geneid | 55325 |
---|---|
ensemblid | ENSG00000109775.11 |
hgncid | 25640 |
symbol | UFSP2 |
name | UFM1 specific peptidase 2 |
refseq_nuc | NM_018359.5 |
refseq_prot | NP_060829.2 |
ensembl_nuc | ENST00000264689.11 |
ensembl_prot | ENSP00000264689.6 |
mane_status | MANE Select |
chr | chr4 |
start | 185399537 |
end | 185425964 |
strand | - |
ver | v1.2 |
region | chr4:185399537-185425964 |
region5000 | chr4:185394537-185430964 |
regionname0 | UFSP2_chr4_185399537_185425964 |
regionname5000 | UFSP2_chr4_185394537_185430964 |
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 | 469 | 290 | 88 | 47 | 98 | 12 | 43 | 76 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0002 | 0/0 | 469 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0003 | 0/0 | 469 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0004 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0005 | 0/0 | 469 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0006 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0007 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0008 | 0/0 | 469 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1410 | 264 | 76 | 46 | 87 | 12 | 41 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0002 | 0/0 | 1410 | 16 | 3 | 1 | 10 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0003 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0004 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0005 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0006 | 0/0 | 1410 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0007 | 0/0 | 1410 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0008 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0009 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0010 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0011 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0012 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0013 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
c0014 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
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 | 952 | 121 | 12 | 30 | 54 | 9 | 16 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0002 | 0/1 | 952 | 57 | 28 | 14 | 4 | 2 | 8 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0003 | 0/0 | 952 | 41 | 15 | 1 | 18 | 1 | 6 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0004 | 0/0 | 952 | 25 | 3 | 0 | 19 | 0 | 3 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0005 | 0/0 | 952 | 24 | 20 | 3 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0006 | 0/0 | 952 | 11 | 6 | 2 | 1 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0007 | 0/0 | 952 | 4 | 0 | 0 | 2 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0008 | 0/0 | 952 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0009 | 0/0 | 952 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0010 | 0/0 | 952 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0011 | 1/0 | 952 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0012 | 0/0 | 952 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0013 | 0/0 | 952 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0014 | 0/0 | 952 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0015 | 0/0 | 952 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0016 | 0/0 | 952 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0017 | 0/0 | 952 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0018 | 0/0 | 952 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0019 | 0/0 | 952 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0020 | 0/0 | 952 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
t0021 | 0/0 | 952 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
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 | 20 | 1 | 8 | 7 | 2 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0002 | 0/0 | 7 | 0 | 0 | 2 | 0 | 5 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0003 | 0/0 | 7 | 2 | 2 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0004 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0005 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0012 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1410 | 264 | 76 | 46 | 87 | 12 | 41 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0002 | 0/0 | 1410 | 16 | 3 | 1 | 10 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0004 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0005 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0006 | 0/0 | 1410 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0008 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0010 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0002c0003 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0003c0007 | 0/0 | 1410 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0004c0012 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0005c0011 | 0/0 | 1410 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0006c0013 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0007c0009 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0008c0014 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2361 | 116 | 11 | 30 | 51 | 9 | 15 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0002 | 0/1 | 2361 | 50 | 22 | 13 | 4 | 2 | 8 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0003 | 0/0 | 2361 | 41 | 15 | 1 | 18 | 1 | 6 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0004 | 0/0 | 2361 | 18 | 3 | 0 | 12 | 0 | 3 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0005 | 0/0 | 2361 | 20 | 18 | 1 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0006 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0007 | 0/0 | 2361 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0008 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0009 | 0/0 | 2361 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0010 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0011 | 1/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0012 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0014 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0015 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0016 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0017 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0018 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0019 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0020 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0001t0021 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0002t0004 | 0/0 | 2361 | 7 | 0 | 0 | 7 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0002t0006 | 0/0 | 2361 | 7 | 3 | 1 | 1 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0002t0007 | 0/0 | 2361 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0004t0002 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0005t0006 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0006t0005 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0008t0013 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0001c0010t0001 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0002c0003t0002 | 0/0 | 2361 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0003c0007t0005 | 0/0 | 2361 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0004c0012t0001 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0005c0011t0002 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0006c0013t0001 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0007c0009t0001 | 0/0 | 2361 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
a0008c0014t0001 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | copy fasta | chr4 | 185394537 | 185430964 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 1 | 8 | 7 | 2 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0003 | 0/0 | 7 | 2 | 2 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0004 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0005 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0002 | 0/0 | 7 | 0 | 0 | 2 | 0 | 5 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0011g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0014g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0016g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0017g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0019g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0020g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0001t0021g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0002t0007g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0004t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0005t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0005t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0006t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0008t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0001c0010t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0002c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0002c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0002c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0003c0007t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0003c0007t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0004c0012t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0005c0011t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0006c0013t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0007c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
