 0/0 | 7596 | 15 | 0 | 0 | 15 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0003c0005t0011 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0004c0006t0007 | 0/0 | 7596 | 6 | 0 | 0 | 6 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0005c0007t0001 | 0/0 | 7596 | 4 | 4 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0006c0008t0003 | 0/0 | 7597 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0007c0010t0001 | 0/0 | 7596 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0008c0011t0008 | 0/0 | 7596 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0009c0012t0001 | 0/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0010c0013t0005 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0011c0018t0002 | 0/0 | 7597 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0012c0017t0001 | 0/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
a0013c0016t0013 | 0/0 | 7597 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | copy fasta | chr6 | 145879807 | 145969358 |
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 | 5 | 0 | 1 | 4 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0012g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0015g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0016g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0013 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0009g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0009t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0014t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0015t0014g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0019t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0020t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0006c0008t0003g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0007c0010t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0008c0011t0008g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0009c0012t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0010c0013t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0011c0018t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0012c0017t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0013c0016t0013g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0002 | g0199 | EUR | FIN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00609 | hp1 | a0003 | c0005 | t0001 | g0180 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0213 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0279 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0280 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01081 | hp1 | a0002 | c0004 | t0003 | g0269 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01081 | hp2 | a0006 | c0008 | t0003 | g0042 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01433 | hp1 | a0001 | c0003 | t0005 | g0053 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0041 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0013 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0041 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01884 | hp1 | a0002 | c0004 | t0003 | g0264 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01891 | hp2 | a0001 | c0003 | t0003 | g0258 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02040 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0277 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02056 | hp1 | a0001 | c0019 | t0001 | g0109 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02074 | hp1 | a0001 | c0014 | t0001 | g0161 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02132 | hp2 | a0003 | c0005 | t0001 | g0176 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02135 | hp1 | a0003 | c0005 | t0001 | g0175 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02135 | hp2 | a0004 | c0006 | t0007 | g0045 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02145 | hp1 | a0002 | c0004 | t0003 | g0265 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02145 | hp2 | a0001 | c0003 | t0003 | g0256 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02155 | hp1 | a0003 | c0005 | t0001 | g0178 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02155 | hp2 | a0004 | c0006 | t0007 | g0008 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02165 | hp1 | a0003 | c0005 | t0011 | g0181 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02451 | hp2 | a0006 | c0008 | t0003 | g0042 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02572 | hp2 | a0001 | c0003 | t0005 | g0051 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0230 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02630 | hp2 | a0002 | c0004 | t0003 | g0007 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0281 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02717 | hp1 | a0001 | c0003 | t0005 | g0050 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02717 | hp2 | a0001 | c0003 | t0009 | g0261 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02723 | hp1 | a0002 | c0004 | t0003 | g0007 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02735 | hp1 | a0009 | c0012 | t0001 | g0094 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02735 | hp2 | a0013 | c0016 | t0013 | g0218 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02809 | hp1 | a0005 | c0007 | t0001 | g0093 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02809 | hp2 | a0001 | c0003 | t0005 | g0049 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02818 | hp2 | a0001 | c0003 | t0005 | g0054 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02886 | hp2 | a0002 | c0004 | t0003 | g0271 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02895 | hp2 | a0001 | c0003 | t0005 | g0014 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02896 | hp2 | a0002 | c0004 | t0003 | g0043 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02897 | hp1 | a0002 | c0004 | t0003 | g0043 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02897 | hp2 | a0001 | c0003 | t0005 | g0014 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02965 | hp1 | a0010 | c0013 | t0005 | g0056 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02970 | hp2 | a0002 | c0004 | t0003 | g0262 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02976 | hp2 | a0002 | c0004 | t0003 | g0272 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03017 | hp2 | a0001 | c0020 | t0001 | g0060 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0255 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03041 | hp2 | a0001 | c0003 | t0005 | g0009 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0276 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03195 | hp1 | a0001 | c0003 | t0003 | g0257 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03195 | hp2 | a0001 | c0003 | t0005 | g0057 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03209 | hp1 | a0001 | c0003 | t0005 | g0055 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03209 | hp2 | a0001 | c0015 | t0014 | g0253 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0260 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0227 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03453 | hp1 | a0001 | c0003 | t0005 | g0052 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03453 | hp2 | a0001 | c0003 | t0003 | g0259 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03486 | hp1 | a0001 | c0003 | t0003 | g0254 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03540 | hp2 | a0005 | c0007 | t0001 | g0092 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03579 | hp1 | a0002 | c0004 | t0003 | g0263 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03579 | hp2 | a0005 | c0007 | t0001 | g0091 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0214 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0044 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03669 | hp2 | a0012 | c0017 | t0001 | g0100 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0283 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0206 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0226 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0278 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18612 | hp1 | a0003 | c0005 | t0001 | g0174 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18747 | hp1 | a0001 | c0001 | t0010 | g0081 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18906 | hp1 | a0005 | c0007 | t0001 | g0090 | AFR | YRI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18906 | hp2 | a0002 | c0004 | t0003 | g0266 | AFR | YRI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18952 | hp2 | a0001 | c0009 | t0001 | g0087 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18953 | hp1 | a0008 | c0011 | t0008 | g0029 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18963 | hp1 | a0004 | c0006 | t0007 | g0046 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18977 | hp2 | a0001 | c0009 | t0001 | g0064 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18984 | hp1 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18986 | hp1 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18986 | hp2 | a0003 | c0005 | t0001 | g0118 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19002 | hp1 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19002 | hp2 | a0004 | c0006 | t0007 | g0008 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19003 | hp2 | a0004 | c0006 | t0007 | g0047 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19007 | hp1 | a0008 | c0011 | t0008 | g0029 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19043 | hp2 | a0001 | c0003 | t0005 | g0048 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19055 | hp2 | a0003 | c0005 | t0001 | g0177 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19056 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19057 | hp2 | a0003 | c0005 | t0001 | g0179 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19065 | hp2 | a0007 | c0010 | t0001 | g0032 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19066 | hp2 | a0011 | c0018 | t0002 | g0231 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19074 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19081 | hp2 | a0004 | c0006 | t0007 | g0008 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19085 | hp1 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19087 | hp1 | a0007 | c0010 | t0001 | g0032 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20129 | hp1 | a0002 | c0004 | t0003 | g0268 | AFR | ASW | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ASW | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20752 | hp1 | a0001 | c0001 | t0012 | g0243 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0207 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0282 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0250 | SAS | GIH | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01123 | hp2 | a0002 | c0004 | t0003 | g0007 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02109 | hp1 | a0002 | c0004 | t0003 | g0270 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02486 | hp1 | a0002 | c0004 | t0003 | g0007 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02559 | hp2 | a0002 | c0004 | t0003 | g0267 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG06807 | hp2 | a0001 | c0003 | t0005 | g0009 | AFR | USA | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0232 | REF | REF | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0009 | g0234 | REF | REF | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145921337
|
C | T | 1 | a0011 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.3838G>A | p.Val1280Met | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/30 | 4498/7596 | 3838/5052 | 1280/1683 | chr6 | 145921337 | ||
chr6:145921378
|
G | A | 1 | a0010 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.3797C>T | p.Thr1266Ile | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/30 | 4457/7596 | 3797/5052 | 1266/1683 | chr6 | 145921378 | ||
chr6:145921385
|
C | T | 1 | a0012 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3790G>A | p.Gly1264Ser | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/30 | 4450/7596 | 3790/5052 | 1264/1683 | chr6 | 145921385 | ||
chr6:145922780
|
T | C | 2 | a0003a0007 | 18 | HG00609.hp1 HG02040.hp2 HG02132.hp2 others(15): Show |
missense_variant | MODERATE | c.3602A>G | p.Asn1201Ser | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/30 | 4262/7596 | 3602/5052 | 1201/1683 | chr6 | 145922780 | ||
chr6:145922825
|
C | T | 1 | a0013 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.3557G>A | p.Cys1186Tyr | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/30 | 4217/7596 | 3557/5052 | 1186/1683 | chr6 | 145922825 | ||
chr6:145941835
|
G | T | 1 | a0006 | 2 | HG01081.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.2278C>A | p.His760Asn | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/30 | 2938/7596 | 2278/5052 | 760/1683 | chr6 | 145941835 | ||
chr6:145943474
|
A | G | 1 | a0007 | 2 | NA19065.hp2 NA19087.hp1 |
missense_variant | MODERATE | c.1907T>C | p.Leu636Pro | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2567/7596 | 1907/5052 | 636/1683 | chr6 | 145943474 | ||
chr6:145943606
|
A | C | 1 | a0002 | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
missense_variant | MODERATE | c.1775T>G | p.Phe592Cys | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2435/7596 | 1775/5052 | 592/1683 | chr6 | 145943606 | ||
chr6:145952478
|
C | T | 1 | a0009 | 1 | HG02735.hp1 | missense_variant&splice_region_variant | MODERATE | c.634G>A | p.Val212Ile | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/30 | 1294/7596 | 634/5052 | 212/1683 | chr6 | 145952478 | ||
chr6:145954829
|
T | C | 1 | a0008 | 2 | NA18953.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.494A>G | p.Lys165Arg | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/30 | 1154/7596 | 494/5052 | 165/1683 | chr6 | 145954829 | ||
chr6:145954847
|
T | G | 1 | a0004 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
missense_variant | MODERATE | c.476A>C | p.Asp159Ala | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/30 | 1136/7596 | 476/5052 | 159/1683 | chr6 | 145954847 | ||
chr6:145955144
|
C | T | 1 | a0005 | 4 | HG02809.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.179G>A | p.Ser60Asn | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/30 | 839/7596 | 179/5052 | 60/1683 | chr6 | 145955144 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145910484
|
T | C | 1 | a0001c0019 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.4479A>G | p.Ser1493Ser | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/30 | 5139/7596 | 4479/5052 | 1493/1683 | chr6 | 145910484 | ||
chr6:145913508
|
G | A | 17 | a0001c0001a0001c0003a0001c0009others(14): Show | 283 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(280): Show |
synonymous_variant | LOW | c.4296C>T | p.Cys1432Cys | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/30 | 4956/7596 | 4296/5052 | 1432/1683 | chr6 | 145913508 | ||
chr6:145940766
|
A | G | 1 | a0001c0015 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2526T>C | p.Asn842Asn | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/30 | 3186/7596 | 2526/5052 | 842/1683 | chr6 | 145940766 | ||
chr6:145943344
|
C | T | 1 | a0001c0014 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.2037G>A | p.Lys679Lys | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2697/7596 | 2037/5052 | 679/1683 | chr6 | 145943344 | ||
chr6:145943452
|
T | G | 1 | a0001c0020 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1929A>C | p.Val643Val | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2589/7596 | 1929/5052 | 643/1683 | chr6 | 145943452 | ||
chr6:145946315
|
C | T | 1 | a0001c0009 | 2 | NA18952.hp2 NA18977.hp2 |
synonymous_variant | LOW | c.1239G>A | p.Pro413Pro | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 7/30 | 1899/7596 | 1239/5052 | 413/1683 | chr6 | 145946315 | ||
chr6:145950340
|
A | G | 4 | a0001c0003a0002c0004a0006c0008others(1): Show | 42 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(39): Show |
synonymous_variant | LOW | c.906T>C | p.Pro302Pro | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/30 | 1566/7596 | 906/5052 | 302/1683 | chr6 | 145950340 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145884837
|
G | T | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1854C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1854 | chr6 | 145884837 | |||||
chr6:145884865
|
G | A | 3 | a0001c0001t0004a0001c0001t0006a0001c0001t0012 | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1826C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1826 | chr6 | 145884865 | |||||
chr6:145884950
|
A | T | 1 | a0008c0011t0008 | 2 | NA18953.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1741T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1741 | chr6 | 145884950 | |||||
chr6:145885137
|
A | G | 1 | a0001c0001t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1554T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1554 | chr6 | 145885137 | |||||
chr6:145885458
|
G | C | 1 | a0001c0001t0010 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1233 | chr6 | 145885458 | |||||
chr6:145886119
|
A | C | 1 | a0013c0016t0013 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 572 | chr6 | 145886119 | |||||
chr6:145886329
|
A | G | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(7): Show | 124 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*362T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 362 | chr6 | 145886329 | |||||
chr6:145886366
|
G | GT | 16 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(13): Show | 171 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*324dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 324 | chr6 | 145886366 | |||||
chr6:145886372
|
T | G | 1 | a0004c0006t0007 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*319A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 319 | chr6 | 145886372 | |||||
chr6:145886427
|
A | G | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*264T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 264 | chr6 | 145886427 | |||||