a0008c0014t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | GBR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00408 | hp2 | a0001 | c0002 | t0004 | g0133 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00544 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00639 | hp1 | a0001 | c0002 | t0006 | g0096 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00642 | hp2 | a0003 | c0007 | t0005 | g0106 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01081 | hp2 | a0005 | c0011 | t0002 | g0043 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0092 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01934 | hp1 | a0003 | c0007 | t0005 | g0109 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02015 | hp2 | a0006 | c0013 | t0001 | g0186 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02055 | hp1 | a0008 | c0014 | t0001 | g0200 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02055 | hp2 | a0002 | c0003 | t0002 | g0079 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02083 | hp2 | a0004 | c0012 | t0001 | g0184 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02145 | hp1 | a0001 | c0004 | t0002 | g0013 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0107 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02165 | hp2 | a0001 | c0002 | t0006 | g0111 | EAS | CDX | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0108 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02451 | hp1 | a0002 | c0003 | t0002 | g0081 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02523 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02572 | hp1 | a0001 | c0005 | t0006 | g0025 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02615 | hp2 | a0001 | c0005 | t0006 | g0025 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02735 | hp2 | a0007 | c0009 | t0001 | g0194 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02818 | hp1 | a0001 | c0006 | t0005 | g0029 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02818 | hp2 | a0001 | c0004 | t0002 | g0013 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02970 | hp2 | a0002 | c0003 | t0002 | g0084 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03017 | hp2 | a0001 | c0001 | t0009 | g0040 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03130 | hp1 | a0001 | c0004 | t0002 | g0013 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03130 | hp2 | a0001 | c0002 | t0006 | g0094 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0105 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03486 | hp1 | a0001 | c0002 | t0006 | g0110 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03491 | hp1 | a0001 | c0002 | t0006 | g0095 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0090 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0203 | AFR | ESN | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03579 | hp1 | a0001 | c0006 | t0005 | g0029 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03654 | hp1 | a0001 | c0002 | t0006 | g0097 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03704 | hp2 | a0001 | c0001 | t0020 | g0206 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0045 | SAS | PJL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03834 | hp2 | a0001 | c0001 | t0014 | g0046 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0101 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0122 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0124 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04184 | hp2 | a0001 | c0001 | t0016 | g0125 | SAS | BEB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0207 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18970 | hp2 | a0001 | c0001 | t0017 | g0129 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18973 | hp1 | a0001 | c0001 | t0019 | g0130 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18975 | hp1 | a0001 | c0010 | t0001 | g0146 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0135 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19064 | hp1 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19064 | hp2 | a0001 | c0002 | t0007 | g0031 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19065 | hp2 | a0001 | c0002 | t0004 | g0132 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19083 | hp1 | a0001 | c0002 | t0007 | g0031 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ASW | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0060 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02109 | hp1 | a0001 | c0001 | t0015 | g0113 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02486 | hp1 | a0001 | c0005 | t0006 | g0091 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG03471 | hp2 | a0001 | c0001 | t0018 | g0116 | AFR | MSL | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA18955 | hp2 | a0001 | c0002 | t0004 | g0134 | EAS | JPT | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA20300 | hp2 | a0001 | c0001 | t0021 | g0139 | AFR | USA | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA21309 | hp1 | a0001 | c0008 | t0013 | g0070 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | LWK | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0005 | REF | REF | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0011 | g0039 | REF | REF | UFSP2_chr4_185394537_185430964 | UFSP2 | chr4 | 185394537 | 185430964 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185403591
|
A | G | 1 | a0005 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1226T>C | p.Leu409Pro | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/12 | 1322/2361 | 1226/1410 | 409/469 | chr4 | 185403591 | ||
chr4:185408335
|
C | G | 1 | a0002 | 3 | HG02055.hp2 HG02451.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.932G>C | p.Cys311Ser | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 8/12 | 1028/2361 | 932/1410 | 311/469 | chr4 | 185408335 | ||
chr4:185413748
|
G | A | 1 | a0004 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.809C>T | p.Pro270Leu | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/12 | 905/2361 | 809/1410 | 270/469 | chr4 | 185413748 | ||
chr4:185415221
|
T | G | 1 | a0006 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.618A>C | p.Lys206Asn | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/12 | 714/2361 | 618/1410 | 206/469 | chr4 | 185415221 | ||
chr4:185415276
|
A | G | 1 | a0007 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.563T>C | p.Met188Thr | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/12 | 659/2361 | 563/1410 | 188/469 | chr4 | 185415276 | ||
chr4:185418466
|
T | C | 1 | a0003 | 2 | HG00642.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.308A>G | p.Lys103Arg | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/12 | 404/2361 | 308/1410 | 103/469 | chr4 | 185418466 | ||
chr4:185418667
|
T | C | 1 | a0008 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.186A>G | p.Ile62Met | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 3/12 | 282/2361 | 186/1410 | 62/469 | chr4 | 185418667 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185403521
|
A | G | 1 | a0001c0004 | 3 | HG02145.hp1 HG02818.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1296T>C | p.Ala432Ala | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/12 | 1392/2361 | 1296/1410 | 432/469 | chr4 | 185403521 | ||
chr4:185407965
|
G | T | 1 | a0001c0010 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.1092C>A | p.Ile364Ile | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/12 | 1188/2361 | 1092/1410 | 364/469 | chr4 | 185407965 | ||
chr4:185415311
|
T | C | 2 | a0001c0002a0001c0005 | 19 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(16): Show |
synonymous_variant | LOW | c.528A>G | p.Gln176Gln | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/12 | 624/2361 | 528/1410 | 176/469 | chr4 | 185415311 | ||
chr4:185418495
|
T | C | 1 | a0001c0005 | 3 | HG02486.hp1 HG02572.hp1 HG02615.hp2 |
synonymous_variant | LOW | c.279A>G | p.Glu93Glu | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/12 | 375/2361 | 279/1410 | 93/469 | chr4 | 185418495 | ||
chr4:185418616
|
A | G | 1 | a0001c0006 | 2 | HG02818.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.237T>C | p.Ser79Ser | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 3/12 | 333/2361 | 237/1410 | 79/469 | chr4 | 185418616 | ||
chr4:185418625
|
A | G | 1 | a0001c0008 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.228T>C | p.Thr76Thr | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 3/12 | 324/2361 | 228/1410 | 76/469 | chr4 | 185418625 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185399647
|
C | A | 1 | a0001c0001t0015 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*745G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 745 | chr4 | 185399647 | |||||
chr4:185399726
|
A | G | 3 | a0001c0001t0003a0001c0001t0018a0001c0001t0021 | 43 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*666T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 666 | chr4 | 185399726 | |||||
chr4:185399736
|
G | A | 1 | a0001c0001t0009 | 2 | HG03017.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*656C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 656 | chr4 | 185399736 | |||||
chr4:185399752
|
C | G | 3 | a0001c0001t0003a0001c0001t0015a0001c0001t0021 | 43 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*640G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 640 | chr4 | 185399752 | |||||
chr4:185399808
|
G | A | 1 | a0001c0001t0008 | 2 | HG02145.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*584C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 584 | chr4 | 185399808 | |||||
chr4:185399816
|
C | T | 1 | a0001c0001t0017 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 576 | chr4 | 185399816 | |||||
chr4:185399913
|
C | T | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(15): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*479G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 479 | chr4 | 185399913 | |||||
chr4:185399927
|
G | C | 1 | a0001c0001t0014 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 465 | chr4 | 185399927 | |||||
chr4:185399978
|
A | T | 1 | a0001c0008t0013 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 414 | chr4 | 185399978 | |||||
chr4:185400055
|
C | T | 1 | a0001c0001t0010 | 2 | HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*337G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 337 | chr4 | 185400055 | |||||
chr4:185400062
|
T | C | 1 | a0001c0001t0019 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 330 | chr4 | 185400062 | |||||
chr4:185400128
|
C | T | 6 | a0001c0001t0005a0001c0001t0008a0001c0001t0016others(3): Show | 28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 264 | chr4 | 185400128 | |||||
chr4:185400293
|
C | G | 10 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(7): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*99G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 99 | chr4 | 185400293 | |||||
chr4:185400308
|
A | G | 1 | a0001c0001t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 12/12 | 84 | chr4 | 185400308 | |||||
chr4:185425886
|
G | A | 1 | a0001c0001t0015 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 18 | chr4 | 185425886 | |||||
chr4:185425901
|
G | A | 9 | a0001c0001t0001a0001c0001t0010a0001c0001t0020others(6): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 33 | chr4 | 185425901 | |||||
chr4:185425919
|
G | C | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(14): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 51 | chr4 | 185425919 | |||||
chr4:185425938
|
T | C | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
5_prime_UTR_variant | MODIFIER | c.-70A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/12 | 70 | chr4 | 185425938 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:185400493
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1324-15G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400493 | ||||||
chr4:185400635
|
C | A | 1 | a0001c0001t0003g0059 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1324-157G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400635 | ||||||
chr4:185400662
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1324-184A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400662 | ||||||
chr4:185400708
|
A | G | 5 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(2): Show | 5 | HG01081.hp2 HG01433.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324-230T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400708 | ||||||
chr4:185400725
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1324-247A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400725 | ||||||
chr4:185400848
|
G | T | 30 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1324-370C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400848 | ||||||
chr4:185400880
|
T | G | 1 | a0001c0001t0002g0022 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1324-402A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400880 | ||||||
chr4:185400895
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1324-417G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185400895 | ||||||
chr4:185401202
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1324-724C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401202 | ||||||
chr4:185401259
|
A | G | 1 | a0001c0001t0005g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1324-781T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401259 | ||||||
chr4:185401349
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1324-871A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401349 | ||||||
chr4:185401442
|
C | A | 1 | a0001c0001t0004g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1324-964G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401442 | ||||||
chr4:185401458
|
G | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1324-980C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401458 | ||||||
chr4:185401462
|
C | T | 1 | a0001c0001t0005g0104 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1324-984G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401462 | ||||||
chr4:185401483
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1324-1005A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401483 | ||||||
chr4:185401587
|
A | C | 1 | a0001c0001t0002g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1324-1109T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401587 | ||||||
chr4:185401633
|
T | G | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1324-1155A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401633 | ||||||
chr4:185401833
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1324-1355G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185401833 | ||||||
chr4:185402017
|
C | T | 3 | a0001c0001t0002g0049a0001c0004t0002g0013a0002c0003t0002g0079 | 5 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+1477G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402017 | ||||||
chr4:185402055
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1323+1439T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402055 | ||||||
chr4:185402096
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1323+1398G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402096 | ||||||
chr4:185402140
|
CCTT | C | 28 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(25): Show | 43 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.1323+1351_1323+135 others(7): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402140 | ||||||
chr4:185402153
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1323+1341T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402153 | ||||||
chr4:185402154
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1323+1340G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402154 | ||||||
chr4:185402287
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0085 | 3 | HG03239.hp1 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1323+1207T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402287 | ||||||
chr4:185402294
|
A | G | 19 | a0001c0001t0005g0008a0001c0001t0005g0016a0001c0001t0005g0026others(16): Show | 28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.1323+1200T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402294 | ||||||
chr4:185402361
|
G | GA | 6 | a0001c0001t0001g0176a0001c0001t0001g0198a0001c0001t0002g0069others(3): Show | 6 | HG00741.hp1 HG02615.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+1132dupT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402361 | ||||||
chr4:185402439
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1323+1055G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402439 | ||||||
chr4:185402507
|
C | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1323+987G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402507 | ||||||
chr4:185402627
|
C | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1323+867G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402627 | ||||||
chr4:185402896
|
T | C | 1 | a0001c0001t0020g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1323+598A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402896 | ||||||
chr4:185402986
|
C | T | 1 | a0001c0002t0006g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1323+508G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185402986 | ||||||
chr4:185403034
|
C | T | 1 | a0001c0001t0015g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1323+460G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403034 | ||||||
chr4:185403146
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1323+348A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403146 | ||||||
chr4:185403255
|
C | T | 20 | a0001c0001t0004g0017a0001c0001t0004g0030a0001c0001t0004g0117others(17): Show | 24 | HG00408.hp2 HG00544.hp1 HG02523.hp1 others(21): Show |