chr6:145886521
|
A | C | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 170 | chr6 | 145886521 | |||||
chr6:145886550
|
T | C | 3 | a0001c0001t0015a0001c0001t0016a0001c0015t0014 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 141 | chr6 | 145886550 | |||||
chr6:145886661
|
C | T | 1 | a0001c0001t0012 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 30 | chr6 | 145886661 | |||||
chr6:145963790
|
C | T | 1 | a0001c0001t0015 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8468 | chr6 | 145963790 | |||||
chr6:145963827
|
G | A | 1 | a0003c0005t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8505 | chr6 | 145963827 | |||||
chr6:145964065
|
C | G | 1 | a0004c0006t0007 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-367G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8743 | chr6 | 145964065 | |||||
chr6:145964068
|
C | A | 13 | a0001c0001t0001a0001c0001t0010a0001c0009t0001others(10): Show | 181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
5_prime_UTR_variant | MODIFIER | c.-370G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8746 | chr6 | 145964068 | |||||
chr6:145964069
|
C | T | 13 | a0001c0001t0001a0001c0001t0010a0001c0009t0001others(10): Show | 181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
5_prime_UTR_variant | MODIFIER | c.-371G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8747 | chr6 | 145964069 | |||||
chr6:145964078
|
T | G | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG02055.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-380A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8756 | chr6 | 145964078 | |||||
chr6:145964089
|
G | T | 2 | a0001c0003t0005a0010c0013t0005 | 15 | HG01433.hp1 HG02572.hp2 HG02717.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-391C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8767 | chr6 | 145964089 | |||||
chr6:145964302
|
GT | G | 1 | a0001c0001t0006 | 8 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-605delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8981 | chr6 | 145964302 | |||||
chr6:145964303
|
TC | T | 1 | a0004c0006t0007 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-606delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8982 | chr6 | 145964303 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145886844
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4956-57T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145886844 | ||||||
chr6:145886975
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.4956-188A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145886975 | ||||||
chr6:145886984
|
T | G | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4956-197A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145886984 | ||||||
chr6:145887027
|
G | C | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4956-240C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887027 | ||||||
chr6:145887265
|
T | A | 3 | a0001c0001t0001g0123a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG00738.hp1 HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4956-478A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887265 | ||||||
chr6:145887529
|
G | GT | 14 | a0001c0001t0001g0097a0001c0001t0002g0193a0001c0001t0002g0196others(11): Show | 16 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.4955+490dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887529 | ||||||
chr6:145887532
|
TG | T | 5 | a0001c0001t0002g0195a0001c0001t0002g0209a0001c0001t0002g0274others(2): Show | 5 | HG02109.hp2 HG02976.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4955+487delC | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887532 | ||||||
chr6:145887533
|
G | GT | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 47 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.4955+486dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | ||||||
chr6:145887533
|
G | GTT | 6 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0098others(3): Show | 6 | HG01981.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4955+485_4955+486d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | ||||||
chr6:145887533
|
G | T | 98 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0150others(95): Show | 128 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.4955+487C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | ||||||
chr6:145887533
|
GT | G | 13 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0003t0003g0260others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4955+486delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | ||||||
chr6:145887535
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4955+485A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887535 | ||||||
chr6:145887606
|
G | A | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4955+414C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887606 | ||||||
chr6:145887627
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4955+393G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887627 | ||||||
chr6:145887628
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4955+392C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887628 | ||||||
chr6:145887639
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4955+381C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887639 | ||||||
chr6:145887655
|
C | T | 1 | a0001c0002t0002g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4955+365G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887655 | ||||||
chr6:145887673
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4955+347G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887673 | ||||||
chr6:145887687
|
A | G | 1 | a0001c0003t0003g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4955+333T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887687 | ||||||
chr6:145887801
|
T | G | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4955+219A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887801 | ||||||
chr6:145888237
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4875-137C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888237 | ||||||
chr6:145888287
|
A | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0119 | 3 | HG00642.hp1 HG01257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4875-187T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888287 | ||||||
chr6:145888534
|
C | T | 23 | a0001c0001t0001g0027a0001c0001t0001g0099a0001c0001t0001g0170others(20): Show | 28 | HG00735.hp1 HG01081.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.4875-434G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888534 | ||||||
chr6:145888626
|
C | T | 32 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(29): Show | 40 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.4875-526G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888626 | ||||||
chr6:145888890
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4875-790C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888890 | ||||||
chr6:145888893
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4875-793A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888893 | ||||||
chr6:145888927
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4875-827C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888927 | ||||||
chr6:145888975
|
T | C | 1 | a0005c0007t0001g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4875-875A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888975 | ||||||
chr6:145889004
|
G | A | 18 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(15): Show | 22 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.4875-904C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889004 | ||||||
chr6:145889397
|
A | G | 1 | a0001c0002t0002g0201 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4875-1297T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889397 | ||||||
chr6:145889488
|
T | C | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4875-1388A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889488 | ||||||
chr6:145889527
|
C | A | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4875-1427G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889527 | ||||||
chr6:145889863
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4875-1763G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889863 | ||||||
chr6:145889964
|
G | A | 1 | a0001c0003t0003g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4875-1864C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889964 | ||||||
chr6:145890009
|
T | C | 1 | a0001c0002t0002g0200 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4875-1909A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890009 | ||||||
chr6:145890047
|
A | C | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4875-1947T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890047 | ||||||
chr6:145890069
|
C | G | 2 | a0001c0003t0005g0014a0001c0003t0005g0051 | 3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4875-1969G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890069 | ||||||
chr6:145890248
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(279): Show | 353 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(350): Show |
intron_variant | MODIFIER | c.4875-2148G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890248 | ||||||
chr6:145890290
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4875-2190G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890290 | ||||||
chr6:145890339
|
T | A | 2 | a0004c0006t0007g0008a0004c0006t0007g0045 | 4 | HG02135.hp2 HG02155.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4875-2239A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890339 | ||||||
chr6:145890386
|
T | A | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4875-2286A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890386 | ||||||
chr6:145890488
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4875-2388G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890488 | ||||||
chr6:145890499
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4875-2399A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890499 | ||||||
chr6:145890697
|
T | C | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4874+2518A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890697 | ||||||
chr6:145890787
|
G | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2428C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890787 | ||||||
chr6:145890867
|
G | C | 1 | a0006c0008t0003g0042 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4874+2348C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890867 | ||||||
chr6:145890924
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2291G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890924 | ||||||
chr6:145890929
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2286A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890929 | ||||||
chr6:145890963
|
T | A | 1 | a0001c0001t0002g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2252A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890963 | ||||||
chr6:145890964
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2251A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890964 | ||||||
chr6:145890977
|
GGATGACT others(4): Show |
G | 1 | a0001c0001t0002g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2227_4874+223 others(15): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890977 | ||||||
chr6:145890989
|
T | A | 1 | a0001c0001t0002g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2226A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890989 | ||||||
chr6:145890999
|
G | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2216C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890999 | ||||||
chr6:145891115
|
A | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+2100T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891115 | ||||||
chr6:145891149
|
A | G | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4874+2066T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891149 | ||||||
chr6:145891202
|
T | C | 135 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0036others(132): Show | 173 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(170): Show |
intron_variant | MODIFIER | c.4874+2013A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891202 | ||||||
chr6:145891459
|
A | G | 2 | a0003c0005t0001g0033a0003c0005t0001g0179 | 3 | NA18986.hp1 NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4874+1756T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891459 | ||||||
chr6:145891501
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4874+1714G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891501 | ||||||
chr6:145891537
|
C | T | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+1678G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891537 | ||||||
chr6:145891591
|
T | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+1624A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891591 | ||||||
chr6:145891621
|
G | A | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4874+1594C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891621 | ||||||
chr6:145891773
|
T | C | 1 | a0001c0003t0003g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4874+1442A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891773 | ||||||
chr6:145892192
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+1023G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892192 | ||||||
chr6:145892519
|
G | A | 12 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(9): Show | 16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4874+696C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892519 | ||||||
chr6:145892569
|
TC | T | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0003t0003g0257 | 3 | HG02615.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+645delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892569 | ||||||
chr6:145892570
|
C | T | 130 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(127): Show | 168 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(165): Show |
intron_variant | MODIFIER | c.4874+645G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892570 | ||||||
chr6:145892596
|
A | G | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4874+619T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892596 | ||||||
chr6:145893008
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4874+207C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145893008 | ||||||
chr6:145893427
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0127 | 2 | NA18950.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.4696-34C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893427 | ||||||
chr6:145893446
|
AGTAT | A | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0015t0014g0253 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4696-57_4696-54del others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893446 | ||||||
chr6:145893517
|
C | A | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4696-124G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893517 | ||||||
chr6:145893564
|
A | C | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4696-171T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893564 | ||||||
chr6:145893617
|
T | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4696-224A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893617 | ||||||
chr6:145893749
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4696-356G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893749 | ||||||
chr6:145893772
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0116a0001c0001t0001g0159 | 3 | HG01928.hp2 NA18998.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.4695+378G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893772 | ||||||
chr6:145893773
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4695+377C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893773 | ||||||
chr6:145893788
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0150 | 3 | HG02572.hp1 HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.4695+362C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893788 | ||||||
chr6:145893901
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4695+249A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893901 | ||||||
chr6:145893907
|
C | G | 1 | a0001c0001t0015g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4695+243G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893907 | ||||||
chr6:145894082
|
G | A | 1 | a0001c0001t0004g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4695+68C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145894082 | ||||||
chr6:145894083
|
C | A | 1 | a0001c0001t0004g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4695+67G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145894083 | ||||||
chr6:145894130
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0086 | 3 | HG02965.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4695+20C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145894130 | ||||||
chr6:145894420
|
G | GT | 113 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0001g0131others(110): Show | 147 | HG00280.hp1 HG00609.hp2 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.4609-185dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894420 | ||||||
chr6:145894420
|
G | GTT | 23 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0002t0002g0202others(20): Show | 27 | HG01081.hp2 HG01123.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.4609-186_4609-185d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894420 | ||||||
chr6:145894420
|
G | T | 1 | a0001c0001t0004g0238 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4609-184C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894420 | ||||||
chr6:145894582
|
C | G | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4608+303G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894582 | ||||||
chr6:145894674
|