intron_variant | MODIFIER | c.1323+239G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403255 | ||||||
chr4:185403398
|
C | T | 1 | a0001c0008t0013g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1323+96G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403398 | ||||||
chr4:185403483
|
T | C | 30 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1323+11A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 11/11 | chr4 | 185403483 | ||||||
chr4:185403687
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1199-69A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403687 | ||||||
chr4:185403966
|
C | CA | 61 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(58): Show | 96 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1199-349dupT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | ||||||
chr4:185403966
|
C | CAA | 19 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0147others(16): Show | 23 | HG00642.hp1 HG01433.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1199-350_1199-349d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | ||||||
chr4:185403966
|
C | CAAA | 14 | a0001c0001t0001g0175a0001c0001t0001g0185a0001c0001t0004g0017others(11): Show | 18 | HG00544.hp1 HG01884.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1199-351_1199-349d others(5): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | ||||||
chr4:185403966
|
C | CAAAA | 10 | a0001c0001t0004g0115a0001c0001t0004g0118a0001c0001t0004g0121others(7): Show | 10 | HG00408.hp2 HG02738.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.1199-352_1199-349d others(6): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403966 | ||||||
chr4:185403976
|
AAC | A | 25 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(22): Show | 40 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1199-360_1199-359d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403976 | ||||||
chr4:185403977
|
AC | A | 4 | a0001c0001t0002g0069a0001c0001t0003g0057a0001c0001t0003g0060others(1): Show | 4 | HG02615.hp1 HG02647.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199-360delG | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403977 | ||||||
chr4:185403978
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1199-360G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403978 | ||||||
chr4:185403988
|
C | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1199-370G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185403988 | ||||||
chr4:185404042
|
A | G | 1 | a0001c0001t0015g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1199-424T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404042 | ||||||
chr4:185404075
|
G | T | 1 | a0001c0001t0005g0016 | 3 | HG01975.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1199-457C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404075 | ||||||
chr4:185404275
|
T | C | 38 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(35): Show | 53 | HG00544.hp2 HG00639.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1199-657A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404275 | ||||||
chr4:185404293
|
G | GT | 39 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(36): Show | 58 | HG00544.hp2 HG00642.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1199-676dupA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404293 | ||||||
chr4:185404293
|
G | GTT | 7 | a0001c0001t0002g0042a0001c0001t0002g0047a0001c0001t0005g0100others(4): Show | 7 | HG01433.hp2 HG02572.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1199-677_1199-676d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404293 | ||||||
chr4:185404293
|
GT | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1199-676delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404293 | ||||||
chr4:185404413
|
A | G | 4 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0123others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-795T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404413 | ||||||
chr4:185404560
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1199-942C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404560 | ||||||
chr4:185404615
|
T | C | 2 | a0001c0001t0002g0049a0001c0004t0002g0013 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-997A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404615 | ||||||
chr4:185404658
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA19054.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1199-1040G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404658 | ||||||
chr4:185404689
|
G | C | 2 | a0001c0001t0002g0049a0001c0004t0002g0013 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-1071C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185404689 | ||||||
chr4:185405002
|
C | CT | 111 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(108): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1198+777dupA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405002 | ||||||
chr4:185405059
|
A | G | 1 | a0008c0014t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198+721T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405059 | ||||||
chr4:185405163
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1198+617T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405163 | ||||||
chr4:185405173
|
T | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0158 | 3 | HG00408.hp1 HG02135.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1198+607A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405173 | ||||||
chr4:185405173
|
T | TG | 2 | a0001c0001t0003g0006a0001c0001t0003g0051 | 5 | HG02074.hp1 HG02083.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198+606_1198+607i others(3): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405173 | ||||||
chr4:185405225
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1198+555A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405225 | ||||||
chr4:185405487
|
C | A | 1 | a0001c0001t0004g0123 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1198+293G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405487 | ||||||
chr4:185405511
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1198+269G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405511 | ||||||
chr4:185405555
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1198+225C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405555 | ||||||
chr4:185405570
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1198+210G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405570 | ||||||
chr4:185405617
|
A | G | 30 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198+163T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405617 | ||||||
chr4:185405705
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1198+75T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405705 | ||||||
chr4:185405743
|
A | T | 1 | a0001c0008t0013g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1198+37T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 10/11 | chr4 | 185405743 | ||||||
chr4:185405868
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1122-12G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185405868 | ||||||
chr4:185405898
|
A | G | 1 | a0001c0002t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1122-42T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185405898 | ||||||
chr4:185405952
|
G | A | 2 | a0001c0001t0008g0105a0001c0001t0008g0107 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1122-96C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185405952 | ||||||
chr4:185406079
|
C | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1122-223G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406079 | ||||||
chr4:185406285
|
C | G | 1 | a0001c0001t0003g0014 | 3 | HG02040.hp2 HG02132.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1122-429G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406285 | ||||||
chr4:185406359
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1122-503T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406359 | ||||||
chr4:185406389
|
G | T | 2 | a0001c0001t0002g0049a0001c0004t0002g0013 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-533C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406389 | ||||||
chr4:185406606
|
C | T | 3 | a0001c0001t0003g0021a0001c0001t0003g0058a0001c0001t0003g0061 | 4 | HG02723.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-750G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406606 | ||||||
chr4:185406636
|
C | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0050a0001c0001t0003g0056others(1): Show | 5 | NA18942.hp1 NA18945.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122-780G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185406636 | ||||||
chr4:185407017
|
CT | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(123): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1121+918delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | ||||||
chr4:185407017
|
CTT | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0177a0001c0001t0001g0179others(9): Show | 14 | HG01070.hp2 HG01256.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1121+917_1121+918d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | ||||||
chr4:185407017
|
CTTT | C | 27 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(24): Show | 42 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.1121+916_1121+918d others(5): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | ||||||
chr4:185407017
|
CTTTT | C | 19 | a0001c0001t0005g0008a0001c0001t0005g0016a0001c0001t0005g0026others(16): Show | 28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.1121+915_1121+918d others(6): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407017 | ||||||
chr4:185407048
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1121+888T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407048 | ||||||
chr4:185407056
|
G | GT | 45 | a0001c0001t0001g0152a0001c0001t0002g0004a0001c0001t0002g0005others(42): Show | 70 | HG00544.hp2 HG00733.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.1121+879dupA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407056 | ||||||
chr4:185407057
|
T | G | 1 | a0001c0001t0005g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1121+879A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407057 | ||||||
chr4:185407082
|
G | T | 1 | a0001c0001t0001g0166 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1121+854C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407082 | ||||||
chr4:185407125
|
A | G | 30 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1121+811T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407125 | ||||||
chr4:185407137
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1121+799T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407137 | ||||||
chr4:185407318
|
T | C | 1 | a0001c0008t0013g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1121+618A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407318 | ||||||
chr4:185407333
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1121+603G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407333 | ||||||
chr4:185407345
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1121+591G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407345 | ||||||
chr4:185407439
|
T | A | 8 | a0001c0001t0006g0092a0001c0002t0006g0094a0001c0002t0006g0095others(5): Show | 8 | HG00639.hp1 HG01106.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+497A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407439 | ||||||
chr4:185407550
|
C | G | 1 | a0001c0006t0005g0029 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1121+386G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407550 | ||||||
chr4:185407601
|
TAA | T | 30 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 45 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1121+333_1121+334d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407601 | ||||||
chr4:185407756
|
C | T | 1 | a0008c0014t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+180G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407756 | ||||||
chr4:185407853
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+83C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 9/11 | chr4 | 185407853 | ||||||
chr4:185408066
|
T | C | 19 | a0001c0001t0005g0008a0001c0001t0005g0016a0001c0001t0005g0026others(16): Show | 28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.997-6A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 8/11 | chr4 | 185408066 | ||||||
chr4:185408258
|
G | A | 2 | a0001c0001t0002g0069a0001c0008t0013g0070 | 2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.996+13C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 8/11 | chr4 | 185408258 | ||||||
chr4:185408730
|
A | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0051a0001c0001t0003g0054others(1): Show | 7 | HG00544.hp2 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-295T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408730 | ||||||
chr4:185408807
|
C | T | 1 | a0001c0002t0006g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.832-372G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408807 | ||||||
chr4:185408927
|
G | A | 29 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(26): Show | 44 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.832-492C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408927 | ||||||
chr4:185408946
|
T | C | 1 | a0001c0001t0005g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.832-511A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185408946 | ||||||
chr4:185409006
|
C | T | 2 | a0001c0001t0003g0052a0001c0001t0003g0053 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.832-571G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409006 | ||||||
chr4:185409018
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.832-583A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409018 | ||||||
chr4:185409043
|
G | C | 1 | a0001c0002t0006g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.832-608C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409043 | ||||||
chr4:185409258
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.832-823T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409258 | ||||||
chr4:185409261
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.832-826C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409261 | ||||||
chr4:185409285
|
T | G | 2 | a0001c0001t0002g0049a0001c0004t0002g0013 | 4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-850A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409285 | ||||||
chr4:185409324
|
T | C | 31 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(28): Show | 46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.832-889A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409324 | ||||||
chr4:185409980
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.832-1545A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185409980 | ||||||
chr4:185410021
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.832-1586A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410021 | ||||||
chr4:185410041
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.832-1606A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410041 | ||||||
chr4:185410045
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.832-1610T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410045 | ||||||
chr4:185410332
|
G | A | 1 | a0001c0008t0013g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-1897C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410332 | ||||||
chr4:185410669
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01070.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.832-2234C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410669 | ||||||
chr4:185410849
|
G | GGGA | 2 | a0001c0005t0006g0025a0001c0005t0006g0091 | 3 | HG02486.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.832-2417_832-2415d others(5): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410849 | ||||||
chr4:185410945
|
C | CA | 33 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0182others(30): Show | 38 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.832-2511dupT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410945 | ||||||
chr4:185410945
|
C | CAA | 81 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.832-2512_832-2511d others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185410945 | ||||||
chr4:185411119
|
GT | G | 21 | a0001c0001t0002g0112a0001c0001t0004g0017a0001c0001t0004g0030others(18): Show | 25 | HG00408.hp2 HG00544.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.831+2606delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411119 | ||||||
chr4:185411132
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(179): Show | 262 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.831+2594A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411132 | ||||||
chr4:185411259
|
AT | A | 2 | a0001c0001t0005g0027a0001c0001t0005g0102 | 3 | HG02922.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.831+2466delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411259 | ||||||
chr4:185411315
|
G | A | 13 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(10): Show | 22 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.831+2411C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411315 | ||||||
chr4:185411453
|
G | A | 27 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(24): Show | 42 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.831+2273C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411453 | ||||||
chr4:185411576
|
A | C | 13 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(10): Show | 22 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.831+2150T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411576 | ||||||
chr4:185411590
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0035others(8): Show | 17 | HG00597.hp1 HG00738.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.831+2136T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411590 | ||||||