A | C | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4608+211T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894674 | ||||||
chr6:145895048
|
C | T | 133 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(130): Show | 171 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(168): Show |
intron_variant | MODIFIER | c.4516-71G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895048 | ||||||
chr6:145895193
|
G | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-216C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895193 | ||||||
chr6:145895243
|
G | A | 133 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(130): Show | 171 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(168): Show |
intron_variant | MODIFIER | c.4516-266C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895243 | ||||||
chr6:145895272
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4516-295A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895272 | ||||||
chr6:145895473
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4516-496C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895473 | ||||||
chr6:145895537
|
G | GT | 55 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0070others(52): Show | 76 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4516-561dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895537 | ||||||
chr6:145895614
|
G | C | 1 | a0001c0002t0002g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4516-637C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895614 | ||||||
chr6:145895652
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4516-675A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895652 | ||||||
chr6:145895655
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4516-678G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895655 | ||||||
chr6:145896015
|
A | G | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4516-1038T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896015 | ||||||
chr6:145896172
|
A | G | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4516-1195T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896172 | ||||||
chr6:145896434
|
C | T | 137 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0001g0172others(134): Show | 176 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(173): Show |
intron_variant | MODIFIER | c.4516-1457G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896434 | ||||||
chr6:145896514
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0152 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.4516-1537G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896514 | ||||||
chr6:145896530
|
A | G | 1 | a0001c0001t0004g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4516-1553T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896530 | ||||||
chr6:145896633
|
T | C | 96 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(93): Show | 124 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.4516-1656A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896633 | ||||||
chr6:145896968
|
T | G | 2 | a0002c0004t0003g0267a0002c0004t0003g0271 | 2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4516-1991A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896968 | ||||||
chr6:145897045
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4516-2068T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897045 | ||||||
chr6:145897199
|
A | T | 1 | a0001c0001t0012g0243 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4516-2222T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897199 | ||||||
chr6:145897203
|
T | A | 137 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0001g0172others(134): Show | 176 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(173): Show |
intron_variant | MODIFIER | c.4516-2226A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897203 | ||||||
chr6:145897210
|
A | C | 91 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(88): Show | 119 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.4516-2233T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897210 | ||||||
chr6:145897265
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-2288G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897265 | ||||||
chr6:145897850
|
T | C | 1 | a0001c0002t0002g0214 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4516-2873A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897850 | ||||||
chr6:145897913
|
T | C | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4516-2936A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897913 | ||||||
chr6:145898028
|
A | G | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4516-3051T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898028 | ||||||
chr6:145898042
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4516-3065C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898042 | ||||||
chr6:145898081
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0160 | 4 | NA18990.hp1 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.4516-3104C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898081 | ||||||
chr6:145898096
|
T | C | 48 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0005others(45): Show | 69 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4516-3119A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898096 | ||||||
chr6:145898397
|
T | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(171): Show | 223 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4516-3420A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898397 | ||||||
chr6:145898447
|
ATT | A | 65 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(62): Show | 88 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.4516-3472_4516-347 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898447 | ||||||
chr6:145898626
|
T | C | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4516-3649A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898626 | ||||||
chr6:145898723
|
C | A | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4516-3746G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898723 | ||||||
chr6:145898727
|
C | T | 1 | a0001c0002t0002g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4516-3750G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898727 | ||||||
chr6:145898751
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4516-3774T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898751 | ||||||
chr6:145898759
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4516-3782G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898759 | ||||||
chr6:145898908
|
C | T | 1 | a0001c0002t0002g0197 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4516-3931G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898908 | ||||||
chr6:145899114
|
G | A | 101 | a0001c0001t0001g0062a0001c0001t0002g0036a0001c0001t0002g0037others(98): Show | 131 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.4516-4137C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899114 | ||||||
chr6:145899273
|
C | A | 96 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(93): Show | 124 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.4516-4296G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899273 | ||||||
chr6:145899318
|
T | C | 1 | a0001c0003t0003g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4516-4341A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899318 | ||||||
chr6:145899324
|
G | A | 1 | a0001c0001t0001g0019 | 2 | HG00438.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.4516-4347C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899324 | ||||||
chr6:145899622
|
G | C | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4516-4645C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899622 | ||||||
chr6:145900046
|
C | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(215): Show | 269 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.4516-5069G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900046 | ||||||
chr6:145900160
|
C | T | 1 | a0001c0003t0003g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4516-5183G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900160 | ||||||
chr6:145900383
|
C | G | 1 | a0001c0001t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4516-5406G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900383 | ||||||
chr6:145900423
|
T | C | 1 | a0001c0019t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4516-5446A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900423 | ||||||
chr6:145900466
|
C | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4516-5489G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900466 | ||||||
chr6:145900483
|
G | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4516-5506C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900483 | ||||||
chr6:145900617
|
A | G | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4516-5640T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900617 | ||||||
chr6:145900712
|
T | C | 20 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(17): Show | 24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.4516-5735A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900712 | ||||||
chr6:145901100
|
A | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-6123T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901100 | ||||||
chr6:145901200
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG01346.hp2 HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4516-6223C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901200 | ||||||
chr6:145901473
|
G | C | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4516-6496C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901473 | ||||||
chr6:145901656
|
A | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4516-6679T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901656 | ||||||
chr6:145901669
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-6692G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901669 | ||||||
chr6:145901738
|
AAC | A | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4516-6763_4516-676 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901738 | ||||||
chr6:145901795
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0110 | 2 | HG01361.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4516-6818A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901795 | ||||||
chr6:145901910
|
C | T | 1 | a0001c0001t0010g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4516-6933G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901910 | ||||||
chr6:145902217
|
T | G | 1 | a0001c0003t0005g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4516-7240A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902217 | ||||||
chr6:145902240
|
T | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-7263A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902240 | ||||||
chr6:145902310
|
A | C | 1 | a0001c0001t0002g0037 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4516-7333T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902310 | ||||||
chr6:145902405
|
G | A | 1 | a0001c0003t0003g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4516-7428C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902405 | ||||||
chr6:145902505
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4516-7528A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902505 | ||||||
chr6:145902640
|
G | GA | 100 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0190others(97): Show | 130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4516-7664dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902640 | ||||||
chr6:145902700
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-7723C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902700 | ||||||
chr6:145903219
|
C | T | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4515+7229G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903219 | ||||||
chr6:145903342
|
TA | T | 27 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(24): Show | 32 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.4515+7105delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903342 | ||||||
chr6:145903343
|
A | T | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+7105T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903343 | ||||||
chr6:145903369
|
A | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+7079T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903369 | ||||||
chr6:145903408
|
G | A | 20 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(17): Show | 24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.4515+7040C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903408 | ||||||
chr6:145903412
|
T | C | 1 | a0001c0002t0002g0212 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4515+7036A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903412 | ||||||
chr6:145903427
|
CAG | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.4515+7019_4515+702 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903427 | ||||||
chr6:145903510
|
C | T | 1 | a0005c0007t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4515+6938G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903510 | ||||||
chr6:145903570
|
T | C | 2 | a0001c0003t0005g0014a0001c0003t0005g0051 | 3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4515+6878A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903570 | ||||||
chr6:145903775
|
C | T | 1 | a0001c0001t0004g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4515+6673G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903775 | ||||||
chr6:145903976
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4515+6472C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903976 | ||||||
chr6:145904012
|
T | C | 4 | a0002c0004t0003g0264a0002c0004t0003g0269a0002c0004t0003g0270others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.4515+6436A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904012 | ||||||
chr6:145904088
|
G | T | 1 | a0001c0001t0002g0195 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4515+6360C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904088 | ||||||
chr6:145904135
|
C | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(147): Show | 183 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.4515+6313G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904135 | ||||||
chr6:145904187
|
C | T | 1 | a0001c0019t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4515+6261G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904187 | ||||||
chr6:145904483
|
G | A | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4515+5965C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904483 | ||||||
chr6:145904539
|
A | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4515+5909T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904539 | ||||||
chr6:145904626
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+5822C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904626 | ||||||
chr6:145904687
|
G | A | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4515+5761C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904687 | ||||||
chr6:145904731
|
T | C | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+5717A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904731 | ||||||
chr6:145904834
|
G | T | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+5614C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904834 | ||||||
chr6:145904835
|
C | A | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+5613G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904835 | ||||||
chr6:145904878
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4515+5570C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904878 | ||||||
chr6:145904900
|
A | G | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4515+5548T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904900 | ||||||
chr6:145904952
|
C | A | 20 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(17): Show | 24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.4515+5496G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904952 | ||||||
chr6:145905225
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+5223C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905225 | ||||||
chr6:145905371
|
C | T | 1 | a0001c0001t0004g0237 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4515+5077G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905371 | ||||||
chr6:145905400
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0136 | 2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.4515+5048A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905400 | ||||||
chr6:145905453
|
T | C | 1 | a0001c0002t0002g0211 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4515+4995A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905453 | ||||||
chr6:145905617
|
T | C | 1 | a0001c0002t0002g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4515+4831A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905617 | ||||||
chr6:145905739
|
T | C | 1 | a0011c0018t0002g0231 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4515+4709A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905739 | ||||||
chr6:145905753
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+4695A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905753 | ||||||
chr6:145905870
|
C | A | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4515+4578G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905870 | ||||||
chr6:145906118
|
A | G | 1 | a0001c0001t0004g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4515+4330T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145906118 | ||||||
chr6:145906419
|
C | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 6 | NA18943.hp2 NA18962.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.4515+4029G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145906419 | ||||||
chr6:145906896
|
G | A | 1 | a0001c0003t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4515+3552C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145906896 | ||||||