chr4:185411622
|
A | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+2104T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185411622 | ||||||
chr4:185412000
|
A | G | 1 | a0001c0002t0006g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.831+1726T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412000 | ||||||
chr4:185412026
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.831+1700C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412026 | ||||||
chr4:185412067
|
A | G | 4 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0123others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+1659T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412067 | ||||||
chr4:185412232
|
T | C | 1 | a0001c0001t0006g0092 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.831+1494A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412232 | ||||||
chr4:185412318
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.831+1408T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412318 | ||||||
chr4:185412329
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.831+1397A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412329 | ||||||
chr4:185412753
|
G | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | NA18986.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.831+973C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412753 | ||||||
chr4:185412820
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.831+906C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412820 | ||||||
chr4:185412915
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.831+811G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412915 | ||||||
chr4:185412984
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.831+742C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412984 | ||||||
chr4:185412985
|
G | C | 1 | a0001c0001t0005g0104 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.831+741C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185412985 | ||||||
chr4:185413015
|
T | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+711A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413015 | ||||||
chr4:185413037
|
G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.831+689C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413037 | ||||||
chr4:185413130
|
T | C | 19 | a0001c0001t0005g0008a0001c0001t0005g0016a0001c0001t0005g0026others(16): Show | 28 | HG00642.hp2 HG01934.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.831+596A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413130 | ||||||
chr4:185413235
|
A | T | 1 | a0001c0001t0003g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.831+491T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413235 | ||||||
chr4:185413237
|
A | C | 1 | a0001c0001t0003g0051 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.831+489T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413237 | ||||||
chr4:185413240
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.831+486A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413240 | ||||||
chr4:185413486
|
A | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+240T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413486 | ||||||
chr4:185413571
|
T | C | 29 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(26): Show | 44 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.831+155A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413571 | ||||||
chr4:185413645
|
A | G | 31 | a0001c0001t0002g0069a0001c0001t0003g0002a0001c0001t0003g0006others(28): Show | 46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.831+81T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 7/11 | chr4 | 185413645 | ||||||
chr4:185414092
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.685-220C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414092 | ||||||
chr4:185414428
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.685-556A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414428 | ||||||
chr4:185414456
|
A | G | 1 | a0001c0001t0005g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685-584T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414456 | ||||||
chr4:185414538
|
G | A | 1 | a0001c0002t0006g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.684+617C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414538 | ||||||
chr4:185414552
|
G | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.684+603C>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414552 | ||||||
chr4:185414588
|
C | T | 10 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0042others(7): Show | 17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+567G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414588 | ||||||
chr4:185414718
|
T | A | 1 | a0001c0001t0005g0028 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.684+437A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414718 | ||||||
chr4:185414779
|
C | T | 1 | a0001c0001t0002g0004 | 5 | HG00733.hp1 HG01074.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+376G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414779 | ||||||
chr4:185414923
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 6 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+232G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 6/11 | chr4 | 185414923 | ||||||
chr4:185415395
|
CAATAAAG others(42): Show |
C | 2 | a0001c0001t0002g0069a0001c0008t0013g0070 | 2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.492-97_492-49delAA others(47): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415395 | ||||||
chr4:185415418
|
A | T | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.492-71T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415418 | ||||||
chr4:185415429
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(178): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.492-82C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415429 | ||||||
chr4:185415467
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.492-120C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415467 | ||||||
chr4:185415514
|
T | C | 13 | a0001c0002t0004g0032a0001c0002t0004g0132a0001c0002t0004g0133others(10): Show | 15 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.492-167A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415514 | ||||||
chr4:185415679
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.491+31T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 5/11 | chr4 | 185415679 | ||||||
chr4:185415873
|
T | C | 1 | a0001c0001t0015g0113 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.334-6A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185415873 | ||||||
chr4:185415922
|
A | G | 1 | a0001c0001t0007g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.334-55T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185415922 | ||||||
chr4:185415990
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-123G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185415990 | ||||||
chr4:185416045
|
G | A | 2 | a0001c0001t0008g0105a0001c0001t0008g0107 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.334-178C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416045 | ||||||
chr4:185416383
|
C | A | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-516G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416383 | ||||||
chr4:185416600
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0143a0001c0001t0001g0152 | 4 | HG02015.hp1 HG02602.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-733G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416600 | ||||||
chr4:185416600
|
CGT | C | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-735_334-734del others(2): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416600 | ||||||
chr4:185416643
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.334-776C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416643 | ||||||
chr4:185416833
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.334-966T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185416833 | ||||||
chr4:185417052
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.334-1185G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417052 | ||||||
chr4:185417090
|
TAAGTG | T | 14 | a0001c0001t0004g0017a0001c0001t0004g0030a0001c0001t0004g0117others(11): Show | 17 | HG02698.hp2 HG02738.hp1 HG04199.hp2 others(14): Show |
intron_variant | MODIFIER | c.334-1228_334-1224d others(7): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417090 | ||||||
chr4:185417604
|
C | T | 31 | a0001c0001t0004g0017a0001c0001t0004g0030a0001c0001t0004g0114others(28): Show | 35 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.333+837G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417604 | ||||||
chr4:185417677
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0149a0001c0001t0001g0205 | 6 | HG02132.hp2 NA18962.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+764A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417677 | ||||||
chr4:185417769
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.333+672G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417769 | ||||||
chr4:185417836
|
G | A | 30 | a0001c0001t0002g0049a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 47 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+605C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417836 | ||||||
chr4:185417920
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.333+521A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417920 | ||||||
chr4:185417944
|
C | T | 2 | a0001c0001t0008g0105a0001c0001t0008g0107 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.333+497G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417944 | ||||||
chr4:185417961
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.333+480A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185417961 | ||||||
chr4:185418047
|
A | AACAC | 3 | a0001c0001t0018g0116a0001c0005t0006g0025a0001c0005t0006g0091 | 4 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+390_333+393dup others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(5): Show |
3 | a0001c0001t0001g0199a0001c0001t0003g0068a0002c0003t0002g0084 | 3 | HG02970.hp1 HG02970.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.333+382_333+393dup others(12): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(7): Show |
26 | a0001c0001t0001g0037a0001c0001t0001g0195a0001c0001t0001g0196others(23): Show | 30 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.333+380_333+393dup others(14): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(9): Show |
13 | a0001c0001t0001g0012a0001c0001t0001g0140a0001c0001t0001g0189others(10): Show | 16 | HG00733.hp2 HG01106.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.333+378_333+393dup others(16): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(11): Show |
88 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0018others(85): Show | 137 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.333+376_333+393dup others(18): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(13): Show |
23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0145others(20): Show | 31 | HG01074.hp2 HG01255.hp1 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.333+374_333+393dup others(20): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(15): Show |
9 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0002g0023others(6): Show | 11 | HG00140.hp2 HG01515.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(22): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(17): Show |
6 | a0001c0001t0002g0003a0001c0001t0002g0022a0001c0001t0002g0069others(3): Show | 13 | HG01192.hp2 HG01243.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(24): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(19): Show |
7 | a0001c0001t0002g0007a0001c0001t0002g0076a0001c0001t0005g0103others(4): Show | 10 | HG00642.hp2 HG00741.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(26): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(21): Show |
3 | a0001c0001t0005g0008a0001c0001t0005g0016a0001c0001t0005g0028 | 9 | HG01975.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(28): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(23): Show |
5 | a0001c0001t0005g0026a0001c0001t0005g0098a0001c0001t0005g0100others(2): Show | 6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+393_333+394ins others(30): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | AACACACA others(27): Show |
2 | a0001c0001t0005g0027a0001c0001t0005g0099 | 3 | HG02809.hp2 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.333+393_333+394ins others(34): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.333+393_333+394ins others(17): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.333+393_333+394ins others(19): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418047
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0002g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333+393_333+394ins others(21): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418047 | ||||||
chr4:185418068
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.333+372_333+373ins others(17): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418068 | ||||||
chr4:185418068
|
A | ACACACAC others(16): Show |
1 | a0001c0001t0003g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.333+372_333+373ins others(23): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418068 | ||||||
chr4:185418069
|
A | C | 10 | a0001c0001t0002g0005a0001c0001t0002g0041a0001c0001t0002g0042others(7): Show | 13 | HG01081.hp2 HG01255.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.333+372T>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418069 | ||||||
chr4:185418069
|
A | T | 1 | a0001c0001t0002g0004 | 5 | HG00733.hp1 HG01074.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+372T>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418069 | ||||||
chr4:185418071
|
C | CACACACA others(4): Show |
10 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(7): Show | 17 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.333+369_333+370ins others(11): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418071 | ||||||
chr4:185418080
|
C | T | 30 | a0001c0001t0002g0049a0001c0001t0003g0002a0001c0001t0003g0006others(27): Show | 47 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+361G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418080 | ||||||
chr4:185418143
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.333+298A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418143 | ||||||
chr4:185418164
|
T | C | 2 | a0001c0001t0008g0105a0001c0001t0008g0107 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.333+277A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418164 | ||||||
chr4:185418295
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.333+146T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418295 | ||||||
chr4:185418430
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.333+11T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 4/11 | chr4 | 185418430 | ||||||
chr4:185419154
|
T | C | 11 | a0001c0002t0004g0032a0001c0002t0004g0132a0001c0002t0004g0133others(8): Show | 13 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-384A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419154 | ||||||
chr4:185419195
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.83-425C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419195 | ||||||
chr4:185419200
|
G | C | 1 | a0001c0001t0001g0201 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.83-430C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419200 | ||||||
chr4:185419225
|
G | A | 1 | a0001c0001t0012g0090 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.83-455C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419225 | ||||||
chr4:185419256
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.83-486G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419256 | ||||||
chr4:185419377
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.83-607C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419377 | ||||||
chr4:185419382
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.83-612C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419382 | ||||||
chr4:185419410
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.83-640T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419410 | ||||||
chr4:185419709
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.83-939A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419709 | ||||||
chr4:185419723
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.83-953A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419723 | ||||||
chr4:185419818
|
T | C | 1 | a0001c0001t0001g0038 | 2 | HG00140.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.83-1048A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185419818 | ||||||
chr4:185420006
|
G | A | 12 | a0001c0002t0004g0032a0001c0002t0004g0132a0001c0002t0004g0133others(9): Show | 13 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-1236C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420006 | ||||||
chr4:185420080
|
T | C | 1 | a0001c0001t0003g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.83-1310A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420080 | ||||||
chr4:185420183
|
GT | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.83-1414delA | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420183 | ||||||
chr4:185420299
|
T | A | 1 | a0001c0001t0002g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.83-1529A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420299 | ||||||
chr4:185420655
|
C | T | 1 | a0001c0002t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82+1830G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420655 | ||||||
chr4:185420771
|
T | C | 1 | a0001c0002t0006g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82+1714A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420771 | ||||||
chr4:185420846
|