chr6:145907279
|
A | C | 1 | a0001c0003t0009g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4515+3169T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907279 | ||||||
chr6:145907308
|
A | G | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4515+3140T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907308 | ||||||
chr6:145907766
|
T | C | 1 | a0001c0003t0005g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4515+2682A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907766 | ||||||
chr6:145907785
|
AAAAACAA others(3): Show |
A | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4515+2653_4515+266 others(14): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907785 | ||||||
chr6:145907785
|
AAAAACAA others(8): Show |
A | 12 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(9): Show | 16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4515+2648_4515+266 others(19): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907785 | ||||||
chr6:145907831
|
C | G | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4515+2617G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907831 | ||||||
chr6:145907941
|
G | A | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4515+2507C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907941 | ||||||
chr6:145908184
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4515+2264A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908184 | ||||||
chr6:145908303
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+2145A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908303 | ||||||
chr6:145908393
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4515+2055G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908393 | ||||||
chr6:145908403
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+2045A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908403 | ||||||
chr6:145908503
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4515+1945G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908503 | ||||||
chr6:145908506
|
C | T | 1 | a0002c0004t0003g0262 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4515+1942G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908506 | ||||||
chr6:145908767
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+1681C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908767 | ||||||
chr6:145908948
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4515+1500C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908948 | ||||||
chr6:145909000
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4515+1448T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909000 | ||||||
chr6:145909096
|
C | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4515+1352G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909096 | ||||||
chr6:145909101
|
A | G | 3 | a0001c0003t0005g0049a0001c0003t0005g0052a0001c0003t0005g0053 | 3 | HG01433.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4515+1347T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909101 | ||||||
chr6:145909193
|
T | C | 2 | a0001c0001t0004g0236a0001c0001t0004g0240 | 2 | NA19088.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.4515+1255A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909193 | ||||||
chr6:145909196
|
T | C | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4515+1252A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909196 | ||||||
chr6:145909318
|
T | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4515+1130A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909318 | ||||||
chr6:145909407
|
G | A | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4515+1041C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909407 | ||||||
chr6:145909699
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+749G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909699 | ||||||
chr6:145909769
|
GA | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4515+678delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909769 | ||||||
chr6:145909832
|
T | C | 1 | a0001c0003t0005g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4515+616A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909832 | ||||||
chr6:145909843
|
T | A | 12 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(9): Show | 16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4515+605A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909843 | ||||||
chr6:145909981
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4515+467G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909981 | ||||||
chr6:145910334
|
C | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4515+114G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145910334 | ||||||
chr6:145910426
|
A | G | 1 | a0003c0005t0011g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4515+22T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145910426 | ||||||
chr6:145911167
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4327-531C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911167 | ||||||
chr6:145911189
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4327-553A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911189 | ||||||
chr6:145911211
|
C | T | 1 | a0001c0003t0005g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4327-575G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911211 | ||||||
chr6:145911222
|
C | A | 1 | a0001c0001t0015g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4327-586G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911222 | ||||||
chr6:145911267
|
G | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4327-631C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911267 | ||||||
chr6:145911327
|
G | A | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4327-691C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911327 | ||||||
chr6:145911413
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-777C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911413 | ||||||
chr6:145911668
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4327-1032G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911668 | ||||||
chr6:145911685
|
T | G | 1 | a0001c0001t0016g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4327-1049A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911685 | ||||||
chr6:145911690
|
A | ATAG | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1055_4327-105 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911690 | ||||||
chr6:145911692
|
T | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1056A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911692 | ||||||
chr6:145911697
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1061G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911697 | ||||||
chr6:145911698
|
A | AGAAAG | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1063_4327-106 others(9): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911698 | ||||||
chr6:145911827
|
C | T | 1 | a0001c0002t0002g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4327-1191G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911827 | ||||||
chr6:145911842
|
A | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4327-1206T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911842 | ||||||
chr6:145911931
|
T | C | 8 | a0001c0001t0002g0037a0001c0001t0002g0209a0001c0001t0002g0217others(5): Show | 9 | HG01070.hp2 HG01346.hp1 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.4327-1295A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911931 | ||||||
chr6:145912028
|
A | G | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4327-1392T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912028 | ||||||
chr6:145912083
|
G | T | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4326+1395C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912083 | ||||||
chr6:145912106
|
GC | G | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4326+1371delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912106 | ||||||
chr6:145912202
|
A | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4326+1276T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912202 | ||||||
chr6:145912237
|
G | T | 1 | a0001c0001t0004g0250 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4326+1241C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912237 | ||||||
chr6:145912266
|
GA | G | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4326+1211delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912266 | ||||||
chr6:145912382
|
A | C | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4326+1096T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912382 | ||||||
chr6:145912425
|
A | G | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4326+1053T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912425 | ||||||
chr6:145912850
|
G | GAT | 15 | a0001c0001t0001g0119a0001c0001t0001g0155a0002c0004t0003g0007others(12): Show | 19 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.4326+626_4326+627d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912850 | ||||||
chr6:145912875
|
T | A | 7 | a0001c0002t0002g0035a0001c0002t0002g0183a0001c0002t0002g0184others(4): Show | 8 | NA18950.hp1 NA18953.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.4326+603A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912875 | ||||||
chr6:145912894
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4326+584A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912894 | ||||||
chr6:145912909
|
G | A | 1 | a0002c0004t0003g0265 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4326+569C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912909 | ||||||
chr6:145913061
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.4326+417C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913061 | ||||||
chr6:145913167
|
T | C | 1 | a0001c0001t0004g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4326+311A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913167 | ||||||
chr6:145913178
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4326+300G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913178 | ||||||
chr6:145913285
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4326+193A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913285 | ||||||
chr6:145913399
|
G | A | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4326+79C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913399 | ||||||
chr6:145913585
|
G | A | 3 | a0001c0002t0002g0035a0001c0002t0002g0183a0001c0002t0002g0188 | 4 | NA18950.hp1 NA18959.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.4255-36C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913585 | ||||||
chr6:145913795
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-246G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913795 | ||||||
chr6:145913797
|
T | C | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4255-248A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913797 | ||||||
chr6:145913853
|
A | G | 1 | a0001c0001t0004g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4255-304T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913853 | ||||||
chr6:145913883
|
A | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-334T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913883 | ||||||
chr6:145913931
|
A | C | 3 | a0001c0002t0002g0034a0001c0002t0002g0040a0001c0002t0002g0224 | 5 | NA18956.hp1 NA18988.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.4255-382T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913931 | ||||||
chr6:145913936
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4255-387A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913936 | ||||||
chr6:145914163
|
T | C | 1 | a0001c0002t0002g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4255-614A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914163 | ||||||
chr6:145914245
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4255-696G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914245 | ||||||
chr6:145914291
|
A | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(1): Show | 4 | NA18991.hp2 NA19011.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.4255-742T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914291 | ||||||
chr6:145914461
|
T | C | 1 | a0001c0002t0002g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4255-912A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914461 | ||||||
chr6:145914490
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4255-941T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914490 | ||||||
chr6:145914708
|
G | C | 2 | a0001c0009t0001g0064a0001c0009t0001g0087 | 2 | NA18952.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.4255-1159C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914708 | ||||||
chr6:145914771
|
G | T | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4255-1222C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914771 | ||||||
chr6:145914877
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4255-1328C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914877 | ||||||
chr6:145914969
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4255-1420A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914969 | ||||||
chr6:145915105
|
A | C | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4255-1556T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915105 | ||||||
chr6:145915186
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-1637G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915186 | ||||||
chr6:145915237
|
T | TAA | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-1690_4255-168 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915237 | ||||||
chr6:145915352
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 44 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4255-1803A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915352 | ||||||
chr6:145915820
|
TTTAC | T | 104 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(101): Show | 126 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.4255-2275_4255-227 others(8): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915820 | ||||||
chr6:145915824
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4255-2275G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915824 | ||||||
chr6:145915930
|
ATTCTC | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4254+2196_4254+220 others(9): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915930 | ||||||
chr6:145916069
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4254+2062A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916069 | ||||||
chr6:145916209
|
T | C | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4254+1922A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916209 | ||||||
chr6:145916360
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4254+1771A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916360 | ||||||
chr6:145916421
|
A | G | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4254+1710T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916421 | ||||||
chr6:145916510
|
TA | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4254+1620delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916510 | ||||||
chr6:145916821
|
C | T | 1 | a0001c0001t0004g0236 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4254+1310G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916821 | ||||||
chr6:145916896
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(142): Show | 177 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.4254+1235G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916896 | ||||||
chr6:145917009
|
C | T | 1 | a0001c0003t0005g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4254+1122G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917009 | ||||||
chr6:145917047
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0171 | 3 | HG02723.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4254+1084G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917047 | ||||||
chr6:145917135
|
T | C | 1 | a0001c0001t0002g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4254+996A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917135 | ||||||
chr6:145917166
|
T | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.4254+965A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917166 | ||||||
chr6:145917196
|
T | C | 8 | a0001c0001t0001g0028a0001c0001t0001g0061a0001c0001t0001g0144others(5): Show | 9 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.4254+935A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917196 | ||||||
chr6:145917311
|
G | A | 2 | a0001c0003t0003g0255a0006c0008t0003g0042 | 3 | HG01081.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4254+820C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917311 | ||||||
chr6:145917391
|
C | T | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4254+740G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917391 | ||||||
chr6:145917412
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4254+719G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917412 | ||||||
chr6:145917571
|
G | A | 1 | a0001c0002t0002g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4254+560C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917571 | ||||||
chr6:145917595
|
G | GA | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4254+535dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917595 | ||||||
chr6:145917797
|
T | C | 1 | a0001c0002t0002g0215 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4254+334A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917797 | ||||||
chr6:145917807
|
A | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4254+324T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917807 | ||||||
chr6:145917988
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4254+143A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917988 | ||||||
chr6:145918109
|
T | C | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4254+22A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145918109 | ||||||
chr6:145918400
|
GA | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 6 | HG01993.hp1 NA18954.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.4153-169delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918400 | ||||||
chr6:145918401
|
A | AT | 4 | a0001c0001t0001g0162a0002c0004t0003g0043a0002c0004t0003g0270others(1): Show | 6 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4153-170dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918401 | ||||||
chr6:145918445
|
A | G | 1 | a0006c0008t0003g0042 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4153-213T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918445 | ||||||
chr6:145918538
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4153-306G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918538 | ||||||
chr6:145918681
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4153-449A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918681 | ||||||
chr6:145919104
|
C | T | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4152+244G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145919104 | ||||||
chr6:145919249
|
C | G | 1 | a0002c0004t0003g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4152+99G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145919249 | ||||||
chr6:145919501
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4009-10A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919501 | ||||||
chr6:145919570
|
CAA | C | 7 | a0001c0001t0002g0036a0001c0001t0002g0190a0001c0001t0002g0191others(4): Show | 8 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.4009-81_4009-80del others(2): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919570 | ||||||
chr6:145919700
|
T | G | 1 | a0002c0004t0003g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4009-209A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919700 | ||||||
chr6:145919713
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4009-222T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919713 | ||||||
chr6:145919771
|
C | T | 2 | a0001c0001t0004g0249a0001c0001t0004g0250 | 2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.4009-280G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919771 | ||||||
chr6:145919771
|
CTT | C | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0016g0277 | 3 | HG02055.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4009-282_4009-281d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919771 | ||||||
chr6:145919880
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4009-389A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919880 | ||||||
chr6:145919935
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4009-444A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919935 | ||||||
chr6:145920061
|
T | C | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4009-570A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920061 | ||||||
chr6:145920105
|
A | G | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4009-614T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920105 | ||||||
chr6:145920323
|
A | G | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4009-832T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920323 | ||||||
chr6:145920336
|
A | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(188): Show | 234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.4008+831T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920336 | ||||||
chr6:145920379
|
G | A | 1 | a0001c0002t0002g0200 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4008+788C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920379 | ||||||
chr6:145920494
|
ATC | A | 5 | a0001c0001t0001g0083a0004c0006t0007g0008a0004c0006t0007g0045others(2): Show | 7 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.4008+671_4008+672d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920494 | ||||||
chr6:145920575
|
A | AT | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4008+591_4008+592i others(3): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920575 | ||||||
chr6:145920862
|
A | G | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0015t0014g0253 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4008+305T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920862 | ||||||
chr6:145921516
|
C | A | 1 | a0001c0001t0001g0168 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3783-124G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921516 | ||||||
chr6:145921540
|
GT | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(177): Show | 222 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.3783-149delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921540 | ||||||
chr6:145921553
|
TA | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0145 | 3 | HG02559.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3783-162delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921553 | ||||||
chr6:145921554
|
A | T | 1 | a0001c0001t0002g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3783-162T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921554 | ||||||
chr6:145921691
|
G | C | 1 | a0001c0002t0002g0223 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3783-299C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921691 | ||||||
chr6:145921767
|
A | G | 2 | a0001c0003t0005g0050a0001c0003t0005g0054 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3783-375T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921767 | ||||||
chr6:145921806
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.3783-414G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921806 | ||||||
chr6:145921820
|
T | G | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.3783-428A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921820 | ||||||
chr6:145921935
|
T | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.3782+351A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921935 | ||||||
chr6:145921940
|
A | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.3782+346T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921940 | ||||||
chr6:145921964
|
C | G | 1 | a0001c0002t0002g0208 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3782+322G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921964 | ||||||
chr6:145921974
|
T | G | 3 | a0003c0005t0001g0033a0003c0005t0001g0118a0003c0005t0001g0179 | 4 | NA18986.hp1 NA18986.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782+312A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921974 | ||||||
chr6:145922025
|
G | C | 20 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(17): Show | 24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.3782+261C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145922025 | ||||||
chr6:145922049
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0171 | 3 | HG02723.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3782+237T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145922049 | ||||||
chr6:145922071
|
T | C | 1 | a0001c0002t0002g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3782+215A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145922071 | ||||||
chr6:145922390
|
C | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3720-42G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/29 | chr6 | 145922390 | ||||||
chr6:145922445
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.3720-97G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/29 | chr6 | 145922445 | ||||||
chr6:145922583
|
T | C | 2 | a0001c0003t0005g0014a0001c0003t0005g0051 | 3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3719+80A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/29 | chr6 | 145922583 | ||||||
chr6:145922855
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3546-19G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922855 | ||||||
chr6:145922876
|
G | A | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3546-40C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922876 | ||||||
chr6:145922880
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3546-44T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922880 | ||||||
chr6:145922912
|
T | C | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.3546-76A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922912 | ||||||
chr6:145922940
|
T | C | 1 | a0001c0003t0003g0256 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3546-104A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922940 | ||||||
chr6:145922941
|
T | A | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3546-105A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922941 | ||||||
chr6:145922945
|
G | GT | 177 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(174): Show | 217 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.3546-110dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922945 | ||||||
chr6:145922945
|
G | GTT | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3546-111_3546-110d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922945 | ||||||
chr6:145922992
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.3546-156T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922992 | ||||||
chr6:145923049
|
T | C | 1 | a0001c0001t0006g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3546-213A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923049 | ||||||
chr6:145923138
|
G | A | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3546-302C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923138 | ||||||
chr6:145923245
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0099a0001c0001t0001g0170 | 4 | HG00735.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.3545+398C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923245 | ||||||
chr6:145923572
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3545+71T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923572 | ||||||
chr6:145923607
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.3545+36T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923607 | ||||||
chr6:145923904
|
G | T | 2 | a0003c0005t0001g0033a0003c0005t0001g0118 | 3 | NA18986.hp1 NA18986.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3403-119C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145923904 | ||||||
chr6:145923910
|
C | G | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0015t0014g0253 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3403-125G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145923910 | ||||||
chr6:145924015
|
G | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 264 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.3403-230C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924015 | ||||||
chr6:145924038
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0131 | 5 | HG03942.hp2 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.3403-253A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924038 | ||||||
chr6:145924096
|
A | G | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3403-311T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924096 | ||||||
chr6:145924097
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3403-312A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924097 | ||||||
chr6:145924136
|
A | G | 1 | a0001c0001t0004g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3403-351T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924136 | ||||||
chr6:145924140
|
A | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3403-355T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924140 | ||||||
chr6:145924144
|
C | T | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3403-359G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924144 | ||||||
chr6:145924292
|
AGT | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.3402+445_3402+446d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924292 | ||||||
chr6:145924886
|
T | A | 2 | a0001c0003t0005g0055a0010c0013t0005g0056 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3295-40A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145924886 | ||||||
chr6:145925005
|
A | G | 1 | a0004c0006t0007g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3295-159T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925005 | ||||||
chr6:145925048
|
A | T | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3295-202T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925048 | ||||||
chr6:145925075
|
A | G | 18 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(15): Show | 22 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.3295-229T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925075 | ||||||
chr6:145925216
|
T | C | 1 | a0004c0006t0007g0046 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3295-370A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925216 | ||||||
chr6:145925320
|
G | A | 1 | a0010c0013t0005g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3295-474C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925320 | ||||||
chr6:145925341
|
T | TAC | 32 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0151others(29): Show | 37 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3295-497_3295-496d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
T | TACAC | 23 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0002g0274others(20): Show | 30 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3295-499_3295-496d others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
T | TACACAC | 32 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 41 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.3295-501_3295-496d others(8): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0088others(4): Show | 7 | HG00544.hp2 HG01069.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.3295-503_3295-496d others(10): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
T | TACACACA others(3): Show |
82 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 103 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.3295-505_3295-496d others(12): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
T | TACACACA others(5): Show |
18 | a0001c0001t0001g0028a0001c0001t0001g0061a0001c0001t0001g0098others(15): Show | 19 | HG00558.hp2 HG00738.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3295-507_3295-496d others(14): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
T | TACACACA others(7): Show |
2 | a0001c0020t0001g0060a0005c0007t0001g0091 | 2 | HG03017.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3295-509_3295-496d others(16): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925341
|
TAC | T | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0002t0002g0220 | 3 | HG02055.hp2 HG03098.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.3295-497_3295-496d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | ||||||
chr6:145925368
|
A | ACACACAC others(5): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0076a0001c0001t0001g0079others(1): Show | 5 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.3295-523_3295-522i others(14): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925368 | ||||||
chr6:145925371
|
T | C | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3295-525A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925371 | ||||||
chr6:145925463
|
T | C | 2 | a0001c0002t0002g0226a0001c0002t0002g0227 | 2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3295-617A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925463 | ||||||
chr6:145925491
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3295-645A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925491 | ||||||
chr6:145925544
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3294+660A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925544 | ||||||
chr6:145925595
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3294+609G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925595 | ||||||
chr6:145925653
|
C | T | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3294+551G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925653 | ||||||
chr6:145925759
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3294+445G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925759 | ||||||
chr6:145925868
|
A | G | 1 | a0001c0014t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3294+336T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925868 | ||||||
chr6:145925911
|
A | C | 2 | a0001c0002t0002g0004a0001c0002t0002g0039 | 7 | HG00609.hp2 NA18952.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.3294+293T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925911 | ||||||
chr6:145925918
|
T | C | 1 | a0001c0001t0004g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3294+286A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925918 | ||||||
chr6:145926356
|
C | T | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3202-60G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926356 | ||||||
chr6:145926368
|
T | C | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3202-72A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926368 | ||||||
chr6:145926399
|
T | C | 1 | a0001c0002t0002g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3202-103A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926399 | ||||||
chr6:145926484
|
G | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3202-188C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926484 | ||||||
chr6:145926814
|
T | C | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3201+375A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926814 | ||||||
chr6:145926817
|
A | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+372T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926817 | ||||||
chr6:145926830
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0006g0279a0001c0001t0006g0280 | 3 | HG00642.hp2 HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3201+359G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926830 | ||||||
chr6:145926910
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+279G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926910 | ||||||