T | C | 29 | a0001c0001t0002g0049a0001c0001t0003g0002a0001c0001t0003g0006others(26): Show | 46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.82+1639A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420846 | ||||||
chr4:185420847
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.82+1638A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420847 | ||||||
chr4:185420928
|
T | G | 1 | a0001c0001t0005g0028 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.82+1557A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420928 | ||||||
chr4:185420976
|
T | C | 1 | a0001c0008t0013g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82+1509A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185420976 | ||||||
chr4:185421122
|
GCTGA | G | 3 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0018g0116 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.82+1359_82+1362del others(4): Show |
UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421122 | ||||||
chr4:185421373
|
T | C | 31 | a0001c0001t0002g0049a0001c0001t0002g0069a0001c0001t0003g0002others(28): Show | 48 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.82+1112A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421373 | ||||||
chr4:185421388
|
G | A | 1 | a0001c0008t0013g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82+1097C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421388 | ||||||
chr4:185421693
|
C | T | 1 | a0001c0001t0005g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+792G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421693 | ||||||
chr4:185421701
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(118): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.82+784G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185421701 | ||||||
chr4:185422228
|
T | C | 2 | a0001c0001t0010g0203a0001c0001t0010g0207 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.82+257A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 2/11 | chr4 | 185422228 | ||||||
chr4:185422706
|
T | C | 13 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(10): Show | 21 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.4-143A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422706 | ||||||
chr4:185422761
|
T | G | 15 | a0001c0001t0004g0017a0001c0001t0004g0126a0001c0001t0004g0127others(12): Show | 19 | HG00408.hp2 HG00544.hp1 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.4-198A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422761 | ||||||
chr4:185422811
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4-248G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422811 | ||||||
chr4:185422825
|
A | G | 13 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(10): Show | 21 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.4-262T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422825 | ||||||
chr4:185422903
|
A | AG | 202 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.4-341dupC | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422903 | ||||||
chr4:185422936
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4-373C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422936 | ||||||
chr4:185422976
|
A | G | 1 | a0001c0001t0005g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4-413T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185422976 | ||||||
chr4:185423034
|
T | G | 2 | a0001c0001t0002g0069a0001c0008t0013g0070 | 2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4-471A>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423034 | ||||||
chr4:185423139
|
G | A | 44 | a0001c0001t0002g0049a0001c0001t0003g0002a0001c0001t0003g0006others(41): Show | 65 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.4-576C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423139 | ||||||
chr4:185423148
|
C | T | 20 | a0001c0001t0002g0112a0001c0001t0005g0008a0001c0001t0005g0016others(17): Show | 29 | HG00642.hp2 HG00733.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.4-585G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423148 | ||||||
chr4:185423361
|
T | C | 1 | a0003c0007t0005g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4-798A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423361 | ||||||
chr4:185423379
|
G | A | 1 | a0001c0006t0005g0029 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4-816C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423379 | ||||||
chr4:185423563
|
TA | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(88): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.4-1001delT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423563 | ||||||
chr4:185423648
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4-1085A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423648 | ||||||
chr4:185423813
|
TAC | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0074a0001c0001t0002g0075 | 3 | HG01258.hp2 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4-1252_4-1251delGT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185423813 | ||||||
chr4:185424031
|
T | C | 3 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0018g0116 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4-1468A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424031 | ||||||
chr4:185424100
|
G | C | 6 | a0001c0001t0003g0015a0001c0001t0003g0064a0001c0001t0003g0065others(3): Show | 8 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-1537C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424100 | ||||||
chr4:185424140
|
CA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.4-1578delT | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424140 | ||||||
chr4:185424229
|
C | T | 3 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0018g0116 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3+1637G>A | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424229 | ||||||
chr4:185424230
|
G | A | 26 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0014others(23): Show | 41 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.3+1636C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424230 | ||||||
chr4:185424252
|
G | A | 1 | a0001c0002t0006g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3+1614C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424252 | ||||||
chr4:185424374
|
A | G | 11 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0041others(8): Show | 18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.3+1492T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424374 | ||||||
chr4:185424577
|
G | A | 29 | a0001c0001t0002g0049a0001c0001t0003g0002a0001c0001t0003g0006others(26): Show | 46 | HG00544.hp2 HG01109.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.3+1289C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424577 | ||||||
chr4:185424626
|
C | A | 2 | a0001c0001t0002g0069a0001c0008t0013g0070 | 2 | HG02615.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3+1240G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424626 | ||||||
chr4:185424689
|
T | A | 1 | a0001c0002t0006g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3+1177A>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424689 | ||||||
chr4:185424716
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3+1150C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424716 | ||||||
chr4:185424879
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3+987A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424879 | ||||||
chr4:185424998
|
C | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(180): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.3+868G>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185424998 | ||||||
chr4:185425085
|
C | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.3+781G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425085 | ||||||
chr4:185425315
|
T | C | 2 | a0001c0002t0004g0135a0001c0002t0004g0136 | 2 | NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3+551A>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425315 | ||||||
chr4:185425372
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3+494C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425372 | ||||||
chr4:185425553
|
G | C | 1 | a0001c0001t0010g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3+313C>G | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425553 | ||||||
chr4:185425570
|
C | A | 1 | a0001c0001t0021g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3+296G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425570 | ||||||
chr4:185425716
|
A | G | 13 | a0001c0001t0001g0138a0001c0001t0002g0004a0001c0001t0002g0005others(10): Show | 20 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.3+150T>C | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425716 | ||||||
chr4:185425749
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3+117C>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425749 | ||||||
chr4:185425834
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3+32G>T | UFSP2 | ENSG00000109775.11 | transcript | ENST00000264689.11 | protein_coding | 1/11 | chr4 | 185425834 |