chr6:145927008
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+181C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927008 | ||||||
chr6:145927041
|
T | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(188): Show | 234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.3201+148A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927041 | ||||||
chr6:145927084
|
G | C | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3201+105C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927084 | ||||||
chr6:145927105
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+84G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927105 | ||||||
chr6:145927533
|
T | C | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0015t0014g0253 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3113-256A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927533 | ||||||
chr6:145927571
|
C | T | 14 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0038others(11): Show | 27 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(24): Show |
intron_variant | MODIFIER | c.3113-294G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927571 | ||||||
chr6:145927576
|
G | C | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3113-299C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927576 | ||||||
chr6:145927705
|
A | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3113-428T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927705 | ||||||
chr6:145927727
|
C | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(188): Show | 234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.3113-450G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927727 | ||||||
chr6:145927798
|
T | G | 1 | a0006c0008t0003g0042 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3113-521A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927798 | ||||||
chr6:145927915
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3113-638T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927915 | ||||||
chr6:145928049
|
C | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02886.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3113-772G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928049 | ||||||
chr6:145928209
|
TG | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0150 | 3 | HG02572.hp1 HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3113-933delC | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928209 | ||||||
chr6:145928310
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3113-1033C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928310 | ||||||
chr6:145928392
|
A | T | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1115T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928392 | ||||||
chr6:145928393
|
A | T | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1116T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928393 | ||||||
chr6:145928394
|
AAAAGGTA others(14): Show |
A | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1138_3113-111 others(25): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928394 | ||||||
chr6:145928642
|
A | T | 1 | a0004c0006t0007g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3113-1365T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928642 | ||||||
chr6:145928695
|
G | A | 2 | a0005c0007t0001g0090a0005c0007t0001g0091 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3113-1418C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928695 | ||||||
chr6:145928837
|
C | G | 1 | a0003c0005t0001g0175 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3113-1560G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928837 | ||||||
chr6:145928851
|
GAGA | G | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1577_3113-157 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928851 | ||||||
chr6:145928889
|
C | T | 12 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(9): Show | 16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3113-1612G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928889 | ||||||
chr6:145929019
|
A | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.3113-1742T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929019 | ||||||
chr6:145929059
|
A | G | 2 | a0005c0007t0001g0090a0005c0007t0001g0091 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3113-1782T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929059 | ||||||
chr6:145929242
|
C | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3113-1965G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929242 | ||||||
chr6:145929311
|
G | C | 1 | a0001c0002t0002g0212 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3113-2034C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929311 | ||||||
chr6:145929577
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3113-2300T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929577 | ||||||
chr6:145929743
|
T | A | 1 | a0001c0001t0012g0243 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3113-2466A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929743 | ||||||
chr6:145929811
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(142): Show | 177 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.3113-2534A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929811 | ||||||
chr6:145929823
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(144): Show | 180 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.3113-2546T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929823 | ||||||
chr6:145929847
|
G | A | 1 | a0001c0001t0015g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3113-2570C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929847 | ||||||
chr6:145929972
|
G | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.3113-2695C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929972 | ||||||
chr6:145930078
|
C | T | 1 | a0001c0002t0002g0219 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3113-2801G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930078 | ||||||
chr6:145930280
|
G | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18943.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.3112+2777C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930280 | ||||||
chr6:145930364
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3112+2693A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930364 | ||||||
chr6:145930376
|
CAT | C | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3112+2679_3112+268 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930376 | ||||||
chr6:145930439
|
T | C | 2 | a0001c0001t0006g0279a0001c0001t0006g0280 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.3112+2618A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930439 | ||||||
chr6:145930493
|
A | C | 1 | a0003c0005t0011g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3112+2564T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930493 | ||||||
chr6:145930696
|
T | G | 2 | a0001c0002t0002g0207a0001c0002t0002g0213 | 2 | HG00639.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3112+2361A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930696 | ||||||
chr6:145930902
|
G | A | 33 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(30): Show | 41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3112+2155C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930902 | ||||||
chr6:145930926
|
T | C | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3112+2131A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930926 | ||||||
chr6:145931196
|
C | T | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3112+1861G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931196 | ||||||
chr6:145931328
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3112+1729C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931328 | ||||||
chr6:145931359
|
A | C | 1 | a0001c0001t0002g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3112+1698T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931359 | ||||||
chr6:145931439
|
G | A | 1 | a0004c0006t0007g0047 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3112+1618C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931439 | ||||||
chr6:145931498
|
G | A | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3112+1559C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931498 | ||||||
chr6:145931538
|
A | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0085 | 2 | HG00280.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.3112+1519T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931538 | ||||||
chr6:145931890
|
CT | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(178): Show | 222 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.3112+1166delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931890 | ||||||
chr6:145931890
|
CTT | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+1165_3112+116 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931890 | ||||||
chr6:145932009
|
G | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0147 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3112+1048C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932009 | ||||||
chr6:145932041
|
AT | A | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0015t0014g0253 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3112+1015delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932041 | ||||||
chr6:145932190
|
A | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0071others(1): Show | 4 | NA18991.hp2 NA19011.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.3112+867T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932190 | ||||||
chr6:145932285
|
T | C | 1 | a0001c0002t0002g0214 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3112+772A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932285 | ||||||
chr6:145932314
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.3112+743G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932314 | ||||||
chr6:145932480
|
AACACTAT others(6): Show |
A | 2 | a0001c0002t0002g0201a0001c0002t0002g0215 | 2 | HG01255.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3112+564_3112+576d others(15): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932480 | ||||||
chr6:145932503
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+554G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932503 | ||||||
chr6:145932507
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3112+550G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932507 | ||||||
chr6:145932513
|
G | C | 1 | a0001c0002t0002g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3112+544C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932513 | ||||||
chr6:145932541
|
G | A | 1 | a0006c0008t0003g0042 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3112+516C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932541 | ||||||
chr6:145932741
|
T | G | 2 | a0001c0002t0002g0226a0001c0002t0002g0227 | 2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3112+316A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932741 | ||||||
chr6:145932787
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+270G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932787 | ||||||
chr6:145932838
|
ATGTT | A | 24 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(21): Show | 29 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.3112+215_3112+218d others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932838 | ||||||
chr6:145932847
|
T | A | 1 | a0001c0001t0002g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3112+210A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932847 | ||||||
chr6:145932964
|
T | TC | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.3112+92dupG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932964 | ||||||
chr6:145933224
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2991-46C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933224 | ||||||
chr6:145933376
|
T | C | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2991-198A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933376 | ||||||
chr6:145933565
|
C | G | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2991-387G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933565 | ||||||
chr6:145933669
|
T | C | 1 | a0006c0008t0003g0042 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2991-491A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933669 | ||||||
chr6:145933911
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2991-733G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933911 | ||||||
chr6:145933943
|
A | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.2991-765T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933943 | ||||||
chr6:145934011
|
T | A | 14 | a0001c0001t0016g0277a0001c0003t0005g0009a0001c0003t0005g0014others(11): Show | 18 | HG01081.hp2 HG01433.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2991-833A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934011 | ||||||
chr6:145934114
|
G | C | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2990+793C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934114 | ||||||
chr6:145934130
|
G | A | 2 | a0001c0001t0004g0249a0001c0001t0004g0250 | 2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2990+777C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934130 | ||||||
chr6:145934193
|
C | T | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2990+714G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934193 | ||||||
chr6:145934194
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2990+713C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934194 | ||||||
chr6:145934230
|
G | A | 12 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(9): Show | 15 | HG01433.hp1 HG02572.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2990+677C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934230 | ||||||
chr6:145934339
|
G | T | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2990+568C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934339 | ||||||
chr6:145934423
|
GC | G | 101 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 123 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.2990+483delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934423 | ||||||
chr6:145934473
|
T | TAAATA | 25 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 32 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.2990+429_2990+433d others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934473
|
T | TAAATAAA others(3): Show |
17 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0062others(14): Show | 18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2990+424_2990+433d others(12): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934473
|
T | TAAATAAA others(8): Show |
107 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(104): Show | 133 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.2990+419_2990+433d others(17): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934473
|
T | TAAATAAA others(13): Show |
13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0137others(10): Show | 14 | HG01496.hp1 HG01515.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.2990+414_2990+433d others(22): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934473
|
T | TAAATAAA others(18): Show |
16 | a0001c0003t0003g0257a0001c0003t0003g0258a0001c0003t0005g0009others(13): Show | 20 | HG01433.hp1 HG01891.hp2 HG02809.hp2 others(17): Show |
intron_variant | MODIFIER | c.2990+409_2990+433d others(27): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934473
|
T | TAAATAAA others(23): Show |
9 | a0001c0015t0014g0253a0002c0004t0003g0007a0002c0004t0003g0264others(6): Show | 12 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2990+404_2990+433d others(32): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934473
|
T | TAAATAAA others(28): Show |
2 | a0001c0003t0005g0050a0001c0003t0005g0054 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2990+399_2990+433d others(37): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | ||||||
chr6:145934507
|
T | TAAAATAA others(9): Show |
4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2990+399_2990+400i others(18): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934507 | ||||||
chr6:145934508
|
A | AAAATAAA others(7): Show |
1 | a0001c0001t0001g0072 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2990+398_2990+399i others(16): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934508 | ||||||
chr6:145934613
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2990+294A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934613 | ||||||
chr6:145934658
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2990+249C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934658 | ||||||
chr6:145934808
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2990+99G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934808 | ||||||
chr6:145935174
|
G | C | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2734-11C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935174 | ||||||
chr6:145935179
|
G | GA | 17 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0003t0003g0254others(14): Show | 20 | HG00738.hp1 HG01433.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.2734-17dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935179 | ||||||
chr6:145935179
|
GA | G | 5 | a0001c0002t0002g0183a0004c0006t0007g0008a0004c0006t0007g0045others(2): Show | 7 | HG02135.hp2 HG02155.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.2734-17delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935179 | ||||||
chr6:145935194
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2734-31T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935194 | ||||||
chr6:145935498
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2570-57C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935498 | ||||||
chr6:145935661
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2570-220T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935661 | ||||||
chr6:145935879
|
T | G | 3 | a0001c0001t0015g0276a0001c0001t0016g0277a0001c0015t0014g0253 | 3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2570-438A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935879 | ||||||
chr6:145935928
|
T | C | 1 | a0001c0001t0016g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2570-487A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935928 | ||||||
chr6:145935954
|
TAC | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-515_2570-514d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935954 | ||||||
chr6:145936029
|
G | C | 1 | a0001c0001t0016g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2570-588C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936029 | ||||||
chr6:145936065
|
T | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0245a0001c0001t0004g0246 | 6 | NA18951.hp2 NA18955.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2570-624A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936065 | ||||||
chr6:145936209
|
G | A | 1 | a0001c0002t0002g0251 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2570-768C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936209 | ||||||
chr6:145936352
|
G | A | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.2570-911C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936352 | ||||||
chr6:145936466
|
A | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-1025T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936466 | ||||||
chr6:145936467
|
T | C | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2570-1026A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936467 | ||||||
chr6:145936625
|
G | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.2570-1184C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936625 | ||||||
chr6:145936668
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-1227G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936668 | ||||||
chr6:145936725
|
C | T | 1 | a0001c0001t0006g0281 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2570-1284G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936725 | ||||||
chr6:145936775
|
T | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-1334A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936775 | ||||||
chr6:145936938
|
G | A | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2570-1497C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936938 | ||||||
chr6:145936964
|
C | T | 1 | a0001c0003t0005g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2570-1523G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936964 | ||||||
chr6:145936976
|
A | ATCT | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0015g0276 | 3 | HG02615.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2570-1538_2570-153 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936976 | ||||||
chr6:145936978
|
C | CT | 6 | a0001c0001t0002g0191a0001c0002t0002g0013a0001c0002t0002g0203others(3): Show | 8 | HG01516.hp1 HG02257.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2570-1538dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | ||||||
chr6:145936978
|
CT | C | 12 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0070others(9): Show | 13 | HG01993.hp2 HG02735.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.2570-1538delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | ||||||
chr6:145936978
|
CTT | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 194 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.2570-1539_2570-153 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | ||||||
chr6:145936978
|
CTTT | C | 18 | a0001c0001t0001g0107a0001c0001t0001g0143a0001c0001t0001g0170others(15): Show | 22 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2570-1540_2570-153 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | ||||||
chr6:145936979
|
T | TTC | 6 | a0001c0001t0002g0193a0001c0001t0016g0277a0004c0006t0007g0008others(3): Show | 8 | HG02055.hp2 HG02135.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.2570-1539_2570-153 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936979 | ||||||
chr6:145936980
|
T | TC | 3 | a0001c0001t0002g0036a0001c0001t0002g0194a0001c0001t0002g0195 | 4 | HG02109.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2570-1540_2570-153 others(5): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936980 | ||||||
chr6:145936982
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0070others(4): Show | 7 | HG02965.hp1 HG03209.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.2570-1541A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936982 | ||||||
chr6:145936983
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 194 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.2570-1542A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936983 | ||||||
chr6:145936984
|
T | C | 18 | a0001c0001t0001g0143a0001c0001t0001g0170a0001c0003t0003g0255others(15): Show | 22 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2570-1543A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936984 | ||||||
chr6:145937022
|
C | T | 14 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0038others(11): Show | 27 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(24): Show |
intron_variant | MODIFIER | c.2570-1581G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937022 | ||||||
chr6:145937042
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2570-1601C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937042 | ||||||
chr6:145937086
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2570-1645G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937086 | ||||||
chr6:145937183
|
C | G | 1 | a0001c0019t0001g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2570-1742G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937183 | ||||||
chr6:145937370
|
C | G | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2570-1929G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937370 | ||||||
chr6:145937397
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18956.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2570-1956T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937397 | ||||||
chr6:145937602
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 4 | HG01255.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.2570-2161C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937602 | ||||||
chr6:145937915
|
T | TAAC | 14 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0038others(11): Show | 27 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(24): Show |
intron_variant | MODIFIER | c.2570-2475_2570-247 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937915 | ||||||
chr6:145938369
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2569+2354G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938369 | ||||||
chr6:145938486
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2569+2237T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938486 | ||||||
chr6:145938567
|
T | C | 3 | a0001c0002t0002g0034a0001c0002t0002g0040a0001c0002t0002g0224 | 5 | NA18956.hp1 NA18988.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569+2156A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938567 | ||||||
chr6:145938645
|
G | A | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2569+2078C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938645 | ||||||
chr6:145938874
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2569+1849T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938874 | ||||||
chr6:145938877
|
C | G | 1 | a0001c0001t0004g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2569+1846G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938877 | ||||||
chr6:145939146
|
A | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2569+1577T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939146 | ||||||
chr6:145939298
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2569+1425A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939298 | ||||||
chr6:145939400
|
A | G | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2569+1323T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939400 | ||||||
chr6:145939546
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2569+1177T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939546 | ||||||
chr6:145939617
|
C | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.2569+1106G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939617 | ||||||
chr6:145939837
|
A | C | 1 | a0001c0001t0015g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2569+886T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939837 | ||||||
chr6:145939880
|
T | C | 1 | a0003c0005t0001g0174 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2569+843A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939880 | ||||||
chr6:145940098
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18966.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2569+625A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940098 | ||||||
chr6:145940135
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2569+588G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940135 | ||||||
chr6:145940203
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2569+520G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940203 | ||||||
chr6:145940305
|
T | A | 1 | a0001c0001t0006g0281 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2569+418A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940305 | ||||||
chr6:145940323
|
C | G | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2569+400G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940323 | ||||||
chr6:145940370
|
A | AC | 39 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2569+352dupG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940370 | ||||||
chr6:145940507
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2569+216G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940507 | ||||||
chr6:145940663
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0152 | 2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2569+60A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940663 | ||||||
chr6:145940717
|
C | A | 3 | a0001c0002t0002g0034a0001c0002t0002g0040a0001c0002t0002g0224 | 5 | NA18956.hp1 NA18988.hp1 NA18998.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2569+6G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940717 | ||||||
chr6:145940871
|
T | C | 1 | a0001c0002t0002g0182 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2491-70A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/29 | chr6 | 145940871 | ||||||
chr6:145941557
|
C | T | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2490+66G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/29 | chr6 | 145941557 | ||||||
chr6:145941561
|
G | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 274 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(271): Show |
intron_variant | MODIFIER | c.2490+62C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/29 | chr6 | 145941561 | ||||||
chr6:145941954
|
C | T | 2 | a0001c0001t0004g0041a0001c0001t0004g0235 | 3 | HG01515.hp2 HG01517.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2239-80G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145941954 | ||||||
chr6:145942016
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2239-142T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942016 | ||||||
chr6:145942178
|
T | A | 1 | a0001c0003t0005g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2239-304A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942178 | ||||||
chr6:145942323
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2239-449A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942323 | ||||||
chr6:145942571
|
T | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0099others(2): Show | 7 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2238+572A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942571 | ||||||
chr6:145942690
|
A | G | 1 | a0001c0002t0002g0189 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2238+453T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942690 | ||||||
chr6:145942750
|
G | A | 12 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(9): Show | 15 | HG01433.hp1 HG02572.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2238+393C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942750 | ||||||
chr6:145942935
|
T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 264 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.2238+208A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942935 | ||||||
chr6:145943002
|
C | A | 1 | a0001c0003t0003g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2238+141G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145943002 | ||||||
chr6:145943073
|
G | C | 2 | a0001c0003t0005g0055a0010c0013t0005g0056 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2238+70C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145943073 | ||||||
chr6:145943096
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0063 | 3 | HG00741.hp1 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2238+47C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145943096 | ||||||
chr6:145943884
|
T | C | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1579-82A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145943884 | ||||||
chr6:145944043
|
G | T | 2 | a0001c0003t0003g0254a0001c0003t0003g0256 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1579-241C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944043 | ||||||
chr6:145944078
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1579-276T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944078 | ||||||
chr6:145944204
|
C | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.1579-402G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944204 | ||||||
chr6:145944263
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579-461G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944263 | ||||||
chr6:145944499
|
A | C | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1579-697T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944499 | ||||||
chr6:145944500
|
GGTCGAAC others(1): Show |
G | 92 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1579-706_1579-699d others(10): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944500 | ||||||
chr6:145944510
|
G | C | 92 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1579-708C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944510 | ||||||
chr6:145944511
|
G | T | 92 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(89): Show | 113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1579-709C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944511 | ||||||
chr6:145945036
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.1578+345A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145945036 | ||||||
chr6:145945273
|
T | G | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1578+108A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145945273 | ||||||
chr6:145946039
|
G | T | 1 | a0001c0003t0005g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1321+194C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 7/29 | chr6 | 145946039 | ||||||
chr6:145946172
|
G | T | 7 | a0001c0002t0002g0035a0001c0002t0002g0183a0001c0002t0002g0184others(4): Show | 8 | NA18950.hp1 NA18953.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1321+61C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 7/29 | chr6 | 145946172 | ||||||
chr6:145946737
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.1213-396T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946737 | ||||||
chr6:145946743
|
AT | A | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1213-403delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946743 | ||||||
chr6:145946753
|
T | A | 2 | a0001c0002t0002g0226a0001c0002t0002g0227 | 2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1213-412A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946753 | ||||||
chr6:145946754
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1213-413T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946754 | ||||||
chr6:145946840
|
G | C | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1213-499C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946840 | ||||||
chr6:145946859
|
T | A | 1 | a0001c0001t0002g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1213-518A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946859 | ||||||
chr6:145947094
|
A | G | 18 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(15): Show | 22 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1212+399T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947094 | ||||||
chr6:145947243
|
C | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01515.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1212+250G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947243 | ||||||
chr6:145947301
|
C | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212+192G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947301 | ||||||
chr6:145947382
|
C | T | 2 | a0001c0003t0003g0259a0001c0003t0003g0260 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1212+111G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947382 | ||||||
chr6:145947487
|
T | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
splice_region_variant&intron_variant | LOW | c.1212+6A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947487 | ||||||
chr6:145947674
|
T | C | 1 | a0001c0003t0003g0256 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1062-31A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 5/29 | chr6 | 145947674 | ||||||
chr6:145947883
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1062-240C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 5/29 | chr6 | 145947883 | ||||||
chr6:145948045
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+227C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 5/29 | chr6 | 145948045 | ||||||
chr6:145948456
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.983-106A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948456 | ||||||
chr6:145948685
|
T | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-335A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948685 | ||||||
chr6:145948746
|
T | C | 1 | a0001c0003t0003g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.983-396A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948746 | ||||||
chr6:145948805
|
G | A | 1 | a0001c0002t0002g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.983-455C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948805 | ||||||
chr6:145948891
|
A | G | 1 | a0001c0003t0003g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.983-541T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948891 | ||||||
chr6:145948955
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-605G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948955 | ||||||
chr6:145948985
|
T | C | 1 | a0006c0008t0003g0042 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.983-635A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948985 | ||||||
chr6:145948998
|
A | G | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-648T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948998 | ||||||
chr6:145949311
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.982+953T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145949311 | ||||||
chr6:145950041
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.982+223A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145950041 | ||||||
chr6:145950197
|
C | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+67G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145950197 | ||||||
chr6:145950533
|
T | G | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.764-51A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950533 | ||||||
chr6:145950563
|
A | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-81T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950563 | ||||||
chr6:145950740
|
T | TA | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.764-259dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950740 | ||||||
chr6:145950841
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.764-359G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950841 | ||||||
chr6:145950847
|
AGAAGCTG others(4): Show |
A | 149 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(146): Show | 182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.764-376_764-366del others(11): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950847 | ||||||
chr6:145950878
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-396A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950878 | ||||||
chr6:145950917
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.764-435C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950917 | ||||||
chr6:145951177
|
T | C | 1 | a0011c0018t0002g0231 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.764-695A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951177 | ||||||
chr6:145951438
|
A | G | 1 | a0001c0002t0002g0034 | 2 | NA18988.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.763+911T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951438 | ||||||
chr6:145951467
|
T | C | 1 | a0001c0009t0001g0087 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.763+882A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951467 | ||||||
chr6:145951523
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.763+826G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951523 | ||||||
chr6:145951655
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.763+694G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951655 | ||||||
chr6:145952122
|
A | G | 2 | a0001c0003t0003g0257a0001c0003t0003g0258 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.763+227T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952122 | ||||||
chr6:145952169
|
T | C | 1 | a0001c0001t0002g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.763+180A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952169 | ||||||
chr6:145952183
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.763+166T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952183 | ||||||
chr6:145952214
|
A | G | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.763+135T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952214 | ||||||
chr6:145952562
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.634-84A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952562 | ||||||
chr6:145952633
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.634-155G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952633 | ||||||
chr6:145952829
|
CAGA | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0171 | 3 | HG02723.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.634-354_634-352del others(3): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952829 | ||||||
chr6:145952885
|
T | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0061a0001c0001t0001g0144others(4): Show | 8 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.634-407A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952885 | ||||||
chr6:145953285
|
G | A | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.634-807C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953285 | ||||||
chr6:145953443
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0063 | 4 | HG00741.hp1 HG02451.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.634-965G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953443 | ||||||
chr6:145953595
|
A | C | 3 | a0001c0003t0003g0259a0001c0003t0003g0260a0001c0003t0009g0261 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.633+1095T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953595 | ||||||
chr6:145953686
|
T | C | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.633+1004A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953686 | ||||||
chr6:145953826
|
T | C | 1 | a0001c0002t0002g0233 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.633+864A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953826 | ||||||
chr6:145953920
|
G | A | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.633+770C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953920 | ||||||
chr6:145953998
|
CA | C | 19 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(16): Show | 23 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.633+691delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953998 | ||||||
chr6:145954093
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.633+597G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954093 | ||||||
chr6:145954137
|
GA | G | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.633+552delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954137 | ||||||
chr6:145954166
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(279): Show | 353 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(350): Show |
intron_variant | MODIFIER | c.633+524T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954166 | ||||||
chr6:145954217
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.633+473T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954217 | ||||||
chr6:145954259
|
G | A | 13 | a0002c0004t0003g0007a0002c0004t0003g0043a0002c0004t0003g0262others(10): Show | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.633+431C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954259 | ||||||
chr6:145954435
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.633+255C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954435 | ||||||
chr6:145954585
|
T | C | 2 | a0001c0001t0015g0276a0001c0001t0016g0277 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.633+105A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954585 | ||||||
chr6:145955644
|
A | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-32-290T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955644 | ||||||
chr6:145955735
|
C | T | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-381G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955735 | ||||||
chr6:145955753
|
T | G | 2 | a0001c0001t0006g0282a0001c0001t0006g0283 | 2 | HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-32-399A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955753 | ||||||
chr6:145955955
|
T | C | 6 | a0001c0001t0004g0041a0001c0001t0004g0235a0001c0001t0004g0247others(3): Show | 7 | HG01074.hp1 HG01109.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-601A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955955 | ||||||
chr6:145956195
|
C | T | 13 | a0001c0003t0005g0009a0001c0003t0005g0014a0001c0003t0005g0048others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-841G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956195 | ||||||
chr6:145956558
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-32-1204C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956558 | ||||||
chr6:145956626
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-32-1272T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956626 | ||||||
chr6:145956691
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.-32-1337G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956691 | ||||||
chr6:145956757
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-32-1403A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956757 | ||||||
chr6:145957117
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-1763C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957117 | ||||||
chr6:145957365
|
T | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-32-2011A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957365 | ||||||
chr6:145957784
|
T | C | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-2430A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957784 | ||||||
chr6:145957823
|
T | C | 106 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(103): Show | 128 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.-32-2469A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957823 | ||||||
chr6:145957926
|
T | A | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-32-2572A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957926 | ||||||
chr6:145957962
|
G | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.-32-2608C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957962 | ||||||
chr6:145957995
|
GAGACTTC others(8): Show |
G | 3 | a0001c0003t0003g0259a0001c0003t0003g0260a0001c0003t0009g0261 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-2656_-32-2642d others(17): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957995 | ||||||
chr6:145958227
|
C | T | 25 | a0001c0001t0004g0006a0001c0001t0004g0041a0001c0001t0004g0235others(22): Show | 30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-2873G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958227 | ||||||
chr6:145958302
|
A | G | 3 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256 | 3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-32-2948T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958302 | ||||||
chr6:145958466
|
C | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-32-3112G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958466 | ||||||
chr6:145958828
|
C | CATTT | 3 | a0001c0001t0001g0061a0002c0004t0003g0262a0002c0004t0003g0263 | 3 | HG02630.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-32-3478_-32-3475d others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958828 | ||||||
chr6:145958962
|
A | C | 1 | a0001c0020t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-32-3608T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958962 | ||||||
chr6:145959001
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-32-3647A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959001 | ||||||
chr6:145959055
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-32-3701A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959055 | ||||||
chr6:145959370
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-32-4016G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959370 | ||||||
chr6:145959374
|
T | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 6 | HG01993.hp1 NA18954.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-4020A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959374 | ||||||
chr6:145959513
|
CT | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.-32-4160delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959513 | ||||||
chr6:145959654
|
G | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(188): Show | 234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.-33+4077C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959654 | ||||||
chr6:145959655
|
C | T | 2 | a0001c0001t0004g0041a0001c0001t0004g0235 | 3 | HG01515.hp2 HG01517.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-33+4076G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959655 | ||||||
chr6:145959833
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0158 | 4 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+3898G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959833 | ||||||
chr6:145960009
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+3722A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960009 | ||||||
chr6:145960210
|
GCAATGGT | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-33+3514_-33+3520d others(9): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960210 | ||||||
chr6:145960231
|
T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 264 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.-33+3500A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960231 | ||||||
chr6:145960232
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-33+3499C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960232 | ||||||
chr6:145960402
|
G | A | 1 | a0001c0003t0005g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+3329C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960402 | ||||||
chr6:145960493
|
T | A | 1 | a0001c0002t0002g0251 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-33+3238A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960493 | ||||||
chr6:145960676
|
A | T | 1 | a0001c0002t0002g0182 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-33+3055T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960676 | ||||||
chr6:145960847
|
C | T | 1 | a0003c0005t0001g0174 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-33+2884G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960847 | ||||||
chr6:145960925
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.-33+2806T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960925 | ||||||
chr6:145960944
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33+2787A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960944 | ||||||
chr6:145961012
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-33+2719A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961012 | ||||||
chr6:145961059
|
G | A | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33+2672C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961059 | ||||||
chr6:145961195
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-33+2536C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961195 | ||||||
chr6:145961202
|
C | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0160others(8): Show | 15 | HG02074.hp1 NA18942.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+2529G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961202 | ||||||
chr6:145961263
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-33+2468A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961263 | ||||||
chr6:145961493
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-33+2238A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961493 | ||||||
chr6:145961552
|
A | G | 21 | a0001c0003t0003g0254a0001c0003t0003g0255a0001c0003t0003g0256others(18): Show | 25 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-33+2179T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961552 | ||||||
chr6:145961685
|
G | A | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33+2046C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961685 | ||||||
chr6:145962206
|
G | A | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+1525C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145962206 | ||||||
chr6:145962538
|
G | A | 1 | a0001c0015t0014g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33+1193C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145962538 | ||||||
chr6:145962783
|
A | G | 4 | a0004c0006t0007g0008a0004c0006t0007g0045a0004c0006t0007g0046others(1): Show | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+948T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145962783 | ||||||
chr6:145963379
|
G | A | 1 | a0003c0005t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-33+352C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963379 | ||||||
chr6:145963424
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 176 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.-33+307T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963424 | ||||||
chr6:145963485
|
T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(185): Show | 231 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(228): Show |
intron_variant | MODIFIER | c.-33+246A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963485 | ||||||
chr6:145963544
|
T | C | 11 | a0003c0005t0001g0003a0003c0005t0001g0033a0003c0005t0001g0174others(8): Show | 17 | HG00609.hp1 HG02040.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+187A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963544 | ||||||
chr6:145963607
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+124C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963607 | ||||||
chr6:145963681
|
G | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-33+50C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963681 | ||||||
chr6:145963682
|
C | A | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-33+49G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963682 |